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Sample records for all-pm monolithic fs

  1. Monolithic stabilized Yb-fiber All-PM laser directly delivering nJ-level femtosecond pulses

    DEFF Research Database (Denmark)

    Turchinovich, Dmitry; Liu, Xiaomin; Lægsgaard, Jesper

    2008-01-01

    We present a monolithic, self-starting, all-PM, stabilized Yb-fiber laser, pulse-compressed in a hollow-core PM photonic crystal fiber, providing the 370 fs pulses of 4 nJ energy with high mode quality.......We present a monolithic, self-starting, all-PM, stabilized Yb-fiber laser, pulse-compressed in a hollow-core PM photonic crystal fiber, providing the 370 fs pulses of 4 nJ energy with high mode quality....

  2. Monolithic all-PM femtosecond Yb-fiber laser stabilized with a narrow-band fiber Bragg grating and pulse-compressed in a hollow-core photonic crystal fiber

    DEFF Research Database (Denmark)

    Turchinovich, Dmitry; Liu, Xiaomin; Lægsgaard, Jesper

    2008-01-01

    We report on an environmentally stable self-starting monolithic (i.e. without any free-space coupling) all-polarization-maintaining (PM) femtosecond Yb-fiber laser, stabilized against Q-switching by a narrow-band fiber Bragg grating and modelocked using a semiconductor saturable absorber mirror....... The laser output is compressed in a spliced-on hollow-core PM photonic crystal fiber, thus providing direct end-of-the-fiber delivery of pulses of around 370 fs duration and 4 nJ energy with high mode quality. Tuning the pump power of the end amplifier of the laser allows for the control of output pulse...

  3. Monolithic spectrometer

    Science.gov (United States)

    Rajic, Slobodan; Egert, Charles M.; Kahl, William K.; Snyder, Jr., William B.; Evans, III, Boyd M.; Marlar, Troy A.; Cunningham, Joseph P.

    1998-01-01

    A monolithic spectrometer is disclosed for use in spectroscopy. The spectrometer is a single body of translucent material with positioned surfaces for the transmission, reflection and spectral analysis of light rays.

  4. SeaWiFS

    Data.gov (United States)

    Washington University St Louis — SEAWiFS_US is a high resolution (1km) satellite dataset derived from the eight wavelength SEAWiFS sensor. The dataset also includes the aerosol reflectance over the...

  5. Monoliths in Bioprocess Technology

    Directory of Open Access Journals (Sweden)

    Vignesh Rajamanickam

    2015-04-01

    Full Text Available Monolithic columns are a special type of chromatography column, which can be used for the purification of different biomolecules. They have become popular due to their high mass transfer properties and short purification times. Several articles have already discussed monolith manufacturing, as well as monolith characteristics. In contrast, this review focuses on the applied aspect of monoliths and discusses the most relevant biomolecules that can be successfully purified by them. We describe success stories for viruses, nucleic acids and proteins and compare them to conventional purification methods. Furthermore, the advantages of monolithic columns over particle-based resins, as well as the limitations of monoliths are discussed. With a compilation of commercially available monolithic columns, this review aims at serving as a ‘yellow pages’ for bioprocess engineers who face the challenge of purifying a certain biomolecule using monoliths.

  6. Long all-active monolithic mode-locked lasers with surface-etched bragg gratings

    DEFF Research Database (Denmark)

    Larsson, David; Yvind, Kresten; Hvam, Jørn Märcher

    2007-01-01

    We have fabricated 4.4-mm-long monolithic InAlGaAsP–InP mode-locked lasers with integrated deeply surface etched distributed Bragg reflector (DBR) mirrors. The lasers produce 3.7-ps transform-limited Gaussian pulses with 10-mW average output power and 250-fs absolute timing jitter. The performance...

  7. Monolithic microwave integrated circuits

    Science.gov (United States)

    Pucel, R. A.

    Monolithic microwave integrated circuits (MMICs), a new microwave technology which is expected to exert a profound influence on microwave circuit designs for future military systems as well as for the commercial and consumer markets, is discussed. The book contains an historical discussion followed by a comprehensive review presenting the current status in the field. The general topics of the volume are: design considerations, materials and processing considerations, monolithic circuit applications, and CAD, measurement, and packaging techniques. All phases of MMIC technology are covered, from design to testing.

  8. Embedded-monolith armor

    Science.gov (United States)

    McElfresh, Michael W.; Groves, Scott E; Moffet, Mitchell L.; Martin, Louis P.

    2016-07-19

    A lightweight armor system utilizing a face section having a multiplicity of monoliths embedded in a matrix supported on low density foam. The face section is supported with a strong stiff backing plate. The backing plate is mounted on a spall plate.

  9. Monolithic MACS micro resonators

    Science.gov (United States)

    Lehmann-Horn, J. A.; Jacquinot, J.-F.; Ginefri, J. C.; Bonhomme, C.; Sakellariou, D.

    2016-10-01

    Magic Angle Coil Spinning (MACS) aids improving the intrinsically low NMR sensitivity of heterogeneous microscopic samples. We report on the design and testing of a new type of monolithic 2D MACS resonators to overcome known limitations of conventional micro coils. The resonators' conductors were printed on dielectric substrate and tuned without utilizing lumped element capacitors. Self-resonance conditions have been computed by a hybrid FEM-MoM technique. Preliminary results reported here indicate robust mechanical stability, reduced eddy currents heating and negligible susceptibility effects. The gain in B1 /√{ P } is in agreement with the NMR sensitivity enhancement according to the principle of reciprocity. A sensitivity enhancement larger than 3 has been achieved in a monolithic micro resonator inside a standard 4 mm rotor at 500 MHz. These 2D resonators could offer higher performance micro-detection and ease of use of heterogeneous microscopic substances such as biomedical samples, microscopic specimens and thin film materials.

  10. Bioaffinity chromatography on monolithic supports

    NARCIS (Netherlands)

    Tetala, K.K.R.; Beek, van T.A.

    2010-01-01

    Affinity chromatography on monolithic supports is a powerful analytical chemical platform because it allows for fast analyses, small sample volumes, strong enrichment of trace biomarkers and applications in microchips. In this review, the recent research using monolithic materials in the field of bi

  11. Design of monoliths through their mechanical properties.

    Science.gov (United States)

    Podgornik, Aleš; Savnik, Aleš; Jančar, Janez; Krajnc, Nika Lendero

    2014-03-14

    Chromatographic monoliths have several interesting properties making them attractive supports for analytics but also for purification, especially of large biomolecules and bioassemblies. Although many of monolith features were thoroughly investigated, there is no data available to predict how monolith mechanical properties affect its chromatographic performance. In this work, we investigated the effect of porosity, pore size and chemical modification on methacrylate monolith compression modulus. While a linear correlation between pore size and compression modulus was found, the effect of porosity was highly exponential. Through these correlations it was concluded that chemical modification affects monolith porosity without changing the monolith skeleton integrity. Mathematical model to describe the change of monolith permeability as a function of monolith compression modulus was derived and successfully validated for monoliths of different geometries and pore sizes. It enables the prediction of pressure drop increase due to monolith compressibility for any monolith structural characteristics, such as geometry, porosity, pore size or mobile phase properties like viscosity or flow rate, based solely on the data of compression modulus and structural data of non-compressed monolith. Furthermore, it enables simple determination of monolith pore size at which monolith compressibility is the smallest and the most robust performance is expected. Data of monolith compression modulus in combination with developed mathematical model can therefore be used for the prediction of monolith permeability during its implementation but also to accelerate the design of novel chromatographic monoliths with desired hydrodynamic properties for particular application.

  12. Porous polymer monolithic col

    Directory of Open Access Journals (Sweden)

    Lydia Terborg

    2015-05-01

    Full Text Available A new approach has been developed for the preparation of mixed-mode stationary phases to separate proteins. The pore surface of monolithic poly(glycidyl methacrylate-co-ethylene dimethacrylate capillary columns was functionalized with thiols and coated with gold nanoparticles. The final mixed mode surface chemistry was formed by attaching, in a single step, alkanethiols, mercaptoalkanoic acids, and their mixtures on the free surface of attached gold nanoparticles. Use of these mixtures allowed fine tuning of the hydrophobic/hydrophilic balance. The amount of attached gold nanoparticles according to thermal gravimetric analysis was 44.8 wt.%. This value together with results of frontal elution enabled calculation of surface coverage with the alkanethiol and mercaptoalkanoic acid ligands. Interestingly, alkanethiols coverage in a range of 4.46–4.51 molecules/nm2 significantly exceeded that of mercaptoalkanoic acids with 2.39–2.45 molecules/nm2. The mixed mode character of these monolithic stationary phases was for the first time demonstrated in the separations of proteins that could be achieved in the same column using gradient elution conditions typical of reverse phase (using gradient of acetonitrile in water and ion exchange chromatographic modes (applying gradient of salt in water, respectively.

  13. High-Power and Low-Noise 10-GHz All-Active Monolithic Mode-Locked Lasers with Surface Etched Bragg Grating

    DEFF Research Database (Denmark)

    Larsson, David; Yvind, Kresten; Hvam, Jørn Märcher

    2007-01-01

    We have fabricated 4.4 mm long monolithic InAlGaAsP/InP mode-locked lasers with integrated deeply surface etched DBR-mirrors. The lasers produce 3.7 ps transform-limited Gaussian pulses with 10 mW average power and 250 fs timing jitter.......We have fabricated 4.4 mm long monolithic InAlGaAsP/InP mode-locked lasers with integrated deeply surface etched DBR-mirrors. The lasers produce 3.7 ps transform-limited Gaussian pulses with 10 mW average power and 250 fs timing jitter....

  14. Monolithic microchannel heatsink

    Science.gov (United States)

    Benett, William J.; Beach, Raymond J.; Ciarlo, Dino R.

    1996-01-01

    A silicon wafer has slots sawn in it that allow diode laser bars to be mounted in contact with the silicon. Microchannels are etched into the back of the wafer to provide cooling of the diode bars. To facilitate getting the channels close to the diode bars, the channels are rotated from an angle perpendicular to the diode bars which allows increased penetration between the mounted diode bars. This invention enables the fabrication of monolithic silicon microchannel heatsinks for laser diodes. The heatsinks have low thermal resistance because of the close proximity of the microchannels to the laser diode being cooled. This allows high average power operation of two-dimensional laser diode arrays that have a high density of laser diode bars and therefore high optical power density.

  15. Monolithic Fuel Fabrication Process Development

    Energy Technology Data Exchange (ETDEWEB)

    C. R. Clark; N. P. Hallinan; J. F. Jue; D. D. Keiser; J. M. Wight

    2006-05-01

    The pursuit of a high uranium density research reactor fuel plate has led to monolithic fuel, which possesses the greatest possible uranium density in the fuel region. Process developments in fabrication development include friction stir welding tool geometry and cooling improvements and a reduction in the length of time required to complete the transient liquid phase bonding process. Annealing effects on the microstructures of the U-10Mo foil and friction stir welded aluminum 6061 cladding are also examined.

  16. Pressure drop in CIM disk monolithic columns.

    Science.gov (United States)

    Mihelic, Igor; Nemec, Damjan; Podgornik, Ales; Koloini, Tine

    2005-02-11

    Pressure drop analysis in commercial CIM disk monolithic columns is presented. Experimental measurements of pressure drop are compared to hydrodynamic models usually employed for prediction of pressure drop in packed beds, e.g. free surface model and capillary model applying hydraulic radius concept. However, the comparison between pressure drop in monolith and adequate packed bed give unexpected results. Pressure drop in a CIM disk monolithic column is approximately 50% lower than in an adequate packed bed of spheres having the same hydraulic radius as CIM disk monolith; meaning they both have the same porosity and the same specific surface area. This phenomenon seems to be a consequence of the monolithic porous structure which is quite different in terms of the pore size distribution and parallel pore nonuniformity compared to the one in conventional packed beds. The number of self-similar levels for the CIM monoliths was estimated to be between 1.03 and 2.75.

  17. Graphene-supported metal oxide monolith

    Energy Technology Data Exchange (ETDEWEB)

    Worsley, Marcus A.; Baumann, Theodore F.; Biener, Juergen; Biener, Monika A.; Wang, Yinmin; Ye, Jianchao; Tylski, Elijah

    2017-01-10

    A composition comprising at least one graphene-supported metal oxide monolith, said monolith comprising a three-dimensional structure of graphene sheets crosslinked by covalent carbon bonds, wherein the graphene sheets are coated by at least one metal oxide such as iron oxide or titanium oxide. Also provided is an electrode comprising the aforementioned graphene-supported metal oxide monolith, wherein the electrode can be substantially free of any carbon-black and substantially free of any binder.

  18. Highly-stable monolithic femtosecond Yb-fiber laser system based on photonic crystal fibers

    DEFF Research Database (Denmark)

    Liu, Xiaomin; Lægsgaard, Jesper; Turchinovich, Dmitry

    2010-01-01

    A self-starting, passively stabilized, monolithic all polarizationmaintaining femtosecond Yb-fiber master oscillator / power amplifier with very high operational and environmental stability is demonstrated. The system is based on the use of two different photonic crystal fibers. One is used...... in the oscillator cavity for dispersion balancing and nonlinear optical limiting, and another one is used for low nonlinearity final pulse recompression. The chirped-pulse amplification and recompression of the 232-fs, 45-pJ/pulse oscillator output yields a final direct fiber-end delivery of 7.3-nJ energy pulses...

  19. Monolithically integrated absolute frequency comb laser system

    Energy Technology Data Exchange (ETDEWEB)

    Wanke, Michael C.

    2016-07-12

    Rather than down-convert optical frequencies, a QCL laser system directly generates a THz frequency comb in a compact monolithically integrated chip that can be locked to an absolute frequency without the need of a frequency-comb synthesizer. The monolithic, absolute frequency comb can provide a THz frequency reference and tool for high-resolution broad band spectroscopy.

  20. Nanosecond monolithic CMOS readout cell

    Science.gov (United States)

    Souchkov, Vitali V.

    2004-08-24

    A pulse shaper is implemented in monolithic CMOS with a delay unit formed of a unity gain buffer. The shaper is formed of a difference amplifier having one input connected directly to an input signal and a second input connected to a delayed input signal through the buffer. An elementary cell is based on the pulse shaper and a timing circuit which gates the output of an integrator connected to the pulse shaper output. A detector readout system is formed of a plurality of elementary cells, each connected to a pixel of a pixel array, or to a microstrip of a plurality of microstrips, or to a detector segment.

  1. Compact monolithic capacitive discharge unit

    Science.gov (United States)

    Roesler, Alexander W.; Vernon, George E.; Hoke, Darren A.; De Marquis, Virginia K.; Harris, Steven M.

    2007-06-26

    A compact monolithic capacitive discharge unit (CDU) is disclosed in which a thyristor switch and a flyback charging circuit are both sandwiched about a ceramic energy storage capacitor. The result is a compact rugged assembly which provides a low-inductance current discharge path. The flyback charging circuit preferably includes a low-temperature co-fired ceramic transformer. The CDU can further include one or more ceramic substrates for enclosing the thyristor switch and for holding various passive components used in the flyback charging circuit. A load such as a detonator can also be attached directly to the CDU.

  2. Microfluidic devices and methods including porous polymer monoliths

    Science.gov (United States)

    Hatch, Anson V; Sommer, Gregory J; Singh, Anup K; Wang, Ying-Chih; Abhyankar, Vinay V

    2014-04-22

    Microfluidic devices and methods including porous polymer monoliths are described. Polymerization techniques may be used to generate porous polymer monoliths having pores defined by a liquid component of a fluid mixture. The fluid mixture may contain iniferters and the resulting porous polymer monolith may include surfaces terminated with iniferter species. Capture molecules may then be grafted to the monolith pores.

  3. Monolithic Continuous-Flow Bioreactors

    Science.gov (United States)

    Stephanopoulos, Gregory; Kornfield, Julia A.; Voecks, Gerald A.

    1993-01-01

    Monolithic ceramic matrices containing many small flow passages useful as continuous-flow bioreactors. Ceramic matrix containing passages made by extruding and firing suitable ceramic. Pores in matrix provide attachment medium for film of cells and allow free movement of solution. Material one not toxic to micro-organisms grown in reactor. In reactor, liquid nutrients flow over, and liquid reaction products flow from, cell culture immobilized in one set of channels while oxygen flows to, and gaseous reaction products flow from, culture in adjacent set of passages. Cells live on inner surfaces containing flowing nutrient and in pores of walls of passages. Ready access to nutrients and oxygen in channels. They generate continuous high yield characteristic of immobilized cells, without large expenditure of energy otherwise incurred if necessary to pump nutrient solution through dense biomass as in bioreactors of other types.

  4. Monolithic cells for solar fuels.

    Science.gov (United States)

    Rongé, Jan; Bosserez, Tom; Martel, David; Nervi, Carlo; Boarino, Luca; Taulelle, Francis; Decher, Gero; Bordiga, Silvia; Martens, Johan A

    2014-12-07

    Hybrid energy generation models based on a variety of alternative energy supply technologies are considered the best way to cope with the depletion of fossil energy resources and to limit global warming. One of the currently missing technologies is the mimic of natural photosynthesis to convert carbon dioxide and water into chemical fuel using sunlight. This idea has been around for decades, but artificial photosynthesis of organic molecules is still far away from providing real-world solutions. The scientific challenge is to perform in an efficient way the multi-electron transfer reactions of water oxidation and carbon dioxide reduction using holes and single electrons generated in an illuminated semiconductor. In this tutorial review the design of photoelectrochemical (PEC) cells that combine solar water oxidation and CO2 reduction is discussed. In such PEC cells simultaneous transport and efficient use of light, electrons, protons and molecules has to be managed. It is explained how efficiency can be gained by compartmentalisation of the water oxidation and CO2 reduction processes by proton exchange membranes, and monolithic concepts of artificial leaves and solar membranes are presented. Besides transferring protons from the anode to the cathode compartment the membrane serves as a molecular barrier material to prevent cross-over of oxygen and fuel molecules. Innovative nano-organized multimaterials will be needed to realise practical artificial photosynthesis devices. This review provides an overview of synthesis techniques which could be used to realise monolithic multifunctional membrane-electrode assemblies, such as Layer-by-Layer (LbL) deposition, Atomic Layer Deposition (ALD), and porous silicon (porSi) engineering. Advances in modelling approaches, electrochemical techniques and in situ spectroscopies to characterise overall PEC cell performance are discussed.

  5. Anisotropically structured magnetic aerogel monoliths

    Science.gov (United States)

    Heiligtag, Florian J.; Airaghi Leccardi, Marta J. I.; Erdem, Derya; Süess, Martin J.; Niederberger, Markus

    2014-10-01

    Texturing of magnetic ceramics and composites by aligning and fixing of colloidal particles in a magnetic field is a powerful strategy to induce anisotropic chemical, physical and especially mechanical properties into bulk materials. If porosity could be introduced, anisotropically structured magnetic materials would be the perfect supports for magnetic separations in biotechnology or for magnetic field-assisted chemical reactions. Aerogels, combining high porosity with nanoscale structural features, offer an exceptionally large surface area, but they are difficult to magnetically texture. Here we present the preparation of anatase-magnetite aerogel monoliths via the assembly of preformed nanocrystallites. Different approaches are proposed to produce macroscopic bodies with gradient-like magnetic segmentation or with strongly anisotropic magnetic texture.Texturing of magnetic ceramics and composites by aligning and fixing of colloidal particles in a magnetic field is a powerful strategy to induce anisotropic chemical, physical and especially mechanical properties into bulk materials. If porosity could be introduced, anisotropically structured magnetic materials would be the perfect supports for magnetic separations in biotechnology or for magnetic field-assisted chemical reactions. Aerogels, combining high porosity with nanoscale structural features, offer an exceptionally large surface area, but they are difficult to magnetically texture. Here we present the preparation of anatase-magnetite aerogel monoliths via the assembly of preformed nanocrystallites. Different approaches are proposed to produce macroscopic bodies with gradient-like magnetic segmentation or with strongly anisotropic magnetic texture. Electronic supplementary information (ESI) available: Digital photographs of dispersions and gels with different water-to-ethanol ratios; magnetic measurements of an anatase aerogel containing 0.25 mol% Fe3O4 nanoparticles; XRD patterns of the iron oxide and

  6. Controlling S2 terminal using FS software

    Science.gov (United States)

    Xue, Zhuhe

    New S2FS software for controlling S2 terminal of Sheshan station has been developed. It works under Field System software. All S2 operation commands are incorporated in a station program. The interface of SWT computer and S2 terminal is RS232 interface. S2FS software is designed by using Shell and C language. It has been used in VSOP experiments.

  7. Monolithic Time Delay Integrated APD Arrays Project

    Data.gov (United States)

    National Aeronautics and Space Administration — The overall goal of the proposed program by Epitaxial Technologies is to develop monolithic time delay integrated avalanche photodiode (APD) arrays with sensitivity...

  8. Hollow-fiber compression of visible, 200 fs laser pulses to 40 fs pulse duration.

    Science.gov (United States)

    Procino, I; Velotta, R; Altucci, C; Amoruso, S; Bruzzese, R; Wang, X; Tosa, V; Sansone, G; Vozzi, C; Nisoli, M

    2007-07-01

    We demonstrate the use of a very simple, compact, and versatile method, based on the hollow-fiber compression technique, to shorten the temporal length of visible laser pulses of 100-300 fs to pulse durations shorter than approximately 50 fs. In particular, 200 fs, frequency-doubled, Nd:glass laser pulses (527 nm) were spectrally broadened to final bandwidths as large as 25 nm by nonlinear propagation through an Ar-filled hollow fiber. A compact, dispersive, prism-pair compressor was then used to produce as short as 40 fs, 150 microJ pulses. A very satisfactory agreement between numerical simulations and measurements is found.

  9. Monolithic multinozzle emitters for nanoelectrospray mass spectrometry

    Science.gov (United States)

    Wang, Daojing; Yang, Peidong; Kim, Woong; Fan, Rong

    2011-09-20

    Novel and significantly simplified procedures for fabrication of fully integrated nanoelectrospray emitters have been described. For nanofabricated monolithic multinozzle emitters (NM.sup.2 emitters), a bottom up approach using silicon nanowires on a silicon sliver is used. For microfabricated monolithic multinozzle emitters (M.sup.3 emitters), a top down approach using MEMS techniques on silicon wafers is used. The emitters have performance comparable to that of commercially-available silica capillary emitters for nanoelectrospray mass spectrometry.

  10. A monolithically integrated dual-mode laser for photonic microwave generation and all-optical clock recovery

    Science.gov (United States)

    Yu, Liqiang; Zhou, Daibing; Zhao, Lingjuan

    2014-09-01

    We demonstrate a monolithically integrated dual-mode laser (DML) with narrow-beat-linewidth and wide-beat-tunability. Using a monolithic DFB laser subjected to amplified feedback, photonic microwave generation of up to 45 GHz is obtained with higher than 15 GHz beat frequency tunability. Thanks to the high phase correlation of the two modes and the narrow mode linewidth, a RF linewidth of lower than 50 kHz is measured. Simulations are also carried out to illustrate the dual-mode beat characteristic. Furthermore, using the DML, an all-optical clock recovery for 40  Gbaud NRZ-QPSK signals is demonstrated. Timing jitter of lower than 363 fs (integrated within a frequency range from 100 Hz to 1 GHz) is obtained.

  11. Monolithically integrated Ge CMOS laser

    Science.gov (United States)

    Camacho-Aguilera, Rodolfo

    2014-02-01

    Ge-on-Si devices are explored for photonic integration. Through the development of better growth techniques, monolithic integration, laser design and prototypes, it was possible to probe Ge light emitters with emphasis on lasers. Preliminary worked shows thermal photonic behavior capable of enhancing lamination at high temperatures. Increase luminescence is observed up to 120°C from L-band contribution. Higher temperatures show contribution from Δ -band. The increase carrier thermal contribution suggests high temperature applications for Ge light emitters. A Ge electrically pumped laser was probed under 0.2% biaxial strain and doping concentration ~4.5×1019cm-3 n-type. Ge pnn lasers exhibit a gain >1000cm-1 with 8mW power output, presenting a spectrum range of over 200nm, making Ge the ideal candidate for Si photonics. Large temperatures fluctuations and process limit the present device. Theoretically a gain of >4000cm- gain is possible with a threshold of as low as 1kA/cm2. Improvements in Ge work

  12. Fracture resistance of monolithic zirconia molar crowns with reduced thickness

    OpenAIRE

    Nakamura, Keisuke; Harada, A.; Inagaki, R.; Kanno, Taro; Niwano, Y; Milleding, Percy; Ørtengren, Ulf Thore

    2015-01-01

    This is the accepted manuscript version. Published version is available at Acta Odontologica Scandinavica Objectives. The purpose of the present study was to analyze the relationship between fracture load of monolithic zirconia crowns and axial/occlusal thickness, and to evaluate the fracture resistance of monolithic zirconia crowns with reduced thickness in comparison with that of monolithic lithium disilicate crowns with regular thickness. Materials and methods. Monolithic zi...

  13. Modified monolithic silica capillary for preconcentration of catecholamines

    Institute of Scientific and Technical Information of China (English)

    Wei Chang; Tusyo-shi Komazu

    2009-01-01

    Preconcentration of catecholamines by the modified monolithic silica in the capillary was investigated in this study. In order to achieve a microchip-based method for determining catecholamines in the saliva, the monolithic silica was fabricated in the capillary and the monolithic silica was chemically modified by on-column reaction with phenylboronate. Different modified methods were compared. The concentration conditions were optimized. This study indicates the applicability of the modified monolithic silica capillary when it was used to concentrate catecholamines.

  14. Modified monolithic silica capillary for preconcentration of catecholamines

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Preconcentration of catecholamines by the modified monolithic silica in the capillary was investigated in this study. In order to achieve a microchip-based method for determining catecholamines in the saliva,the monolithic silica was fabricated in the capillary and the monolithic silica was chemically modified by on-column reaction with phenylboronate. Different modified methods were compared. The concentration conditions were optimized. This study indicates the applicability of the modified monolithic sili...

  15. Carbon Fiber Composite Monoliths as Catalyst Supports

    Energy Technology Data Exchange (ETDEWEB)

    Contescu, Cristian I [ORNL; Gallego, Nidia C [ORNL; Pickel, Joseph M [ORNL; Blom, Douglas Allen [ORNL; Burchell, Timothy D [ORNL

    2006-01-01

    Carbon fiber composite monoliths are rigid bodies that can be activated to a large surface area, have tunable porosity, and proven performance in gas separation and storage. They are ideal as catalyst supports in applications where a rigid support, with open structure and easy fluid access is desired. We developed a procedure for depositing a dispersed nanoparticulate phase of molybdenum carbide (Mo2C) on carbon composite monoliths in the concentration range of 3 to 15 wt% Mo. The composition and morphology of this phase was characterized using X-ray diffraction and electron microscopy, and a mechanism was suggested for its formation. Molybdenum carbide is known for its catalytic properties that resemble those of platinum group metals, but at a lower cost. The materials obtained are expected to demonstrate catalytic activity in a series of hydrocarbon reactions involving hydrogen transfer. This project demonstrates the potential of carbon fiber composite monoliths as catalyst supports.

  16. Carbon Fiber Composite Monoliths for Catalyst Supports

    Energy Technology Data Exchange (ETDEWEB)

    Contescu, Cristian I [ORNL; Gallego, Nidia C [ORNL; Pickel, Joseph M [ORNL; Blom, Douglas Allen [ORNL; Burchell, Timothy D [ORNL

    2006-01-01

    Carbon fiber composite monoliths are rigid bodies that can be activated to a large surface area, have tunable porosity, and proven performance in gas separation and storage. They are ideal as catalyst supports in applications where a rigid support, with open structure and easy fluid access is desired. We developed a procedure for depositing a dispersed nanoparticulate phase of molybdenum carbide (Mo2C) on carbon composite monoliths in the concentration range of 3 to 15 wt% Mo. The composition and morphology of this phase was characterized using X-ray diffraction and electron microscopy, and a mechanism was suggested for its formation. Molybdenum carbide is known for its catalytic properties that resemble those of platinum group metals, but at a lower cost. The materials obtained are expected to demonstrate catalytic activity in a series of hydrocarbon reactions involving hydrogen transfer. This project demonstrates the potential of carbon fiber composite monoliths as catalyst supports.

