WorldWideScience

Sample records for all-pm monolithic fs

  1. 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

    . 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......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...

  2. All-PM fiber, net normal cavity, Tm-doped fiber laser

    Science.gov (United States)

    Aguergaray, Claude

    2016-03-01

    We demonstrate herein a PM-fiber based cavity design capable of supporting many different pulse dynamics, such as soliton propagation or dissipative solitons in a dispersion managed cavity. By changing the dispersion of the fiber Bragg grating of the cavity we modify the net cavity dispersion, and thus stimulate various pulse dynamics. In particular we demonstrate the first net normal cavity, all-PM, all-fiber, dipersion managed cavity operating the in the 2μm range. Furthermore, we also demonstrate an all-fiber all-PM MOPA system capable of delivering up to 6 W of average power at 16 MHz by direct amplification of 70 ps long narrowband pulses. The amplifier stages are not fully saturated and are currently limited by the pump power available.

  3. Switchable dual-pulse-shape mode-locked figure-eight all-PM fibre master oscillator with 0.5 W-level average output

    Science.gov (United States)

    Kobtsev, Sergey; Ivanenko, Aleksey; Fedotov, Yurii; Smirnov, Sergey V.; Golubtsov, Artur; Khripunov, Sergey

    2016-03-01

    For the first time a method for switching between generation of single- and double-scale pulses has been demonstrated in a mode-locked figure-eight NALM-based all-PM-fibre Yb master oscillator by adjustment of two pumps power. Introduction into a F8 configuration of a non-linear amplifying loop mirror with two active media not only ensured relatively high average output power of the master oscillator (> 0.5 W at 22-MHz repetition rate), but also allowed switching laser operation from one pulse type (single-scale with duration of <10 ps) to another - femtosecond clusters with envelope width of 16 ps and sub-pulse duration <200 fs.

  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. Surface modified aerogel monoliths

    Science.gov (United States)

    Leventis, Nicholas (Inventor); Johnston, James C. (Inventor); Kuczmarski, Maria A. (Inventor); Meador, Mary Ann B. (Inventor)

    2013-01-01

    This invention comprises reinforced aerogel monoliths such as silica aerogels having a polymer coating on its outer geometric surface boundary, and to the method of preparing said aerogel monoliths. The polymer coatings on the aerogel monoliths are derived from polymer precursors selected from the group consisting of isocyanates as a precursor, precursors of epoxies, and precursors of polyimides. The coated aerogel monoliths can be modified further by encapsulating the aerogel with the polymer precursor reinforced with fibers such as carbon or glass fibers to obtain mechanically reinforced composite encapsulated aerogel monoliths.

  7. FS CMa type binaries

    CERN Document Server

    Miroshnichenko, Anatoly

    2015-01-01

    FS CMa type stars is a group of ~70 objects formerly known as unclassified stars with the B[e] phenomenon. Their very strong emission-line spectra in combination with a nearly main-sequence luminosity suggest the binary nature for them. They possess strong IR excesses due to radiation of circumstellar dust that implies a compact distribution probably in a circumbinary disk. Our long-term spectroscopic monitoring revealed neutral metal lines, which always include that of Li I 6708 \\AA, in the spectra of some FS CMa objects indicating the presence of a cool star. We present a summary of our results with a first overview of FS CMa type binaries and review possible implications for the nature and evolutionary status of the entire group.

  8. FS65 Disposition Option Report

    Energy Technology Data Exchange (ETDEWEB)

    Wenz, Tracy R. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2015-09-25

    This report outlines the options for dispositioning the MOX fuel stored in FS65 containers at LANL. Additional discussion regarding the support equipment for loading and unloading the FS65 transport containers is included at the end of the report.

  9. 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...

  10. 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.

  11. Embedded-monolith armor

    Energy Technology Data Exchange (ETDEWEB)

    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.

  12. 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.

  13. 948 kHz repetition rate, picosecond pulse duration, all-PM 1.03 μm mode-locked fiber laser based on nonlinear polarization evolution

    Science.gov (United States)

    Boivinet, S.; Lecourt, J.-B.; Hernandez, Y.; Fotiadi, A.; Mégret, P.

    2014-05-01

    We present in this study a PM all-fiber laser oscillator passively mode-locked (ML) at 1.03 μm. The laser is based on Nonlinear Polarization Evolution (NPE) in polarization maintaining (PM) fibers. In order to obtain the mode-locking regime, a nonlinear reflective mirror including a fibered polarizer, a long fiber span and a fibered Faraday mirror (FM) is inserted in a Fabry-Perot laser cavity. In this work we explain the principles of operation of this original laser design that permits to generate ultrashort pulses at low repetition (lower that 1MHz) rate with a cavity length of 100 m of fiber. In this experiment, the measured pulse duration is about 6 ps. To our knowledge this is the first all-PM mode-locked laser based on the NPE with a cavity of 100m length fiber and a delivered pulse duration of few picosecondes. Furthermore, the different mode-locked regimes of the laser, i.e. multi-pulse, noise-like mode-locked and single pulse, are presented together with the ways of controlling the apparition of these regimes. When the single pulse mode-locking regime is achieved, the laser delivers linearly polarized pulses in a very stable way. Finally, this study includes numerical results which are obtained with the resolution of the NonLinear Schrodinger Equations (NLSE) with the Split-Step Fourier (SSF) algorithm. This modeling has led to the understanding of the different modes of operation of the laser. In particular, the influence of the peak power on the reflection of the nonlinear mirror and its operation are studied.

  14. 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

  15. 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....

  16. SOI monolithic pixel detector

    Science.gov (United States)

    Miyoshi, T.; Ahmed, M. I.; Arai, Y.; Fujita, Y.; Ikemoto, Y.; Takeda, A.; Tauchi, K.

    2014-05-01

    We are developing monolithic pixel detector using fully-depleted (FD) silicon-on-insulator (SOI) pixel process technology. The SOI substrate is high resistivity silicon with p-n junctions and another layer is a low resistivity silicon for SOI-CMOS circuitry. Tungsten vias are used for the connection between two silicons. Since flip-chip bump bonding process is not used, high sensor gain in a small pixel area can be obtained. In 2010 and 2011, high-resolution integration-type SOI pixel sensors, DIPIX and INTPIX5, have been developed. The characterizations by evaluating pixel-to-pixel crosstalk, quantum efficiency (QE), dark noise, and energy resolution were done. A phase-contrast imaging was demonstrated using the INTPIX5 pixel sensor for an X-ray application. The current issues and future prospect are also discussed.

  17. Optoelectronic devices toward monolithic integration

    Science.gov (United States)

    Ghergia, V.

    1992-12-01

    Starting from the present state of tl art of discrete devices up to the on going realization of monolithic semicorxtuctor integrated prototypes an overview ofoptoelectronic devices for telecom applications is given inchiding a short classification of the different kind of integrated devices. On the future perspective of IBCN distribution network some economica of hybrid and monolithic forms of integration are attempted. lnaflyashoitpresentationoftheactivitiesperformedintbefieldofmonolithic integration by EEC ESPR1T and RACE projects is reported. 1.

  18. Monolithic afocal telescope

    Science.gov (United States)

    Roberts, William T. (Inventor)

    2010-01-01

    An afocal monolithic optical element formed of a shallow cylinder of optical material (glass, polymer, etc.) with fast aspheric surfaces, nominally confocal paraboloids, configured on the front and back surfaces. The front surface is substantially planar, and this lends itself to deposition of multi-layer stacks of thin dielectric and metal films to create a filter for rejecting out-of-band light. However, an aspheric section (for example, a paraboloid) can either be ground into a small area of this surface (for a Cassegrain-type telescope) or attached to the planar surface (for a Gregorian-type telescope). This aspheric section of the surface is then silvered to create the telescope's secondary mirror. The rear surface of the cylinder is figured into a steep, convex asphere (again, a paraboloid in the examples), and also made reflective to form the telescope's primary mirror. A small section of the rear surface (approximately the size of the secondary obscuration, depending on the required field of the telescope) is ground flat to provide an unpowered surface through which the collimated light beam can exit the optical element. This portion of the rear surface is made to transmit the light concentrated by the reflective surfaces, and can support the deposition of a spectral filter.