  17. Development of a monolithic ferrite memory array

    Science.gov (United States)

    Heckler, C. H., Jr.; Bhiwandker, N. C.

    1972-01-01

    The results of the development and testing of ferrite monolithic memory arrays are presented. This development required the synthesis of ferrite materials having special magnetic and physical characteristics and the development of special processes; (1) for making flexible sheets (laminae) of the ferrite composition, (2) for embedding conductors in ferrite, and (3) bonding ferrite laminae together to form a monolithic structure. Major problems encountered in each of these areas and their solutions are discussed. Twenty-two full-size arrays were fabricated and fired during the development of these processes. The majority of these arrays were tested for their memory characteristics as well as for their physical characteristics and the results are presented. The arrays produced during this program meet the essential goals and demonstrate the feasibility of fabricating monolithic ferrite memory arrays by the processes developed.

  18. Eigenpolarization theory of monolithic nonplanar ring oscillators

    Science.gov (United States)

    Nilsson, Alan C.; Gustafson, Eric K.; Byer, Robert L.

    1989-01-01

    Diode-laser-pumped monolithic nonplanar ring oscillators (NPROs) in an applied magnetic field can operate as unidirectional traveling-wave lasers. The diode laser pumping, monolithic construction, and unidirectional oscillation lead to narrow linewidth radiation. Here, a comprehensive theory of the eigenpolarizations of a monolithic NPRO is presented. It is shown how the properties of the integral optical diode that forces unidirectional operation depend on the choice of the gain medium, the applied magnetic field, the output coupler, and the geometry of the nonplanar ring light path. Using optical equivalence theorems to gain insight into the polarization characteristics of the NPRO, a strategy for designing NPROs with low thresholds and large loss nonreciprocities is given. An analysis of the eigenpolarizations for one such NPRO is presented, alternative optimization approaches are considered, and the prospects for further reducing the linewidths of these lasers are briefly discussed.

  19. Physical and chemical sensing using monolithic semiconductor optical transducers

    Science.gov (United States)

    Zappe, Hans P.; Hofstetter, Daniel; Maisenhoelder, Bernd; Moser, Michael; Riel, Peter; Kunz, Rino E.

    1997-09-01

    We present two monolithically integrated optical sensor systems based on semiconductor photonic integrated circuits. These compact, robust and highly functional transducers perform all necessary optical and electro-optical functions on-chip; extension to multi-sensor arrays is easily envisaged. A monolithic Michelson interferometer for high-resolution displacement measurement and a monolithic Mach-Zehnder interferometer for refractometry are discussed.

  20. Increased thermal conductivity monolithic zeolite structures

    Science.gov (United States)

    Klett, James; Klett, Lynn; Kaufman, Jonathan

    2008-11-25

    A monolith comprises a zeolite, a thermally conductive carbon, and a binder. The zeolite is included in the form of beads, pellets, powders and mixtures thereof. The thermally conductive carbon can be carbon nano-fibers, diamond or graphite which provide thermal conductivities in excess of about 100 W/mK to more than 1,000 W/mK. A method of preparing a zeolite monolith includes the steps of mixing a zeolite dispersion in an aqueous colloidal silica binder with a dispersion of carbon nano-fibers in water followed by dehydration and curing of the binder is given.

  1. Characterization of CIM monoliths as enzyme reactors.

    Science.gov (United States)

    Vodopivec, Martina; Podgornik, Ales; Berovic, Marin; Strancar, Ales

    2003-09-25

    The immobilization of the enzymes citrate lyase, malate dehydrogenase, isocitrate dehydrogenase and lactate dehydrogenase to CIM monolithic supports was performed. The long-term stability, reproducibility, and linear response range of the immobilized enzyme reactors were investigated along with the determination of the kinetic behavior of the enzymes immobilized on the CIM monoliths. The Michaelis-Menten constant K(m) and the turnover number k(3) of the immobilized enzymes were found to be flow-unaffected. Furthermore, the K(m) values of the soluble and immobilized enzyme were found to be comparable. Both facts indicate the absence of a diffusional limitation in immobilized CIM enzyme reactors.

  2. Streamlining the RI/FS process

    Energy Technology Data Exchange (ETDEWEB)

    Dumas, L.; Doss, R.C.

    1998-07-01

    In 1994, Pacific Gas and Electric Company (PG and E) contracted with CH2M HILL to manage remedial investigations and feasibility studies (RI/FS) at its former manufactured gas plant (MGP) sites in Chico, Willows, and Marysville, California. These three sites had similar histories, MGP-related contaminants, similar geologic settings, and geographically were close together. Recognizing the advantages that may be gained, both in time and money, by streamlining the RI/FS process, PG and E and CH2M HILL combined the sites into one project. From the start of the project, PG and E and CH2M HILL looked for an implemented changes to the RI/FS process to streamline the project. These changes included combining deliverables, linking field programs at the three sites, and negotiating bulk discounts on laboratory and other services by combining the work to be done at the three sites under one contract. CH2M HILL later proposed additional measures to streamline the project that were eventually adopted by both PG and E and the regulatory agencies. PG and E and CH2M HILL are currently working with the regulatory agencies to negotiate realistic measures to address contaminants in soil and groundwater, and are jointly preparing the FS with the regulatory agencies using a unique means of documentation.

  3. The Three Fs of Classroom Management

    Science.gov (United States)

    Daniels, Mark L.

    2009-01-01

    This article describes a cohesive theory of classroom management, developed by the author. This "three Fs" theory, predicated upon extant empiricism and scholarship vis-a-vis classroom management, was devised and implemented over several semesters within a field-based course at the University of Texas at Austin for preservice mathematics majors…

  4. Epicardial origin of cardiac CFU-Fs.

    Science.gov (United States)

    Slukvin, Igor I

    2011-12-02

    The epicardium has been recognized as a source of cardiovascular progenitors during embryogenesis and postnatal life. In this issue of Cell Stem Cell, Chong et al. (2011) identify cardiac CFU-Fs as cardiac-resident cells of epicardial origin with broad multilineage differentiation potential.

  5. Monolithic Integration of GaN-based LEDs

    Energy Technology Data Exchange (ETDEWEB)

    Ao, Jin-Ping, E-mail: jpao@ee.tokushima-u.ac.jp [Institute of Technology and Science, University of Tokushima 2-1 Minami-Josanjima, Tokushima 770-8506 (Japan)

    2011-02-01

    The technology of monolithically integrated GaN-based light-emitting diodes (LEDs) is reported. First, the technology details to realize monolithic integration are described, including the circuit design for high-voltage and alternating current (AC) operation and the technologies for device isolation. The performances of the fabricated monolithic LED arrays are then demonstrated. A monolithic series array with totally 40 LEDs exhibited expected operation function under AC bias. The operation voltage of the array is 72 V when 20 LEDs were connected in series. Some modified circuit designs for high-voltage operation and other monolithic LED arrays are finally reviewed.

  6. Monolithic pixel detectors for high energy physics

    CERN Document Server

    Snoeys, W

    2013-01-01

    Monolithic pixel detectors integrating sensor matrix and readout in one piece of silicon have revolutionized imaging for consumer applications, but despite years of research they have not yet been widely adopted for high energy physics. Two major requirements for this application, radiation tolerance and low power consumption, require charge collection by drift for the most extreme radiation levels and an optimization of the collected signal charge over input capacitance ratio ( Q / C ). It is shown that monolithic detectors can achieve Q / C for low analog power consumption and even carryout the promise to practically eliminate analog power consumption, but combining suf fi cient Q / C , collection by drift, and integration of readout circuitry within the pixel remains a challenge. An overview is given of different approaches to address this challenge, with possible advantages and disadvantages.

  7. Macroporous Monolithic Polymers: Preparation and Applications

    Directory of Open Access Journals (Sweden)

    Cecilia Inés Alvarez Igarzabal

    2009-12-01

    Full Text Available In the last years, macroporous monolithic materials have been introduced as a new and useful generation of polymers used in different fields. These polymers may be prepared in a simple way from a homogenous mixture into a mold and contain large interconnected pores or channels allowing for high flow rates at moderate pressures. Due to their porous characteristics, they could be used in different processes, such as stationary phases for different types of chromatography, high-throughput bioreactors and in microfluidic chip applications. This review reports the contributions of several groups working in the preparation of different macroporous monoliths and their modification by immobilization of specific ligands on the products for specific purposes.

  8. A monolithic integrated photonic microwave filter

    Science.gov (United States)

    Fandiño, Javier S.; Muñoz, Pascual; Doménech, David; Capmany, José

    2016-12-01

    Meeting the increasing demand for capacity in wireless networks requires the harnessing of higher regions in the radiofrequency spectrum, reducing cell size, as well as more compact, agile and power-efficient base stations that are capable of smoothly interfacing the radio and fibre segments. Fully functional microwave photonic chips are promising candidates in attempts to meet these goals. In recent years, many integrated microwave photonic chips have been reported in different technologies. To the best of our knowledge, none has monolithically integrated all the main active and passive optoelectronic components. Here, we report the first demonstration of a tunable microwave photonics filter that is monolithically integrated into an indium phosphide chip. The reconfigurable radiofrequency photonic filter includes all the necessary elements (for example, lasers, modulators and photodetectors), and its response can be tuned by means of control electric currents. This is an important step in demonstrating the feasibility of integrated and programmable microwave photonic processors.

  9. Monolithically integrated interferometer for optical displacement measurement

    Science.gov (United States)

    Hofstetter, Daniel; Zappe, Hans P.

    1996-01-01

    We discuss the fabrication of a monolithically integrated optical displacement sensors using III-V semiconductor technology. The device is configured as a Michelson interferometer and consists of a distributed Bragg reflector laser, a photodetector and waveguides forming a directional coupler. Using this interferometer, displacements in the 100 nm range could be measured at distances of up to 45 cm. We present fabrication, device results and characterization of the completed interferometer, problems, limitations and future applications will also be discussed.

  10. FLUIDIZED BED STEAM REFORMER MONOLITH FORMATION

    Energy Technology Data Exchange (ETDEWEB)

    Jantzen, C

    2006-12-22

    Fluidized Bed Steam Reforming (FBSR) is being considered as an alternative technology for the immobilization of a wide variety of aqueous high sodium containing radioactive wastes at various DOE facilities in the United States. The addition of clay, charcoal, and a catalyst as co-reactants converts aqueous Low Activity Wastes (LAW) to a granular or ''mineralized'' waste form while converting organic components to CO{sub 2} and steam, and nitrate/nitrite components, if any, to N{sub 2}. The waste form produced is a multiphase mineral assemblage of Na-Al-Si (NAS) feldspathoid minerals with cage-like structures that atomically bond radionuclides like Tc-99 and anions such as SO{sub 4}, I, F, and Cl. The granular product has been shown to be as durable as LAW glass. Shallow land burial requires that the mineralized waste form be able to sustain the weight of soil overburden and potential intrusion by future generations. The strength requirement necessitates binding the granular product into a monolith. FBSR mineral products were formulated into a variety of monoliths including various cements, Ceramicrete, and hydroceramics. All but one of the nine monoliths tested met the <2g/m{sup 2} durability specification for Na and Re (simulant for Tc-99) when tested using the Product Consistency Test (PCT; ASTM C1285). Of the nine monoliths tested the cements produced with 80-87 wt% FBSR product, the Ceramicrete, and the hydroceramic produced with 83.3 wt% FBSR product, met the compressive strength and durability requirements for an LAW waste form.

  11. Update On Monolithic Fuel Fabrication Development

    Energy Technology Data Exchange (ETDEWEB)

    C. R Clark; J. M. Wight; G. C. Knighton; G. A. Moore; J. F. Jue

    2005-11-01

    Efforts to develop a viable monolithic research reactor fuel plate have continued at Idaho National Laboratory. These efforts have concentrated on both fabrication process refinement and scale-up to produce full sized fuel plates. Advancements have been made in the production of U-Mo foil including full sized foils. Progress has also been made in the friction stir welding and transient liquid phase bonding fabrication processes resulting in better bonding, more stable processes and the ability to fabricate larger fuel plates.

  12. An overview of monolithic zirconia in dentistry

    Directory of Open Access Journals (Sweden)

    Özlem Malkondu

    2016-07-01

    Full Text Available Zirconia restorations have been used successfully for years in dentistry owing to their biocompatibility and good mechanical properties. Because of their lack of translucency, zirconia cores are generally veneered with porcelain, which makes restorations weaker due to failure of the adhesion between the two materials. In recent years, all-ceramic zirconia restorations have been introduced in the dental sector with the intent to solve this problem. Besides the elimination of chipping, the reduced occlusal space requirement seems to be a clear advantage of monolithic zirconia restorations. However, scientific evidence is needed to recommend this relatively new application for clinical use. This mini-review discusses the current scientific literature on monolithic zirconia restorations. The results of in vitro studies suggested that monolithic zirconia may be the best choice for posterior fixed partial dentures in the presence of high occlusal loads and minimal occlusal restoration space. The results should be supported with much more in vitro and particularly in vivo studies to obtain a final conclusion.

  13. Preparation of imprinted monolithic column under molecular crowding conditions

    Institute of Scientific and Technical Information of China (English)

    Xiao Xia Li; Xin Liu; Li Hong Bai; Hong Quan Duan; Yan Ping Huang; Zhao Sheng Liu

    2011-01-01

    Molecular crowding is a new concept to obtain molecularly imprinted polymers (MIPs) with greater capacity and selectivity. In this work, molecular crowding agent was firstly applied to the preparation of MIPs monolithic column. A new polymerization system based on molecular crowding surrounding was developed to prepare enrofloxacin-imprinted monolith, which was composed of polystyrene and tetrahydrofuran. The result showed that the monolithic MIPs under molecular crowding conditions presented good molecular recognition for enrofloxacin with an imprinting factor of 3.03.

  14. Monolithic Lumped Element Integrated Circuit (M2LEIC) Transistors.

    Science.gov (United States)

    INTEGRATED CIRCUITS, *MONOLITHIC STRUCTURES(ELECTRONICS), *TRANSISTORS, CHIPS(ELECTRONICS), FABRICATION, EPITAXIAL GROWTH, ULTRAHIGH FREQUENCY, POLYSILICONS, PHOTOLITHOGRAPHY, RADIOFREQUENCY POWER, IMPEDANCE MATCHING .

  15. Preemiad said Rein Raud, fs, Mart Kivastik

    Index Scriptorium Estoniae

    2005-01-01

    Eesti Kultuurkapitali 2004. aasta kirjanduse aastapreemia laureaadid on: Rein Raud ("Hector ja Bernard"), fs (luulekogu "2004"), Mart Kivastik (näidend "Külmetava kunstniku portree"), Jaan Rannap ("Nelja nimega koer"), Toomas Haug ("Troojamäe tõotus"), Harald Rajamets (tõlkeluule kogumik "Pegasos ja peegel"), Antoine Chalvin ("Kalevipoja" tõlge prantsuse keelde"), Ilmar Talve ("Eesti kultuurilugu"), Lauri Sommer (artikkel Uku Masingu käsikirja "Saadik Magellani pilvest" vaimne, ajalis-ruumiline ja elulooline taust), Boris Tuch ("Gorjatshaja desjatka estonskihh pisatelei")

  16. Selective oxidation of cyclohexene through gold functionalized silica monolith microreactors

    Science.gov (United States)

    Alotaibi, Mohammed T.; Taylor, Martin J.; Liu, Dan; Beaumont, Simon K.; Kyriakou, Georgios

    2016-04-01

    Two simple, reproducible methods of preparing evenly distributed Au nanoparticle containing mesoporous silica monoliths are investigated. These Au nanoparticle containing monoliths are subsequently investigated as flow reactors for the selective oxidation of cyclohexene. In the first strategy, the silica monolith was directly impregnated with Au nanoparticles during the formation of the monolith. The second approach was to pre-functionalize the monolith with thiol groups tethered within the silica mesostructure. These can act as evenly distributed anchors for the Au nanoparticles to be incorporated by flowing a Au nanoparticle solution through the thiol functionalized monolith. Both methods led to successfully achieving even distribution of Au nanoparticles along the length of the monolith as demonstrated by ICP-OES. However, the impregnation method led to strong agglomeration of the Au nanoparticles during subsequent heating steps while the thiol anchoring procedure maintained the nanoparticles in the range of 6.8 ± 1.4 nm. Both Au nanoparticle containing monoliths as well as samples with no Au incorporated were tested for the selective oxidation of cyclohexene under constant flow at 30 °C. The Au free materials were found to be catalytically inactive with Au being the minimum necessary requirement for the reaction to proceed. The impregnated Au-containing monolith was found to be less active than the thiol functionalized Au-containing material, attributable to the low metal surface area of the Au nanoparticles. The reaction on the thiol functionalized Au-containing monolith was found to depend strongly on the type of oxidant used: tert-butyl hydroperoxide (TBHP) was more active than H2O2, likely due to the thiol induced hydrophobicity in the monolith.

  17. Isolated sub-10 attosecond pulse generation by a 6-fs driving pulse and a 5-fs subharmonic controlling pulse

    Directory of Open Access Journals (Sweden)

    Yunhui Wang

    2012-06-01

    Full Text Available We theoretically study high-order harmonic generation by quantum path control in a special two-color laser field, which is synthesized by a 6 fs/800 nm fundamental pulse and a weaker 5 fs/1600 nm subharmonic controlling pulse. Single quantum path is selected without optimizing any carrier phase, which not only broadens the harmonic bandwidth to 400 eV, but also enhances the harmonic conversion efficiency in comparison with the short-plus-long scheme, which is based on 5 fs/800 nm driving pulse and 6 fs/1600 nm control pulse. An isolated 8-attosecond pulse is produced with currently available ultrafast laser sources.

  18. Nielsen: Aladdin-Suite, FS89. Maskarade-Overture / Robert Layton

    Index Scriptorium Estoniae

    Layton, Robert

    1996-01-01

    Uuest heliplaadist "Nielsen: Aladdin-Suite, FS89. Maskarade-Overture, Prelude, Act 2. The Cockerels' Dance. Rhapsody Overture: An imaginary journey to the Faroe Islands, FS123. Helios Overture, FS32. Saga-Drom, FS46. Pan and Syrinx, FS87. Gothenburg Symphony Orchestra, Neeme Järvi" DG 447 757-2GH (72 minutes: DDD)

  19. Hydrogel coated monoliths for enzymatic hydrolysis of penicillin G

    NARCIS (Netherlands)

    De Lathouder, K.M.; Smeltink, M.W.; Straathof, A.J.J.; Paasman, M.A.; Van de Sandt, E.J.A.X.; Kapteijn, F.; Moulijn, J.A.

    2008-01-01

    The objective of this work was to develop a hydrogel-coated monolith for the entrapment of penicillin G acylase (E. coli, PGA). After screening of different hydrogels, chitosan was chosen as the carrier material for the preparation of monolithic biocatalysts. This protocol leads to active immobilize

  20. A Monolithic Perovskite Structure for Use as a Magnetic Regenerator

    DEFF Research Database (Denmark)

    Pryds, Nini; Clemens, Frank; Menon, Mohan

    2011-01-01

    A La0.67Ca0.26Sr0.07Mn1.05O3 (LCSM) perovskite was prepared for the first time as a ceramic monolithic regenerator used in a regenerative magnetic refrigeration device. The parameters influencing the extrusion process and the performance of the regenerator, such as the nature of the monolith paste...

  1. Time-based position estimation in monolithic scintillator detectors

    NARCIS (Netherlands)

    Tabacchini, V.; Borghi, G.; Schaart, D.R.

    2015-01-01

    Gamma-ray detectors based on bright monolithic scintillation crystals coupled to pixelated photodetectors are currently being considered for several applications in the medical imaging field. In a typical monolithic detector, both the light intensity and the time of arrival of the earliest scintilla

  2. Energy Absorption of Monolithic and Fibre Reinforced Aluminium Cylinders

    NARCIS (Netherlands)

    De Kanter, J.L.C.G.

    2006-01-01

    Summary accompanying the thesis: Energy Absorption of Monolithic and Fibre Reinforced Aluminium Cylinders by Jens de Kanter This thesis presents the investigation of the crush behaviour of both monolithic aluminium cylinders and externally fibre reinforced aluminium cylinders. The research is based

  3. Components for monolithic fiber chirped pulse amplification laser systems

    Science.gov (United States)

    Swan, Michael Craig

    The first portion of this work develops techniques for generating femtosecond-pulses from conventional fabry-perot laser diodes using nonlinear-spectral-broadening techniques in Yb-doped positive dispersion fiber ampliers. The approach employed an injection-locked fabry-perot laser diode followed by two stages of nonlinear-spectral-broadening to generate sub-200fs pulses. This thesis demonstrated that a 60ps gain-switched fabry-perot laser-diode can be injection-locked to generate a single-longitudinal-mode pulse and compressed by nonlinear spectral broadening to 4ps. Two problems have been identified that must be resolved before moving forward with this approach. First, gain-switched pulses from a standard diode-laser have a number of characteristics not well suited for producing clean self-phase-modulation-broadened pulses, such as an asymmetric temporal shape, which has a long pulse tail. Second, though parabolic pulse formation occurs for any arbitrary temporal input pulse profile, deviation from the optimum parabolic input results in extensively spectrally modulated self-phase-modulation-broadened pulses. In conclusion, the approach of generating self-phase-modulation-broadened pulses from pulsed laser diodes has to be modified from the initial approach explored in this thesis. The first Yb-doped chirally-coupled-core ber based systems are demonstrated and characterized in the second portion of this work. Robust single-mode performance independent of excitation or any other external mode management techniques have been demonstrated in Yb-doped chirally-coupled-core fibers. Gain and power efficiency characteristics are not compromised in any way in this novel fiber structure up to the 87W maximum power achieved. Both the small signal gain at 1064nm of 30.3dB, and the wavelength dependence of the small signal gain were comparable to currently deployed large-mode-area-fiber technology. The efficiencies of the laser and amplifier were measured to be 75% and 54

  4. Monolithic aerogels with nanoporous crystalline phases

    Science.gov (United States)

    Daniel, Christophe; Guerra, Gaetano

    2015-05-01

    High porosity monolithic aerogels with nanoporous crystalline phases can be obtained from syndiotactic polystyrene and poly(2,6-dimethyl-1,4-phenylene)oxide thermoreversible gels by removing the solvent with supercritical CO2. The presence of crystalline nanopores in the aerogels based on these polymers allows a high uptake associated with a high selectivity of volatile organic compounds from vapor phase or aqueous solutions even at very low activities. The sorption and the fast kinetics make these materials particularly suitable as sorption medium to remove traces of pollutants from water and moist air.

  5. A new large area monolithic silicon telescope

    CERN Document Server

    Tudisco, S; Cabibbo, M; Cardella, G; De Geronimo, G; Di Pietro, A; Fallica, G; Figuera, P; Musumarra, A; Papa, M; Pappalardo, G S; Rizzo, F; Valvo, G

    1999-01-01

    A new prototype of large area (20x20 mm sup 2) monolithic silicon telescope with an ultrathin DELTA E stage (1 mu m) has been built and tested. A particular mask for the ground electrode has been developed to improve the charge collection reducing the induction between the E and DELTA E stages. A special designed preamplifier has been used for the readout of the signal from the DELTA E stage to overcome the problem of the large input capacitance (40 nF). A rather low energy threshold charge discrimination has been obtained. Small side effects due to the electric field deformation near the ground electrode were observed and quantified.

  6. EST Table: FS920530 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS920530 E_FL_fufe_50K23_F_0 11/12/09 GO hit GO:0047800(cysteamine dioxygenase acti...090992|ref|XP_974899.1| PREDICTED: similar to 2-aminoethanethiol (cysteamine) dioxygenase [Tribolium castaneum] FS920530 fufe ...

  7. EST Table: FS764450 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS764450 E_FL_fcaL_36N15_F_0 10/09/28 42 %/214 aa ref|XP_001945612.1| PREDICTED: similar to glucocerebro...608.1| PREDICTED: similar to putative lysosomal glucocerebrosidase [Tribolium castaneum] FS759318 fcaL ...

  8. EST Table: FS906632 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS906632 E_FL_fufe_08M07_F_0 11/12/09 GO hit GO:0005634(nucleus)|GO:0006974(response to DNA damage stim...2 %/162 aa gi|91087647|ref|XP_973370.1| PREDICTED: similar to Timeless-interacting protein (XTipin) [Tribolium castaneum] FS906632 fufe ...

  9. EST Table: FS919894 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919894 E_FL_fufe_48M03_F_0 10/09/28 41 %/229 aa ref|XP_624752.2| PREDICTED: similar to Niemann-Pic..._967619.2| PREDICTED: similar to niemann-pick C1 [Tribolium castaneum] FS758709 fufe ...

  10. EST Table: FS811017 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS811017 E_FL_fmgV_33J08_F_0 11/12/09 n.h 10/09/28 low homology 10/09/09 36 %/103 a...|gene:AGAP006784 10/09/10 42 %/121 aa gnl|Amel|GB13334-PA 10/09/10 low homology FS811017 fmgV ...

  11. EST Table: FS811019 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS811019 E_FL_fmgV_33J10_F_0 11/12/09 GO hit GO:0003824(catalytic activity)|GO:0006...9/10 34 %/226 aa gi|91075984|ref|XP_970026.1| PREDICTED: similar to AGAP011683-PA [Tribolium castaneum] FS811019 fmgV ...

  12. EST Table: FS871984 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS871984 E_FL_fner_47A02_R_0 11/12/09 n.h 10/09/28 33 %/210 aa gb|ABN58714.1| pol-l... gi|270016726|gb|EFA13172.1| hypothetical protein TcasGA2_TC001813 [Tribolium castaneum] FS871984 fner ...

  13. EST Table: FS819844 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS819844 E_FL_fmgV_05D01_R_0 11/12/09 GO hit GO:0004181(metallocarboxypeptidase act...10 42 %/287 aa gi|91085361|ref|XP_971346.1| PREDICTED: similar to putative carboxypeptidase A-like [Tribolium castaneum] FS819844 fmgV ...

  14. EST Table: FS868268 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS868268 E_FL_fner_36G03_R_0 10/09/28 100 %/133 aa ref|NP_001040212.1| sericotropin... 38 %/131 aa gi|91087441|ref|XP_975685.1| PREDICTED: similar to 13 kDa hemolymph protein a [Tribolium castaneum] FS784478 fner ...

  15. EST Table: FS843095 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS843095 E_FL_fner_17B02_F_0 10/09/28 84 %/185 aa ref|XP_972038.2| PREDICTED: similar to liquid...26|ref|XP_972038.2| PREDICTED: similar to liquid facets [Tribolium castaneum] FS840960 fner ...

  16. EST Table: FS759708 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS759708 E_FL_fcaL_12C07_F_0 10/09/28 48 %/108 aa gb|EFA09250.1| thickveins [Tribol...|XP_970678.1| PREDICTED: similar to thickveins CG14026-PA [Tribolium castaneum] FS936628 fcaL ...

  17. EST Table: FS854714 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS854714 E_FL_fner_49P07_F_0 10/09/28 48 %/108 aa gb|EFA09250.1| thickveins [Tribol...|XP_970678.1| PREDICTED: similar to thickveins CG14026-PA [Tribolium castaneum] FS936628 fner ...

  18. EST Table: FS805538 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS805538 E_FL_fmgV_18D12_F_0 10/09/28 48 %/108 aa gb|EFA09250.1| thickveins [Tribol...|XP_970678.1| PREDICTED: similar to thickveins CG14026-PA [Tribolium castaneum] FS936628 fmgV ...

  19. EST Table: FS733896 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS733896 E_FL_bmmt_22L01_F_0 10/09/28 30 %/251 aa ref|XP_974925.1| PREDICTED: similar to Juvenile.../10 low homology 10/09/10 30 %/251 aa gi|91080979|ref|XP_974925.1| PREDICTED: similar to Juvenile hormone-inducible protein, putative [Tribolium castaneum] FS725285 bmmt ...

  20. EST Table: FS848732 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS848732 E_FL_fner_33A19_F_0 10/09/28 39 %/198 aa ref|XP_971046.2| PREDICTED: similar to antolefin... %/152 aa gnl|Amel|GB16043-PA 10/09/10 39 %/198 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS921551 fner ...

  1. EST Table: FS867121 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS867121 E_FL_fner_33A19_R_0 10/09/28 39 %/198 aa ref|XP_971046.2| PREDICTED: similar to antolefin... %/152 aa gnl|Amel|GB16043-PA 10/09/10 39 %/198 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS752084 fner ...

  2. EST Table: FS918193 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918193 E_FL_fufe_43J18_F_0 10/09/28 39 %/198 aa ref|XP_971046.2| PREDICTED: similar to antolefin... %/152 aa gnl|Amel|GB16043-PA 10/09/10 39 %/198 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS921551 fufe ...

  3. EST Table: FS845801 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS845801 E_FL_fner_24L14_F_0 10/09/28 43 %/155 aa ref|XP_971046.2| PREDICTED: similar to antolefin... %/116 aa gnl|Amel|GB16043-PA 10/09/10 43 %/155 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS921551 fner ...

  4. EST Table: FS905568 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS905568 E_FL_fufe_05H13_F_0 10/09/28 40 %/188 aa ref|XP_971046.2| PREDICTED: similar to antolefin... %/142 aa gnl|Amel|GB16043-PA 10/09/10 40 %/188 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS921551 fufe ...

  5. EST Table: FS896666 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS896666 E_FL_ftes_24D11_R_0 11/12/09 GO hit GO:0003824(catalytic activity)|GO:0005... aa gi|91085015|ref|XP_973533.1| PREDICTED: similar to malate dehydrogenase [Tribolium castaneum] FS896666 ftes ...

  6. EST Table: FS866668 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS866668 E_FL_fner_31M13_R_0 11/12/09 n.h 10/09/28 54 %/126 aa ref|XP_966747.1| PRE.../10 54 %/126 aa gi|91088415|ref|XP_966747.1| PREDICTED: similar to CG32418 CG32418-PA [Tribolium castaneum] FS866668 fner ...

  7. EST Table: FS904669 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS904669 E_FL_fufe_02L06_F_0 10/09/28 39 %/215 aa ref|XP_967337.1| PREDICTED: similar to Serge... %/215 aa gi|91083383|ref|XP_967337.1| PREDICTED: similar to Sergef protein [Tribolium castaneum] FS910504 fufe ...

  8. EST Table: FS811161 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS811161 E_FL_fmgV_33P23_F_0 10/09/28 40 %/212 aa ref|XP_967337.1| PREDICTED: similar to Serge...B17309-PA 10/09/10 40 %/212 aa gi|91083383|ref|XP_967337.1| PREDICTED: similar to Sergef protein [Tribolium castaneum] FS910504 fmgV ...

  9. EST Table: FS810311 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS810311 E_FL_fmgV_31J05_F_0 10/09/28 39 %/186 aa ref|XP_967337.1| PREDICTED: similar to Serge...186 aa gi|91083383|ref|XP_967337.1| PREDICTED: similar to Sergef protein [Tribolium castaneum] FS910504 fmgV ...

  10. EST Table: FS767215 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS767215 E_FL_fcaL_45F03_F_0 10/09/28 44 %/190 aa ref|XP_975194.1| PREDICTED: similar to something about...ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fcaL ...

  11. EST Table: FS913032 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS913032 E_FL_fufe_28A02_F_0 10/09/28 44 %/216 aa ref|XP_975194.1| PREDICTED: similar to something about...A 10/09/10 44 %/216 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fufe ...

  12. EST Table: FS847171 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS847171 E_FL_fner_28J23_F_0 10/09/28 45 %/144 aa ref|XP_971977.1| PREDICTED: similar to reserve...gi|91086211|ref|XP_971977.1| PREDICTED: similar to reserved [Tribolium castaneum] FS918257 fner ...

  13. EST Table: FS908881 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS908881 E_FL_fufe_15I20_F_0 10/09/28 49 %/232 aa ref|XP_971977.1| PREDICTED: similar to reserve...el|GB11583-PA 10/09/10 49 %/232 aa gi|91086211|ref|XP_971977.1| PREDICTED: similar to reserved [Tribolium castaneum] FS918257 fufe ...

  14. EST Table: FS916404 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS916404 E_FL_fufe_38D19_F_0 10/09/28 48 %/244 aa ref|XP_971977.1| PREDICTED: similar to reserve...el|GB11583-PA 10/09/10 48 %/244 aa gi|91086211|ref|XP_971977.1| PREDICTED: similar to reserved [Tribolium castaneum] FS918257 fufe ...

  15. EST Table: FS852221 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS852221 E_FL_fner_42O22_F_0 10/09/28 74 %/189 aa ref|XP_001658413.1| neuroendocrine... differentiation factor [Aedes aegypti] gb|EAT40780.1| neuroendocrine differentiation factor [Aedes aegypti...5 aa gi|91089815|ref|XP_968988.1| PREDICTED: similar to neuroendocrine differentiation factor [Tribolium castaneum] FS765648 fner ...

  16. EST Table: FS845415 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS845415 E_FL_fner_23J15_F_0 10/09/28 42 %/122 aa ref|XP_969763.1| PREDICTED: similar to meteori...a gi|91078226|ref|XP_969763.1| PREDICTED: similar to meteorin [Tribolium castaneum] FS767139 fner ...

  17. EST Table: FS849851 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS849851 E_FL_fner_36C21_F_0 10/09/28 44 %/171 aa ref|XP_969763.1| PREDICTED: similar to meteori...a gi|91078226|ref|XP_969763.1| PREDICTED: similar to meteorin [Tribolium castaneum] FS767139 fner ...

  18. EST Table: FS930966 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS930966 E_FL_fwgP_29M10_F_0 10/09/28 44 %/215 aa ref|XP_969763.1| PREDICTED: similar to meteori...a gi|91078226|ref|XP_969763.1| PREDICTED: similar to meteorin [Tribolium castaneum] FS767139 fwgP ...

  19. EST Table: FS767139 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS767139 E_FL_fcaL_45B09_F_0 11/12/09 n.h 10/09/28 43 %/171 aa ref|XP_969763.1| PREDICTED: similar to meteor...10 43 %/171 aa gi|91078226|ref|XP_969763.1| PREDICTED: similar to meteorin [Tribolium castaneum] FS767139 fcaL ...

  20. EST Table: FS850158 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS850158 E_FL_fner_37A23_F_0 10/09/28 43 %/137 aa ref|XP_969763.1| PREDICTED: similar to meteori...a gi|91078226|ref|XP_969763.1| PREDICTED: similar to meteorin [Tribolium castaneum] FS767139 fner ...

  1. EST Table: FS855797 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS855797 E_FL_fner_52P17_F_0 10/09/28 43 %/137 aa ref|XP_969763.1| PREDICTED: similar to meteori...a gi|91078226|ref|XP_969763.1| PREDICTED: similar to meteorin [Tribolium castaneum] FS767139 fner ...

  2. EST Table: FS827409 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS827409 E_FL_fmgV_26E17_R_0 11/12/09 n.h 10/09/28 42 %/146 aa ref|XP_974840.1| PREDICTED: similar to harmon...27|ref|XP_974840.1| PREDICTED: similar to harmonin [Tribolium castaneum] FS827409 fmgV ...

  3. EST Table: FS911923 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS911923 E_FL_fufe_24L11_F_0 11/12/09 n.h 10/09/28 36 %/206 aa ref|XP_974840.1| PREDICTED: similar to harmon...27|ref|XP_974840.1| PREDICTED: similar to harmonin [Tribolium castaneum] FS911923 fufe ...

  4. Rapid developmental maturation of neocortical FS cell intrinsic excitability.

    Science.gov (United States)

    Goldberg, Ethan M; Jeong, Hyo-Young; Kruglikov, Ilya; Tremblay, Robin; Lazarenko, Roman M; Rudy, Bernardo

    2011-03-01

    Fast-spiking (FS) cells are a prominent subtype of neocortical γ-aminobutyric acidergic interneurons that mediate feed-forward inhibition and the temporal sculpting of information transfer in neural circuits, maintain excitation/inhibition balance, and contribute to network oscillations. FS cell dysfunction may be involved in the pathogenesis of disorders such as epilepsy, autism, and schizophrenia. Mature FS cells exhibit coordinated molecular and cellular specializations that facilitate rapid responsiveness, including brief spikes and sustained high-frequency discharge. We show that these features appear during the second and third postnatal weeks driven by upregulation of K(+) channel subunits of the Kv3 subfamily. The low membrane resistance and fast time constant characteristic of FS cells also appears during this time, driven by expression of a K(+) leak current mediated by K(ir)2 subfamily inward rectifier K(+) channels and TASK subfamily 2-pore K(+) channels. Blockade of this leak produces dramatic depolarization of FS cells suggesting the possibility for potent neuromodulation. Finally, the frequency of FS cell membrane potential oscillations increases during development and is markedly slower in TASK-1/3 knockout mice, suggesting that TASK channels regulate FS cell rhythmogenesis. Our findings imply that some of the effects of acidosis and/or anesthetics on brain function may be due to blockade of TASK channels in FS cells.

  5. EST Table: FS744174 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS744174 E_FL_bmmt_27L11_R_0 10/09/28 62 %/254 aa ref|XP_966408.1| PREDICTED: simil...|Amel|GB13140-PA 10/09/10 62 %/254 aa gi|91091742|ref|XP_966408.1| PREDICTED: similar to AGAP000313-PA isoform 1 [Tribolium castaneum] FS744301 bmmt ...

  6. EST Table: FS882512 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS882512 E_FL_ftes_24I11_F_0 10/09/28 46 %/122 aa ref|XP_968918.2| PREDICTED: similar to william...189241014|ref|XP_968918.2| PREDICTED: similar to williams-beuren syndrome critical region protein [Tribolium castaneum] FS920403 ftes ...

  7. EST Table: FS905741 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS905741 E_FL_fufe_06A07_F_0 10/09/28 31 %/238 aa ref|XP_968918.2| PREDICTED: similar to william...189241014|ref|XP_968918.2| PREDICTED: similar to williams-beuren syndrome critical region protein [Tribolium castaneum] FS920403 fufe ...

  8. EST Table: FS919685 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919685 E_FL_fufe_48B17_F_0 11/12/09 GO hit GO:0005789(endoplasmic reticulum membr...9/10 34 %/234 aa gi|91087517|ref|XP_969270.1| PREDICTED: similar to CG13089 CG13089-PA [Tribolium castaneum] FS919685 fufe ...

  9. EST Table: FS784619 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS784619 E_FL_fcaL_48C03_R_0 10/09/28 64 %/109 aa ref|XP_970998.1| PREDICTED: similar to Evolution...187|ref|XP_970998.1| PREDICTED: similar to Evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial [Tribolium castaneum] FS874188 fcaL ...

  10. EST Table: FS773307 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS773307 E_FL_fcaL_01B18_R_0 10/09/28 51 %/210 aa ref|XP_970998.1| PREDICTED: similar to Evolution...187|ref|XP_970998.1| PREDICTED: similar to Evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial [Tribolium castaneum] FS874188 fcaL ...

  11. EST Table: FS877412 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS877412 E_FL_ftes_09L06_F_0 10/09/28 63 %/108 aa ref|XP_970998.1| PREDICTED: similar to Evolution...94187|ref|XP_970998.1| PREDICTED: similar to Evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial [Tribolium castaneum] FS756091 ftes ...

  12. EST Table: FS919947 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919947 E_FL_fufe_48O15_F_0 11/12/09 GO hit GO:0003924(GTPase activity)|GO:0005515... 56 %/203 aa gnl|Amel|GB16230-PA 10/09/10 55 %/209 aa gi|237820631|ref|NP_001153783.1| Rab-protein 14 [Tribolium castaneum] FS919947 fufe ...

  13. EST Table: FS916979 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS916979 E_FL_fufe_39O23_F_0 10/09/28 42 %/282 aa ref|XP_975212.1| PREDICTED: similar to asteroid...aa gi|91083987|ref|XP_975212.1| PREDICTED: similar to asteroid CG4426-PA [Tribolium castaneum] FS761536 fufe ...

  14. EST Table: FS938903 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS938903 E_FL_fwgP_53F15_F_0 10/09/28 60 %/190 aa ref|XP_968396.2| PREDICTED: similar to failed...0 aa gi|189235487|ref|XP_968396.2| PREDICTED: similar to failed axon connections protein [Tribolium castaneum] FS937483 fwgP ...

  15. EST Table: FS939195 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS939195 E_FL_fwgP_54D09_F_0 10/09/28 59 %/184 aa ref|XP_968396.2| PREDICTED: similar to failed...4 aa gi|189235487|ref|XP_968396.2| PREDICTED: similar to failed axon connections protein [Tribolium castaneum] FS937483 fwgP ...

  16. EST Table: FS919410 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919410 E_FL_fufe_47E05_F_0 11/12/09 GO hit GO:0005515(protein binding) 10/09/28 4...015218|gb|EFA11666.1| hypothetical protein TcasGA2_TC008530 [Tribolium castaneum] FS919410 fufe ...

  17. EST Table: FS913232 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS913232 E_FL_fufe_28J15_F_0 11/12/09 GO hit GO:0003824(catalytic activity)|GO:0009...|189237620|ref|XP_969707.2| PREDICTED: similar to GA10348-PA [Tribolium castaneum] FS913232 fufe ...

  18. EST Table: FS932932 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS932932 E_FL_fwgP_35K07_F_0 10/09/28 72 %/148 aa ref|NP_001166687.1| cuticular pro...mology 10/08/29 n.h 10/09/10 low homology 10/09/10 low homology 10/09/10 low homology FS934632 fwgP ...

  19. EST Table: FS832832 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS832832 E_FL_fmgV_41G24_R_0 11/12/09 GO hit GO:0003824(catalytic activity)|GO:0004...a gnl|Amel|GB18896-PA 10/09/10 39 %/281 aa gi|91091528|ref|XP_970224.1| PREDICTED: similar to beta-glucosidase [Tribolium castaneum] FS832832 fmgV ...

  20. EST Table: FS932732 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS932732 E_FL_fwgP_35B10_F_0 10/09/28 99 %/200 aa ref|NP_001091823.1| poly A bindin...75975.1| PREDICTED: similar to poly A binding protein isoform 4 [Tribolium castaneum] FS932483 fwgP ...

  1. EST Table: FS906357 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS906357 E_FL_fufe_07P06_F_0 10/09/28 89 %/170 aa gb|EFA11544.1| kurtz [Tribolium c...l|GB13683-PA 10/09/10 89 %/170 aa gi|270015096|gb|EFA11544.1| kurtz [Tribolium castaneum] FS911973 fufe ...

  2. EST Table: FS920442 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS920442 E_FL_fufe_50G21_F_0 10/09/28 41 %/229 aa ref|XP_969213.1| PREDICTED: similar to artemis...2-PA 10/09/10 41 %/229 aa gi|91090768|ref|XP_969213.1| PREDICTED: similar to artemis protein [Tribolium castaneum] FS920671 fufe ...

  3. EST Table: FS877907 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS877907 E_FL_ftes_11B10_F_0 10/09/28 42 %/170 aa ref|XP_969213.1| PREDICTED: similar to artemis...2-PA 10/09/10 42 %/170 aa gi|91090768|ref|XP_969213.1| PREDICTED: similar to artemis protein [Tribolium castaneum] FS920671 ftes ...

  4. EST Table: FS920671 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS920671 E_FL_fufe_51C07_F_0 11/12/09 n.h 10/09/28 40 %/240 aa ref|XP_969213.1| PREDICTED: similar to artemi... 40 %/240 aa gi|91090768|ref|XP_969213.1| PREDICTED: similar to artemis protein [Tribolium castaneum] FS920671 fufe ...

  5. EST Table: FS910111 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS910111 E_FL_fufe_19D22_F_0 10/09/28 73 %/268 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 73 %/268 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fufe ...

  6. EST Table: FS908191 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS908191 E_FL_fufe_13H10_F_0 10/09/28 76 %/234 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 76 %/234 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fufe ...

  7. EST Table: FS919087 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919087 E_FL_fufe_46E24_F_0 10/09/28 76 %/246 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 76 %/246 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fufe ...

  8. Fs-laser processing of polydimethylsiloxane

    Energy Technology Data Exchange (ETDEWEB)

    Atanasov, Petar A., E-mail: paatanas@ie.bas.bg; Nedyalkov, Nikolay N. [Institute of Electronics, Bulgarian Academy of Sciences, 72 Tsarigradsko Shose, Sofia 1784 (Bulgaria); Valova, Eugenia I.; Georgieva, Zhenya S.; Armyanov, Stefan A.; Kolev, Konstantin N. [Rostislaw Kaischew Institute of Physical Chemistry, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Block 11, Sofia 1113 (Bulgaria); Amoruso, Salvatore; Wang, Xuan; Bruzzese, Ricardo [CNR-SPIN, Dipartimento di Scienze Fisiche, Universita degli Studi di Napoli Federico II, Complesso Universitario di Monte S. Angelo, Via Cintia, I-80126 Napoli (Italy); Sawczak, Miroslaw; Śliwiński, Gerard [Photophysics Department, The Szewalski Institute, Polish Academy of Sciences, 14 Fiszera St, 80-231 Gdańsk (Poland)

    2014-07-14

    We present an experimental analysis on surface structuring of polydimethylsiloxane films with UV (263 nm) femtosecond laser pulses, in air. Laser processed areas are analyzed by optical microscopy, SEM, and μ-Raman spectroscopy. The laser-treated sample shows the formation of a randomly nanostructured surface morphology. μ-Raman spectra, carried out at both 514 and 785 nm excitation wavelengths, prior and after laser treatment allow evidencing the changes in the sample structure. The influence of the laser fluence on the surface morphology is studied. Finally, successful electro-less metallization of the laser-processed sample is achieved, even after several months from the laser-treatment contrary to previous observation with nanosecond pulses. Our findings address the effectiveness of fs-laser treatment and chemical metallization of polydimethylsiloxane films with perspective technological interest in micro-fabrication devices for MEMS and nano-electromechanical systems.

  9. MarFS-Requirements-Design-Configuration-Admin

    Energy Technology Data Exchange (ETDEWEB)

    Kettering, Brett Michael [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Grider, Gary Alan [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2015-07-08

    This document will be organized into sections that are defined by the requirements for a file system that presents a near-POSIX (Portable Operating System Interface) interface to the user, but whose data is stored in whatever form is most efficient for the type of data being stored. After defining the requirement the design for meeting the requirement will be explained. Finally there will be sections on configuring and administering this file system. More and more, data dominates the computing world. There is a “sea” of data out there in many different formats that needs to be managed and used. “Mar” means “sea” in Spanish. Thus, this product is dubbed MarFS, a file system for a sea of data.

  10. Monolithic columns in plant proteomics and metabolomics.

    Science.gov (United States)

    Rigobello-Masini, Marilda; Penteado, José Carlos Pires; Masini, Jorge Cesar

    2013-03-01

    Since "omics" techniques emerged, plant studies, from biochemistry to ecology, have become more comprehensive. Plant proteomics and metabolomics enable the construction of databases that, with the help of genomics and informatics, show the data obtained as a system. Thus, all the constituents of the system can be seen with their interactions in both space and time. For instance, perturbations in a plant ecosystem as a consequence of application of herbicides or exposure to pollutants can be predicted by using information gathered from these databases. Analytical chemistry has been involved in this scientific evolution. Proteomics and metabolomics are emerging fields that require separation, identification, and quantification of proteins, peptides, and small molecules of metabolites in complex biological samples. The success of this work relies on efficient chromatographic and electrophoretic techniques, and on mass spectrometric detection. This paper reviews recent developments in the use of monolithic columns, focusing on their applications in "top-down" and "bottom-up" approaches, including their use as supports for immobilization of proteolytic enzymes and their use in two-dimensional and multidimensional chromatography. Whereas polymeric columns have been predominantly used for separation of proteins and polypeptides, silica-based monoliths have been more extensively used for separation of small molecules of metabolites. Representative applications in proteomics and in analysis of plant metabolites are given and summarized in tables.

  11. High surface area, high permeability carbon monoliths

    Energy Technology Data Exchange (ETDEWEB)

    Lagasse, R.R.; Schroeder, J.L. [Sandia National Labs., Albuquerque, NM (United States). Organic Materials Processing Dept.

    1994-12-31

    The goal of this work is to prepare carbon monoliths having precisely tailored pore size distribution. Prior studies have demonstrated that poly(acrylonitrile) can be processed into a precursor having tailored macropore structure. Since the macropores were preserved during pyrolysis, this synthetic process provided a route to porous carbon having macropores with size =0.1 to 10{mu}m. No micropores of size <2 nm could be detected in the carbon, however, by nitrogen adsorption. In the present work, the authors have processed a different polymer, poly(vinylidene chloride) into a macroporous precursor, Pyrolysis produced carbon monoliths having macropores derived from the polymer precursor as well as extensive microporosity produced during the pyrolysis of the polymer. One of these carbons had BET surface area of 1,050 m{sup 2}/g and about 1.2 cc/g total pore volume, with about 1/3 of the total pore volume in micropores and the remainder in 1{mu}m macropores. No mesopores in the intermediate size range could be detected by nitrogen adsorption. Carbon materials having high surface area as well as micron size pores have potential applications as electrodes for double layer supercapacitors containing liquid electrolyte, or as efficient media for performing chemical separations.

  12. Catastrophic failure of a monolithic zirconia prosthesis.

    Science.gov (United States)

    Chang, Jae-Seung; Ji, Woon; Choi, Chang-Hoon; Kim, Sunjai

    2015-02-01

    Recently, monolithic zirconia restorations have received attention as an alternative to zirconia veneered with feldspathic porcelain to eliminate chipping failures of veneer ceramics. In this clinical report, a patient with mandibular edentulism received 4 dental implants in the interforaminal area, and a screw-retained monolithic zirconia prosthesis was fabricated. The patient also received a maxillary complete removable dental prosthesis over 4 anterior roots. At the 18-month follow-up, all of the zirconia cylinders were seen to be fractured, and the contacting abutment surfaces had lost structural integrity. The damaged abutments were replaced with new abutments, and a new prosthesis was delivered with a computer-assisted design and computer-assisted manufacturing fabricated titanium framework with denture teeth and denture base resins. At the 6-month recall, the patient did not have any problems. Dental zirconia has excellent physical properties; however, care should be taken to prevent excessive stresses on the zirconia cylinders when a screw-retained zirconia restoration is planned as a definitive prosthesis.

  13. Preparation and Characterization of Temperature-responsive Porous Monoliths

    Institute of Scientific and Technical Information of China (English)

    ZHANG, Rongyue; QI, Li; XIN, Peiyong; YANG, Gengliang; CHEN, Yi

    2009-01-01

    A new temperature-responsive porous monolith has been prepared by surface-initiated activators generated by electron transfer atom transfer radical polymerization (AGET ATRP) grafting poly(N-isopropylacrylamide) (PNIPAAm) within the pores of the porous polymer monolith. The grafting copolymerization was carried out by a method based on a continuous flow-through technique without special deoxygenation procedure needed in the general ATRP. The addition of ascorbic acid could counteract the oxidation effect of oxygen diffusing into the reaction system. The resulting grafted monolith was characterized by a mercury intrusion method and the size of macropore was 3.65 μm, which was suitable for flow through the monolith for HPLC. The thermally responsive property of the grafted monolith was evaluated by HPLC using steroids with various hydrophobicities as probes. Through determination of retention factor of each steroid on the grafted monolith at different temperatures using water as mobile phase, it was found that the slope of the plot of retention factor of each steroid versus the temperature changed around the low critical solution temperature (LCST, 32 ℃) of PNIPAAm in water. It was relative to the grafted PNIPAAm temperature sensitivity that a hydrophobic and hydrophilic alternation would take place around its LCST.Based on this thermally responsive property, the grafted monolith was used as stationary phase for HPLC and to separate the steroids using water as mobile phase by changing the column temperature. As a mobile phase, water is much better than organic solvents concerning the environment.

  14. Influence of different carbon monolith preparation parameters on pesticide adsorption

    Directory of Open Access Journals (Sweden)

    Vukčević Marija

    2013-01-01

    Full Text Available The capacity of carbon monolith for pesticide removal from water, and the mechanism of pesticide interaction with carbon surface were examined. Different carbon monolith samples were obtained by varying the carbonization and activation parameters. In order to examine the role of surface oxygen groups in pesticide adsorption, carbon monolith surface was functionalized by chemical treatment in HNO3, H2O2 and KOH. The surface properties of the obtained samples were investigated by BET surface area, pore size distribution and temperature-programmed desorption. Adsorption of pesticides from aqueous solution onto activated carbon monolith samples was studied by using five pesticides belonging to different chemical groups (acetamiprid, dimethoate, nicosulfuron, carbofuran and atrazine. Presented results show that higher temperature of carbonization and the amount of activating agent allow obtaining microporous carbon monolith with higher amount of surface functional groups. Adsorption properties of the activated carbon monolith were more readily affected by the amount of the surface functional groups than by specific surface area. Results obtained by carbon monolith functionalisation showed that π-π interactions were the main force for adsorption of pesticides with aromatic structure, while acidic groups play an important role in adsorption of pesticides with no aromatic ring in the chemical structure.

  15. Hierarchically Structured Monolithic ZSM-5 through Macroporous Silica Gel Zeolitization

    Institute of Scientific and Technical Information of China (English)

    Lei Qian; Zhao Tianbo; Li Fengyan; Zong Baoning; Tong Yangchuan

    2006-01-01

    The hierarchically structured ZSM-5 monolith was prepared through transforming the skeletons of the macroporous silica gel into ZSM-5 by the steam-assisted conversion method. The morphology and monolithic shapes of macroporous silica gel were well preserved. The hierarchically structured ZSM-5 monolith exhibited the hierarchical porosity, with mesopores and macropores existing inside the macroporous silica gel, and micropores formed by the ZSM-5. The products have been characterized properly by using the XRD, SEM and N2 adsorption-desorption methods.

  16. Preparation of carbon monoliths from orange peel for NOx retention

    Directory of Open Access Journals (Sweden)

    Liliana Giraldo

    2014-12-01

    Full Text Available A series of monoliths are prepared from orange peels and chemically activated with H3PO4, KOH, ZnCl2, and water vapor without a binder. The monoliths were characterized by N2 adsorption-desorption isotherms at 77 K, Boehm titrations and XPS. Thereafter, monoliths were tested for their ability to establish NOx retention. The results show that the retention capacities of NOx were a function of the textural properties and chemistries. The carbons synthesized with ZnCl2 and KOH retained similar amounts of NOx.

  17. On monolithic stability and reinforcement analysis of high arch dams

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Monolithic stability safety and reinforcement based on monolithic stability are very important for arch dam design.In this paper,the issue is addressed based on deformation reinforcement theory.In this approach,plastic complementary energy norm can be taken as safety Index for monolithic stability.According to deformation reinforcement theory,the areas where unbalanced force exists require reinforcement,and the required reinforcement forces are just the unbalanced forces with opposite direction.Results show that areas with unbalanced force mainly concentrate in dam-toes,dam-heels and faults.

  18. Preliminary comparison of monolithic and aperture optics for XRMF

    Energy Technology Data Exchange (ETDEWEB)

    Havrilla, G.J.; Worley, C.G.

    1997-08-01

    Comparisons between standard aperture optics and a custom designed monolithic capillary x-ray optic for the Kevex Omicron are presented. The results demonstrate the feasibility of retrofitting an Omicron with a monolithic capillary. Increased flux is observed especially at lower energies which results in an increase in sensitivity and potentially an increase in spatial resolution. Alignment is a critical factor in achieving optimal performance of the monolithic capillary. Further improvements in flux output, spot size and overall sensitivity are expected with better alignment.

  19. A decoupled monolithic projection method for natural convection problems

    Science.gov (United States)

    Pan, Xiaomin; Kim, Kyoungyoun; Lee, Changhoon; Choi, Jung-Il

    2016-06-01

    We propose an efficient monolithic numerical procedure based on a projection method for solving natural convection problems. In the present monolithic method, the buoyancy, linear diffusion, and nonlinear convection terms are implicitly advanced by applying the Crank-Nicolson scheme in time. To avoid an otherwise inevitable iterative procedure in solving the monolithic discretized system, we use a linearization of the nonlinear convection terms and approximate block lower-upper (LU) decompositions along with approximate factorization. Numerical simulations demonstrate that the proposed method is more stable and computationally efficient than other semi-implicit methods, preserving temporal second-order accuracy.