  19. Monolithic metal oxide transistors.

    Science.gov (United States)

    Choi, Yongsuk; Park, Won-Yeong; Kang, Moon Sung; Yi, Gi-Ra; Lee, Jun-Young; Kim, Yong-Hoon; Cho, Jeong Ho

    2015-04-28

    We devised a simple transparent metal oxide thin film transistor architecture composed of only two component materials, an amorphous metal oxide and ion gel gate dielectric, which could be entirely assembled using room-temperature processes on a plastic substrate. The geometry cleverly takes advantage of the unique characteristics of the two components. An oxide layer is metallized upon exposure to plasma, leading to the formation of a monolithic source-channel-drain oxide layer, and the ion gel gate dielectric is used to gate the transistor channel effectively at low voltages through a coplanar gate. We confirmed that the method is generally applicable to a variety of sol-gel-processed amorphous metal oxides, including indium oxide, indium zinc oxide, and indium gallium zinc oxide. An inverter NOT logic device was assembled using the resulting devices as a proof of concept demonstration of the applicability of the devices to logic circuits. The favorable characteristics of these devices, including (i) the simplicity of the device structure with only two components, (ii) the benign fabrication processes at room temperature, (iii) the low-voltage operation under 2 V, and (iv) the excellent and stable electrical performances, together support the application of these devices to low-cost portable gadgets, i.e., cheap electronics. PMID:25777338

  20. High peak-power monolithic femtosecond ytterbium fiber chirped pulse amplifier with a spliced-on hollow core fiber compressor.

    Science.gov (United States)

    Verhoef, A J; Jespersen, K; Andersen, T V; Grüner-Nielsen, L; Flöry, T; Zhu, L; Baltuška, A; Fernández, A

    2014-07-14

    We demonstrate a monolithic Yb-fiber chirped pulse amplifier that uses a dispersion matched fiber stretcher and a spliced-on hollow core photonic bandgap fiber compressor. For an output energy of 77 nJ, 220 fs pulses with 92% of the energy contained in the main pulse, can be obtained with minimal nonlinearities in the system. 135 nJ pulses are obtained with 226 fs duration and 82 percent of the energy in the main pulse. Due to the good dispersion match of the stretcher to the hollow core photonic bandgap fiber compressor, the duration of the output pulses is within 10% of the Fourier limited duration. PMID:25090494

  1. 34-fs, all-fiber all-polarization-maintaining single-mode pulse nonlinear amplifier.

    Science.gov (United States)

    Yu, Jia; Feng, Ye; Cai, Yajun; Li, Xiaohui; Hu, Xiaohong; Zhang, Wei; Duan, Lina; Yang, Zhi; Wang, Yishan; Liu, Yuanshan; Zhao, Wei

    2016-07-25

    We present an all-fiber all-polarization-maintaining (PM) single mode (SM) fiber pulse nonlinear amplification system. The seed laser with a repetition rate of 200 MHz is amplified by two-section erbium-doped PM gain fibers with different peak-absorption rate. The amplified pulse duration can be compressed into 34-fs with 320-mW output power, which corresponds to 1.6-nJ pulse energy and approximate 23.5-kW peak power. In addition, the amplified and compressed pulse is further coupled into the high nonlinear fiber and an octave-spanning supercontinuum generation can be obtained. To the best of our knowledge, it is the highest peak power and the shortest pulse duration obtained in the field of all-fiber all-PM SM pulse-amplification systems. PMID:27464117

  2. Monolithic fiber optic sensor assembly

    Energy Technology Data Exchange (ETDEWEB)

    Sanders, Scott

    2015-02-10

    A remote sensor element for spectrographic measurements employs a monolithic assembly of one or two fiber optics to two optical elements separated by a supporting structure to allow the flow of gases or particulates therebetween. In a preferred embodiment, the sensor element components are fused ceramic to resist high temperatures and failure from large temperature changes.

  3. In situ Fabrication of Monolithic Copper Azide

    Science.gov (United States)

    Li, Bing; Li, Mingyu; Zeng, Qingxuan; Wu, Xingyu

    2016-04-01

    Fabrication and characterization of monolithic copper azide were performed. The monolithic nanoporous copper (NPC) with interconnected pores and nanoparticles was prepared by decomposition and sintering of the ultrafine copper oxalate. The preferable monolithic NPC can be obtained through decomposition and sintering at 400°C for 30 min. Then, the available monolithic NPC was in situ reacted with the gaseous HN3 for 24 h and the monolithic NPC was transformed into monolithic copper azide. Additionally, the copper particles prepared by electrodeposition were also reacted with the gaseous HN3 under uniform conditions as a comparison. The fabricated monolithic copper azide was characterized by Fourier transform infrared (FTIR), inductively coupled plasma-optical emission spectrometry (ICP-OES), and differential scanning calorimetry (DSC).

  4. Protective Skins for Aerogel Monoliths

    Science.gov (United States)

    Leventis, Nicholas; Johnston, James C.; Kuczmarski, Maria A.; Meador, Ann B.

    2007-01-01

    A method of imparting relatively hard protective outer skins to aerogel monoliths has been developed. Even more than aerogel beads, aerogel monoliths are attractive as thermal-insulation materials, but the commercial utilization of aerogel monoliths in thermal-insulation panels has been inhibited by their fragility and the consequent difficulty of handling them. Therefore, there is a need to afford sufficient protection to aerogel monoliths to facilitate handling, without compromising the attractive bulk properties (low density, high porosity, low thermal conductivity, high surface area, and low permittivity) of aerogel materials. The present method was devised to satisfy this need. The essence of the present method is to coat an aerogel monolith with an outer polymeric skin, by painting or spraying. Apparently, the reason spraying and painting were not attempted until now is that it is well known in the aerogel industry that aerogels collapse in contact with liquids. In the present method, one prevents such collapse through the proper choice of coating liquid and process conditions: In particular, one uses a viscous polymer precursor liquid and (a) carefully controls the amount of liquid applied and/or (b) causes the liquid to become cured to the desired hard polymeric layer rapidly enough that there is not sufficient time for the liquid to percolate into the aerogel bulk. The method has been demonstrated by use of isocyanates, which, upon exposure to atmospheric moisture, become cured to polyurethane/polyurea-type coats. The method has also been demonstrated by use of commercial epoxy resins. The method could also be implemented by use of a variety of other resins, including polyimide precursors (for forming high-temperature-resistant protective skins) or perfluorinated monomers (for forming coats that impart hydrophobicity and some increase in strength).

  5. A monolithic RF transceiver for DC-OFDM UWB

    Institute of Scientific and Technical Information of China (English)

    陈云锋; 周涵超; 朱宁; 李宁; 任俊彦; 李巍; 傅海鹏; 高亭; 陈丹凤; 周锋; 蔡德望; 李丹; 牛杨杨

    2012-01-01

    This paper presents a first monolithic RF transceiver for DC-OFDM UWB applications.The proposed direct-conversion transceiver integrates all the building blocks including two receiver (Rx) cores,two transmitter (Tx) cores and a dual-carrier frequency synthesizer (DC-FS) as well as a 3-wire serial peripheral interface (SPI) to set the operating status of the transceiver.The ESD-protected chip is fabricated by a TSMC 0.13-μm RF CMOS process with a die size of 4.5 × 3.6 mm2.The measurement results show that the wideband Rx achieves an NF of 5-6.2 dB,a max gain of 76-84 dB with 64-dB variable gain,an in-/out-of-band IIP3 of -6/+4 dBm and an input loss S11 of <-10 in all bands.The Tx achieves an LOLRR/IMGRR of-34/-33 dBc,a typical OIP3 of+6 dBm and a maximum output power of -5 dBm.The DC-FS outputs two separate carriers simultaneously with an inter-band hopping time of < 1.2 ns.The full chip consumes a maximum current of 420 mA under a 1.2-V supply.

  6. Monolithic cell for frequency conversion

    International Nuclear Information System (INIS)

    We report the successful design, assembly, and operation of a single cell for frequency conversion of Nd:glass laser radiation from lambda = 1054 nm to lambda = 351 nm. Our approach combines the highly energy-efficient polarization mismatch scheme previously conceived and developed with the simplicity of the tandem crystal approach recently demonstrated. The resultant monolithic conversion cell consists of two KDP Type II crystals, assembled with tuning axes orthogonal and contained between a single pair of windows. An index-matching liquid is used to eliminate reflections from all internal surfaces. In this paper we describe a simple birefringence-sensitive method for marking and orienting circular doubler and mixer crystals with tuning axes orthogonal to better than 60 seconds of arc. The monolithic cell design is described, with emphasis on the chemical compatibility of component materials (crystals, spacers, seals, and metal surfaces) with index-matching liquids. A comparison between Halocarbon and Koolase index-matching fluids, after several months of operation (greater than 400 shots), shows the latter to exhibit better long-term, photochemical stability. The performance of the monolithic cell is superior to that of separate doubler and mixer cells. It exhibits better long-term pointing stability and produces a cleaner 3 #betta# beam

  7. Synthesis of high porosity, monolithic alumina aerogels

    Energy Technology Data Exchange (ETDEWEB)

    Poco, J F; Satcher, J H; Hrubesh, L W

    2000-09-20

    Many non-silica aerogels are notably weak and fragile in monolithic form. Particularly, few monolithic aerogels with densities less than 50kg/m3 have any significant strength. It is especially difficult to prepare uncracked monoliths of pure alumina aerogels that are robust and moisture stable. In this paper, we discuss the synthesis of strong, stable, monolithic, high porosity (>98% porous) alumina aerogels, using a two-step sol-gel process. The alumina aerogels have a polycrystalline morphology that results in enhanced physical properties. Most of the measured physical properties of the alumina aerogels are superior to those for silica aerogels for equivalent densities.