  20. Machining distortion prediction of aerospace monolithic components

    Institute of Scientific and Technical Information of China (English)

    Yun-bo BI; Qun-lin CHENG; Hui-yue DONG; Ying-lin KE

    2009-01-01

    To predict the distortion of aerospace monolithic components.a model is established to simulate the numerical control (NC)milling process using 3D finite element method(FEM).In this model,the cutting layer is simplified firstly.Then,the models of cutting force and cutting temperature are established to gain the cutting loads,which are applied to the mesh model of the part.Finally,a prototype of machining simulation environment is developed to simulate the milling process of a spar.Key factors influencing the distortion,such as initial residual stress,cutting loads,fixture layout,cutting sequence,and tool path are considered all together.The total distortion of the spar is predicted and an experiment is conducted to validate the numerical results.It is found that the maximum discrepancy between the simulation results and experiment values is 19.0%

  1. A monolithic thin film electrochromic window

    Energy Technology Data Exchange (ETDEWEB)

    Goldner, R.B.; Arntz, F.O.; Berera, G.; Haas, T.E.; Wong, K.K. (Tufts Univ., Medford, MA (United States). Electro-Optics Technology Center); Wei, G. (Mobil Solar Energy Corp., Billerica, MA (United States)); Yu, P.C. (PPG Industries, Inc., Monroeville, PA (United States))

    1991-01-01

    Three closely related thin film solid state ionic devices that are potentially important for applications are: electrochromic smart windows, high energy density thin film rechargeable batteries, and thin film electrochemical sensors. Each usually has at least on mixed ion/electron conductor, an electron-blocking ion conductor, and an ion-blocking electron conductor, and many of the technical issues associated with thin film solid state ionics are common to all three devices. Since the electrochromic window has the added technical requirement of electrically-controlled optical modulation, (over the solar spectrum), and since research at the authors' institution has focused primarily on the window structure, this paper will address the electrochromic window, and particularly a monolithic variable reflectivity electrochromic window, as an illustrative example of some of the challenges and opportunities that are confronting the thin film solid state ionics community. 33 refs.

  2. A monolithic thin film electrochromic window

    Energy Technology Data Exchange (ETDEWEB)

    Goldner, R.B.; Arntz, F.O.; Berera, G.; Haas, T.E.; Wong, K.K. [Tufts Univ., Medford, MA (United States). Electro-Optics Technology Center; Wei, G. [Mobil Solar Energy Corp., Billerica, MA (United States); Yu, P.C. [PPG Industries, Inc., Monroeville, PA (United States)

    1991-12-31

    Three closely related thin film solid state ionic devices that are potentially important for applications are: electrochromic smart windows, high energy density thin film rechargeable batteries, and thin film electrochemical sensors. Each usually has at least on mixed ion/electron conductor, an electron-blocking ion conductor, and an ion-blocking electron conductor, and many of the technical issues associated with thin film solid state ionics are common to all three devices. Since the electrochromic window has the added technical requirement of electrically-controlled optical modulation, (over the solar spectrum), and since research at the authors` institution has focused primarily on the window structure, this paper will address the electrochromic window, and particularly a monolithic variable reflectivity electrochromic window, as an illustrative example of some of the challenges and opportunities that are confronting the thin film solid state ionics community. 33 refs.

  3. Monolithically Peltier-cooled laser diodes

    Energy Technology Data Exchange (ETDEWEB)

    Hava, S.; Hunsperger, R.G.; Sequeira, H.B.

    1984-04-01

    A new method of cooling a GaAs/GaAlAs laser in an optical integrated circuit or on a discrete chip, by adding an integral thermoelectric (Peltier) cooling and heat spreading device to the laser, is presented. This cooling both reduces and stabilizes the laser junction temperature to minimize such deleterious effects as wavelength drift due to heating. A unified description of the electrical and thermal properties of a monolithic semiconductor mesa structure is given. Here it is shown that an improvement in thermal characteristics is obtained by depositing a relatively thick metallic layer, and by using this layer as a part of an active Peltier structure. Experimental results reveal a 14-percent increase in emitted power (external quantum efficiency) due to passive heat spreading and a further 8-percent if its Peltier cooler is operated. Fabrication techniques used to obtain devices exhibiting the above performance characteristics are given. 21 references.

  4. LSST primary/tertiary monolithic mirror

    Science.gov (United States)

    Sebag, J.; Gressler, W.; Liang, M.; Neill, D.; Araujo-Hauck, C.; Andrew, J.; Angeli, G.; Cho, M.; Claver, C.; Daruich, F.; Gessner, C.; Hileman, E.; Krabbendam, V.; Muller, G.; Poczulp, G.; Repp, R.; Wiecha, O.; Xin, B.; Kenagy, K.; Martin, H. M.; Tuell, M. T.; West, S. C.

    2016-08-01

    At the core of the Large Synoptic Survey Telescope (LSST) three-mirror optical design is the primary/tertiary (M1M3) mirror that combines these two large mirrors onto one monolithic substrate. The M1M3 mirror was spin cast and polished at the Steward Observatory Mirror Lab at The University of Arizona (formerly SOML, now the Richard F. Caris Mirror Lab at the University of Arizona (RFCML)). Final acceptance of the mirror occurred during the year 2015 and the mirror is now in storage while the mirror cell assembly is being fabricated. The M1M3 mirror will be tested at RFCML after integration with its mirror cell before being shipped to Chile.

  5. Solid oxide fuel cell having monolithic core

    Science.gov (United States)

    Ackerman, J. P.; Young, J. E.

    1983-10-01

    A solid oxide fuel cell is described for electrochemically combining fuel and oxidant for generating galvanic output, wherein the cell core has an array of electrolyte and interconnect walls that are substantially devoid of any composite inert materials for support. The core is monolithic, where each electrolyte wall consists of thin layers of cathode and anode materials sandwiching a thin layer of electrolyte material. The electrolyte walls are arranged and backfolded between adjacent interconnect walls operable to define a plurality of core passageways alternately arranged where the inside faces have only the anode material or only the cathode material exposed. Each layer of the electrolyte and interconnect materials 0.002 to 0.01 cm thick; and each layer of the cathode and anode materials is 0.002 to 0.05 cm thick.

  6. Strongly Semicontinuous Domains and Semi-FS Domains

    Directory of Open Access Journals (Sweden)

    Qingyu He

    2014-01-01

    Full Text Available We are mainly concerned with some special kinds of semicontinuous domains and relationships between them. New concepts of strongly semicontinuous domains, meet semicontinuous domains and semi-FS domains are introduced. It is shown that a dcpo L is strongly semicontinuous if and only if L is semicontinuous and meet semicontinuous. It is proved that semi-FS domains are strongly semicontinuous. Some interpolation properties of semiway-below relations in (strongly semicontinuous bc-domains are given. In terms of these properties, it is proved that strongly semicontinuous bc-domains, in particular strongly semicontinuous lattices, are all semi-FS domains.

  7. Monolithic CMOS pixel detector for international linear collider vertex detection

    Indian Academy of Sciences (India)

    J E Brau; O Igonkina; N Sinew; D Strom; C Baltay; W Emmet; H Neal; D Rabinowitz

    2007-12-01

    A monolithic CMS pixel detector is under development for an ILC experiment. This chronopixel array provides a time stamp resolution of one bunch crossing, a critical feature for background suppression. The status of this effort is summarized.

  8. Monolithic Rare Earth Doped PTR Glass Laser Project

    Data.gov (United States)

    National Aeronautics and Space Administration — The main goal of the project is to demonstrate the feasibility of a monolithic solid state laser on the basis of PTR glass co-doped with luminescent rare earth ions....

  9. Plant oil-based shape memory polymer using acrylic monolith

    Directory of Open Access Journals (Sweden)

    T. Tsujimoto

    2015-09-01

    Full Text Available This article deals with the synthesis of a plant oil-based material using acrylic monolith. An acrylic monolith bearing oxirane groups was prepared via simple technique that involved the dissolution of poly(glycidyl methacrylate-comethyl methacrylate (PGMA in ethanolic – aqueous solution by heating and subsequent cooling. The PGMA monolith had topologically porous structure, which was attributed to the phase separation of the polymer solution. The PGMA monolith was impregnated by epoxidized soybean oil (ESO containing thermally-latent catalyst, and the subsequent curing produced a crosslinked material with relatively good transparency. The Young’s modulus and the tensile strength of polyESO/PGMA increased compared with the ESO homopolymer. The strain at break of polyESO/PGMA was larger than that of the ESO homopolymer and crosslinked PGMA. Furthermore, polyESO/PGMA exhibited good shape memory-recovery behavior.

  10. Reliability Analysis and Optimal Design of Monolithic Vertical Wall Breakwaters

    DEFF Research Database (Denmark)

    Sørensen, John Dalsgaard; Burcharth, Hans F.; Christiani, E.

    1994-01-01

    Reliability analysis and reliability-based design of monolithic vertical wall breakwaters are considered. Probabilistic models of the most important failure modes, sliding failure, failure of the foundation and overturning failure are described . Relevant design variables are identified and relia......Reliability analysis and reliability-based design of monolithic vertical wall breakwaters are considered. Probabilistic models of the most important failure modes, sliding failure, failure of the foundation and overturning failure are described . Relevant design variables are identified...

  11. Sol-Gel Synthesis of Non-Silica Monolithic Materials

    Directory of Open Access Journals (Sweden)

    Bartłomiej Gaweł

    2010-04-01

    Full Text Available Monolithic materials have become very popular because of various applications, especially within chromatography and catalysis. Large surface areas and multimodal porosities are great advantages for these applications. New sol-gel preparation methods utilizing phase separation or nanocasting have opened the possibility for preparing materials of other oxides than silica. In this review, we present different synthesis methods for inorganic, non-silica monolithic materials. Some examples of application of the materials are also included.

  12. Extended Leach Testing of Simulated LAW Cast Stone Monoliths

    Energy Technology Data Exchange (ETDEWEB)

    Serne, R. Jeffrey [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Westsik, Joseph H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Williams, Benjamin D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Jung, H. B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Wang, Guohui [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-07-09

    This report describes the results from long-term laboratory leach tests performed at Pacific Northwest National Laboratory (PNNL) for Washington River Protection Solutions (WRPS) to evaluate the release of key constituents from monoliths of Cast Stone prepared with four simulated low-activity waste (LAW) liquid waste streams. Specific objectives of the Cast Stone long-term leach tests described in this report focused on four activities: 1. Extending the leaching times for selected ongoing EPA-1315 tests on monoliths made with LAW simulants beyond the conventional 63-day time period up to 609 days reported herein (with some tests continuing that will be documented later) in an effort to evaluate long-term leaching properties of Cast Stone to support future performance assessment activities. 2. Starting new EPA-1315 leach tests on archived Cast Stone monoliths made with four LAW simulants using two leachants (deionized water [DIW] and simulated Hanford Integrated Disposal Facility (IDF) Site vadose zone pore water [VZP]). 3. Evaluating the impacts of varying the iodide loading (starting iodide concentrations) in one LAW simulant (7.8 M Na Hanford Tank Waste Operations Simulator (HTWOS) Average) by manufacturing new Cast Stone monoliths and repeating the EPA-1315 leach tests using DIW and the VZP leachants. 4. Evaluating the impacts of using a non-pertechnetate form of Tc that is present in some Hanford tanks. In this activity one LAW simulant (7.8 M Na HTWOS Average) was spiked with a Tc(I)-tricarbonyl gluconate species and then solidified into Cast Stone monoliths. Cured monoliths were leached using the EPA-1315 leach protocol with DIW and VZP. The leach results for the Tc-Gluconate Cast Stone monoliths were compared to Cast Stone monoliths pertechnetate.

  13. EST Table: FS796464 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ar to putative lysosomal glucocerebrosidase [Tribolium castaneum] 10/09/09 32 %/334 aa FBpp0237202|DvirGJ227...milar to putative lysosomal glucocerebrosidase [Tribolium castaneum] FS796494 ffbm ...

  14. EST Table: FS759318 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 25 aa ref|XP_975608.1| PREDICTED: similar to putative lysosomal glucocerebrosidas...%/225 aa gi|91087345|ref|XP_975608.1| PREDICTED: similar to putative lysosomal glucocerebrosidase [Tribolium castaneum] FS759318 fcaL ...

  15. Destruction of PCDD/Fs by gliding arc discharges

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    PCDD/Fs have been become a serious issue because of their lexicological effects and associated adverse health implications. In this study, the gliding arc plasma was tested for treatment of polychlorinated dibenzo-p-dioxins (PCDDs) and pol ychlorinated dibenzofurans (PCDFs), which was synthesized from pentachlorophenol in atmospheric condition at 350℃ with or without the catalysis of CuCh-From the experiment, we found that the destruction efficiency of PCDD/F homologues after gliding was discharge ranged from 25% to 79%. This result demonstrates that gliding arc plasma is an effective technology to decompose PCDDs/Fs in flue gas. A plausible degradation mechanism for PCDD/Fs by gliding arc was discussed. Finally, a multistage reactor structure of gliding arc was proposed to upgrade removal efficiency for PCDD/Fs.

  16. Nonlinear light propagation in fs laser-written waveguide arrays

    Directory of Open Access Journals (Sweden)

    Szameit A.

    2013-11-01

    Full Text Available We report on recent achievements in the field of nonlinear light propagation in fs laser-written waveguide lattices. Particular emphasis is thereby given on discrete solitons in such systems.

  17. EST Table: FS879118 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available milar to Ubiquitin-conjugating enzyme E2-17 kDa (Ubiquitin-protein ligase) (Ubiquitin carrier protein) (Protein effet...se) (Ubiquitin carrier protein) (Protein effete) [Tribolium castaneum] FS793905 ftes ...

  18. EST Table: FS748350 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available PREDICTED: similar to fetal alzheimer antigen, falz [Nasonia vitripennis] 10/09/08 37 %/193 aa FBpp0290563|E...811424.1| PREDICTED: similar to fetal alzheimer antigen, falz [Tribolium castaneum] FS748350 caL- ...

  19. EST Table: FS731272 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available DICTED: similar to Protein SDA1 homolog (Mystery protein 45A) [Tribolium castaneum] gb|EFA00563.1| hypotheti...imilar to Protein SDA1 homolog (Mystery protein 45A) [Tribolium castaneum] FS731272 bmmt ...

  20. EST Table: FS745067 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available DICTED: similar to Protein SDA1 homolog (Mystery protein 45A) [Tribolium castaneum] gb|EFA00563.1| hypotheti...imilar to Protein SDA1 homolog (Mystery protein 45A) [Tribolium castaneum] FS745067 bmmt ...

  1. EST Table: FS929848 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available DICTED: similar to Low density lipoprotein receptor adapter protein 1 (Autosomal recessive hypercholesterole...1| PREDICTED: similar to Low density lipoprotein receptor adapter protein 1 (Autosomal recessive hypercholesterolemia protein) isoform 1 [Tribolium castaneum] FS929848 fwgP ...

  2. EST Table: FS936166 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ar to Low density lipoprotein receptor adapter protein 1 (Autosomal recessive hypercholesterolemia protein) ... similar to Low density lipoprotein receptor adapter protein 1 (Autosomal recessive hypercholesterolemia protein) isoform 1 [Tribolium castaneum] FS929848 fwgP ...

  3. Mechanically stable, hierarchically porous Cu3(btc)2 (HKUST-1) monoliths via direct conversion of copper(II) hydroxide-based monoliths.

    Science.gov (United States)

    Moitra, Nirmalya; Fukumoto, Shotaro; Reboul, Julien; Sumida, Kenji; Zhu, Yang; Nakanishi, Kazuki; Furukawa, Shuhei; Kitagawa, Susumu; Kanamori, Kazuyoshi

    2015-02-28

    The synthesis of highly crystalline macro-meso-microporous monolithic Cu3(btc)2 (HKUST-1; btc(3-) = benzene-1,3,5-tricarboxylate) is demonstrated by direct conversion of Cu(OH)2-based monoliths while preserving the characteristic macroporous structure. The high mechanical strength of the monoliths is promising for possible applications to continuous flow reactors.

  4. EST Table: FS926683 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS926683 E_FL_fwgP_17C05_F_0 10/09/28 92 %/204 aa ref|NP_001164152.1| held out wings...0 %/173 aa gnl|Amel|GB13678-PA 10/09/10 92 %/204 aa gi|270002790|gb|EEZ99237.1| held out wings [Tribolium castaneum] FS761805 fwgP ...

  5. EST Table: FS837816 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS837816 E_FL_fner_02D05_F_0 10/09/28 55 %/109 aa ref|XP_968887.1| PREDICTED: similar to cleft...gnl|Amel|GB16225-PA 10/09/10 55 %/109 aa gi|91081299|ref|XP_968887.1| PREDICTED: similar to cleft lip and palate transmembrane protein 1 [Tribolium castaneum] FS920349 fner ...

  6. EST Table: FS725996 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS725996 E_FL_bmmt_06E05_F_0 10/09/28 55 %/109 aa ref|XP_968887.1| PREDICTED: similar to cleft...gnl|Amel|GB16225-PA 10/09/10 55 %/109 aa gi|91081299|ref|XP_968887.1| PREDICTED: similar to cleft lip and palate transmembrane protein 1 [Tribolium castaneum] FS920349 bmmt ...

  7. EST Table: FS750430 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS750430 E_ET_caL-_01H08_R_0 10/09/28 65 %/149 aa ref|NP_001130045.1| flightin [Bom...byx mori] gb|ACI96114.1| flightin [Bombyx mori] 10/09/08 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 low homology FS783611 caL- ...

  8. EST Table: FS745476 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS745476 E_ET_caL-_01H08_F_0 10/09/28 57 %/128 aa ref|NP_001130045.1| flightin [Bom...byx mori] gb|ACI96114.1| flightin [Bombyx mori] 10/09/08 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS763751 caL- ...

  9. EST Table: FS802051 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS802051 E_FL_fmgV_08I20_F_0 10/09/28 62 %/109 aa ref|XP_001664237.1| breast cancer metastasis...-suppressor [Aedes aegypti] gb|EAT33713.1| breast cancer metastasis-suppressor [Aedes aegypti] 10...0 59 %/107 aa gi|91080755|ref|XP_966988.1| PREDICTED: similar to breast cancer metastasis-suppressor 1 [Tribolium castaneum] FS939099 fmgV ...

  10. EST Table: FS918672 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918672 E_FL_fufe_45B07_F_0 10/09/28 57 %/175 aa ref|XP_001664237.1| breast cancer metastasis...-suppressor [Aedes aegypti] gb|EAT33713.1| breast cancer metastasis-suppressor [Aedes aegypti] 10...0 57 %/173 aa gi|91080755|ref|XP_966988.1| PREDICTED: similar to breast cancer metastasis-suppressor 1 [Tribolium castaneum] FS939099 fufe ...

  11. EST Table: FS808745 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS808745 E_FL_fmgV_27D04_F_0 10/09/28 32 %/212 aa ref|XP_001865385.1| niemann-Pick ...C1 protein [Culex quinquefasciatus] gb|EDS41634.1| niemann-Pick C1 protein [Culex quinquefasciatus] 10/09/09.../10 30 %/210 aa gi|189241956|ref|XP_967619.2| PREDICTED: similar to niemann-pick C1 [Tribolium castaneum] FS803743 fmgV ...

  12. EST Table: FS766125 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available similar to Myosin-IA (MIA) (Brush border myosin IA) (BBMIA) [Tribolium castaneum] FS929464 fcaL ... ...FS766125 E_FL_fcaL_41P06_F_0 10/09/28 63 %/144 aa ref|XP_966392.1| PREDICTED: simil...ar to Myosin-IA (MIA) (Brush border myosin IA) (BBMIA) [Tribolium castaneum] gb|EFA08265.1| hypothetical pro

  13. EST Table: FS811016 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS811016 E_FL_fmgV_33J07_F_0 11/12/09 GO hit GO:0005328(neurotransmitter:sodium sym...66 aa gnl|Amel|GB18422-PA 10/09/10 57 %/127 aa gi|270012260|gb|EFA08708.1| hypothetical protein TcasGA2_TC006379 [Tribolium castaneum] FS811016 fmgV ...

  14. EST Table: FS861101 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS861101 E_FL_fner_15B20_R_0 11/12/09 GO hit GO:0005576(extracellular region) 10/09...K lipoprotein precursor [Bombyx mori] 10/09/11 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS861101 fner ...

  15. EST Table: FS919842 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919842 E_FL_fufe_48J09_F_0 11/12/09 GO hit GO:0003735(structural constituent of r...-1|gene:AGAP000508 10/09/10 60 %/164 aa gnl|Amel|GB10944-PA 10/09/10 60 %/187 aa gi|189236859|ref|XP_974352.2| PREDICTED: similar to GA18397-PA [Tribolium castaneum] FS919842 fufe ...

  16. EST Table: FS894471 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS894471 E_FL_ftes_15C05_R_0 10/09/28 47 %/260 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...DICTED: similar to Outer dense fiber protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS893448 ftes ...

  17. EST Table: FS901584 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS901584 E_FL_ftes_43M21_R_0 10/09/28 35 %/178 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...DICTED: similar to Outer dense fiber protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS893448 ftes ...

  18. EST Table: FS893822 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS893822 E_FL_ftes_12P11_R_0 10/09/28 47 %/258 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...DICTED: similar to Outer dense fiber protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS893448 ftes ...

  19. EST Table: FS790109 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 86181|ref|XP_971039.1| PREDICTED: similar to scaffold protein salvador (shar-pei) [Tribolium castaneum] FS920136 ffbm ... ...ar to scaffold protein salvador (shar-pei) [Tribolium castaneum] 10/09/09 31 %/225 aa FBpp0159976|DmojGI1075...FS790109 E_FL_ffbm_02K08_F_0 10/09/28 37 %/312 aa ref|XP_971039.1| PREDICTED: simil

  20. EST Table: FS935751 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 86181|ref|XP_971039.1| PREDICTED: similar to scaffold protein salvador (shar-pei) [Tribolium castaneum] FS920136 fwgP ... ...ar to scaffold protein salvador (shar-pei) [Tribolium castaneum] 10/09/13 30 %/208 aa FBpp0159976|DmojGI1075...FS935751 E_FL_fwgP_43P13_F_0 10/09/28 37 %/295 aa ref|XP_971039.1| PREDICTED: simil

  1. EST Table: FS768368 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS768368 E_FL_fcaL_48N17_F_0 10/09/28 78 %/215 aa ref|NP_001161754.1| integrin beta...otein|X:14937399:14948907:1|gene:INTB 10/09/10 40 %/194 aa gnl|Amel|GB19541-PA 10/09/10 43 %/192 aa gi|270014241|gb|EFA10689.1| myospheroid [Tribolium castaneum] FS932451 fcaL ...

  2. EST Table: FS844440 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS844440 E_FL_fner_20M15_F_0 10/09/28 100 %/207 aa gb|ACY95331.1| ribosomal protein...0 90 %/207 aa gnl|Amel|GB17629-PA 10/09/10 88 %/207 aa gi|91083393|ref|XP_967983.1| PREDICTED: similar to ribosomal protein L8e [Tribolium castaneum] FS794442 fner ...

  3. EST Table: FS738267 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS738267 E_FL_bmmt_11C08_R_0 10/09/28 80 %/137 aa gb|ACT36277.1| antitrypsin isofor...m 2 [Bombyx mori] gb|ACT36279.1| antitrypsin isoform 4 [Bombyx mori] 10/09/07 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS783140 bmmt ...

  4. EST Table: FS905729 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS905729 E_FL_fufe_05P17_F_0 10/09/28 64 %/289 aa ref|XP_968073.1| PREDICTED: similar to Longevity...gene:AGAP001761 10/09/10 n.h 10/09/10 64 %/289 aa gi|91087843|ref|XP_968073.1| PREDICTED: similar to Longevity assurance gene 1 CG3576-PB [Tribolium castaneum] FS764148 fufe ...

  5. EST Table: FS771867 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS771867 E_FL_fcaL_23K08_F_0 10/09/28 87 %/139 aa ref|XP_001659698.1| liquid facets... [Aedes aegypti] gb|EAT39088.1| liquid facets [Aedes aegypti] 10/09/08 88 %/136 aa FBpp0227429|DvirGJ13012-P... %/143 aa gi|189240526|ref|XP_972038.2| PREDICTED: similar to liquid facets [Tribolium castaneum] FS840960 fcaL ...

  6. EST Table: FS840960 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS840960 E_FL_fner_11A09_F_0 11/12/09 n.h 10/09/28 87 %/139 aa ref|XP_001659698.1| liquid... facets [Aedes aegypti] gb|EAT39088.1| liquid facets [Aedes aegypti] 10/09/10 88 %/136 aa FBpp0227429|...A 10/09/10 84 %/143 aa gi|189240526|ref|XP_972038.2| PREDICTED: similar to liquid facets [Tribolium castaneum] FS840960 fner ...

  7. EST Table: FS896014 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS896014 E_FL_ftes_20I10_R_0 10/09/28 46 %/262 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...DICTED: similar to Outer dense fiber protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS893448 ftes ...

  8. EST Table: FS801980 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS801980 E_FL_fmgV_08F19_F_0 10/09/28 42 %/152 aa ref|XP_001648294.1| Juvenile horm...one-inducible protein, putative [Aedes aegypti] gb|EAT44634.1| Juvenile hormone-inducible protein, putative ...|GB15308-PA 10/09/10 34 %/148 aa gi|91080979|ref|XP_974925.1| PREDICTED: similar to Juvenile hormone-inducible protein, putative [Tribolium castaneum] FS808716 fmgV ...

  9. EST Table: FS816465 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS816465 E_FL_fmgV_48K22_F_0 10/09/28 43 %/181 aa ref|XP_001648294.1| Juvenile horm...one-inducible protein, putative [Aedes aegypti] gb|EAT44634.1| Juvenile hormone-inducible protein, putative ...|GB15308-PA 10/09/10 37 %/178 aa gi|91080979|ref|XP_974925.1| PREDICTED: similar to Juvenile hormone-inducible protein, putative [Tribolium castaneum] FS808716 fmgV ...

  10. EST Table: FS913793 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS913793 E_FL_fufe_30F13_F_0 10/09/28 41 %/299 aa ref|XP_001648294.1| Juvenile horm...one-inducible protein, putative [Aedes aegypti] gb|EAT44634.1| Juvenile hormone-inducible protein, putative ...|GB15308-PA 10/09/10 38 %/286 aa gi|91080979|ref|XP_974925.1| PREDICTED: similar to Juvenile hormone-inducible protein, putative [Tribolium castaneum] FS808716 fufe ...

  11. EST Table: FS760335 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS760335 E_FL_fcaL_14A08_F_0 10/09/28 42 %/192 aa ref|XP_001648294.1| Juvenile horm...one-inducible protein, putative [Aedes aegypti] gb|EAT44634.1| Juvenile hormone-inducible protein, putative ...|GB15308-PA 10/09/10 38 %/184 aa gi|91080979|ref|XP_974925.1| PREDICTED: similar to Juvenile hormone-inducible protein, putative [Tribolium castaneum] FS808716 fcaL ...

  12. EST Table: FS747012 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS747012 E_ET_caL-_07O17_F_0 10/09/28 39 %/183 aa ref|XP_971046.2| PREDICTED: similar to antolefin... %/135 aa gnl|Amel|GB16043-PA 10/09/10 39 %/183 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS921551 caL- ...

  13. EST Table: FS752084 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available P_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS752084 caL- ... ...FS752084 E_ET_caL-_07O17_R_0 11/12/09 n.h 10/09/28 39 %/198 aa ref|XP_971046.2| PREDICTED: similar to antole...finin [Tribolium castaneum] 10/09/08 34 %/152 aa FBpp0116483|DanaGF13291-PA 10/08/2

  14. EST Table: FS899341 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS899341 E_FL_ftes_34E24_R_0 10/09/28 39 %/198 aa ref|XP_971046.2| PREDICTED: similar to antolefin...0 low homology 10/09/10 39 %/152 aa gnl|Amel|GB16043-PA 10/09/10 39 %/198 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS752084 ftes ...

  15. EST Table: FS864234 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS864234 E_FL_fner_24L14_R_0 10/09/28 38 %/198 aa ref|XP_971046.2| PREDICTED: similar to antolefin...0 low homology 10/09/10 39 %/152 aa gnl|Amel|GB16043-PA 10/09/10 38 %/198 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS752084 fner ...

  16. EST Table: FS930987 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS930987 E_FL_fwgP_29N09_F_0 10/09/28 64 %/130 aa ref|XP_001865018.1| suppression of tumorigen...icity [Culex quinquefasciatus] gb|EDS41077.1| suppression of tumorigenicity [Culex quinquefasciat...09/10 62 %/130 aa gi|91091438|ref|XP_972410.1| PREDICTED: similar to suppression of tumorigenicity [Tribolium castaneum] FS881106 fwgP ...

  17. EST Table: FS881106 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS881106 E_FL_ftes_20G18_F_0 11/12/09 n.h 10/09/28 52 %/186 aa ref|XP_001865018.1| suppression of tumorigen...icity [Culex quinquefasciatus] gb|EDS41077.1| suppression of tumorigenicity [Culex q...B15913-PA 10/09/10 50 %/186 aa gi|91091438|ref|XP_972410.1| PREDICTED: similar to suppression of tumorigenicity [Tribolium castaneum] FS881106 ftes ...

  18. EST Table: FS910504 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS910504 E_FL_fufe_20G20_F_0 11/12/09 n.h 10/09/28 39 %/248 aa ref|XP_967337.1| PREDICTED: similar to Serge.../244 aa gnl|Amel|GB17309-PA 10/09/10 39 %/248 aa gi|91083383|ref|XP_967337.1| PREDICTED: similar to Sergef protein [Tribolium castaneum] FS910504 fufe ...

  19. EST Table: FS895931 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS895931 E_FL_ftes_20D04_R_0 10/09/28 48 %/263 aa ref|XP_975194.1| PREDICTED: similar to something about.../309 aa gnl|Amel|GB19080-PA 10/09/10 48 %/263 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 ftes ...

  20. EST Table: FS773374 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS773374 E_FL_fcaL_01E22_R_0 10/09/28 46 %/259 aa ref|XP_975194.1| PREDICTED: similar to something about.../265 aa gnl|Amel|GB19080-PA 10/09/10 46 %/259 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 fcaL ...

  1. EST Table: FS918452 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918452 E_FL_fufe_44G17_F_0 10/09/28 46 %/244 aa ref|XP_975194.1| PREDICTED: similar to something about.../253 aa gnl|Amel|GB19080-PA 10/09/10 46 %/244 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fufe ...

  2. EST Table: FS771043 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS771043 E_FL_fcaL_21B10_F_0 10/09/28 50 %/102 aa ref|XP_975194.1| PREDICTED: similar to something about.../109 aa gnl|Amel|GB19080-PA 10/09/10 50 %/102 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fcaL ...

  3. EST Table: FS783759 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS783759 E_FL_fcaL_45F03_R_0 10/09/28 49 %/292 aa ref|XP_975194.1| PREDICTED: similar to something about.../298 aa gnl|Amel|GB19080-PA 10/09/10 49 %/292 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 fcaL ...

  4. EST Table: FS787334 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS787334 E_FL_fcaL_21B10_R_0 10/09/28 47 %/229 aa ref|XP_975194.1| PREDICTED: similar to something about.../235 aa gnl|Amel|GB19080-PA 10/09/10 47 %/229 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 fcaL ...

  5. EST Table: FS756160 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS756160 E_FL_fcaL_01E22_F_0 10/09/28 45 %/124 aa ref|XP_975194.1| PREDICTED: similar to something about.../134 aa gnl|Amel|GB19080-PA 10/09/10 45 %/124 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fcaL ...

  6. EST Table: FS881026 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS881026 E_FL_ftes_20D04_F_0 10/09/28 48 %/142 aa ref|XP_975194.1| PREDICTED: similar to something about.../146 aa gnl|Amel|GB19080-PA 10/09/10 48 %/142 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 ftes ...

  7. EST Table: FS804514 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS804514 E_FL_fmgV_15G04_F_0 10/09/28 46 %/124 aa ref|XP_975194.1| PREDICTED: similar to something about.../134 aa gnl|Amel|GB19080-PA 10/09/10 46 %/124 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fmgV ...

  8. EST Table: FS877343 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS877343 E_FL_ftes_09I06_F_0 10/09/28 48 %/136 aa ref|XP_975194.1| PREDICTED: similar to something about.../146 aa gnl|Amel|GB19080-PA 10/09/10 48 %/136 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 ftes ...

  9. EST Table: FS772104 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS772104 E_FL_fcaL_24G15_F_0 10/09/28 50 %/114 aa ref|XP_975194.1| PREDICTED: similar to something about.../125 aa gnl|Amel|GB19080-PA 10/09/10 50 %/114 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fcaL ...

  10. EST Table: FS918257 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918257 E_FL_fufe_43N05_F_0 11/12/09 n.h 10/09/28 47 %/253 aa ref|XP_971977.1| PREDICTED: similar to reserv...277 aa gnl|Amel|GB11583-PA 10/09/10 47 %/253 aa gi|91086211|ref|XP_971977.1| PREDICTED: similar to reserved [Tribolium castaneum] FS918257 fufe ...

  11. EST Table: FS822271 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS822271 E_FL_fmgV_11P16_R_0 11/12/09 n.h 10/09/28 75 %/112 aa ref|XP_001656149.1| fetal alzhe...imer antigen, falz [Aedes aegypti] gb|EAT35210.1| fetal alzheimer antigen, falz [Aedes aegypti] 1...8 %/115 aa gi|189240808|ref|XP_001811424.1| PREDICTED: similar to fetal alzheimer antigen, falz [Tribolium castaneum] FS822271 fmgV ...

  12. EST Table: FS742012 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS742012 E_FL_bmmt_21K17_R_0 11/12/09 n.h 10/09/28 54 %/122 aa ref|XP_970450.1| PRE...gnl|Amel|GB11088-PA 10/09/10 54 %/122 aa gi|91084727|ref|XP_970450.1| PREDICTED: similar to CG3655 CG3655-PB [Tribolium castaneum] FS742012 bmmt ...

  13. EST Table: FS803120 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS803120 E_FL_fmgV_11I07_F_0 10/09/28 74 %/111 aa ref|NP_001034501.1| extradenticle... [Tribolium castaneum] emb|CAD57734.1| extradenticle [Tribolium castaneum] 10/09/09 68 %/113 aa FBpp0123364|...XD_ANOGA 10/09/10 low homology 10/09/10 74 %/111 aa gi|38490515|emb|CAD57734.1| extradenticle [Tribolium castaneum] FS924788 fmgV ...

  14. EST Table: FS871957 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS871957 E_FL_fner_46O21_R_0 11/12/09 n.h 10/09/28 47 %/211 aa gb|EFA02106.1| hypot...0809 10/09/10 49 %/213 aa gnl|Amel|GB16525-PA 10/09/10 47 %/211 aa gi|270005658|gb|EFA02106.1| hypothetical protein TcasGA2_TC007750 [Tribolium castaneum] FS871957 fner ...

  15. EST Table: FS849566 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS849566 E_FL_fner_35F20_F_0 10/09/28 57 %/111 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/11 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 low homology FS915193 fner ...

  16. EST Table: FS916464 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS916464 E_FL_fufe_38G11_F_0 10/09/28 54 %/242 aa ref|XP_972061.1| PREDICTED: similar to thymus... 10/09/10 58 %/212 aa gnl|Amel|GB19831-PA 10/09/10 54 %/242 aa gi|91078858|ref|XP_972061.1| PREDICTED: similar to thymus-specific serine protease [Tribolium castaneum] FS916293 fufe ...

  17. EST Table: FS770700 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS770700 E_FL_fcaL_20A18_F_0 10/09/28 99 %/164 aa ref|NP_001091766.1| fructose 1,6-...8 aa gnl|Amel|GB19460-PA 10/09/10 78 %/163 aa gi|270008484|gb|EFA04932.1| hypothetical protein TcasGA2_TC014998 [Tribolium castaneum] FS797404 fcaL ...

  18. EST Table: FS770170 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS770170 E_FL_fcaL_18G15_F_0 10/09/28 69 %/163 aa ref|NP_001166694.1| cuticular pro...0 %/135 aa gnl|Amel|GB12600-PA 10/09/10 46 %/136 aa gi|270001940|gb|EEZ98387.1| hypothetical protein TcasGA2_TC000851 [Tribolium castaneum] FS768607 fcaL ...

  19. EST Table: FS766762 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS766762 E_FL_fcaL_43O18_F_0 10/09/28 66 %/124 aa ref|NP_001165864.1| extended syna...2 aa gnl|Amel|GB16451-PA 10/09/10 66 %/124 aa gi|288869514|ref|NP_001165864.1| extended synaptotagmin-like protein 2a [Tribolium castaneum] FS756117 fcaL ...

  20. EST Table: FS734952 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS734952 E_FL_bmmt_01L24_R_0 10/09/28 44 %/134 aa ref|XP_970577.1| PREDICTED: similar to ganglios...2 10/09/10 n.h 10/09/10 44 %/134 aa gi|91078536|ref|XP_970577.1| PREDICTED: similar to ganglioside-induced differentiation-associated-protein 1 [Tribolium castaneum] FS741586 bmmt ...

  1. EST Table: FS820105 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS820105 E_FL_fmgV_05P05_R_0 10/09/28 43 %/144 aa ref|XP_970577.1| PREDICTED: similar to ganglios...2 10/09/10 n.h 10/09/10 43 %/144 aa gi|91078536|ref|XP_970577.1| PREDICTED: similar to ganglioside-induced differentiation-associated-protein 1 [Tribolium castaneum] FS741586 fmgV ...

  2. EST Table: FS823467 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS823467 E_FL_fmgV_15E11_R_0 10/09/28 40 %/161 aa ref|XP_970577.1| PREDICTED: similar to ganglios...2 10/09/10 n.h 10/09/10 40 %/161 aa gi|91078536|ref|XP_970577.1| PREDICTED: similar to ganglioside-induced differentiation-associated-protein 1 [Tribolium castaneum] FS741586 fmgV ...

  3. EST Table: FS740251 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS740251 E_FL_bmmt_16L03_R_0 10/09/28 42 %/143 aa ref|XP_970577.1| PREDICTED: similar to ganglios...2 10/09/10 n.h 10/09/10 42 %/143 aa gi|91078536|ref|XP_970577.1| PREDICTED: similar to ganglioside-induced differentiation-associated-protein 1 [Tribolium castaneum] FS741586 bmmt ...

  4. EST Table: FS743781 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS743781 E_FL_bmmt_26K02_R_0 10/09/28 45 %/125 aa ref|XP_970577.1| PREDICTED: similar to ganglios...2 10/09/10 n.h 10/09/10 45 %/125 aa gi|91078536|ref|XP_970577.1| PREDICTED: similar to ganglioside-induced differentiation-associated-protein 1 [Tribolium castaneum] FS741586 bmmt ...

  5. EST Table: FS734992 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS734992 E_FL_bmmt_01N18_R_0 10/09/28 45 %/125 aa ref|XP_970577.1| PREDICTED: similar to ganglios...2 10/09/10 n.h 10/09/10 45 %/125 aa gi|91078536|ref|XP_970577.1| PREDICTED: similar to ganglioside-induced differentiation-associated-protein 1 [Tribolium castaneum] FS741586 bmmt ...

  6. EST Table: FS823499 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS823499 E_FL_fmgV_15F21_R_0 10/09/28 45 %/131 aa ref|XP_970577.1| PREDICTED: similar to ganglios...2 10/09/10 n.h 10/09/10 45 %/131 aa gi|91078536|ref|XP_970577.1| PREDICTED: similar to ganglioside-induced differentiation-associated-protein 1 [Tribolium castaneum] FS741586 fmgV ...

  7. EST Table: FS739740 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS739740 E_FL_bmmt_15E02_R_0 10/09/28 43 %/144 aa ref|XP_970577.1| PREDICTED: similar to ganglios...2 10/09/10 n.h 10/09/10 43 %/144 aa gi|91078536|ref|XP_970577.1| PREDICTED: similar to ganglioside-induced differentiation-associated-protein 1 [Tribolium castaneum] FS741586 bmmt ...

  8. EST Table: FS860601 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS860601 E_FL_fner_13L02_R_0 10/09/28 69 %/112 aa ref|NP_001091750.1| ribosomal pro...#protein_id:AAK27864.1 10/09/10 60 %/110 aa AGAP007740-PA Protein|3R:173065:17380...1| PREDICTED: similar to 60S acidic ribosomal protein P1 [Tribolium castaneum] FS784781 fner ...

  9. EST Table: FS918214 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918214 E_FL_fufe_43K22_F_0 10/09/28 53 %/199 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fufe ...

  10. EST Table: FS730803 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS730803 E_FL_bmmt_19O18_F_0 10/09/28 54 %/206 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 bmmt ...

  11. EST Table: FS897753 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS897753 E_FL_ftes_28E17_R_0 10/09/28 47 %/256 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...DICTED: similar to Outer dense fiber protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS893448 ftes ...

  12. EST Table: FS903628 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS903628 E_FL_ftes_51L18_R_0 10/09/28 47 %/257 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...DICTED: similar to Outer dense fiber protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS893448 ftes ...

  13. EST Table: FS887803 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS887803 E_FL_ftes_40G04_F_0 10/09/28 35 %/122 aa ref|XP_967620.1| PREDICTED: similar to anopheles stephen... %/149 aa gnl|Amel|GB19565-PA 10/09/10 35 %/122 aa gi|91093471|ref|XP_967620.1| PREDICTED: similar to anopheles stephensi ubiquitin, putative [Tribolium castaneum] FS914988 ftes ...

  14. EST Table: FS900811 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS900811 E_FL_ftes_40G04_R_0 10/09/28 35 %/117 aa ref|XP_967620.1| PREDICTED: similar to anopheles stephen... %/144 aa gnl|Amel|GB19565-PA 10/09/10 35 %/117 aa gi|91093471|ref|XP_967620.1| PREDICTED: similar to anopheles stephensi ubiquitin, putative [Tribolium castaneum] FS788262 ftes ...

  15. EST Table: FS915066 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915066 E_FL_fufe_34C05_F_0 10/09/28 35 %/122 aa ref|XP_967620.1| PREDICTED: similar to anopheles stephen... %/149 aa gnl|Amel|GB19565-PA 10/09/10 35 %/122 aa gi|91093471|ref|XP_967620.1| PREDICTED: similar to anopheles stephensi ubiquitin, putative [Tribolium castaneum] FS914988 fufe ...

  16. EST Table: FS854155 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS854155 E_FL_fner_48F23_F_0 10/09/28 35 %/122 aa ref|XP_967620.1| PREDICTED: similar to anopheles stephen... %/149 aa gnl|Amel|GB19565-PA 10/09/10 35 %/122 aa gi|91093471|ref|XP_967620.1| PREDICTED: similar to anopheles stephensi ubiquitin, putative [Tribolium castaneum] FS914988 fner ...

  17. EST Table: FS934225 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS934225 E_FL_fwgP_39G18_F_0 10/09/28 34 %/122 aa ref|XP_967620.1| PREDICTED: similar to anopheles stephen... %/149 aa gnl|Amel|GB19565-PA 10/09/10 34 %/122 aa gi|91093471|ref|XP_967620.1| PREDICTED: similar to anopheles stephensi ubiquitin, putative [Tribolium castaneum] FS914988 fwgP ...

  18. EST Table: FS923067 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS923067 E_FL_fwgP_06H12_F_0 10/09/28 39 %/164 aa ref|XP_975114.2| PREDICTED: similar to almond...|Amel|GB17827-PA 10/09/10 39 %/164 aa gi|189239453|ref|XP_975114.2| PREDICTED: similar to almondex CG12127-PA [Tribolium castaneum] FS916326 fwgP ...

  19. EST Table: FS838350 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS838350 E_FL_fner_03K13_F_0 10/09/28 84 %/180 aa ref|XP_001651215.1| vitellogenin,... putative [Aedes aegypti] gb|EAT42854.1| vitellogenin, putative [Aedes aegypti] 10/09/10 70 %/207 aa FBpp027...gi|91086835|ref|XP_974078.1| PREDICTED: similar to vitellogenin, putative [Tribolium castaneum] FS729194 fner ...

  20. EST Table: FS922886 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922886 E_FL_fwgP_05P03_F_0 10/09/28 84 %/198 aa ref|XP_001847442.1| vitellogenin ...[Culex quinquefasciatus] gb|EDS26195.1| vitellogenin [Culex quinquefasciatus] 10/09/13 72 %/197 aa FBpp02478...206 aa gi|91086835|ref|XP_974078.1| PREDICTED: similar to vitellogenin, putative [Tribolium castaneum] FS729194 fwgP ...

  1. EST Table: FS938859 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS938859 E_FL_fwgP_53D14_F_0 10/09/28 92 %/249 aa ref|NP_001037309.1| vitellogenin ...rt=VH; Flags: Precursor dbj|BAA02444.1| vitellogenin precursor [Bombyx mori] dbj|BAA06397.1| vitellogenin [B...2654|ref|XP_970210.1| PREDICTED: similar to vitellogenin [Tribolium castaneum] FS939370 fwgP ...

  2. EST Table: FS824678 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available f|XP_971868.2| PREDICTED: similar to esophageal cancer associated protein [Tribolium castaneum] FS824678 fmgV ... ...phageal cancer associated protein [Nasonia vitripennis] 10/09/10 39 %/103 aa FBpp01...FS824678 E_FL_fmgV_18K16_R_0 11/12/09 n.h 10/09/28 46 %/114 aa ref|XP_001604914.1| PREDICTED: similar to eso

  3. EST Table: FS892940 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 108 aa gi|91094187|ref|XP_970998.1| PREDICTED: similar to Evolutionarily conserved signaling intermediate in Toll pathway, mitochondrial [Tribolium castaneum] FS892940 ftes ... ...FS892940 E_FL_ftes_09L06_R_0 11/12/09 n.h 10/09/28 63 %/108 aa ref|XP_970998.1| PREDICTED: similar to Evolut...ionarily conserved signaling intermediate in Toll pathway, mitochondrial [Tribolium

  4. EST Table: FS881403 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS881403 E_FL_ftes_21E11_F_0 11/12/09 GO hit GO:0005515(protein binding)|GO:0008270...niProt:Q 9U3L0#protein_id:CAB54207.1 10/09/10 n.h 10/09/10 n.h 10/09/10 low homology FS881403 ftes ...

  5. EST Table: FS880988 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS880988 E_FL_ftes_20B09_F_0 10/09/28 71 %/202 aa ref|XP_001648944.1| dendritic cel...ubunit M; Short=eIF3m gb|EAT44291.1| dendritic cell protein [Aedes aegypti] 10/09/11 66 %/198 aa FBpp0276999...91954|ref|XP_968265.1| PREDICTED: similar to dendritic cell protein [Tribolium castaneum] FS916297 ftes ...

  6. EST Table: FS839662 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS839662 E_FL_fner_07F07_F_0 10/09/28 69 %/186 aa ref|XP_001648944.1| dendritic cel...ubunit M; Short=eIF3m gb|EAT44291.1| dendritic cell protein [Aedes aegypti] 10/09/10 65 %/183 aa FBpp0276999...|XP_968265.1| PREDICTED: similar to dendritic cell protein [Tribolium castaneum] FS916297 fner ...

  7. EST Table: FS851964 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS851964 E_FL_fner_42D09_F_0 10/09/28 71 %/204 aa ref|XP_001648944.1| dendritic cel...ubunit M; Short=eIF3m gb|EAT44291.1| dendritic cell protein [Aedes aegypti] 10/09/11 66 %/201 aa FBpp0276999...91954|ref|XP_968265.1| PREDICTED: similar to dendritic cell protein [Tribolium castaneum] FS916297 fner ...

  8. EST Table: FS932249 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS932249 E_FL_fwgP_33K22_F_0 10/09/28 69 %/188 aa ref|XP_001648944.1| dendritic cel...ubunit M; Short=eIF3m gb|EAT44291.1| dendritic cell protein [Aedes aegypti] 10/09/13 65 %/185 aa FBpp0276999...|XP_968265.1| PREDICTED: similar to dendritic cell protein [Tribolium castaneum] FS916297 fwgP ...

  9. EST Table: FS846539 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS846539 E_FL_fner_26N03_F_0 10/09/28 70 %/190 aa ref|XP_001648944.1| dendritic cel...ubunit M; Short=eIF3m gb|EAT44291.1| dendritic cell protein [Aedes aegypti] 10/09/10 65 %/187 aa FBpp0276999...|XP_968265.1| PREDICTED: similar to dendritic cell protein [Tribolium castaneum] FS916297 fner ...

  10. EST Table: FS913523 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS913523 E_FL_fufe_29I07_F_0 10/09/28 74 %/270 aa ref|XP_001648944.1| dendritic cel...ubunit M; Short=eIF3m gb|EAT44291.1| dendritic cell protein [Aedes aegypti] 10/09/12 69 %/267 aa FBpp0276999...91954|ref|XP_968265.1| PREDICTED: similar to dendritic cell protein [Tribolium castaneum] FS916297 fufe ...

  11. EST Table: FS774579 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS774579 E_FL_fcaL_05D18_R_0 10/09/28 60 %/153 aa ref|NP_001164203.1| cannonball [T...ribolium castaneum] gb|EFA04573.1| cannonball [Tribolium castaneum] 10/09/08 49 %/161 aa FBpp0170014|DmojGI2...%/153 aa gi|270008125|gb|EFA04573.1| cannonball [Tribolium castaneum] FS786025 fcaL ...

  12. EST Table: FS825912 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS825912 E_FL_fmgV_22B23_R_0 10/09/28 65 %/235 aa ref|NP_001164203.1| cannonball [T...ribolium castaneum] gb|EFA04573.1| cannonball [Tribolium castaneum] 10/09/10 57 %/236 aa FBpp0170014|DmojGI2...%/235 aa gi|270008125|gb|EFA04573.1| cannonball [Tribolium castaneum] FS786025 fmgV ...

  13. EST Table: FS803374 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS803374 E_FL_fmgV_12D12_F_0 10/09/28 45 %/149 aa ref|XP_973163.1| PREDICTED: similar to jump...46 %/150 aa gnl|Amel|GB14856-PA 10/09/10 45 %/149 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 fmgV ...

  14. EST Table: FS822360 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS822360 E_FL_fmgV_12D12_R_0 10/09/28 46 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...46 %/151 aa gnl|Amel|GB14856-PA 10/09/10 46 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS891321 fmgV ...

  15. EST Table: FS787608 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS787608 E_FL_fcaL_21P07_R_0 10/09/28 46 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...46 %/151 aa gnl|Amel|GB14856-PA 10/09/10 46 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS891321 fcaL ...

  16. EST Table: FS847583 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS847583 E_FL_fner_29M11_F_0 10/09/28 45 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...45 %/151 aa gnl|Amel|GB14856-PA 10/09/10 45 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 fner ...

  17. EST Table: FS923051 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS923051 E_FL_fwgP_06G17_F_0 10/09/28 45 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...45 %/151 aa gnl|Amel|GB14856-PA 10/09/10 45 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 fwgP ...

  18. EST Table: FS895588 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS895588 E_FL_ftes_18N10_R_0 10/09/28 46 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...46 %/151 aa gnl|Amel|GB14856-PA 10/09/10 46 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS891321 ftes ...

  19. EST Table: FS844168 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS844168 E_FL_fner_20A08_F_0 10/09/28 45 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...45 %/151 aa gnl|Amel|GB14856-PA 10/09/10 45 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 fner ...

  20. EST Table: FS880548 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS880548 E_FL_ftes_18N10_F_0 10/09/28 45 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...45 %/151 aa gnl|Amel|GB14856-PA 10/09/10 45 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 ftes ...

  1. EST Table: FS862828 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS862828 E_FL_fner_20A08_R_0 10/09/28 46 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...46 %/151 aa gnl|Amel|GB14856-PA 10/09/10 46 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS891321 fner ...

  2. EST Table: FS865993 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS865993 E_FL_fner_29M11_R_0 10/09/28 46 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...46 %/151 aa gnl|Amel|GB14856-PA 10/09/10 46 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS891321 fner ...

  3. EST Table: FS875608 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS875608 E_FL_ftes_04F20_F_0 10/09/28 45 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...45 %/151 aa gnl|Amel|GB14856-PA 10/09/10 45 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 ftes ...

  4. EST Table: FS928974 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS928974 E_FL_fwgP_23N08_F_0 10/09/28 45 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...45 %/151 aa gnl|Amel|GB14856-PA 10/09/10 45 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 fwgP ...

  5. EST Table: FS891805 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS891805 E_FL_ftes_04F20_R_0 10/09/28 46 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...46 %/151 aa gnl|Amel|GB14856-PA 10/09/10 46 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS891321 ftes ...

  6. EST Table: FS874950 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS874950 E_FL_ftes_02G24_F_0 10/09/28 45 %/153 aa ref|XP_973163.1| PREDICTED: similar to jump...45 %/151 aa gnl|Amel|GB14856-PA 10/09/10 45 %/153 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 ftes ...

  7. EST Table: FS771324 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS771324 E_FL_fcaL_21P07_F_0 10/09/28 46 %/146 aa ref|XP_973163.1| PREDICTED: similar to jump...45 %/146 aa gnl|Amel|GB14856-PA 10/09/10 46 %/146 aa gi|91086783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 fcaL ...

  8. EST Table: FS795245 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS795245 E_FL_ffbm_17L22_F_0 10/09/28 100 %/173 aa ref|NP_001093312.1| gloverin 3 [...Bombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  9. EST Table: FS792011 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS792011 E_FL_ffbm_08H19_F_0 10/09/28 100 %/173 aa ref|NP_001093312.1| gloverin 3 [...Bombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  10. EST Table: FS792609 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS792609 E_FL_ffbm_10C20_F_0 10/09/28 100 %/173 aa ref|NP_001093312.1| gloverin 3 [...Bombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  11. EST Table: FS793269 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS793269 E_FL_ffbm_12A24_F_0 10/09/28 82 %/146 aa ref|NP_001093312.1| gloverin 3 [B...ombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  12. EST Table: FS841256 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS841256 E_FL_fner_11N20_F_0 10/09/28 100 %/173 aa ref|NP_001093312.1| gloverin 3 [...Bombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/10 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 fner ...

  13. EST Table: FS859964 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS859964 E_FL_fner_11N20_R_0 10/09/28 99 %/173 aa ref|NP_001093312.1| gloverin 3 [B...ombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/11 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS789236 fner ...

  14. EST Table: FS796763 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS796763 E_FL_ffbm_22C21_F_0 10/09/28 99 %/162 aa ref|NP_001093312.1| gloverin 3 [B...ombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  15. EST Table: FS793562 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS793562 E_FL_ffbm_12P11_F_0 10/09/28 100 %/173 aa ref|NP_001093312.1| gloverin 3 [...Bombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  16. EST Table: FS799323 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS799323 E_FL_ffbm_29O13_F_0 10/09/28 99 %/172 aa ref|NP_001093312.1| gloverin 3 [B...ombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  17. EST Table: FS797046 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS797046 E_FL_ffbm_22P20_F_0 10/09/28 100 %/173 aa ref|NP_001093312.1| gloverin 3 [...Bombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  18. EST Table: FS792731 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS792731 E_FL_ffbm_10I07_F_0 10/09/28 85 %/162 aa ref|NP_001093312.1| gloverin 3 [B...ombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  19. EST Table: FS781921 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS781921 E_FL_fcaL_39B11_R_0 11/12/09 n.h 10/09/28 50 %/189 aa ref|XP_001662178.1| ...A 10/09/10 44 %/172 aa gi|91078880|ref|XP_972914.1| PREDICTED: similar to THUMP domain-containing protein 1 [Tribolium castaneum] FS781921 fcaL ...

  20. EST Table: FS772493 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS772493 E_FL_fcaL_25K03_F_0 10/09/28 99 %/180 aa ref|NP_001040437.1| muscular prot...ein 20 [Bombyx mori] gb|ABF51386.1| muscular protein 20 [Bombyx mori] 10/09/08 60 %/171 aa FBpp0235584|DvirG.../179 aa gi|91077564|ref|XP_972465.1| PREDICTED: similar to muscular protein 20 [Tribolium castaneum] FS765856 fcaL ...

  1. EST Table: FS742806 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS742806 E_FL_bmmt_23P01_R_0 10/09/28 45 %/155 aa gb|ACN52067.1| insect intestinal mucin 3 [Mamestra configu...rata] 10/09/07 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS740161 bmmt ...

  2. EST Table: FS731466 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS731466 E_FL_bmmt_30M21_F_0 10/09/28 46 %/205 aa gb|ACN52067.1| insect intestinal mucin 3 [Mamestra configu...rata] 10/09/03 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS733323 bmmt ...