  8. 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.

  9. Adsorption over polyacrylonitrile based carbon monoliths

    Science.gov (United States)

    Nandi, Mahasweta; Dutta, Arghya; Patra, Astam Kumar; Bhaumik, Asim; Uyama, Hiroshi

    2013-02-01

    Highly porous activated carbon monoliths have been prepared from mesoporous polyacrylonitrile (PAN) monolith as the carbon precursor. The mesoporous PAN monoliths are fabricated by a unique and facile template-free method which on carbonization gives N-doped activated carbon monoliths. The carbonization is achieved via two step thermal process which includes pretreatment in air leading to cyclization and subsequent aromatization of the PAN moieties followed by carbonization in a mixture of argon and carbon dioxide to give a layered carbon framework. Nitrogen sorption experiments carried over these carbon monoliths revealed high surface area (ca. 2500 m2g-1) for these materials with precise micropore size distribution. The activated carbons show extraordinarily high CO2 capture capacity and the uptake up to 3 bar has been found to be as high as 22.5 and 10.6 mmol/g at 273 K and 298 K, respectively.

  10. CernVM-FS - beyond LHC computing

    Science.gov (United States)

    Condurache, C.; Collier, I.

    2014-06-01

    In the last three years the CernVM File System has transformed the distribution of experiment software to WLCG sites. CernVM-FS removes the need for local installations jobs and performant network fileservers at sites and it often improves performance at the same time. Now established and proven to work at scale, CernVM-FS is beginning to perform a similar role for non-LHC computing. The deployment of CernVM-FS service at RAL Tier-1 is presented, as well as the proposed development of a network of Stratum-0 and Stratum-1 replicas somewhat modelled upon the infrastructure developed to support the WLCG computing. A case study of one non-LHC Virtual Organization is also included, describing their use of the CernVM-FS Stratum-0 service, along with a web interface intended to be used as a tool to upload software at Stratum-0 sites.

  11. 260 fs and 1 nJ pulse generation from a compact, mode-locked Tm-doped fiber laser.

    Science.gov (United States)

    Sobon, Grzegorz; Sotor, Jaroslaw; Pasternak, Iwona; Krajewska, Aleksandra; Strupinski, Wlodek; Abramski, Krzysztof M

    2015-11-30

    We report on generation of 260 fs-short pulses with energy of 1.1 nJ from a fully fiberized, monolithic Tm-doped fiber laser system. The design comprises a simple, graphene-based ultrafast oscillator and an integrated all-fiber chirped pulse amplifier (CPA). The system generates 110 mW of average power at 100.25 MHz repetition rate and central wavelength of 1968 nm. This is, to our knowledge, the highest pulse energy generated from a fully fiberized sub-300 fs Tm-doped laser, without the necessity of using grating-based dispersion compensation. Such compact, robust and cost-effective system might serve as a seed source for nonlinear frequency conversion or mid-infrared supercontinuum generation. PMID:26698769

  12. 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.

  13. 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.

  14. 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

  15. 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...

  16. Activated carbon monoliths for methane storage

    Science.gov (United States)

    Chada, Nagaraju; Romanos, Jimmy; Hilton, Ramsey; Suppes, Galen; Burress, Jacob; Pfeifer, Peter

    2012-02-01

    The use of adsorbent storage media for natural gas (methane) vehicles allows for the use of non-cylindrical tanks due to the decreased pressure at which the natural gas is stored. The use of carbon powder as a storage material allows for a high mass of methane stored for mass of sample, but at the cost of the tank volume. Densified carbon monoliths, however, allow for the mass of methane for volume of tank to be optimized. In this work, different activated carbon monoliths have been produced using a polymeric binder, with various synthesis parameters. The methane storage was studied using a home-built, dosing-type instrument. A monolith with optimal parameters has been fabricated. The gravimetric excess adsorption for the optimized monolith was found to be 161 g methane for kg carbon.

  17. 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.

  18. Monolithically integrated waveguide-coupled silica microtoroids

    CERN Document Server

    Richter, Jens; Witzens, Jeremy

    2015-01-01

    We report on the design and fabrication of a new type of microtoroid high-Q silica resonators monolithically coupled to on-chip silicon nanowire waveguides. In order to enable monolithic waveguide coupling, the microtoroid geometry is inverted such that the resonator is formed by thermal reflow at the circumference of a hole etched in a suspended SiO2 membrane. This configuration is shown to be conducive to integration with a fully functional Silicon Photonics technology platform.

  19. Monolithic JFET preamplifier for ionization chamber calorimeter

    International Nuclear Information System (INIS)

    A monolithic charge sensitive preamplifier using exclusively n-channel diffused JFETs has been designed and is now being fabricated by INTERFET Corp. by means of a dielectrically isolated process which allows preserving as much as possible the technology upon which discrete JFETs are based. A first prototype built by means of junction isolated process has been delivered. The characteristics of monolithically integrated JFETs compare favorably with discrete devices. First results of tests of a preamplifier which uses these devices are reported

  20. 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.

  1. Methacrylate Polymer Monoliths for Separation Applications

    Directory of Open Access Journals (Sweden)

    Robert J. Groarke

    2016-06-01

    Full Text Available This review summarizes the development of methacrylate-based polymer monoliths for separation science applications. An introduction to monoliths is presented, followed by the preparation methods and characteristics specific to methacrylate monoliths. Both traditional chemical based syntheses and emerging additive manufacturing methods are presented along with an analysis of the different types of functional groups, which have been utilized with methacrylate monoliths. The role of methacrylate based porous materials in separation science in industrially important chemical and biological separations are discussed, with particular attention given to the most recent developments and challenges associated with these materials. While these monoliths have been shown to be useful for a wide variety of applications, there is still scope for exerting better control over the porous architectures and chemistries obtained from the different fabrication routes. Conclusions regarding this previous work are drawn and an outlook towards future challenges and potential developments in this vibrant research area are presented. Discussed in particular are the potential of additive manufacturing for the preparation of monolithic structures with pre-defined multi-scale porous morphologies and for the optimization of surface reactive chemistries.

  2. 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…

  3. 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

    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 zirconia crowns (Lava Plus Zirconia, 3M/ESPE) with specified axial/occlusal thicknesses and lithium disilica...

  4. 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.

  5. 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...

  6. 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.

  7. 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.

  8. 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.

  9. UPDATE ON MONOLITHIC FUEL FABRICATION METHODS

    Energy Technology Data Exchange (ETDEWEB)

    C. R. Clark; J. F. Jue; G. A. Moore; N. P. Hallinan; B. H. Park; D. E. Burkes

    2006-10-01

    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. Progress at INL has led to fabrication of hot isostatic pressed uranium-molybdenum bearing monolithic fuel plates. These miniplates are part of the RERTR-8 miniplate irradiation test. Further progress has also been made on friction stir weld processing which has been used to fabricate full size fuel plates which will be irradiated in the ATR and OSIRIS reactors.

  10. Monolithic JFET preamplifier for ionization chamber calorimeter

    International Nuclear Information System (INIS)

    A monolithic charge sensitive preamplifier using exclusively n-channel diffused JFETs has been designed and is now being fabricated by INTERFET Corp. by means of a dielectrically isolated process which allows preserving as much as possible the technology upon which discrete JFETs are based. A first prototype built by means of junction isolated process has been delivered. The characteristics of monolithically integrated JFETs compare favorably with discrete devices. First results of tests of a preamplifier which uses these devices are reported. 4 refs

  11. 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")

  12. 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.

  13. 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.

  14. Monolithic Optical-To-Electronic Receiver

    Science.gov (United States)

    Kunath, Richard; Mactaggert, Ross

    1994-01-01

    Monolithic optoelectronic integrated circuit converts multiplexed digital optical signals into electrical signals, separates, and distributes them to intended destinations. Developed to deliver phase and amplitude commands to monolithic microwave integrated circuits (MMIC's) at elements of millimeter-wave phased-array antenna from single optical fiber driven by external array controller. Also used in distribution of high-data-rate optical communications in local-area networks (LAN's). Notable features include options for optical or electrical clock inputs; outputs for raw data, addresses, and instructions for diagnosis; and optical-signal-detection circuit used to reduce power consumption by 80 percent between data-transmission times. Chip fabricated by processes available at many major semiconductor foundries. Distribution of digital signals in aircraft, automobiles, and ships potential application.

  15. Comparison of soil-monolith extraction techniques

    Science.gov (United States)

    Meissner, R.; Rupp, H.; Weller, U.; Vogel, H.-J.

    2009-04-01

    In the international literature the term „lysimeter" is used for different objectives, e.g. suction cups, fluxmeters, etc. According to our understanding it belongs to the direct methods to measure water and solute fluxes in soil. Depending on the scientific task the shape and dimensions of the lysimeter as well as the type of filling (disturbed or undisturbed) and the specific instrumentation can be different. In any case where water dynamics or solute transport in natural soil is considered, lysimeters should be filled with 'undisturbed' monoliths which are large enough to contain the small scale heterogeneity of a site since flow and transport is highly sensitive to soil structure. Furthermore, lysimeters with vegetation should represent the natural crop inventory and the maximum root penetration depth should be taken into account. The aim of this contribution is to give an overview about different methods for obtaining undisturbed soil monoliths, in particular about i) techniques for the vertical and ii) for the horizontal extraction and iii) to evaluate the most frequently used procedures based on X-ray tomography images. Minimal disturbance of the soil monolith during extraction and subsequence filling of the lysimeter vessel is of critical importance for establishing flow and transport conditions corresponding approximately to natural field conditions. In the past, several methods were used to extract and fill lysimeter vessels vertically - including hand digging, employing sets of trihedral scaffold with lifting blocks and ballast, or using heavy duty excavators, which could shear and cut large blocks of soil. More recently, technologies have been developed to extract cylindrical soil monoliths by using ramming equipment or screw presses. One of the great disadvantages of the mentioned methods is the compaction or settling of soil that occurs during the "hammering" or "pressing". For this reason a new technology was developed, which cuts the outline of

  16. Solgel-derived photosensitive germanosilicate glass monoliths.

    Science.gov (United States)

    Heaney, A D; Erdogan, T

    2000-12-15

    We demonstrate volume gratings written in solgel-derived, Ge-doped silica monoliths. Glass was fabricated both with and without germanium oxygen deficient center (GODC) defects. The UV absorption and UV-induced index changes of these glasses, with and without hydrogen loading, are reported. The presence of GODC defects greatly enhances the photosensitivity of Ge-doped silica with and without the presence of hydrogen. PMID:18066337

  17. 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.

  18. 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.

  19. 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.

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. EST Table: FS917025 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917025 E_FL_fufe_40B06_F_0 11/12/09 GO hit GO:0016020(membrane) 10/09/28 94 %/274.../09/10 82 %/271 aa gi|91082327|ref|XP_974606.1| PREDICTED: similar to prohibitin protein WPH [Tribolium castaneum] FS917025 fufe ...

  9. 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 ...

  10. 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 ...

  11. EST Table: FS909890 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909890 E_FL_fufe_18J09_F_0 10/09/28 56 %/214 aa ref|XP_001810630.1| PREDICTED: si...GB15377-PA 10/09/10 56 %/214 aa gi|189237082|ref|XP_001810630.1| PREDICTED: similar to CG14722 CG14722-PA [Tribolium castaneum] FS908860 fufe ...

  12. EST Table: FS909071 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909071 E_FL_fufe_16C04_F_0 11/12/09 GO hit GO:0003924(GTPase activity)|GO:0005525...ref|XP_973240.2| PREDICTED: similar to mitochondrial elongation factor G2 [Tribolium castaneum] FS909071 fufe ...

  13. EST Table: FS909052 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909052 E_FL_fufe_16B09_F_0 10/09/28 68 %/145 aa ref|XP_970438.1| PREDICTED: simil...8 %/145 aa gi|91080473|ref|XP_970438.1| PREDICTED: similar to IMP1 inner mitochondrial membrane peptidase-like [Tribolium castaneum] FS929080 fufe ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. 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 ...

  20. EST Table: FS920155 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS920155 E_FL_fufe_49I16_F_0 11/12/09 GO hit GO:0004175(endopeptidase activity)|GO:...|Amel|GB10411-PA 10/09/10 87 %/232 aa gi|189237685|ref|XP_969117.2| PREDICTED: similar to proteasome beta-subunit [Tribolium castaneum] FS920155 fufe ...

  1. EST Table: FS728588 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS728588 E_FL_bmmt_13K09_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 bmmt ...

  2. EST Table: FS853491 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS853491 E_FL_fner_46I09_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 fner ...

  3. EST Table: FS840331 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS840331 E_FL_fner_09D19_F_0 10/09/28 52 %/148 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/148 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 fner ...

  4. EST Table: FS917878 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917878 E_FL_fufe_42K11_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 fufe ...

  5. EST Table: FS915661 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915661 E_FL_fufe_36A05_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 fufe ...

  6. EST Table: FS881695 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS881695 E_FL_ftes_22C03_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 ftes ...

  7. EST Table: FS908653 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS908653 E_FL_fufe_14N17_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 fufe ...

  8. EST Table: FS887231 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS887231 E_FL_ftes_38K16_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 ftes ...

  9. EST Table: FS734382 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS734382 E_FL_bmmt_28B11_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 bmmt ...

  10. EST Table: FS729732 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS729732 E_FL_bmmt_16N22_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 bmmt ...

  11. EST Table: FS915047 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915047 E_FL_fufe_34B04_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 fufe ...

  12. EST Table: FS725701 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS725701 E_FL_bmmt_05G09_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 bmmt ...

  13. EST Table: FS883210 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS883210 E_FL_ftes_26I20_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 ftes ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. 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 ...

  20. 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 ...

  1. EST Table: FS762412 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS762412 E_FL_fcaL_30I19_F_0 10/09/28 79 %/104 aa ref|XP_970822.2| PREDICTED: similar to Darkener of apricot...9/10 79 %/104 aa gi|189241909|ref|XP_970822.2| PREDICTED: similar to Darkener of apricot CG33553-PG [Tribolium castaneum] FS918661 fcaL ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. 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 ...

  7. EST Table: FS908032 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS908032 E_FL_fufe_12P21_F_0 10/09/28 75 %/250 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 75 %/250 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fufe ...

  8. EST Table: FS852098 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS852098 E_FL_fner_42J11_F_0 10/09/28 75 %/223 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 75 %/223 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fner ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. EST Table: FS919062 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919062 E_FL_fufe_46D19_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 fufe ...

  14. 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.

  15. 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.

  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. 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

  18. Monolithic LTCC seal frame and lid

    Energy Technology Data Exchange (ETDEWEB)

    Krueger, Daniel S.; Peterson, Kenneth A.; Stockdale, Dave; Duncan, James Brent; Riggs, Bristen

    2016-06-21

    A method for forming a monolithic seal frame and lid for use with a substrate and electronic circuitry comprises the steps of forming a mandrel from a ceramic and glass based material, forming a seal frame and lid block from a ceramic and glass based material, creating a seal frame and lid by forming a compartment and a plurality of sidewalls in the seal frame and lid block, placing the seal frame and lid on the mandrel such that the mandrel fits within the compartment, and cofiring the seal frame and lid block.

  19. 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.

  20. Fibrous monoliths: Economic ceramic matrix composites from powders [Final report

    Energy Technology Data Exchange (ETDEWEB)

    Rigali, Mark; Sutaria, Manish; Mulligan, Anthony; Creegan, Peter; Cipriani, Ron

    1999-05-26

    The project was to develop and perform pilot-scale production of fibrous monolith composites. The principal focus of the program was to develop damage-tolerant, wear-resistant tooling for petroleum drilling applications and generate a basic mechanical properties database on fibrous monolith composites.

  1. 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

  2. Media Presentation Synchronisation for Non-monolithic Rendering Architectures

    NARCIS (Netherlands)

    Vaishnavi, I.; Bulterman, D.C.A.; Cesar Garcia, P.S.; Gao, B.