  3. EST Table: FS734325 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS734325 E_FL_bmmt_23O20_F_0 10/09/28 46 %/205 aa gb|ACN52067.1| insect intestinal mucin 3 [Mamestra configu...rata] 10/09/03 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS733323 bmmt ...

  4. EST Table: FS741790 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS741790 E_FL_bmmt_21A21_R_0 10/09/28 48 %/172 aa gb|ACN52067.1| insect intestinal mucin 3 [Mamestra configu...rata] 10/09/07 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS740161 bmmt ...

  5. EST Table: FS743730 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS743730 E_FL_bmmt_26H21_R_0 10/09/28 49 %/178 aa gb|ACN52067.1| insect intestinal mucin 3 [Mamestra configu...rata] 10/09/07 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS740161 bmmt ...

  6. EST Table: FS745261 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS745261 E_FL_bmmt_30M21_R_0 10/09/28 45 %/135 aa gb|ACN52067.1| insect intestinal mucin 3 [Mamestra configu...rata] 10/09/08 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS740161 bmmt ...

  7. EST Table: FS728748 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS728748 E_FL_bmmt_14B19_F_0 10/09/28 46 %/205 aa gb|ACN52067.1| insect intestinal mucin 3 [Mamestra configu...rata] 10/09/03 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS733323 bmmt ...

  8. EST Table: FS732832 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS732832 E_FL_bmmt_27K04_F_0 10/09/28 69 %/163 aa ref|XP_974883.1| PREDICTED: simil...gnl|Amel|GB14192-PA 10/09/10 69 %/163 aa gi|91083327|ref|XP_974883.1| PREDICTED: similar to 39S ribosomal protein L15, mitochondrial [Tribolium castaneum] FS914543 bmmt ...

  9. EST Table: FS853077 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS853077 E_FL_fner_45F16_F_0 10/09/28 78 %/203 aa ref|XP_001847239.1| arsenical pump-driving...: Full=Arsenite-stimulated ATPase; AltName: Full=Arsenical pump-driving ATPase homolog gb|EDS45868.1| arsenical pump-driving...5|ref|XP_974589.1| PREDICTED: similar to arsenical pump-driving atpase [Tribolium castaneum] FS918630 fner ...

  10. EST Table: FS932533 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS932533 E_FL_fwgP_34I10_F_0 10/09/28 96 %/124 aa ref|NP_001129358.1| osiris 21 [Bo...mbyx mori] gb|ACI23616.1| osiris 21 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 low homology 10/09/10 n.h 10/09/10 n.h FS930345 fwgP ...

  11. EST Table: FS934649 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS934649 E_FL_fwgP_40K10_F_0 10/09/28 31 %/210 aa ref|NP_001129360.1| osiris 9 [Bom...byx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 low homology 10/09/10 n.h 10/09/10 n.h FS923180 fwgP ...

  12. EST Table: FS813184 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS813184 E_FL_fmgV_39K08_F_0 10/09/28 76 %/238 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 76 %/238 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fmgV ...

  13. EST Table: FS911686 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS911686 E_FL_fufe_23P16_F_0 11/12/09 n.h 10/09/28 74 %/268 aa ref|XP_970542.1| PREDICTED: similar to brix...aa gnl|Amel|GB12626-PA 10/09/10 74 %/268 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fufe ...

  14. EST Table: FS776725 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS776725 E_FL_fcaL_12C20_R_0 10/09/28 72 %/185 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 72 %/185 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS825195 fcaL ...

  15. EST Table: FS892222 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS892222 E_FL_ftes_06F11_R_0 11/12/09 n.h 10/09/28 50 %/224 aa ref|XP_395189.3| PRE...el|GB15458-PA 10/09/10 42 %/238 aa gi|91083381|ref|XP_967258.1| PREDICTED: similar to AGAP009881-PA [Tribolium castaneum] FS892222 ftes ...

  16. Monoliths: A Review of the Basics, Preparation Methods and Their Relevance to Oxidation

    Directory of Open Access Journals (Sweden)

    Sandeeran Govender

    2017-02-01

    Full Text Available Considerable research has been conducted on monolithic catalysts for various applications. Strategies toward coating monoliths are of equal interest and importance. In this paper, the preparation of monoliths and monolithic catalysts have been summarized. More specifically, a brief explanation for the manufacturing of ceramic and metallic monoliths has been provided. Also, different methods for coating γ-alumina, as a secondary support, are included. Techniques used to deposit metal-based species, zeolites and carbon onto monoliths are discussed. Furthermore, monoliths extruded with metal oxides, zeolites and carbon are described. The main foci are on the reasoning and understanding behind the preparation of monolithic catalysts. Ideas and concerns are also contributed to encourage better approaches when designing these catalysts. More importantly, the relevance of monolithic structures to reactions, such as the selective oxidation of alkanes, catalytic combustion for power generation and the preferential oxidation of carbon monoxide, has been described.

  17. Polymethacrylate monolithic and hybrid particle-monolithic columns for reversed-phase and hydrophilic interaction capillary liquid chromatography.

    Science.gov (United States)

    Jandera, Pavel; Urban, Jirí; Skeríková, Veronika; Langmaier, Pavel; Kubícková, Romana; Planeta, Josef

    2010-01-01

    We prepared hybrid particle-monolithic polymethacrylate columns for micro-HPLC by in situ polymerization in fused silica capillaries pre-packed with 3-5microm C(18) and aminopropyl silica bonded particles, using polymerization mixtures based on laurylmethacrylate-ethylene dimethacrylate (co)polymers for the reversed-phase (RP) mode and [2-(methacryloyloxy)ethyl]-dimethyl-(3-sulfopropyl) zwitterionic (co)polymers for the hydrophilic interaction (HILIC) mode. The hybrid particle-monolithic columns showed reduced porosity and hold-up volumes, approximately 2-2.5 times lower in comparison to the pure monolithic columns prepared in the whole volume of empty capillaries. The elution volumes of sample compounds are also generally lower in comparison to packed or pure monolithic columns. The efficiency and permeability of the hybrid columns are intermediate in between the properties of the reference pure monolithic and particle-packed columns. The chemistries of the embedded solid particles and of the interparticle monolithic moiety in the hybrid capillary columns contribute to the retention to various degrees, affecting the selectivity of separation. Some hybrid columns provided improved separations of proteins in comparison to the reference particle-packed columns in the reversed-phase mode. Zwitterionic hybrid particle-monolithic columns show dual mode retention HILIC/RP behaviour depending on the composition of the mobile phase and allow separations of polar compounds such as phenolic acids in the HILIC mode at lower concentrations of acetonitrile and, often in shorter analysis time in comparison to particle-packed and full-volume monolithic columns.

  18. Biasable, Balanced, Fundamental Submillimeter Monolithic Membrane Mixer

    Science.gov (United States)

    Siegel, Peter; Schlecht, Erich; Mehdi, Imran; Gill, John; Velebir, James; Tsang, Raymond; Dengler, Robert; Lin, Robert

    2010-01-01

    This device is a biasable, submillimeter-wave, balanced mixer fabricated using JPL s monolithic membrane process a simplified version of planar membrane technology. The primary target application is instrumentation used for analysis of atmospheric constituents, pressure, temperature, winds, and other physical and chemical properties of the atmospheres of planets and comets. Other applications include high-sensitivity gas detection and analysis. This innovation uses a balanced configuration of two diodes allowing the radio frequency (RF) signal and local oscillator (LO) inputs to be separated. This removes the need for external diplexers that are inherently narrowband, bulky, and require mechanical tuning to change frequency. Additionally, this mixer uses DC bias-ability to improve its performance and versatility. In order to solve problems relating to circuit size, the GaAs membrane process was created. As much of the circuitry as possible is fabricated on-chip, making the circuit monolithic. The remainder of the circuitry is precision-machined into a waveguide block that holds the GaAs circuit. The most critical alignments are performed using micron-scale semiconductor technology, enabling wide bandwidth and high operating frequencies. The balanced mixer gets superior performance with less than 2 mW of LO power. This can be provided by a simple two-stage multiplier chain following an amplifier at around 90 GHz. Further, the diodes are arranged so that they can be biased. Biasing pushes the diodes closer to their switching voltage, so that less LO power is required to switch the diodes on and off. In the photo, the diodes are at the right end of the circuit. The LO comes from the waveguide at the right into a reduced-height section containing the diodes. Because the diodes are in series to the LO signal, they are both turned on and off simultaneously once per LO cycle. Conversely, the RF signal is picked up from the RF waveguide by the probe at the left, and flows

  19. Dedicated monolithic infrared spectrometer for process monitoring

    Science.gov (United States)

    Chadha, Suneet; Kyle, William; Bolduc, Roy A.; Curtiss, Lawrence E.

    1999-12-01

    Foster-Miller has leveraged its innovations in IR fiber- optic probes and the recent development of a miniature spectrometer to build a novel IR sensor system for process applications. The developed sensor systems is a low-cost alternative to process FTIR and filter based systems. A monolithic wedge-grating optic provides the spectral dispersion with low cost thermopile point or array detectors picking off the diffracted wavelengths from the optic. The integrated optic provides spectral discrimination between 3- 12 micrometers with resolution at 8 cm-1 or better and high overall optical throughput. The device has a fixed cylindrical grating uniquely bonded to the edge of a ZnSe conditioning 'wedge'. The conditioning optic overcomes limitations of concave gratings as it accepts high angle light at the narrow end of the wedge and progressively conditions it to be near normal to the grating. On return, the diffracted wavelengths are concentrated on the discrete or array detector elements by the wedge, providing throughput comparable to that of an FTIR. The miniature spectrometer coupled to flow through liquid cells or multipass gas cells provides significant cost advantage over conventional sampling methodologies. Currently, we are investigating process applications for the petroleum and dairy markets. The sensor system eliminates the cost, complexity, reliability and bandwidth/resolution problems associated with either Fabry Perot or Michelson Interferometer based approaches for low-cost process applications.

  20. The Advanced Virgo monolithic fused silica suspension

    Energy Technology Data Exchange (ETDEWEB)

    Aisa, D.; Aisa, S.; Campeggi, C.; Colombini, M. [University of Perugia and INFN Perugia (Italy); Conte, A. [University of Roma Sapienza and INFN Roma (Italy); Farnesini, L. [University of Perugia and INFN Perugia (Italy); Majorana, E.; Mezzani, F. [University of Roma Sapienza and INFN Roma (Italy); Montani, M. [University of Urbino and INFN Firenze (Italy); Naticchioni, L.; Perciballi, M. [University of Roma Sapienza and INFN Roma (Italy); Piergiovanni, F. [University of Urbino and INFN Firenze (Italy); Piluso, A. [University of Perugia and INFN Perugia (Italy); Puppo, P., E-mail: paola.puppo@roma1.infn.it [University of Roma Sapienza and INFN Roma (Italy); Rapagnani, P. [University of Roma Sapienza and INFN Roma (Italy); Travasso, F. [University of Perugia and INFN Perugia (Italy); Vicerè, A. [University of Urbino and INFN Firenze (Italy); Vocca, H. [University of Perugia and INFN Perugia (Italy)

    2016-07-11

    The detection of gravitational waves is one of the most challenging prospects faced by experimental physicists. Suspension thermal noise is an important noise source at operating frequencies between approximately 10 and 30 Hz, and represents a limit to the sensitivity of the ground based interferometric gravitational wave detectors. Its effects can be reduced by minimizing the losses and by optimizing the geometry of the suspension fiber as well as its attachment system. In this proceeding we will describe the mirrors double stage monolithic suspension system to be used in the Advanced Virgo (AdV) detector. We also present the results of the thermal noise study, performed with the help of a finite elements model, taking into account the precise geometry of the fibers attachment systems on the suspension elements. We shall demonstrate the suitability of this suspension for installation in AdV. - Highlights: • Suspension system design for the test masses of the gravitational wave detectors. • Finite element model studies. • Suspension thermal noise studies.

  1. Monolithic supports with unique geometries and enhanced mass transfer.

    Energy Technology Data Exchange (ETDEWEB)

    Stuecker, John Nicholas; Ferrizz, Robert Matthew; Cesarano, Joseph, III; Miller, James Edward

    2004-01-01

    The catalytic combustion of natural gas has been the topic of much research over the past decade. Interest in this technology results from a desire to decrease or eliminate the emissions of harmful nitrogen oxides (NOX) from gas turbine power plants. A low-pressure drop catalyst support, such as a ceramic monolith, is ideal for this high-temperature, high-flow application. A drawback to the traditional honeycomb monoliths under these operating conditions is poor mass transfer to the catalyst surface in the straight-through channels. 'Robocasting' is a unique process developed at Sandia National Laboratories that can be used to manufacture ceramic monoliths with alternative 3-dimensional geometries, providing tortuous pathways to increase mass transfer while maintaining low pressure drops. This report details the mass transfer effects for novel 3-dimensional robocast monoliths, traditional honeycomb-type monoliths, and ceramic foams. The mass transfer limit is experimentally determined using the probe reaction of CO oxidation over a Pt / {gamma}-Al{sub 2}O{sub 3} catalyst, and the pressure drop is measured for each monolith sample. Conversion versus temperature data is analyzed quantitatively using well-known dimensionless mass transfer parameters. The results show that, relative to the honeycomb monolith support, considerable improvement in mass transfer efficiency is observed for robocast samples synthesized using an FCC-like geometry of alternating rods. Also, there is clearly a trade-off between enhanced mass transfer and increased pressure drop, which can be optimized depending on the particular demands of a given application.

  2. ADVANCED GASIFICATION MERCURY/TRACE METAL CONTROL WITH MONOLITH TRAPS

    Energy Technology Data Exchange (ETDEWEB)

    Mark A. Musich; Michael L. Swanson; Grant E. Dunham; Joshua J. Stanislowski

    2010-07-31

    Two Corning monoliths and a non-carbon-based material have been identified as potential additives for mercury capture in syngas at temperatures above 400°F and pressure of 600 psig. A new Corning monolith formulation, GR-F1-2189, described as an active sample appeared to be the best monolith tested to date. The Corning SR Liquid monolith concept continues to be a strong candidate for mercury capture. Both monolith types allowed mercury reduction to below 5-μg/m3 (~5 ppb), a current U.S. Department of Energy (DOE) goal for trace metal control. Preparation methods for formulating the SR Liquid monolith impacted the ability of the monolith to capture mercury. The Energy & Environmental Research Center (EERC)-prepared Noncarbon Sorbents 1 and 2 appeared to offer potential for sustained and significant reduction of mercury concentration in the simulated fuel gas. The Noncarbon Sorbent 1 allowed sustained mercury reduction to below 5-μg/m3 (~5 ppb). The non-carbon-based sorbent appeared to offer the potential for regeneration, that is, desorption of mercury by temperature swing (using nitrogen and steam at temperatures above where adsorption takes place). A Corning cordierite monolith treated with a Group IB metal offered limited potential as a mercury sorbent. However, a Corning carbon-based monolith containing prereduced metallic species similar to those found on the noncarbon sorbents did not exhibit significant or sustained mercury reduction. EERC sorbents prepared with Group IB and IIB selenide appeared to have some promise for mercury capture. Unfortunately, these sorbents also released Se, as was evidenced by the measurement of H2Se in the effluent gas. All sorbents tested with arsine or hydrogen selenide, including Corning monoliths and the Group IB and IIB metal-based materials, showed an ability to capture arsine or hydrogen selenide at 400°F and 600 psig. Based on current testing, the noncarbon metal-based sorbents appear to be the most effective arsine

  3. Recent advances in polymer monoliths for ion-exchange chromatography.

    Science.gov (United States)

    Nordborg, Anna; Hilder, Emily F

    2009-05-01

    The use of polymeric materials in ion-exchange chromatography applications is advantageous because of their typically high mechanical stability and tolerance of a wide range of pH conditions. The possibility of using polymeric monoliths in ion-exchange chromatography is therefore obvious and many of the same strategies developed for polymeric particles have been adapted for use with polymeric monoliths. In this review different strategies for the synthesis of polymeric monoliths with ion-exchange functionality are discussed. The incorporation of ion-exchange functionality by co-polymerization is included, as also are different post-polymerization alterations to the monolith surface such as grafting. The formulations and strategies presented include materials intended for use in analytical separations in ion-exchange chromatography, sample pre-treatment or enrichment applications, and materials for capillary electrochromatography. Finally, examples of the use of polymeric monoliths in ion-exchange chromatography applications are included with examples published in the years 2003 to 2008.

  4. New Graphene Form of Nanoporous Monolith for Excellent Energy Storage.

    Science.gov (United States)

    Bi, Hui; Lin, Tianquan; Xu, Feng; Tang, Yufeng; Liu, Zhanqiang; Huang, Fuqiang

    2016-01-13

    Extraordinary tubular graphene cellular material of a tetrahedrally connected covalent structure was very recently discovered as a new supermaterial with ultralight, ultrastiff, superelastic, and excellent conductive characteristics, but no high specific surface area will keep it from any next-generation energy storage applications. Herein, we prepare another new graphene monolith of mesoporous graphene-filled tubes instead of hollow tubes in the reported cellular structure. This graphene nanoporous monolith is also composed of covalently bonded carbon network possessing high specific surface area of ∼1590 m(2) g(-1) and electrical conductivity of ∼32 S cm(-1), superior to graphene aerogels and porous graphene forms self-assembled by graphene oxide. This 3D graphene monolith can support over 10 000 times its own weight, significantly superior to CNT and graphene cellular materials with a similar density. Furthermore, pseudocapacitance-active functional groups are introduced into the new nanoporous graphene monolith as an electrode material in electrochemical capacitors. Surprisingly, the electrode of 3D mesoporous graphene has a specific capacitance of 303 F g(-1) and maintains over 98% retention after 10 000 cycles, belonging to the list for the best carbon-based active materials. The macroscopic mesoporous graphene monolith suggests the great potential as an electrode for supercapacitors in energy storage areas.

  5. Monolithic View of Galaxy Formation and Evolution

    Directory of Open Access Journals (Sweden)

    Cesare Chiosi

    2014-07-01

    Full Text Available We review and critically discuss the current understanding of galaxy formation and evolution limited to Early Type Galaxies (ETGs as inferred from the observational data and briefly contrast the hierarchical and quasi-monolithic paradigms of formation and evolution. Since in Cold Dark Matter (CDM cosmogony small scale structures typically collapse early and form low-mass haloes that subsequently can merge to assembly larger haloes, galaxies formed in the gravitational potential well of a halo are also expected to merge thus assembling their mass hierarchically. Mergers should occur all over the Hubble time and large mass galaxies should be in place only recently. However, recent observations of high redshift galaxies tell a different story: massive ETGs are already in place at high redshift. To this aim, we propose here a revision of the quasi-monolithic scenario as an alternative to the hierarchical one, in which mass assembling should occur in early stages of a galaxy lifetime and present recent models of ETGs made of Dark and Baryonic Matter in a Λ-CDM Universe that obey the latter scheme. The galaxies are followed from the detachment from the linear regime and Hubble flow at z ≥ 20 down to the stage of nearly complete assembly of the stellar content (z ∼ 2 − 1 and beyond.  It is found that the total mass (Mh = MDM + MBM and/or initial over-density of the proto-galaxy drive the subsequent star formation histories (SFH. Massive galaxies (Mh ~ _1012M⊙ experience a single, intense burst of star formation (with rates ≥ 103M⊙/yr at early epochs, consistently with observations, with a weak dependence on the initial over-density; intermediate mass haloes (Mh~_ 1010 − 1011M⊙ have star formation histories that strongly depend on their initial over-density; finally, low mass haloes (Mh ~_ 109M⊙ always have erratic, burst-like star forming histories. The present-day properties (morphology, structure, chemistry and photometry of the

  6. Monolithic Solid Oxide Fuel Cell development

    Science.gov (United States)

    Myles, K. M.; McPheeters, C. C.

    1989-12-01

    The Monolithic Solid Oxide Fuel Cell (MSOFC) is an oxide-ceramic structure in which appropriate electronic and ionic conductors are fabricated in a honeycomb shape similar to a block of corrugated paperboard. These electronic and ionic conductors are arranged to provide short conduction paths to minimize resistive losses. The power density achievable with the MSOFC is expected to be about 8 kW/kg or 4 kW/L, at fuel efficienceis over 50 percent, because of small cell size and low resistive losses in the materials. The MSOFC operates in the range of 700 to 1000 C, at which temperatures rapid reform of hydrocarbon fuels is expected within the nickel-YSZ fuel channels. Tape casting and hot roll calendering are used to fabricate the MSOFC structure. The performance of the MSOFC has improved significantly during the course of development. The limitation of this system, based on materials resistance alone without interfacial resistances, is 0.093 ohm-sq cm area-specific resistance (ASR). The current typical performance of MSOFC single cells is characterized by ASRs of about 0.4 to 0.5 ohm-sq cm. With further development the ASR is expected to be reduced below 0.2 ohm-sq cm, which will result in power levels greater than 1.4 W/sq cm. The feasibility of the MSOFC concept was proven, and the performance was dramatically improved. The differences in thermal expansion coefficients and firing shrinkages among the fuel cell materials were minimized. As a result of good matching of these properties, the MSOFC structure was successfully fabricated with few defects, and the system shows excellent promise for development into a practical power source.

  7. GlusterFS One Storage Server to Rule Them All

    Energy Technology Data Exchange (ETDEWEB)

    Boyer, Eric B. [Los Alamos National Laboratory; Broomfield, Matthew C. [Los Alamos National Laboratory; Perrotti, Terrell A. [Los Alamos National Laboratory

    2012-07-30

    GlusterFS is a Linux based distributed file system, designed to be highly scalable and serve many clients. Some reasons to use GlusterFS are: No centralized metadata server, Scalability, Open Source, Dynamic and live service modifications, Can be used over Infiniband or Ethernet, Can be tuned for speed and/or resilience and Flexible administration. It's useful for enterprise environments - virtualization; high performance computing (HPC) and it works with Mac, Linux and Windows clients. Conclusions are: (1) GlusterFS proved to have widespread capabilities as a virtual file system; (2) Scalability is very dependent upon the underlying hardware; (3) Lack of built-in encryption and security paradigm; and (4) Best suited in a general purpose computing environment.

  8. Schedule Optimization Study, Hanford RI/FS Program

    Energy Technology Data Exchange (ETDEWEB)

    1992-12-01

    A Schedule Optimization Study (SOS) of the US Department of Energy (DOE) Hanford Site Remedial Investigation/Feasibility Study (RI/FS) Program was conducted by an independent team of professionals from other federal agencies and the private sector experienced in environmental restoration. This team spent two weeks at Hanford in September 1992 examining the reasons for the lengthy RI/FS process at Hanford and developing recommendations to expedite the process. The need for the study arose out of a schedule dispute regarding the submission of the 1100-EM-1 Operable Unit RI/FS Work Plan. This report documents the study called for in the August 29, 1991, Dispute Resolution Committee Decision Statement. Battelle's Environmental Management Operations (EMO) coordinated the effort for DOE's Richland Field Office (RL).

  9. Monolithic fuel cell based power source for burst power generation

    Science.gov (United States)

    Fee, D. C.; Blackburn, P. E.; Busch, D. E.; Dees, D. W.; Dusek, J.; Easler, T. E.; Ellingson, W. A.; Flandermeyer, B. K.; Fousek, R. J.; Heiberger, J. J.

    A unique fuel cell coupled with a low power nuclear reactor presents an attractive approach for SDI burst power requirements. The monolithic fuel cell looks attractive for space applications and represents a quantum jump in fuel cell technology. Such a breakthrough in design is the enabling technology for lightweight, low volume power sources for space based pulse power systems. The monolith is unique among fuel cells in being an all solid state device. The capability for miniaturization, inherent in solid state devices, gives the low volume required for space missions. In addition, the solid oxide fuel cell technology employed in the monolith has high temperature reject heat and can be operated in either closed or open cycles. Both these features are attractive for integration into a burst power system.

  10. A Possible Astronomically Aligned Monolith at Gardom's Edge

    CERN Document Server

    Brown, D; Bemand, E

    2012-01-01

    A unique triangular shaped monolith located within the Peak District National Park at Gardom's Edge could be intentionally astronomically aligned. It is set within a landscape rich in late Neolithic and Bronze Age remains. We show that the stone is most likely in its original orientation owing to its clear signs of erosion and associated to the time period of the late Neolithic. It is tilted towards South and its North side slopes at an angle equal to the maximum altitude of the Sun at mid-summer. This alignment emphasizes the changing declinations of the Sun during the seasons as well as giving an indication of mid-summers day. This functionality is achieved by an impressive display of light and shadow on the North-facing side of the Monolith. Together with other monuments in the close vicinity the monolith would have represented an ideal marker or social arena for seasonal gatherings for the else dispersed small communities.

  11. MONOLITHIC FUEL FABRICATION PROCESS DEVELOPMENT AT THE IDAHO NATIONAL LABORATORY_

    Energy Technology Data Exchange (ETDEWEB)

    G. A. Moore; F. J. Rice; N. E. Woolstenhulme; J-F. Jue; B. H. Park; S. E. Steffler; N. P. Hallinan; M. D. Chapple; M. C. Marshall; B. L. Mackowiak; C. R. Clark; B. H. Rabin

    2009-11-01

    Full-size/prototypic U10Mo monolithic fuel-foils and aluminum clad fuel plates are being developed at the Idaho National Laboratory’s (INL) Materials and Fuels Complex (MFC). These efforts are focused on realizing Low Enriched Uranium (LEU) high density monolithic fuel plates for use in High Performance Research and Test Reactors. The U10Mo fuel foils under development afford a fuel meat density of ~16 gU/cc and thus have the potential to facilitate LEU conversions without any significant reactor-performance penalty. An overview is provided of the ongoing monolithic UMo fuel development effort, including application of a zirconium barrier layer on fuel foils, fabrication scale-up efforts, and development of complex/graded fuel foils. Fuel plate clad bonding processes to be discussed include: Hot Isostatic Pressing (HIP) and Friction Bonding (FB).

  12. A Possible Astronomically Aligned Monolith at Gardom's Edge

    Science.gov (United States)

    Brown, Daniel; Alder, Andy; Bemand, Elizabeth

    2015-05-01

    A unique triangular shaped monolith located within the Peak District National Park at Gardom's Edge could be intentionally astronomically aligned. It is set within a landscape rich in late Neolithic and Bronze Age remains. We show that the stone is most likely in its original orientation owing to its clear signs of erosion and associated to the time period of the late Neolithic. It is tilted towards south and its north side slopes at an angle equal to the maximum altitude of the Sun at mid-summer. This alignment emphasizes the changing declinations of the Sun during the seasons as well as giving an indication of mid-summers day. This functionality is achieved by an impressive display of light and shadow on the north facing side of the monolith. Together with other monuments in the close vicinity the monolith would have represented an ideal marker or social arena for seasonal gatherings for the otherwise dispersed small communities.

  13. Preliminary shielding analysis for the CSNS target station monolith

    Institute of Scientific and Technical Information of China (English)

    张斌; 陈义学; 杨寿海; 吴军; 殷雯; 梁天骄; 贾学军

    2010-01-01

    The construction of the China Spallation Neutron Source (CSNS) has been initiated at Dongguan,Guangdong,China.In spallation neutron sources the target station monolith is contaminated by a large number of fast neutrons whose energies can be as large as those of the protons of the proton beam directed towards the tungsten target.A detailed radiation transport analysis of the target station monolith is important for the construction of the CSNS.The analysis is performed using the coupled Monte Carlo and multi-dimensional discrete ordinates method.Successful elimination of the primary ray effects via the two-dimensional uncollided flux and first collision source methodology is also illustrated.The dose at the edge of the monolith is calculated.The results demonstrate that the doses received by the hall staff members are below the required standard limit.

  14. Design of Monolithic Integrator for Strain-to-Frequency Converter

    Directory of Open Access Journals (Sweden)

    Tuan Mohd. Khairi Tuan Mat

    2012-01-01

    Full Text Available Strain-to-Frequency converter (SFC is a one of the analog conditioner tools that converts any strain signal to the frequency signal. The basic concept of SFC is by detecting any changing of strains, then converting the strain to the voltage signal and converting the voltage signal to the frequency signal. This tool consists of 3 main  components which are strain gauge, differential integrator and comparator. This paper presents the designing and analysis of monolithic integrator that to be used in the Strain-toFrequency converter. The primary goal is to design and simulate the performance of monolithic integrator for SFC using GATEWAY Silvaco Electronic Design Automation (S EDA tools and EXPERT software. The performances of SFC using the designed monolithic integrator are also investigated.