    2007-01-01

    Non-monolithic renderers are physically distributed media playback engines. Non-monolithic renderers may use a number of different underlying network connection types to transmit media items belonging to a presentation. There is therefore a need for a media based and inter-network- type synchronizat

  3. 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

  4. Design considerations for monolithic unidirectional planar ring oscillators

    Science.gov (United States)

    Li, Zhenhua; Bao, Guojun; Ge, Yi; Wang, Zhongming; He, Anzhi; Tao, Hailin

    1996-09-01

    In this paper, the characteristics of monolithic unidirectional planar ring oscillator (PROs) are analyzed, and design criteria for PROs with low thresholds and large nonreciprocities are expounded on the basis of the eigenpolarization theory of monolithic nonplanar ring oscillators. A Nd:BGO PRO is designed to take advantage of its large Verdet coefficient.

  5. SeaWiFS Images Fires on Yucatan Peninsula

    Science.gov (United States)

    2002-01-01

    This image from the Sea-viewing Wide Field-of-View Sensor (SeaWiFS) shows dense smoke from fires in the Yucatan peninsula on April 24, 2000. In the El Nino year of 1998 fires in the region emitted enough smoke to cause authorities in Texas to issue air quality warnings. For more information, see: SeaWiFS Project Home Page Global Fire Monitoring 4km2 TRMM Fire Data Image provided by the SeaWiFS Project, NASA/Goddard Space Flight Center, and ORBIMAGE

  6. 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.

  7. 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.

  8. 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.

  9. 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 ...

  10. 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 ...

  11. 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- ...

  12. 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 ...

  13. EST Table: FS929848 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

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

  14. 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 ...

  15. 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- ...

  16. 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- ...

  17. 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 ...

  18. 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 ...

  19. 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 ...

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. 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 ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. 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- ...

  20. 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

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. EST Table: FS888260 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS888260 E_FL_ftes_41L16_F_0 10/09/28 35 %/160 aa ref|NP_001137203.1| bloated tubul...es [Tribolium castaneum] gb|ACH86322.1| bloated tubules [Tribolium castaneum] 10/09/12 32 %/163 aa FBpp01275...:AGAP004932 10/09/10 low homology 10/09/10 35 %/160 aa gi|198386300|gb|ACH86322.1| bloated tubules [Tribolium castaneum] FS928389 ftes ...

  5. EST Table: FS878759 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS878759 E_FL_ftes_13I21_F_0 10/09/28 36 %/150 aa ref|NP_001137203.1| bloated tubul...es [Tribolium castaneum] gb|ACH86322.1| bloated tubules [Tribolium castaneum] 10/09/11 32 %/160 aa FBpp01275...:AGAP004932 10/09/10 low homology 10/09/10 36 %/150 aa gi|198386300|gb|ACH86322.1| bloated tubules [Tribolium castaneum] FS928389 ftes ...

  6. EST Table: FS827862 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS827862 E_FL_fmgV_27J02_R_0 10/09/28 53 %/141 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 53 %/141 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS736242 fmgV ...

  7. EST Table: FS747293 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS747293 E_ET_caL-_09D19_F_0 10/09/28 51 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 51 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 caL- ...

  8. EST Table: FS762894 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS762894 E_FL_fcaL_32A02_F_0 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi...09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 fcaL ...

  9. EST Table: FS827382 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 57 %/109 aa gi|91084063|ref|XP_967668.1| PREDICTED: similar to luciferin-regenerating enzyme [Tribolium castaneum] FS836072 fmgV ... ...FS827382 E_FL_fmgV_26D12_R_0 10/09/28 57 %/109 aa ref|XP_967668.1| PREDICTED: similar to luciferin-regenerat...ing enzyme [Tribolium castaneum] gb|EFA03138.1| hypothetical protein TcasGA2_TC0130

  10. EST Table: FS737575 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available mel|GB18633-PA 10/09/10 60 %/101 aa gi|91084063|ref|XP_967668.1| PREDICTED: similar to luciferin-regenerating enzyme [Tribolium castaneum] FS836072 bmmt ... ...FS737575 E_FL_bmmt_09D02_R_0 10/09/28 60 %/101 aa ref|XP_967668.1| PREDICTED: similar to luciferin-regenerat...ing enzyme [Tribolium castaneum] gb|EFA03138.1| hypothetical protein TcasGA2_TC0130

  11. EST Table: FS735970 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 56 %/111 aa gi|91084063|ref|XP_967668.1| PREDICTED: similar to luciferin-regenerating enzyme [Tribolium castaneum] FS836072 bmmt ... ...FS735970 E_FL_bmmt_04J16_R_0 10/09/28 56 %/111 aa ref|XP_967668.1| PREDICTED: similar to luciferin-regenerat...ing enzyme [Tribolium castaneum] gb|EFA03138.1| hypothetical protein TcasGA2_TC0130

  12. EST Table: FS835284 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 57 %/110 aa gi|91084063|ref|XP_967668.1| PREDICTED: similar to luciferin-regenerating enzyme [Tribolium castaneum] FS836072 fmgV ... ...FS835284 E_FL_fmgV_48D02_R_0 10/09/28 57 %/110 aa ref|XP_967668.1| PREDICTED: similar to luciferin-regenerat...ing enzyme [Tribolium castaneum] gb|EFA03138.1| hypothetical protein TcasGA2_TC0130

  13. 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 ...

  14. 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 ...

  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: 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 ...

  17. 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 ...

  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: 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 ...

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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

  10. 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

  11. EST Table: FS938903 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 0 aa gi|189235487|ref|XP_968396.2| PREDICTED: similar to failed axon connections protein [Tribolium castaneum] FS937483 fwgP ... ...FS938903 E_FL_fwgP_53F15_F_0 10/09/28 60 %/190 aa ref|XP_968396.2| PREDICTED: similar to failed axon connect...ions protein [Tribolium castaneum] 10/09/13 75 %/132 aa FBpp0166084|DmojGI16867-PA

  12. EST Table: FS939195 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 4 aa gi|189235487|ref|XP_968396.2| PREDICTED: similar to failed axon connections protein [Tribolium castaneum] FS937483 fwgP ... ...FS939195 E_FL_fwgP_54D09_F_0 10/09/28 59 %/184 aa ref|XP_968396.2| PREDICTED: similar to failed axon connect...ions protein [Tribolium castaneum] 10/09/13 73 %/126 aa FBpp0286407|DpseGA18298-PA

  13. 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

  14. EST Table: FS883000 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS883000 E_FL_ftes_25O20_F_0 11/12/09 n.h 10/09/28 40 %/206 aa gb|ACE75178.1| conse...gy 10/09/10 46 %/182 aa gnl|Amel|GB16906-PA 10/09/10 39 %/182 aa gi|189238031|ref|XP_966733.2| PREDICTED: similar to T21C9.6 [Tribolium castaneum] FS883000 ftes ...

  15. 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 alzheimer... 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 ...

  16. 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 ...

  17. EST Table: FS849688 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS849688 E_FL_fner_35L09_F_0 10/09/28 77 %/212 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 ...

  18. EST Table: FS789804 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS789804 E_FL_ffbm_01M14_F_0 10/09/28 73 %/331 aa ref|NP_001164155.1| Ras opposite ...P003023 10/09/10 69 %/328 aa gnl|Amel|GB12540-PA 10/09/10 73 %/331 aa gi|282392023|ref|NP_001164155.1| Ras opposite [Tribolium castaneum] FS768412 ffbm ...

  19. 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 ...

  20. EST Table: FS919694 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS919694 E_FL_fufe_48C05_F_0 10/09/28 34 %/248 aa ref|XP_967427.2| PREDICTED: similar to hypoxia... 10/09/10 low homology 10/09/10 34 %/248 aa gi|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia-inducible factor 1 alpha [Tribolium castaneum] FS913906 fufe ...

  1. EST Table: FS922196 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922196 E_FL_fwgP_03O20_F_0 11/12/09 n.h 10/09/28 60 %/157 aa ref|XP_001847098.1| ...nl|Amel|GB13641-PA 10/09/10 59 %/134 aa gi|91078992|ref|XP_974639.1| PREDICTED: similar to mitochondrial 28S ribosomal protein S28 [Tribolium castaneum] FS922196 fwgP ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. 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 ...

  14. 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 ...

  15. 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

  16. 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 ...

  17. EST Table: FS759718 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS759718 E_FL_fcaL_12C20_F_0 10/09/28 73 %/200 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 73 %/200 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fcaL ...