  15. Molecularly imprinted macroporous monolithic materials for protein recognition

    Institute of Scientific and Technical Information of China (English)

    Qi Liang Deng; Yan Li Li; Li Hua Zhang; Yu Kui Zhang

    2011-01-01

    Synthetic materials that can specifically recognize proteins will find wide application in many fields. In this report, bovine serum albumin was chosen as the template protein. Acrylamide and N, N'-methylenebisacrylamide were employed as the functional and cross-linker monomers, respectively. Molecularly imprinted macroporous monolithic materials that can preferentially bind the template protein in an aqueous environment were prepared by combination of molecular imprinting technique and freezing/thawing preparation method. The resulted imprinted macroporous monolithic columns were evaluated by utilizing as stationary phase in high performance liquid chromatography and solid-phase extraction materials. The experimental results indicated that the imprinted macroporous monolithic column exhibited good recognition for template protein, as compared with the control protein (hemoglobin), whereas the non-imprinted polymer (prepared under the same conditions except without addition template protein) had no selective properties.

  16. Preparation of poly(γ-glutamic acid)/hydroxyapatite monolith via biomineralization for bone tissue engineering.

    Science.gov (United States)

    Park, Sung-Bin; Hasegawa, Urara; van der Vlies, André J; Sung, Moon-Hee; Uyama, Hiroshi

    2014-01-01

    A hybrid monolith of poly(γ-glutamic acid) and hydroxyapatite (PGA/HAp monolith) was prepared via biomineralization and used as a macroporous cell scaffold in bone tissue engineering. The PGA monolith having a bimodal pore size distribution was used as a substrate to induce biomineralization. The PGA/HAp monolith was obtained by immersing the PGA monolith in simulated body fluid. Pretreatment with CaCl2 enhanced the apatite-forming ability of the PGA monolith. Murine osteoblastic MC3T3-E1 cells efficiently attached and proliferated on the PGA/HAp monolith. MTT assay showed that both the PGA and PGA/HAp monolith did not have apparent cytotoxicity. Moreover, the PGA and PGA/HAp monoliths adsorbed bone morphogenetic protein-2 (BMP-2) by electrostatic interaction which was slowly released in the medium during cell culture. The PGA/HAp monolith enhanced BMP-2 induced alkaline phosphatase activity compared to the PGA monolith and a polystyrene culture plate. Thus, these PGA/HAp monoliths may have potential in bone tissue engineering.

  17. EST Table: FS939099 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS939099 E_FL_fwgP_53O19_F_0 11/12/09 n.h 10/09/28 57 %/174 aa ref|XP_001664237.1| breast cancer metastasis...-suppressor [Aedes aegypti] gb|EAT33713.1| breast cancer metastasis-suppressor [Aede...33-PA 10/09/10 57 %/171 aa gi|91080755|ref|XP_966988.1| PREDICTED: similar to breast cancer metastasis-suppressor 1 [Tribolium castaneum] FS939099 fwgP ...

  18. EST Table: FS768659 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS768659 E_FL_fcaL_49M03_F_0 10/09/28 35 %/179 aa ref|NP_999487.1| niemann-Pick C1 ...protein precursor [Sus scrofa] sp|P56941.1|NPC1_PIG RecName: Full=Niemann-Pick C1 protein; Flags: Precursor ...gb|AAD47090.1|AF169635_1 Niemann-Pick C disease protein [Sus scrofa] 10/09/08 38 %/177 aa FBpp0147284|DgriGH...f|XP_967619.2| PREDICTED: similar to niemann-pick C1 [Tribolium castaneum] FS758709 fcaL ...

  19. EST Table: FS766641 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS766641 E_FL_fcaL_43I16_F_0 10/09/28 35 %/160 aa ref|NP_999487.1| niemann-Pick C1 ...protein precursor [Sus scrofa] sp|P56941.1|NPC1_PIG RecName: Full=Niemann-Pick C1 protein; Flags: Precursor ...gb|AAD47090.1|AF169635_1 Niemann-Pick C disease protein [Sus scrofa] 10/09/08 37 %/153 aa FBpp0147284|DgriGH...f|XP_967619.2| PREDICTED: similar to niemann-pick C1 [Tribolium castaneum] FS758709 fcaL ...

  20. EST Table: FS936777 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS936777 E_FL_fwgP_47B09_F_0 10/09/28 34 %/182 aa ref|NP_999487.1| niemann-Pick C1 ...protein precursor [Sus scrofa] sp|P56941.1|NPC1_PIG RecName: Full=Niemann-Pick C1 protein; Flags: Precursor ...gb|AAD47090.1|AF169635_1 Niemann-Pick C disease protein [Sus scrofa] 10/09/13 37 %/179 aa FBpp0147284|DgriGH...f|XP_967619.2| PREDICTED: similar to niemann-pick C1 [Tribolium castaneum] FS758709 fwgP ...

  1. EST Table: FS921149 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS921149 E_FL_fufe_53H13_F_0 10/09/28 30 %/250 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...250 aa gi|91078946|ref|XP_974065.1| PREDICTED: similar to Outer dense fiber protein 2 (Outer dense fiber of ...sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS910822 fufe ...

  2. EST Table: FS922922 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922922 E_FL_fwgP_06A21_F_0 11/12/09 n.h 10/09/28 82 %/176 aa ref|NP_001116821.1| 18 wheeler... [Bombyx mori] dbj|BAB85498.1| 18 wheeler [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/...09/10 n.h 10/09/10 36 %/129 aa gi|91076478|ref|XP_972409.1| PREDICTED: similar to 18 wheeler [Tribolium castaneum] FS922922 fwgP ...

  3. EST Table: FS749709 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS749709 E_ET_caL-_19O13_F_0 10/09/28 92 %/228 aa ref|NP_001116821.1| 18 wheeler [B...ombyx mori] dbj|BAB85498.1| 18 wheeler [Bombyx mori] 10/09/08 47 %/148 aa FBpp0235352|DvirGJ20935-PA 10/08/2...Amel|GB15177-PA 10/09/10 51 %/215 aa gi|91076478|ref|XP_972409.1| PREDICTED: similar to 18 wheeler [Tribolium castaneum] FS922922 caL- ...

  4. EST Table: FS799171 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 9/10 34 %/172 aa gnl|Amel|GB13186-PA 10/09/10 40 %/157 aa gi|91086181|ref|XP_971039.1| PREDICTED: similar to scaffold protein salvador (shar-pei) [Tribolium castaneum] FS920136 ffbm ... ...ar to scaffold protein salvador (shar-pei) [Tribolium castaneum] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/0...FS799171 E_FL_ffbm_29H10_F_0 10/09/28 40 %/157 aa ref|XP_971039.1| PREDICTED: simil

  5. EST Table: FS855145 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available Nonsense-mediated mRNA decay protein, putative [Pediculus humanus corporis] gb|EEB15514.1| Nonsense-mediated mRNA decay...0/08/29 51 %/227 aa T25G3.3#CE30306#WBGene00012030#Yeast nonsense-mediated mRNA decay... gi|91091920|ref|XP_967150.1| PREDICTED: similar to nonsense-mediated mrna decay protein [Tribolium castaneum] FS855145 fner ... ...FS855145 E_FL_fner_51C17_F_0 11/12/09 n.h 10/09/28 73 %/230 aa ref|XP_002428252.1|

  6. EST Table: FS808716 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS808716 E_FL_fmgV_27B22_F_0 11/12/09 n.h 10/09/28 43 %/181 aa ref|XP_001648294.1| Juvenile... hormone-inducible protein, putative [Aedes aegypti] gb|EAT44634.1| Juvenile hormone-inducible prote...4 aa gnl|Amel|GB15308-PA 10/09/10 37 %/178 aa gi|91080979|ref|XP_974925.1| PREDICTED: similar to Juvenile hormone-inducible protein, putative [Tribolium castaneum] FS808716 fmgV ...

  7. EST Table: FS921551 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available y 10/09/10 39 %/152 aa gnl|Amel|GB16043-PA 10/09/10 39 %/198 aa gi|189240340|ref|XP_971046.2| PREDICTED: similar to antolefinin [Tribolium castaneum] FS921551 fwgP ... ...FS921551 E_FL_fwgP_02A09_F_0 11/12/09 n.h 10/09/28 39 %/198 aa ref|XP_971046.2| PREDICTED: similar to antole...finin [Tribolium castaneum] 10/09/13 low homology 10/08/29 n.h 10/09/10 low homolog

  8. EST Table: FS757535 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS757535 E_FL_fcaL_05I02_F_0 11/12/09 n.h 10/09/28 39 %/120 aa gb|AAR29593.1| hlucCP+ reporter protein [Repo...rter vector pGL3(R2.2)] 10/09/08 low homology 10/08/28 low homology 10/09/10 low homology 10/09/10 low homology 10/09/10 low homology FS757535 fcaL ...

  9. EST Table: FS924140 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available P010242 10/09/10 low homology 10/09/10 55 %/167 aa gi|91079308|ref|XP_967065.1| PREDICTED: similar to roundabout 1 [Tribolium castaneum] FS924140 fwgP ... ...DICTED: similar to roundabout 1 [Tribolium castaneum] 10/09/13 50 %/181 aa FBpp0197092|DsecGM15615-PA 10/08/...FS924140 E_FL_fwgP_09L01_F_0 11/12/09 n.h 10/09/28 55 %/167 aa ref|XP_967065.1| PRE

  10. Imaging through flesh tissue using fs electronic holographic gating method

    Institute of Scientific and Technical Information of China (English)

    侯比学; 陈国夫; 郝志琦; 丰善; 王淑岩; 王屹山; 王国志

    1999-01-01

    The experimental results of imaging through flesh tissue using fs electronic holographic gating method is reported. In the experiment, Ti: sapphire mode-locked laser is used as light source, of which the repetition rate is 100 MHz, central wavelength 800 mn, duration of pulse 20 fs, output power 80 mW. Tissue is a 7 mm thick chicken slice, and the imaged object is a metal wire with diameter of 0.5 mm. A general CCD is used to record holograms and a clear image of metal wire is obtained. Several relevant problems are discussed.

  11. EST Table: FS847063 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS847063 E_FL_fner_28E20_F_0 10/09/28 90 %/175 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/10 54 %/172 aa FBpp0078827|stai-PC 10/08/29 n.h 10/09/...B18507-PA 10/09/10 54 %/179 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fner ...

  12. EST Table: FS880458 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS880458 E_FL_ftes_18J03_F_0 10/09/28 88 %/150 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/11 54 %/149 aa FBpp0078827|stai-PC 10/08/29 n.h 10/09/...B18507-PA 10/09/10 51 %/154 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 ftes ...

  13. EST Table: FS915165 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915165 E_FL_fufe_34H06_F_0 10/09/28 87 %/256 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/12 47 %/225 aa FBpp0166535|DmojGI17318-PA 10/08/29 n.h...|Amel|GB18507-PA 10/09/10 51 %/264 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fufe ...

  14. EST Table: FS918281 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918281 E_FL_fufe_43O13_F_0 10/09/28 92 %/251 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/12 42 %/257 aa FBpp0144714|DgriGH10808-PA 10/08/29 n.h...|Amel|GB18507-PA 10/09/10 52 %/258 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fufe ...

  15. EST Table: FS912717 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS912717 E_FL_fufe_27A22_F_0 10/09/28 93 %/271 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/12 46 %/271 aa FBpp0144714|DgriGH10808-PA 10/08/29 n.h...|Amel|GB18507-PA 10/09/10 52 %/274 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fufe ...

  16. EST Table: FS884035 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS884035 E_FL_ftes_28P20_F_0 10/09/28 90 %/176 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/12 54 %/172 aa FBpp0078827|stai-PC 10/08/29 n.h 10/09/...B18507-PA 10/09/10 54 %/180 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 ftes ...

  17. EST Table: FS852564 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS852564 E_FL_fner_43O07_F_0 10/09/28 92 %/233 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/11 47 %/225 aa FBpp0166535|DmojGI17318-PA 10/08/29 n.h...|Amel|GB18507-PA 10/09/10 54 %/237 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fner ...

  18. EST Table: FS918793 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918793 E_FL_fufe_45H06_F_0 10/09/28 92 %/247 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/13 43 %/253 aa FBpp0166535|DmojGI17318-PA 10/08/29 n.h...|Amel|GB18507-PA 10/09/10 52 %/256 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fufe ...

  19. EST Table: FS841411 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS841411 E_FL_fner_12E17_F_0 10/09/28 87 %/135 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/10 53 %/133 aa FBpp0078827|stai-PC 10/08/29 n.h 10/09/...B18507-PA 10/09/10 51 %/139 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fner ...

  20. EST Table: FS874636 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS874636 E_FL_ftes_01I14_F_0 10/09/28 88 %/152 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/11 54 %/151 aa FBpp0078827|stai-PC 10/08/29 n.h 10/09/...B18507-PA 10/09/10 51 %/156 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 ftes ...

  1. EST Table: FS919586 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919586 E_FL_fufe_47M17_F_0 10/09/28 93 %/271 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/13 46 %/271 aa FBpp0144714|DgriGH10808-PA 10/08/29 n.h...|Amel|GB18507-PA 10/09/10 53 %/274 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fufe ...

  2. EST Table: FS913761 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS913761 E_FL_fufe_30E02_F_0 10/09/28 79 %/252 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/12 51 %/192 aa FBpp0078829|stai-PA 10/08/29 n.h 10/09/...B18507-PA 10/09/10 49 %/259 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fufe ...

  3. EST Table: FS841247 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS841247 E_FL_fner_11N10_F_0 10/09/28 89 %/162 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/10 54 %/161 aa FBpp0078827|stai-PC 10/08/29 n.h 10/09/...B18507-PA 10/09/10 52 %/166 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fner ...

  4. EST Table: FS874478 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS874478 E_FL_ftes_01B04_F_0 10/09/28 89 %/168 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/11 53 %/167 aa FBpp0078827|stai-PC 10/08/29 n.h 10/09/...B18507-PA 10/09/10 52 %/172 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 ftes ...

  5. EST Table: FS837762 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS837762 E_FL_fner_02A19_F_0 10/09/28 83 %/135 aa ref|NP_001040215.1| stathmin [Bom...byx mori] gb|ABD36259.1| stathmin [Bombyx mori] 10/09/10 60 %/185 aa FBpp0166535|DmojGI17318-PA 10/08/29 n.h...|Amel|GB18507-PA 10/09/10 53 %/130 aa gi|91083957|ref|XP_975021.1| PREDICTED: similar to stathmin [Tribolium castaneum] FS915193 fner ...

  6. EST Table: FS873072 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS873072 E_FL_fner_50B18_R_0 10/09/28 91 %/224 aa ref|NP_001036841.1| Annexin IX is...oform A [Bombyx mori] dbj|BAA92809.1| annexin IX-A [Bombyx mori] 10/09/11 73 %/224 aa FBpp0280989|DpseGA1909...1|gene:ANXB9 10/09/10 62 %/224 aa gnl|Amel|GB16448-PA 10/09/10 73 %/224 aa gi|91092420|ref|XP_967931.1| PREDICTED: similar to Annexin IX CG5730-PC [Tribolium castaneum] FS780436 fner ...

  7. EST Table: FS774145 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS774145 E_FL_fcaL_03N15_R_0 10/09/28 89 %/197 aa ref|NP_001036841.1| Annexin IX is...oform A [Bombyx mori] dbj|BAA92809.1| annexin IX-A [Bombyx mori] 10/09/08 71 %/197 aa FBpp0280989|DpseGA1909...1|gene:ANXB9 10/09/10 60 %/197 aa gnl|Amel|GB16448-PA 10/09/10 71 %/197 aa gi|91092420|ref|XP_967931.1| PREDICTED: similar to Annexin IX CG5730-PC [Tribolium castaneum] FS780436 fcaL ...

  8. EST Table: FS871503 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS871503 E_FL_fner_45K10_R_0 10/09/28 90 %/219 aa ref|NP_001036841.1| Annexin IX is...oform A [Bombyx mori] dbj|BAA92809.1| annexin IX-A [Bombyx mori] 10/09/11 73 %/219 aa FBpp0280989|DpseGA1909...1|gene:ANXB9 10/09/10 61 %/219 aa gnl|Amel|GB16448-PA 10/09/10 73 %/219 aa gi|91092420|ref|XP_967931.1| PREDICTED: similar to Annexin IX CG5730-PC [Tribolium castaneum] FS780436 fner ...

  9. EST Table: FS745241 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS745241 E_FL_bmmt_30L24_R_0 10/09/28 90 %/213 aa ref|NP_001036841.1| Annexin IX is...oform A [Bombyx mori] dbj|BAA92809.1| annexin IX-A [Bombyx mori] 10/09/08 73 %/213 aa FBpp0280989|DpseGA1909...1|gene:ANXB9 10/09/10 61 %/213 aa gnl|Amel|GB16448-PA 10/09/10 73 %/213 aa gi|91092420|ref|XP_967931.1| PREDICTED: similar to Annexin IX CG5730-PC [Tribolium castaneum] FS780436 bmmt ...

  10. EST Table: FS898187 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS898187 E_FL_ftes_29O11_R_0 10/09/28 81 %/240 aa ref|NP_001036841.1| Annexin IX is...oform A [Bombyx mori] dbj|BAA92809.1| annexin IX-A [Bombyx mori] 10/09/12 65 %/241 aa FBpp0280989|DpseGA1909...1|gene:ANXB9 10/09/10 55 %/241 aa gnl|Amel|GB16448-PA 10/09/10 65 %/241 aa gi|91092420|ref|XP_967931.1| PREDICTED: similar to Annexin IX CG5730-PC [Tribolium castaneum] FS780436 ftes ...

  11. EST Table: FS823180 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS823180 E_FL_fmgV_14H20_R_0 10/09/28 33 %/237 aa ref|XP_001868268.1| thymus-specif...ic serine protease [Culex quinquefasciatus] gb|EDS26459.1| thymus-specific serine protease [Culex quinquefas...| PREDICTED: similar to thymus-specific serine protease [Tribolium castaneum] FS826745 fmgV ... ... 32 %/237 aa gnl|Amel|GB17481-PA 10/09/10 31 %/248 aa gi|91078858|ref|XP_972061.1

  12. EST Table: FS909014 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909014 E_FL_fufe_15P13_F_0 10/09/28 34 %/161 aa ref|XP_974840.1| PREDICTED: similar to harmon...um] 10/09/12 n.h 10/08/29 n.h 10/09/10 low homology 10/09/10 n.h 10/09/10 34 %/161 aa gi|91081527|ref|XP_974840.1| PREDICTED: similar to harmonin [Tribolium castaneum] FS911923 fufe ...

  13. EST Table: FS933340 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS933340 E_FL_fwgP_36M17_F_0 10/09/28 34 %/161 aa ref|XP_974840.1| PREDICTED: similar to harmon...um] 10/09/13 n.h 10/08/29 n.h 10/09/10 low homology 10/09/10 n.h 10/09/10 34 %/161 aa gi|91081527|ref|XP_974840.1| PREDICTED: similar to harmonin [Tribolium castaneum] FS911923 fwgP ...

  14. EST Table: FS828086 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS828086 E_FL_fmgV_28D05_R_0 10/09/28 48 %/120 aa ref|XP_974840.1| PREDICTED: similar to harmon...um] 10/09/10 n.h 10/08/29 n.h 10/09/10 low homology 10/09/10 n.h 10/09/10 48 %/120 aa gi|91081527|ref|XP_974840.1| PREDICTED: similar to harmonin [Tribolium castaneum] FS827409 fmgV ...

  15. EST Table: FS915115 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915115 E_FL_fufe_34E16_F_0 11/12/09 n.h 10/09/28 51 %/158 aa ref|XP_315489.2| AGA... 49 %/183 aa FBpp0265444|DyakGE20434-PA 10/08/29 low homology 10/09/10 51 %/158 aa AGAP005486-PA Protein|2L:...09/10 44 %/162 aa gi|91089379|ref|XP_973709.1| PREDICTED: similar to mitochondrial ribosomal protein L50 CG8612-PA [Tribolium castaneum] FS915115 fufe ...

  16. EST Table: FS880101 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS880101 E_FL_ftes_17H24_F_0 10/09/28 91 %/139 aa ref|NP_001040254.1| beadex/dLMO p...rotein [Bombyx mori] gb|ABD36315.1| beadex/dLMO protein [Bombyx mori] 10/09/11 low homology 10/08/29 low hom...ology 10/09/10 low homology 10/09/10 low homology 10/09/10 71 %/119 aa gi|91080717|ref|XP_975367.1| PREDICTED: similar to beadex/dLMO protein [Tribolium castaneum] FS794536 ftes ...

  17. EST Table: FS794131 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS794131 E_FL_ffbm_14J02_F_0 10/09/28 94 %/212 aa ref|NP_001040254.1| beadex/dLMO p...rotein [Bombyx mori] gb|ABD36315.1| beadex/dLMO protein [Bombyx mori] 10/09/09 79 %/158 aa FBpp0125729|DanaG...9 %/150 aa gnl|Amel|GB11268-PA 10/09/10 79 %/183 aa gi|91080717|ref|XP_975367.1| PREDICTED: similar to beadex/dLMO protein [Tribolium castaneum] FS794536 ffbm ...

  18. EST Table: FS928812 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS928812 E_FL_fwgP_23F21_F_0 10/09/28 78 %/134 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS936452 fwgP ...

  19. EST Table: FS920735 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS920735 E_FL_fufe_51F22_F_0 11/12/09 n.h 10/09/28 92 %/229 aa ref|NP_001037168.1| ovarian... serine protease [Bombyx mori] gb|AAL62027.1|AF294884_1 ovarian serine protease [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS920735 fufe ...

  20. EST Table: FS921913 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS921913 E_FL_fwgP_03B17_F_0 10/09/28 54 %/215 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fwgP ...

  1. EST Table: FS804486 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS804486 E_FL_fmgV_15E24_F_0 10/09/28 53 %/199 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fmgV ...

  2. EST Table: FS926804 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS926804 E_FL_fwgP_17H18_F_0 10/09/28 58 %/249 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fwgP ...

  3. EST Table: FS810510 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS810510 E_FL_fmgV_32C08_F_0 10/09/28 57 %/259 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fmgV ...

  4. EST Table: FS800709 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS800709 E_FL_fmgV_04M06_F_0 10/09/28 57 %/262 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fmgV ...

  5. EST Table: FS804646 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS804646 E_FL_fmgV_15M02_F_0 10/09/28 54 %/215 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fmgV ...

  6. EST Table: FS933547 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS933547 E_FL_fwgP_37G10_F_0 10/09/28 56 %/205 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fwgP ...

  7. EST Table: FS807612 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS807612 E_FL_fmgV_24A09_F_0 10/09/28 57 %/266 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fmgV ...

  8. EST Table: FS937969 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS937969 E_FL_fwgP_50K04_F_0 10/09/28 56 %/264 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fwgP ...

  9. EST Table: FS806480 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS806480 E_FL_fmgV_20N06_F_0 10/09/28 57 %/259 aa ref|XP_001659582.1| xaa-pro dipeptidase pepd/pepq(e.coli...) [Aedes aegypti] gb|EAT39285.1| xaa-pro dipeptidase pepd/pepq(e.coli) [Aedes aegypti... aa gi|189233738|ref|XP_971576.2| PREDICTED: similar to xaa-pro dipeptidase pepd/pepq(e.coli) [Tribolium castaneum] FS768084 fmgV ...

  10. EST Table: FS910230 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS910230 E_FL_fufe_19J14_F_0 10/09/28 30 %/250 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...250 aa gi|91078946|ref|XP_974065.1| PREDICTED: similar to Outer dense fiber protein 2 (Outer dense fiber of ...sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS910822 fufe ...

  11. EST Table: FS916459 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS916459 E_FL_fufe_38G06_F_0 10/09/28 30 %/303 aa ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber pro...6 %/182 aa gnl|Amel|GB14311-PA 10/09/10 30 %/303 aa gi|91078946|ref|XP_974065.1| PREDICTED: similar to Outer dense fiber... protein 2 (Outer dense fiber of sperm tails protein 2) (84 kDa outer dense fiber protein) (Cenexin) [Tribolium castaneum] FS910822 fufe ...

  12. EST Table: FS761536 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available /10 40 %/215 aa gi|91083987|ref|XP_975212.1| PREDICTED: similar to asteroid CG4426-PA [Tribolium castaneum] FS761536 fcaL ... ...FS761536 E_FL_fcaL_17N06_F_0 11/12/09 n.h 10/09/28 40 %/215 aa ref|XP_975212.1| PREDICTED: similar to astero...id CG4426-PA [Tribolium castaneum] gb|EFA04435.1| hypothetical protein TcasGA2_TC01

  13. EST Table: FS916297 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS916297 E_FL_fufe_37O18_F_0 11/12/09 n.h 10/09/28 74 %/273 aa ref|XP_001648944.1| dendritic...on factor 3 subunit M; Short=eIF3m gb|EAT44291.1| dendritic cell protein [Aedes aegypti] 10/09/12 70 %/270 a...271 aa gi|91091954|ref|XP_968265.1| PREDICTED: similar to dendritic cell protein [Tribolium castaneum] FS916297 fufe ...

  14. EST Table: FS791278 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS791278 E_FL_ffbm_06E16_F_0 11/12/09 n.h 10/09/28 100 %/173 aa ref|NP_001093312.1| glover...in 3 [Bombyx mori] dbj|BAF63527.1| gloverin3 [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS791278 ffbm ...

  15. EST Table: FS759792 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS759792 E_FL_fcaL_12G09_F_0 10/09/28 89 %/167 aa ref|NP_001036930.1| gloverin 1 [B...ombyx mori] dbj|BAD51473.1| gloverin-like protein 1 [Bombyx mori] 10/09/08 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS798027 fcaL ...

  16. EST Table: FS765856 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS765856 E_FL_fcaL_41C12_F_0 11/12/09 n.h 10/09/28 99 %/182 aa ref|NP_001040437.1| muscular... protein 20 [Bombyx mori] gb|ABF51386.1| muscular protein 20 [Bombyx mori] 10/09/08 61 %/173 aa FBpp...10/09/10 79 %/181 aa gi|91077564|ref|XP_972465.1| PREDICTED: similar to muscular protein 20 [Tribolium castaneum] FS765856 fcaL ...

  17. EST Table: FS931756 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS931756 E_FL_fwgP_32C23_F_0 10/09/28 73 %/261 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 40 %/277 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 38 %/274 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  18. EST Table: FS935181 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS935181 E_FL_fwgP_42D15_F_0 10/09/28 40 %/118 aa ref|NP_001129360.1| osiris 9 [Bom...byx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS935058 fwgP ...

  19. EST Table: FS935773 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS935773 E_FL_fwgP_44A15_F_0 10/09/28 73 %/261 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 40 %/277 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 38 %/274 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  20. EST Table: FS928966 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS928966 E_FL_fwgP_23M22_F_0 10/09/28 83 %/209 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 43 %/226 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 41 %/223 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  1. EST Table: FS938424 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS938424 E_FL_fwgP_51P06_F_0 10/09/28 39 %/128 aa ref|NP_001129360.1| osiris 9 [Bom...byx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS935058 fwgP ...

  2. EST Table: FS933330 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS933330 E_FL_fwgP_36M07_F_0 10/09/28 100 %/103 aa ref|NP_001129360.1| osiris 9 [Bo...mbyx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS930560 fwgP ...

  3. EST Table: FS934228 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS934228 E_FL_fwgP_39G21_F_0 10/09/28 69 %/238 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 40 %/251 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 38 %/247 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  4. EST Table: FS933711 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS933711 E_FL_fwgP_37O05_F_0 10/09/28 73 %/261 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 40 %/277 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 38 %/274 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  5. EST Table: FS938425 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS938425 E_FL_fwgP_51P07_F_0 10/09/28 73 %/259 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 39 %/276 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 38 %/274 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  6. EST Table: FS928195 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS928195 E_FL_fwgP_21J08_F_0 10/09/28 73 %/256 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 40 %/277 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 39 %/268 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  7. EST Table: FS924814 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS924814 E_FL_fwgP_11K20_F_0 10/09/28 39 %/114 aa ref|NP_001129360.1| osiris 9 [Bom...byx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS935058 fwgP ...