  18. EST Table: FS806218 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS806218 E_FL_fmgV_20B08_F_0 10/09/28 74 %/212 aa ref|XP_970542.1| PREDICTED: similar to brix...B12626-PA 10/09/10 74 %/212 aa gi|91090402|ref|XP_970542.1| PREDICTED: similar to brix domain-containing protein 2 [Tribolium castaneum] FS911686 fmgV ...

  19. 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 ...

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. 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 ...

  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. 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.

  16. 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.

  17. 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.

  18. Monolithic fuel injector and related manufacturing method

    Science.gov (United States)

    Ziminsky, Willy Steve; Johnson, Thomas Edward; Lacy, Benjamin; York, William David; Stevenson, Christian Xavier

    2012-05-22

    A monolithic fuel injection head for a fuel nozzle includes a substantially hollow vesicle body formed with an upstream end face, a downstream end face and a peripheral wall extending therebetween, an internal baffle plate extending radially outwardly from a downstream end of the bore, terminating short of the peripheral wall, thereby defining upstream and downstream fuel plenums in the vesicle body, in fluid communication by way of a radial gap between the baffle plate and the peripheral wall. A plurality of integral pre-mix tubes extend axially through the upstream and downstream fuel plenums in the vesicle body and through the baffle plate, with at least one fuel injection hole extending between each of the pre-mix tubes and the upstream fuel plenum, thereby enabling fuel in the upstream plenum to be injected into the plurality of pre-mix tubes. The fuel injection head is formed by direct metal laser sintering.

  19. A monolithic bolometer array suitable for FIRST

    Science.gov (United States)

    Bock, J. J.; LeDuc, H. G.; Lange, A. E.; Zmuidzinas, J.

    1997-01-01

    The development of arrays of infrared bolometers that are suitable for use in the Far Infrared and Submillimeter Telescope (FIRST) mission is reported. The array architecture is based on the silicon nitride micromesh bolometer currently baselined for use in the case of the Planck mission. This architecture allows each pixel to be efficiently coupled to one or both polarizations and to one or more spatial models of radiation. Micromesh structures are currently being developed, coupled with transistor-edge sensors and read out by a SQUID amplifier. If these devices are successful, then the relatively large cooling power available at 300 mK may enable a SQUID-based multiplexer to be integrated on the same wafer as the array, creating a monolithic, fully multiplexed, 2D array with relatively few connections to the sub-Kelvin stage.

  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. HgCdTe monolithic infrared detector

    Energy Technology Data Exchange (ETDEWEB)

    Yakushev, Maxim V.; Dvoretsky, Sergei A.; Kozlov, Alexander I.; Sabinina, Irina V.; Sidorov, Yu.G.; Sorochkin, Alexander V.; Fomin, Boris I.; Aseev, Alexander L. [A.V. Rzhanov Institute of Semiconductor Physics, Siberian Branch RAS, Novosibirsk (Russian Federation)

    2010-06-15

    We report the processes of fabricating monolithic 32 x 32 infrared detector based on (310) HgCdTe/CdTe/ZnTe/ Si photosensitive heterostructure which was grown by a molecular-beam epitaxy technique in the free surface of ROIC cells. Optimum parameters of the technological processes were determined. The minimum temperature of preepitaxial thermal annealing in vacuum of ROIC was determined as 450 C. The dark and photo current-voltage characteristics were measured and analyzed. A good sensitivity of diodes was observed. The product R{sub 0} x A {proportional_to} 10{sup 5} Ohm x cm{sup 2}. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  2. 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.

  3. 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.

  4. 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...

  5. 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.

  6. Chromatographic Properties of Silica-Based Monolithic HPLC Columns

    OpenAIRE

    Smith, Jennifer Houston

    2002-01-01

    Silica-based monolithic HPLC columns contain a novel chromatographic support in which the traditional particulate packing has been replaced with a single, continuous network (monolith) of porous silica. The main advantage of such a network is decreased backpressure due to macropores (2 μm) throughout the network. This allows high flow rates, and hence fast analyses that are unattainable with traditional particulate columns. The Chromolith SpeedROD⠢ (EM Science, Gibbstown NJ) is a commercia...

  7. Monolithic arrays of surface emitting laser NOR logic devices

    OpenAIRE

    Song, J.-I-; Lee, Y. H.; Yoo, J. Y.; Shin, J H; Scherer, A.; Leibenguth, R. E.

    1993-01-01

    Monolithic, cascadable, laser-logic-device arrays have been realized and characterized. The monolithic surface-emitting laser logic (SELL) device consists of an AlGaAs superlattice lasing around 780 nm connected to a heterojunction phototransistor (HPT) in parallel and a resistor in series. Arrays up to 8×8 have been fabricated, and 2×2 arrays show uniform characteristics. The optical logic output is switched off with 40 μW incident optical input.

  8. Characterization of methacrylate chromatographic monoliths bearing affinity ligands.

    Science.gov (United States)

    Černigoj, Urh; Vidic, Urška; Nemec, Blaž; Gašperšič, Jernej; Vidič, Jana; Lendero Krajnc, Nika; Štrancar, Aleš; Podgornik, Aleš

    2016-09-16

    We investigated effect of immobilization procedure and monolith structure on chromatographic performance of methacrylate monoliths bearing affinity ligands. Monoliths of different pore size and various affinity ligands were prepared and characterized using physical and chromatographic methods. When testing protein A monoliths with different protein A ligand densities, a significant nonlinear effect of ligand density on dynamic binding capacity (DBC) for IgG was obtained and accurately described by Langmuir isotherm curve enabling estimation of protein A utilization as a function of ligand density. Maximal IgG binding capacity was found to be at least 12mg/mL exceeding theoretical monolayer adsorption value of 7.8mg/mL assuming hexagonal packing and IgG hydrodynamic diameter of 11nm. Observed discrepancy was explained by shrinkage of IgG during adsorption on protein A experimentally determined through calculated adsorbed IgG layer thickness of 5.4nm from pressure drop data. For monoliths with different pore size maximal immobilized densities of protein A as well as IgG dynamic capacity linearly correlates with monolith surface area indicating constant ligand utilization. Finally, IgGs toward different plasma proteins were immobilized via the hydrazide coupling chemistry to provide oriented immobilization. DBC was found to be flow independent and was increasing with the size of bound protein. Despite DBC was lower than IgG capacity to immobilized protein A, ligand utilization was higher. PMID:27554023

  9. 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.

  10. Monolithic CMOS imaging x-ray spectrometers

    Science.gov (United States)

    Kenter, Almus; Kraft, Ralph; Gauron, Thomas; Murray, Stephen S.

    2014-07-01

    The Smithsonian Astrophysical Observatory (SAO) in collaboration with SRI/Sarnoff is developing monolithic CMOS detectors optimized for x-ray astronomy. The goal of this multi-year program is to produce CMOS x-ray imaging spectrometers that are Fano noise limited over the 0.1-10keV energy band while incorporating the many benefits of CMOS technology. These benefits include: low power consumption, radiation "hardness", high levels of integration, and very high read rates. Small format test devices from a previous wafer fabrication run (2011-2012) have recently been back-thinned and tested for response below 1keV. These devices perform as expected in regards to dark current, read noise, spectral response and Quantum Efficiency (QE). We demonstrate that running these devices at rates ~> 1Mpix/second eliminates the need for cooling as shot noise from any dark current is greatly mitigated. The test devices were fabricated on 15μm, high resistivity custom (~30kΩ-cm) epitaxial silicon and have a 16 by 192 pixel format. They incorporate 16μm pitch, 6 Transistor Pinned Photo Diode (6TPPD) pixels which have ~40μV/electron sensitivity and a highly parallel analog CDS signal chain. Newer, improved, lower noise detectors have just been fabricated (October 2013). These new detectors are fabricated on 9μm epitaxial silicon and have a 1k by 1k format. They incorporate similar 16μm pitch, 6TPPD pixels but have ~ 50% higher sensitivity and much (3×) lower read noise. These new detectors have undergone preliminary testing for functionality in Front Illuminated (FI) form and are presently being prepared for back thinning and packaging. Monolithic CMOS devices such as these, would be ideal candidate detectors for the focal planes of Solar, planetary and other space-borne x-ray astronomy missions. The high through-put, low noise and excellent low energy response, provide high dynamic range and good time resolution; bright, time varying x-ray features could be temporally and

  11. 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

  12. 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 ...

  13. 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 ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. 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 ...

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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

  6. EST Table: FS932894 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS932894 E_FL_fwgP_35I15_F_0 10/09/28 36 %/150 aa ref|NP_001137203.1| bloated tubul...es [Tribolium castaneum] gb|ACH86322.1| bloated tubules [Tribolium castaneum] 10/09/13 32 %/160 aa FBpp01275...:AGAP004932 10/09/10 low homology 10/09/10 36 %/150 aa gi|198386300|gb|ACH86322.1| bloated tubules [Tribolium castaneum] FS928389 fwgP ...

  7. 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 ...

  8. 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

  9. EST Table: FS896726 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS896726 E_FL_ftes_24G17_R_0 10/09/28 70 %/211 aa ref|XP_002424214.1| Arsenical pump-driving... ATPase, putative [Pediculus humanus corporis] gb|EEB11476.1| Arsenical pump-driving ATPase, putati... 67 %/230 aa gnl|Amel|GB18636-PA 10/09/10 69 %/211 aa gi|91081505|ref|XP_974589.1| PREDICTED: similar to arsenical pump-driving atpase [Tribolium castaneum] FS871401 ftes ...

  10. 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

  11. 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 ...

  12. 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 ...

  13. 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 ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. 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 ...

  20. 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 ...

  1. 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 ...

  2. QSAR Studies on PCDD/Fs by Kernel PLS

    Institute of Scientific and Technical Information of China (English)

    TANG Kai-lin; LI Tong-hua; CHEN Kai

    2008-01-01

    QSPR models of PCDD/Fs were generated by means of kernel partial least squares.The molecular distance-edge vector method was used as descriptors to get model I for predicting PCDD/Fs retention behavior.The chlorinated positions were also used and model Ⅱ was obtained.In studied cases,the predictive ability of the KPLS model is comparable or superior to those of PLS and ANN.The results indicate that KPLS can be used as an alternative powerful modeling tool for QSPR studies.

  3. Monolithic JFET preamplifier for ionization chamber calorimeters

    International Nuclear Information System (INIS)

    A prototype preamplifier circuit is presented for use in SSC ionization chamber calorimeters. It consists of a new type of silicon integrated circuit comprised of very low noise junction FET (JFET) components. Presently, monolithic preamplifier circuits for use in highly segmented detectors are made of implanted channel JFETs or MOS devices. While such circuits solve the density problems, they do not perform to the same level of low noise characteristics as found in discrete JFET components. The JFETs which comprise this new integrated circuit preserve the excellent low noise performance normally found only in discrete JFETs. JFETs also are much more radiation resistant and less prone to damage by electromagnetic discharges than MOS transistors. Two innovative fabrication processes are discussed. They solve the difficult gate-to-gate isolation problem needed to manufacture JFET integrated circuits. Both allow the use of an epitaxially formed channel and a diffused gate, as in standard discrete JFET processing. This, presumably, results in JFETs which exhibit lower noise than those made with implanted channels. 11 refs., 9 figs

  4. 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.

  5. 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

  6. EST Table: FS871051 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available aa ref|NP_001139536.1| mortality factor 4-like [Bombyx mori] gb|ABJ99463.1| mrg15-like protein [Bombyx mori...FS871051 E_FL_fner_44F14_R_0 11/12/09 GO hit GO:0005634(nucleus) 10/09/28 100 %/257

  7. EST Table: FS730908 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS730908 E_FL_bmmt_29D15_F_0 10/09/28 31 %/289 aa ref|XP_974925.1| PREDICTED: similar to Juvenile.../10 31 %/268 aa gnl|Amel|GB15308-PA 10/09/10 31 %/289 aa gi|91080979|ref|XP_974925.1| PREDICTED: similar to Juvenile

  8. EST Table: FS933546 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS933546 E_FL_fwgP_37G09_F_0 10/09/28 41 %/186 aa gb|AAD21841.1| trypsin-like serine protease [Ctenocephalid...es felis] 10/09/13 low homology 10/08/29 n.h 10/09/10 37 %/190 aa AGAP004318-PA Pro

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. EST Table: FS932095 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available niofacial development protein 1 [Apis mellifera] 10/09/13 32 %/296 aa FBpp0169615|D...FS932095 E_FL_fwgP_33D17_F_0 11/12/09 n.h 10/09/28 36 %/283 aa ref|XP_001122476.1| PREDICTED: similar to cra

  13. EST Table: FS764147 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS764147 E_FL_fcaL_35O16_F_0 10/09/28 100 %/162 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  14. EST Table: FS767869 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS767869 E_FL_fcaL_47F03_F_0 10/09/28 100 %/162 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  15. EST Table: FS759868 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS759868 E_FL_fcaL_12K02_F_0 10/09/28 100 %/162 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  16. EST Table: FS766446 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS766446 E_FL_fcaL_42P03_F_0 10/09/28 100 %/162 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  17. EST Table: FS762222 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS762222 E_FL_fcaL_29P09_F_0 10/09/28 100 %/162 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  18. EST Table: FS759899 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS759899 E_FL_fcaL_12L13_F_0 10/09/28 100 %/162 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  19. EST Table: FS783042 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS783042 E_FL_fcaL_42P03_R_0 10/09/28 98 %/161 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mori

  20. EST Table: FS778274 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS778274 E_FL_fcaL_17C06_R_0 10/09/28 100 %/137 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  1. EST Table: FS762510 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS762510 E_FL_fcaL_30N10_F_0 10/09/28 100 %/162 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  2. EST Table: FS756751 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS756751 E_FL_fcaL_03B18_F_0 10/09/28 100 %/162 aa ref|NP_001037358.2| time interval... measuring enzyme-esterase A4 [Bombyx mori] dbj|BAF34334.1| time interval measuring enzyme TIME [Bombyx mor

  3. EST Table: FS911738 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS911738 E_FL_fufe_24C09_F_0 10/09/28 57 %/202 aa ref|XP_974840.1| PREDICTED: similar to harmon...10/09/10 57 %/202 aa gi|91081527|ref|XP_974840.1| PREDICTED: similar to harmonin [Tribolium castaneum] AU004664 fufe ...

  4. EST Table: FS735977 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS735977 E_FL_bmmt_04J24_R_0 11/12/09 n.h 10/09/28 36 %/182 aa ref|XP_001865897.1| best...rophin 2,3,4 [Culex quinquefasciatus] gb|EDS42461.1| bestrophin 2,3,4 [Culex quinquefasciatus] 10/09/03

  5. EST Table: FS735493 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS735493 E_FL_bmmt_03E05_R_0 10/09/28 33 %/206 aa ref|NP_001138033.1| bestrophin 1,... isoform B [Drosophila melanogaster] gb|ACL83492.1| bestrophin 1, isoform B [Drosophila melanogaster] 10/09/

  6. EST Table: FS829498 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS829498 E_FL_fmgV_32C07_R_0 10/09/28 34 %/210 aa ref|XP_001656347.1| bestrophin 2,...3,4 [Aedes aegypti] gb|EAT45610.1| bestrophin 2,3,4 [Aedes aegypti] 10/09/10 32 %/234 aa FBpp0113082|Best1-P

  7. EST Table: FS841717 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS841717 E_FL_fner_13C17_F_0 10/09/28 100 %/196 aa ref|NP_001041703.1| receptor for...onfirmed#UniProt:Q21215#protein_id:CAA93 514.1 10/09/10 91 %/196 aa AGAP010173-PA Protein|3R:49908149:49910286:1|gene:AGAP01017

  8. EST Table: FS917517 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917517 E_FL_fufe_41J10_F_0 10/09/28 61 %/218 aa ref|XP_001861467.1| pickel [Culex... quinquefasciatus] gb|EDS35652.1| pickel [Culex quinquefasciatus] 10/09/12 56 %/217 aa FBpp0229973|DvirGJ155

  9. EST Table: FS817517 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS817517 E_FL_fmgV_51J19_F_0 10/09/28 71 %/117 aa ref|NP_001040287.1| vacuolar ATP ...114 aa FBpp0120556|DanaGF17364-PA 10/08/29 41 %/116 aa F46F11.5#CE10604#WBGene00006919#locus:vha-10#vacuolar

  10. EST Table: FS751976 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS751976 E_ET_caL-_07I04_R_0 10/09/28 99 %/153 aa ref|NP_001040427.1| archease [Bom...byx mori] gb|ABF51366.1| archease [Bombyx mori] 10/09/08 71 %/145 aa FBpp0121001|DanaGF17809-PA 10/08/28 43

  11. EST Table: FS865761 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS865761 E_FL_fner_29C02_R_0 11/12/09 n.h 10/09/28 92 %/159 aa ref|NP_001040427.1| arche...ase [Bombyx mori] gb|ABF51366.1| archease [Bombyx mori] 10/09/11 66 %/151 aa FBpp0121001|DanaGF17809-PA