  8. EST Table: FS938632 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS938632 E_FL_fwgP_52J03_F_0 10/09/28 46 %/187 aa ref|NP_001129360.1| osiris 9 [Bom...byx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 34 %/114 aa FBpp0147931|DgriGH14025-PA 10/08/29 n.h 10/09/10 low homology 10/09/10 n.h 10/09/10 n.h FS937505 fwgP ...

  9. EST Table: FS930675 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS930675 E_FL_fwgP_28O10_F_0 10/09/28 40 %/120 aa ref|NP_001129360.1| osiris 9 [Bom...byx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS935058 fwgP ...

  10. EST Table: FS927432 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS927432 E_FL_fwgP_19F11_F_0 10/09/28 83 %/209 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 43 %/226 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 41 %/223 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  11. EST Table: FS934727 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS934727 E_FL_fwgP_40N24_F_0 10/09/28 83 %/209 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 43 %/226 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 41 %/223 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  12. EST Table: FS930504 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS930504 E_FL_fwgP_28G04_F_0 10/09/28 40 %/120 aa ref|NP_001129360.1| osiris 9 [Bom...byx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS935058 fwgP ...

  13. EST Table: FS928483 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS928483 E_FL_fwgP_22G12_F_0 10/09/28 73 %/256 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 40 %/277 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 39 %/268 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  14. EST Table: FS938378 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS938378 E_FL_fwgP_51N02_F_0 10/09/28 40 %/120 aa ref|NP_001129360.1| osiris 9 [Bom...byx mori] gb|ACI23620.1| osiris 9 [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS935058 fwgP ...

  15. EST Table: FS922446 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922446 E_FL_fwgP_04K13_F_0 10/09/28 73 %/261 aa ref|NP_001136223.1| osiris 7 [Bom...byx mori] gb|ACJ12371.1| osiris7 [Bombyx mori] 10/09/13 40 %/277 aa FBpp0255200|DyakGE10190-PA 10/08/29 n.h ...mel|GB13419-PA 10/09/10 38 %/274 aa gi|91091224|ref|XP_967197.1| PREDICTED: similar to osiris 7 [Tribolium castaneum] FS931205 fwgP ...

  16. EST Table: FS922222 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922222 E_FL_fwgP_04A01_F_0 11/12/09 GO hit GO:0003824(catalytic activity)|GO:0004...:Q23528#protein_id :AAA68746.2 10/09/10 45 %/225 aa AGAP007141-PA Protein|2L:43562501:43563392:1|gene:AGAP007141 10/09/10 47 %/222... aa gnl|Amel|GB19856-PA 10/09/10 44 %/259 aa gi|270008174|gb|EFA04622.1| serine protease P145 [Tribolium castaneum] FS922222 fwgP ...

  17. Synthesis of ZSM-5 Monoliths with Hierarchical Porosity

    Institute of Scientific and Technical Information of China (English)

    Tong Yangchuan; Zhao Tianbo; Li Fengyan; Zong Baoning; Wang Yue

    2006-01-01

    A new route to synthesize ZSM-5 monoliths with hierarchical pore structure has been referred to in this stud y. The successful incorporation of the macropores and mesopores within the ZSM-5 structure was achieved through transforming the skeleton of the macroporous silica gel into zeolite ZSM-5 using carbon materials as the transitional template. The ZSM-5 crystal covered part of the macroporous material, and provided micropores to the macroporous silica gel. The structure of carbon monolith was studied after dissolving the silica contained in the carbon/silica composite.

  18. Monolithic Michelson Interferometer as ultra stable wavelength reference

    Science.gov (United States)

    Wan, Xiaoke; Ge, Jian

    2010-07-01

    Ultra-stable Monolithic Michelson interferometer can be an ideal reference for highprecision applications such as RV measurement in planet searching and orbit study. The advantages include wide wavelength range, simple sinusoidal spectral format, and high optical efficiency. In this paper, we report that a monolithic Michelson interferometers has been in-house developed with minimized thermal sensitivity with compensation tuning. With a scanning white light interferometer, the thermal sensitivity is measured ~ 6x10-7/°C at 550 nm and it decreases to zero near 1000 nm. We expect the wideband wavelength reference source to be stabilized better than 0.3 m/s for RV experiments

  19. Numerical Simulation of Fluid Dynamics in a Monolithic Column

    Directory of Open Access Journals (Sweden)

    Kazuhiro Yamamoto

    2017-01-01

    Full Text Available As for the measurement of polycyclic aromatic hydrocarbons (PAHs, ultra-performance liquid chromatography (UPLC is used for PAH identification and densitometry. However, when a solvent containing a substance to be identified passes through a column of UPLC, a dedicated high-pressure-proof device is required. Recently, a liquid chromatography instrument using a monolithic column technology has been proposed to reduce the pressure of UPLC. The present study tested five types of monolithic columns produced in experiments. To simulate the flow field, the lattice Boltzmann method (LBM was used. The velocity profile was discussed to decrease the pressure drop in the ultra-performance liquid chromatography (UPLC system.

  20. A Monolithic Oxide-Based Transversal Thermoelectric Energy Harvester

    Science.gov (United States)

    Teichert, S.; Bochmann, A.; Reimann, T.; Schulz, T.; Dreßler, C.; Udich, S.; Töpfer, J.

    2016-03-01

    We report the fabrication and properties of a monolithic transversal thermoelectric energy harvester based on the combination of a thermoelectric oxide and a metal. The fabrication of the device is done with a ceramic multilayer technology using printing and co-firing processes. Five transversal devices were combined to a meander-like thermoelectric generator. Electrical measurements and finite element calculations were performed to characterize the resulting thermoelectric generator. A maximum experimental electrical power output of 30.2 mW at a temperature difference of {Δ }T = 208 K was found. The prepared monolithic thermoelectric generator provides at {Δ }T = 35 K sufficient energy to drive a simple electronic sensor application.

  1. Paladin Enterprises: Monolithic particle physics models global climate.

    CERN Multimedia

    2002-01-01

    Paladin Enterprises presents a monolithic particle model of the universe which will be used by them to build an economical fusion energy system. The model is an extension of the work done by James Clerk Maxwell. Essentially, gravity is unified with electro-magnetic forces and shown to be a product of a closed loop current system, i.e. a particle - monolithic or sub atomic. This discovery explains rapid global climate changes which are evident in the geological record and also provides an explanation for recent changes in the global climate.

  2. Lectin-carbohydrate interactions on nanoporous gold monoliths.

    Science.gov (United States)

    Tan, Yih Horng; Fujikawa, Kohki; Pornsuriyasak, Papapida; Alla, Allan J; Ganesh, N Vijaya; Demchenko, Alexei V; Stine, Keith J

    2013-07-01

    Monoliths of nanoporous gold (np-Au) were modified with self-assembled monolayers of octadecanethiol (C18-SH), 8-mercaptooctyl α-D-mannopyranoside (αMan-C8-SH), and 8-mercapto-3,6-dioxaoctanol (HO-PEG2-SH), and the loading was assessed using thermogravimetric analysis (TGA). Modification with mixed SAMs containing αMan-C8-SH (at a 0.20 mole fraction in the SAM forming solution) with either octanethiol or HO-PEG2-SH was also investigated. The np-Au monoliths modified with αMan-C8-SH bind the lectin Concanavalin A (Con A), and the additional mass due to bound protein was assessed using TGA analysis. A comparison of TGA traces measured before and after exposure of HO-PEG2-SH modified np-Au to Con A showed that the non-specific binding of Con A was minimal. In contrast, np-Au modified with octanethiol showed a significant mass loss due to non-specifically adsorbed Con A. A significant mass loss was also attributed to binding of Con A to bare np-Au monoliths. TGA revealed a mass loss due to the binding of Con A to np-Au monoliths modified with pure αMan-C8-SH. The use of mass losses determined by TGA to compare the binding of Con A to np-Au monoliths modified by mixed SAMs of αMan-C8-SH and either octanethiol or HO-PEG2-SH revealed that binding to mixed SAM modified surfaces is specific for the mixed SAMs with HO-PEG2-SH but shows a significant contribution from non-specific adsorption for the mixed SAMs with octanethiol. Minimal adsorption of immunoglobulin G (IgG) and peanut agglutinin (PNA) towards the mannoside modified np-Au monoliths was demonstrated. A greater mass loss was found for Con A bound onto the monolith than for either IgG or PNA, signifying that the mannose presenting SAMs in np-Au retain selectivity for Con A. TGA data also provide evidence that Con A bound to the αMan-C8-SH modified np-Au can be eluted by flowing a solution of methyl α-D-mannopyranoside through the structure. The presence of Con A proteins on the modified np-Au surface was

  3. Constitutive Theory Developed for Monolithic Ceramic Materials

    Science.gov (United States)

    Janosik, Lesley A.

    1998-01-01

    with these service conditions by developing a multiaxial viscoplastic constitutive model that accounts for time-dependent hereditary material deformation (such as creep and stress relaxation) in monolithic structural ceramics. Using continuum principles of engineering mechanics, we derived the complete viscoplastic theory from a scalar dissipative potential function.

  4. Polyurea-Based Aerogel Monoliths and Composites

    Science.gov (United States)

    Lee, Je Kyun

    2012-01-01

    aerogel insulation material was developed that will provide superior thermal insulation and inherent radiation protection for government and commercial applications. The rubbery polyureabased aerogel exhibits little dustiness, good flexibility and toughness, and durability typical of the parent polyurea polymer, yet with the low density and superior insulation properties associated with aerogels. The thermal conductivity values of polyurea-based aerogels at lower temperature under vacuum pressures are very low and better than that of silica aerogels. Flexible, rubbery polyurea-based aerogels are able to overcome the weak and brittle nature of conventional inorganic and organic aerogels, including polyisocyanurate aerogels, which are generally prepared with the one similar component to polyurethane rubber aerogels. Additionally, with higher content of hydrogen in their structures, the polyurea rubber-based aerogels will also provide inherently better radiation protection than those of inorganic and carbon aerogels. The aerogel materials also demonstrate good hydrophobicity due to their hydrocarbon molecular structure. There are several strategies to overcoming the drawbacks associated with the weakness and brittleness of silica aerogels. Development of the flexible fiber-reinforced silica aerogel composite blanket has proven to be one promising approach, providing a conveniently fielded form factor that is relatively robust in industrial environments compared to silica aerogel monoliths. However, the flexible, silica aerogel composites still have a brittle, dusty character that may be undesirable, or even intolerable, in certain application environments. Although the cross - linked organic aerogels, such as resorcinol- formaldehyde (RF), polyisocyanurate, and cellulose aerogels, show very high impact strength, they are also very brittle with little elongation (i.e., less rubbery). Also, silica and carbon aerogels are less efficient radiation shielding materials due

  5. Chromatographic comparison of bupivacaine imprinted polymers prepared in crushed monolith, microsphere, silica-based composite and capillary monolith formats.

    Science.gov (United States)

    Oxelbark, Joakim; Legido-Quigley, Cristina; Aureliano, Carla S A; Titirici, Maria-Magdalena; Schillinger, Eric; Sellergren, Börje; Courtois, Julien; Irgum, Knut; Dambies, Laurent; Cormack, Peter A G; Sherrington, David C; De Lorenzi, Ersilia

    2007-08-10

    A comprehensive comparison of five chromatographic stationary phases based on molecularly imprinted polymers is presented. Efficiency, imprinting factors, water compatibility and batch-to-batch reproducibility are discussed for crushed monolith, microspheres, two silica-based composites and capillary monoliths, all imprinted with the local anaesthetic bupivacaine. Synthesis protocol and chromatographic test conditions have been kept fixed within certain limits, in order to provide further insight into the strengths and weaknesses of the different formats. Excluding microparticles, all formats give satisfactory performance, especially in aqueous mobile phases. An assessment of batch-to-batch reproducibility in different mobile phases adds further value to this comparison study.

  6. EST Table: FS905503 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS905503 E_FL_fufe_05E05_F_0 11/12/09 n.h 10/09/28 42 %/180 aa ref|XP_002426758.1| protein singed wings... 2 precursor, putative [Pediculus humanus corporis] gb|EEB14020.1| protein singed wings

  7. EST Table: FS911628 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS911628 E_FL_fufe_23M16_F_0 10/09/28 42 %/180 aa ref|XP_002426758.1| protein singed wings... 2 precursor, putative [Pediculus humanus corporis] gb|EEB14020.1| protein singed wings 2 precursor,

  8. EST Table: FS912142 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS912142 E_FL_fufe_25F22_F_0 10/09/28 42 %/180 aa ref|XP_002426758.1| protein singed wings... 2 precursor, putative [Pediculus humanus corporis] gb|EEB14020.1| protein singed wings 2 precursor,

  9. EST Table: FS825667 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS825667 E_FL_fmgV_21G14_R_0 11/12/09 n.h 10/09/28 42 %/134 aa ref|XP_002426758.1| protein singed wings... 2 precursor, putative [Pediculus humanus corporis] gb|EEB14020.1| protein singed wings

  10. EST Table: FS910236 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS910236 E_FL_fufe_19J20_F_0 10/09/28 42 %/180 aa ref|XP_002426758.1| protein singed wings... 2 precursor, putative [Pediculus humanus corporis] gb|EEB14020.1| protein singed wings 2 precursor,

  11. EST Table: FS916816 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS916816 E_FL_fufe_39H09_F_0 10/09/28 98 %/154 aa ref|NP_001040265.1| phosphohistid...ine phosphatase [Bombyx mori] gb|ABD36332.1| phosphohistidine phosphatase [Bombyx mori] 10/09/12 48 %/130 aa FBpp029216

  12. EST Table: FS937597 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 10 83 %/206 aa gnl|Amel|GB11674-PA 10/09/10 76 %/209 aa gi|91083597|ref|XP_968968.1| PREDICTED: similar to golgi reassembly-stacking protein 2 [Tribolium castaneum] FS915307 fwgP ...

  13. EST Table: FS878154 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 10 82 %/181 aa gnl|Amel|GB11674-PA 10/09/10 76 %/181 aa gi|91083597|ref|XP_968968.1| PREDICTED: similar to golgi reassembly-stacking protein 2 [Tribolium castaneum] FS915307 ftes ...

  14. EST Table: FS920822 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 10 83 %/206 aa gnl|Amel|GB11674-PA 10/09/10 71 %/234 aa gi|91083597|ref|XP_968968.1| PREDICTED: similar to golgi reassembly-stacking protein 2 [Tribolium castaneum] FS915307 fufe ...

  15. EST Table: FS724255 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 10 83 %/206 aa gnl|Amel|GB11674-PA 10/09/10 77 %/209 aa gi|91083597|ref|XP_968968.1| PREDICTED: similar to golgi reassembly-stacking protein 2 [Tribolium castaneum] FS915307 bmmt ...

  16. EST Table: FS911554 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 10 68 %/265 aa gnl|Amel|GB11674-PA 10/09/10 71 %/234 aa gi|91083597|ref|XP_968968.1| PREDICTED: similar to golgi reassembly-stacking protein 2 [Tribolium castaneum] FS915307 fufe ...

  17. EST Table: FS921674 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS921674 E_FL_fwgP_02G01_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  18. EST Table: FS765561 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS765561 E_FL_fcaL_40D21_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  19. EST Table: FS734315 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS734315 E_FL_bmmt_23O07_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  20. EST Table: FS842061 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS842061 E_FL_fner_14C13_F_0 10/09/28 100 %/146 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  1. EST Table: FS728650 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS728650 E_FL_bmmt_13N08_F_0 10/09/28 45 %/162 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  2. EST Table: FS839292 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS839292 E_FL_fner_06E22_F_0 10/09/28 100 %/168 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  3. EST Table: FS922232 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922232 E_FL_fwgP_04A12_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  4. EST Table: FS841521 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS841521 E_FL_fner_12J22_F_0 10/09/28 100 %/166 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  5. EST Table: FS757229 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS757229 E_FL_fcaL_04I18_F_0 10/09/28 99 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  6. EST Table: FS801527 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS801527 E_FL_fmgV_07B09_F_0 10/09/28 100 %/146 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  7. EST Table: FS799544 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS799544 E_FL_fmgV_01I07_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  8. EST Table: FS767754 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS767754 E_FL_fcaL_46P03_F_0 10/09/28 97 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  9. EST Table: FS762107 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS762107 E_FL_fcaL_29J15_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  10. EST Table: FS807394 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS807394 E_FL_fmgV_23G11_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  11. EST Table: FS849318 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS849318 E_FL_fner_34K18_F_0 10/09/28 98 %/168 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  12. EST Table: FS766714 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS766714 E_FL_fcaL_43M05_F_0 10/09/28 99 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  13. EST Table: FS769848 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS769848 E_FL_fcaL_53H04_F_0 10/09/28 99 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  14. EST Table: FS843162 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS843162 E_FL_fner_17E02_F_0 10/09/28 100 %/166 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  15. EST Table: FS807563 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS807563 E_FL_fmgV_23O06_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  16. EST Table: FS909065 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909065 E_FL_fufe_16B22_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  17. EST Table: FS817818 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS817818 E_FL_fmgV_52H08_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  18. EST Table: FS758353 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS758353 E_FL_fcaL_08A24_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  19. EST Table: FS805588 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS805588 E_FL_fmgV_18F17_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  20. EST Table: FS727475 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS727475 E_FL_bmmt_10H14_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  1. EST Table: FS813678 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS813678 E_FL_fmgV_40P23_F_0 10/09/28 99 %/160 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  2. EST Table: FS815997 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS815997 E_FL_fmgV_47G04_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  3. EST Table: FS844955 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS844955 E_FL_fner_22E09_F_0 10/09/28 100 %/166 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  4. EST Table: FS763854 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS763854 E_FL_fcaL_34P15_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  5. EST Table: FS801908 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS801908 E_FL_fmgV_08C10_F_0 10/09/28 100 %/146 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  6. EST Table: FS724828 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS724828 E_FL_bmmt_02O15_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  7. EST Table: FS814316 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS814316 E_FL_fmgV_42L19_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  8. EST Table: FS770229 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS770229 E_FL_fcaL_18J14_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  9. EST Table: FS772713 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS772713 E_FL_fcaL_26E16_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  10. EST Table: FS734009 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS734009 E_FL_bmmt_23A02_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  11. EST Table: FS808271 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS808271 E_FL_fmgV_25N21_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  12. EST Table: FS844912 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS844912 E_FL_fner_22C08_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  13. EST Table: FS765762 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS765762 E_FL_fcaL_40N20_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  14. EST Table: FS801288 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS801288 E_FL_fmgV_06G11_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  15. EST Table: FS888164 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS888164 E_FL_ftes_41H04_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  16. EST Table: FS811208 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS811208 E_FL_fmgV_34B24_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  17. EST Table: FS812927 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS812927 E_FL_fmgV_38O15_F_0 10/09/28 100 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mor

  18. EST Table: FS759325 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS759325 E_FL_fcaL_10P09_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  19. EST Table: FS758897 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS758897 E_FL_fcaL_09K21_F_0 10/09/28 98 %/169 aa ref|NP_001040343.1| peripheral-type benzodiazepine... receptor [Bombyx mori] gb|ABF51223.1| peripheral-type benzodiazepine receptor [Bombyx mori

  20. EST Table: FS906090 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS906090 E_FL_fufe_07B18_F_0 10/09/28 99 %/220 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/12 80 %/222 aa FBpp02346

  1. EST Table: FS841606 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS841606 E_FL_fner_12N15_F_0 10/09/28 100 %/132 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/10 87 %/133 aa FBpp0116

  2. EST Table: FS743516 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS743516 E_FL_bmmt_25O09_R_0 10/09/28 98 %/167 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/07 80 %/167 aa FBpp02771

  3. EST Table: FS850077 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS850077 E_FL_fner_36N05_F_0 10/09/28 99 %/204 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/11 83 %/205 aa FBpp02522

  4. EST Table: FS786649 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS786649 E_FL_fcaL_18O17_R_0 10/09/28 98 %/167 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/09 80 %/167 aa FBpp02771

  5. EST Table: FS853020 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS853020 E_FL_fner_45D02_F_0 10/09/28 99 %/180 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/11 87 %/181 aa FBpp02522

  6. EST Table: FS909348 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909348 E_FL_fufe_16P20_F_0 10/09/28 99 %/220 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/12 80 %/222 aa FBpp02346

  7. EST Table: FS909374 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909374 E_FL_fufe_17B02_F_0 10/09/28 99 %/220 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/12 80 %/222 aa FBpp02346

  8. EST Table: FS764958 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS764958 E_FL_fcaL_38G13_F_0 10/09/28 98 %/220 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/08 80 %/222 aa FBpp02346

  9. EST Table: FS917079 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917079 E_FL_fufe_40D23_F_0 10/09/28 99 %/217 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/12 81 %/213 aa FBpp02346

  10. EST Table: FS868421 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS868421 E_FL_fner_36N05_R_0 10/09/28 98 %/197 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/11 81 %/198 aa FBpp02771

  11. EST Table: FS770331 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS770331 E_FL_fcaL_18O17_F_0 10/09/28 99 %/155 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/08 86 %/156 aa FBpp02522

  12. EST Table: FS763745 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS763745 E_FL_fcaL_34J22_F_0 10/09/28 98 %/202 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/08 83 %/203 aa FBpp02522

  13. EST Table: FS769451 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS769451 E_FL_fcaL_52D16_F_0 10/09/28 96 %/208 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/08 78 %/209 aa FBpp02346

  14. EST Table: FS781715 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS781715 E_FL_fcaL_38G13_R_0 10/09/28 97 %/209 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/08 80 %/210 aa FBpp02771

  15. EST Table: FS878889 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS878889 E_FL_ftes_13O22_F_0 10/09/28 96 %/166 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/11 85 %/167 aa FBpp02522

  16. EST Table: FS780579 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS780579 E_FL_fcaL_34J22_R_0 10/09/28 98 %/202 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/08 80 %/203 aa FBpp02771

  17. EST Table: FS871345 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS871345 E_FL_fner_45D02_R_0 10/09/28 99 %/220 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/11 80 %/221 aa FBpp02346

  18. EST Table: FS876378 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS876378 E_FL_ftes_06K04_F_0 10/09/28 100 %/154 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/11 87 %/155 aa FBpp0252

  19. EST Table: FS912488 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS912488 E_FL_fufe_26G13_F_0 10/09/28 99 %/220 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/12 80 %/222 aa FBpp02346

  20. EST Table: FS785832 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS785832 E_FL_fcaL_52D16_R_0 10/09/28 97 %/118 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/09 78 %/119 aa FBpp02346

  1. EST Table: FS931382 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS931382 E_FL_fwgP_31A18_F_0 10/09/28 100 %/158 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/13 87 %/159 aa FBpp0252

  2. EST Table: FS732209 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS732209 E_FL_bmmt_25O09_F_0 10/09/28 100 %/175 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/03 88 %/176 aa FBpp0252

  3. EST Table: FS910496 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS910496 E_FL_fufe_20G12_F_0 10/09/28 99 %/220 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/12 80 %/222 aa FBpp02346

  4. EST Table: FS917608 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917608 E_FL_fufe_41N17_F_0 10/09/28 99 %/220 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/12 80 %/222 aa FBpp02346

  5. EST Table: FS860309 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS860309 E_FL_fner_12N15_R_0 10/09/28 98 %/165 aa ref|NP_001040402.1| preimplantation... protein [Bombyx mori] gb|ABF51322.1| preimplantation protein [Bombyx mori] 10/09/11 80 %/166 aa FBpp02771

  6. EST Table: FS812727 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 1 aa gnl|Amel|GB16225-PA 10/09/10 49 %/157 aa gi|91081299|ref|XP_968887.1| PREDICTED: similar to cleft lip and palate transmembrane protein 1 [Tribolium castaneum] FS920349 fmgV ...

  7. EST Table: FS765252 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 1 aa gnl|Amel|GB16225-PA 10/09/10 52 %/135 aa gi|91081299|ref|XP_968887.1| PREDICTED: similar to cleft lip and palate transmembrane protein 1 [Tribolium castaneum] FS920349 fcaL ...

  8. EST Table: FS749375 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 0 aa gnl|Amel|GB16225-PA 10/09/10 49 %/156 aa gi|91081299|ref|XP_968887.1| PREDICTED: similar to cleft lip and palate transmembrane protein 1 [Tribolium castaneum] FS920349 caL- ...

  9. EST Table: FS920310 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 6 aa gnl|Amel|GB16225-PA 10/09/10 44 %/202 aa gi|91081299|ref|XP_968887.1| PREDICTED: similar to cleft lip and palate transmembrane protein 1 [Tribolium castaneum] FS920349 fufe ...

  10. EST Table: FS761682 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 6 aa gnl|Amel|GB16225-PA 10/09/10 41 %/212 aa gi|91081299|ref|XP_968887.1| PREDICTED: similar to cleft lip and palate transmembrane protein 1 [Tribolium castaneum] FS920349 fcaL ...

  11. EST Table: FS796494 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 38 aa ref|XP_001945612.1| PREDICTED: similar to glucocerebrosidase, partial [Acyr...9/10 42 %/261 aa gi|91087345|ref|XP_975608.1| PREDICTED: similar to putative lysosomal glucocerebrosidase [Tribolium castaneum] FS796494 ffbm ...

  12. EST Table: FS846041 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS846041 E_FL_fner_25G13_F_0 10/09/28 50 %/132 aa ref|XP_001606590.1| PREDICTED: similar to glucocerebro...el|GB10584-PA 10/09/10 47 %/138 aa gi|91087383|ref|XP_975651.1| PREDICTED: similar to Glucosylceramidase precursor (Beta-glucocerebro

  13. EST Table: FS840242 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available l|Amel|GB10584-PA 10/09/10 47 %/128 aa gi|91087383|ref|XP_975651.1| PREDICTED: similar to Glucosylceramidase precursor (Beta-glucocer...ebrosidase) (Acid beta-glucosidase) (D-glucosyl-N-acylsphingosine glucohydrolase) [Tribolium castaneum] FS796494 fner ...

  14. EST Table: FS758709 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available DICTED: similar to Niemann-Pick Type C-1 CG5722-PA isoform 2 [Apis mellifera] 10/09/08 38 %/193 aa FBpp01472...241956|ref|XP_967619.2| PREDICTED: similar to niemann-pick C1 [Tribolium castaneum] FS758709 fcaL ...

  15. EST Table: FS927097 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS927097 E_FL_fwgP_18F19_F_0 10/09/28 46 %/117 aa ref|XP_001847590.1| Trisn small n...uclear ribonucleoprotein [Culex quinquefasciatus] gb|EDS26491.1| Trisn small nuclear ribonucleoprotein [Cule

  16. EST Table: FS922226 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922226 E_FL_fwgP_04A05_F_0 10/09/28 low homology 10/09/13 low homology 10/08/29 l...ow homology 10/09/10 64 %/100 aa AGAP000444-PA Protein|X:7822875:7823977:-1|gene:AGAP000444 10/09/10 low hom

  17. EST Table: FS740698 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS740698 E_FL_bmmt_17P09_R_0 10/09/28 57 %/105 aa gb|AAT42262.1| cytochrome c oxidase subunit II [Actias sel...ene ningpoana] 10/09/07 41 %/105 aa FBpp0100177|mt:CoII-PA 10/08/28 n.h 10/09/10 n.

  18. EST Table: FS744225 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS744225 E_FL_bmmt_27N17_R_0 10/09/28 58 %/112 aa gb|AAT42262.1| cytochrome c oxidase subunit II [Actias sel...ene ningpoana] 10/09/07 43 %/112 aa FBpp0100177|mt:CoII-PA 10/08/28 n.h 10/09/10 n.

  19. EST Table: FS885385 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS885385 E_FL_ftes_32P04_F_0 10/09/28 54 %/108 aa gb|AAT42262.1| cytochrome c oxidase subunit II [Actias sel...ene ningpoana] 10/09/12 42 %/108 aa FBpp0100177|mt:CoII-PA 10/08/29 n.h 10/09/10 n.

  20. EST Table: FS756340 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 7 %/154 aa ref|NP_001116821.1| 18 wheeler [Bombyx mori] dbj|BAB85498.1| 18 wheeler [Bombyx mori] 10/09/08 44...gi|91076478|ref|XP_972409.1| PREDICTED: similar to 18 wheeler [Tribolium castaneum] FS756340 fcaL ...