  12. EST Table: FS911211 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS911211 E_FL_fufe_22I17_F_0 11/12/09 n.h 10/09/28 91 %/153 aa ref|NP_001040427.1| arche...ase [Bombyx mori] gb|ABF51366.1| archease [Bombyx mori] 10/09/12 64 %/145 aa FBpp0121001|DanaGF17809-PA

  13. EST Table: FS884987 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS884987 E_FL_ftes_31L22_F_0 10/09/28 89 %/123 aa ref|NP_001040427.1| archease [Bom...byx mori] gb|ABF51366.1| archease [Bombyx mori] 10/09/12 64 %/123 aa FBpp0121001|DanaGF17809-PA 10/08/29 36

  14. EST Table: FS795717 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS795717 E_FL_ffbm_19B03_F_0 10/09/28 91 %/153 aa ref|NP_001040427.1| archease [Bom...byx mori] gb|ABF51366.1| archease [Bombyx mori] 10/09/09 64 %/145 aa FBpp0121001|DanaGF17809-PA 10/08/29 38

  15. EST Table: FS746912 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS746912 E_ET_caL-_07I04_F_0 10/09/28 99 %/159 aa ref|NP_001040427.1| archease [Bom...byx mori] gb|ABF51366.1| archease [Bombyx mori] 10/09/08 72 %/151 aa FBpp0121001|DanaGF17809-PA 10/08/28 42

  16. EST Table: FS898689 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS898689 E_FL_ftes_31L22_R_0 10/09/28 90 %/129 aa ref|NP_001040427.1| archease [Bom...byx mori] gb|ABF51366.1| archease [Bombyx mori] 10/09/12 66 %/129 aa FBpp0121001|DanaGF17809-PA 10/08/29 37

  17. EST Table: FS847351 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS847351 E_FL_fner_29C02_F_0 10/09/28 91 %/153 aa ref|NP_001040427.1| archease [Bom...byx mori] gb|ABF51366.1| archease [Bombyx mori] 10/09/10 64 %/145 aa FBpp0121001|DanaGF17809-PA 10/08/29 38

  18. EST Table: FS905677 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS905677 E_FL_fufe_05M22_F_0 10/09/28 45 %/170 aa ref|XP_966671.1| PREDICTED: similar to Deformed...ef|XP_966671.1| PREDICTED: similar to Deformed epidermal autoregulatory factor-1 CG8567-PB [Tribolium castaneum] DC540200 fufe ...

  19. EST Table: FS811111 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS811111 E_FL_fmgV_33N16_F_0 10/09/28 88 %/213 aa ref|NP_001036826.1| serine protea...0246031|DwilGK16888-PA 10/08/29 n.h 10/09/10 34 %/181 aa AGAP010240-PA Protein|3R:51410285:51411157:-1|gene:

  20. EST Table: FS830302 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS830302 E_FL_fmgV_34G24_R_0 10/09/28 84 %/218 aa gb|AAB26023.1| alkaliphilic serin...a] 10/09/10 37 %/203 aa FBpp0173021|DmojGI23804-PA 10/08/29 33 %/222 aa ZK546.15#CE36075#WBGene00006619#locu

  1. EST Table: FS729194 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 82 %/101 aa ref|XP_001651215.1| vitellogenin, putative [Aedes aegypti] gb|EAT42854.1| vitellogenin, putative... aa gnl|Amel|GB12346-PA 10/09/10 69 %/113 aa gi|91086835|ref|XP_974078.1| PREDICTED: similar to vitellogenin, putative [Tribolium castaneum] FS729194 bmmt ...

  2. Spatial Resolution Characterization for AWiFS Multispectral Images

    Science.gov (United States)

    Blonski, Slawomir; Ryan, Robert E.; Pagnutti, Mary; Stanley, Thomas

    2007-01-01

    This viewgraph presentation describes the spatial resolution of the AWiFS multispectral images characterized by an estimation of the Modulation Transfer Function (MTF) at Nyquist frequency. The contents include: 1) MTF Analysis; 2) Target Analysis; 3) "Pulse Target"; 4) "Pulse" Method; 5) Target Images; 6) Bridge Profiles; 7) MTF Calculation; 8) MTF Results; and 9) Results Summary.

  3. EST Table: FS886553 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS886553 E_FL_ftes_36I23_F_0 10/09/28 89 %/179 aa ref|XP_001603203.1| PREDICTED: similar to Ruvb...181 aa C27H6.2#CE43279#WBGene00007784#locus:ruvb-1#Yeast hypothetical 50.5 KD protein like#status:Confirmed#

  4. EST Table: FS765648 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 72 %/182 aa ref|XP_001658413.1| neuroendocrine differentiation factor [Aedes aegypti] gb|EAT40780.1| neuroendocrine... %/191 aa gnl|Amel|GB15107-PA 10/09/10 68 %/187 aa gi|91089815|ref|XP_968988.1| PREDICTED: similar to neuroendocrine differentiation factor [Tribolium castaneum] FS765648 fcaL ...

  5. EST Table: FS904909 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS904909 E_FL_fufe_03G19_F_0 10/09/28 45 %/171 aa ref|XP_001606849.1| PREDICTED: si...10/09/10 45 %/171 aa gnl|Amel|GB18412-PA 10/09/10 42 %/171 aa gi|91091366|ref|XP_972690.1| PREDICTED: simila

  6. EST Table: FS909090 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909090 E_FL_fufe_16C24_F_0 10/09/28 99 %/214 aa ref|NP_001037053.1| clip domain s...erine protease 11 [Bombyx mori] gb|AAN77090.1| masquerade-like serine proteinase homolog [Bombyx mori] dbj|B

  7. EST Table: FS909084 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909084 E_FL_fufe_16C18_F_0 10/09/28 56 %/217 aa ref|XP_001653706.1| glutathione s...ynthetase [Aedes aegypti] gb|EAT39012.1| glutathione synthetase [Aedes aegypti] 10/09/12 54 %/217 aa FBpp024

  8. EST Table: FS907464 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS907464 E_FL_fufe_11E08_F_0 10/09/28 54 %/117 aa ref|XP_001353679.2| GA10602 [Drosophila pseudoobscura... pseudoobscura] gb|EAL29412.2| GA10602 [Drosophila pseudoobscura pseudoobscura] 10/09/12

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. 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

  16. 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

  17. 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

  18. 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

  19. 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

  20. 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

  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. 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 ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. 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 ...

  20. EST Table: FS917216 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917216 E_FL_fufe_40L01_F_0 10/09/28 89 %/136 aa ref|NP_001093316.1| adiponectin r...eceptor [Bombyx mori] gb|ABK57116.2| adiponectin receptor [Bombyx mori] 10/09/12 67 %/191 aa FBpp0083675|CG5

  1. EST Table: FS854153 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS854153 E_FL_fner_48F21_F_0 10/09/28 100 %/103 aa ref|NP_001093316.1| adiponectin ...receptor [Bombyx mori] gb|ABK57116.2| adiponectin receptor [Bombyx mori] 10/09/11 72 %/158 aa FBpp0083675|CG

  2. EST Table: FS905475 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS905475 E_FL_fufe_05C16_F_0 10/09/28 68 %/198 aa ref|XP_001844362.1| adiponectin r...eceptor protein 2 [Culex quinquefasciatus] gb|EDS36702.1| adiponectin receptor protein 2 [Culex quinquefasci

  3. EST Table: FS860390 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS860390 E_FL_fner_13B05_R_0 10/09/28 88 %/161 aa ref|NP_001093316.1| adiponectin r...eceptor [Bombyx mori] gb|ABK57116.2| adiponectin receptor [Bombyx mori] 10/09/11 72 %/161 aa FBpp0151302|Dgr

  4. EST Table: FS769210 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS769210 E_FL_fcaL_51H14_F_0 10/09/28 74 %/176 aa ref|XP_001844362.1| adiponectin r...eceptor protein 2 [Culex quinquefasciatus] gb|EDS36702.1| adiponectin receptor protein 2 [Culex quinquefasci

  5. EST Table: FS762350 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS762350 E_FL_fcaL_30F17_F_0 10/09/28 94 %/112 aa ref|NP_001093316.1| adiponectin r...eceptor [Bombyx mori] gb|ABK57116.2| adiponectin receptor [Bombyx mori] 10/09/08 69 %/167 aa FBpp0083675|CG5

  6. EST Table: FS905957 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available e)|GO:0006886(intracellular protein transport) 10/09/28 52 %/144 aa ref|XP_969934.1| PREDICTED: similar to maggi.../10 low homology 10/09/10 low homology 10/09/10 52 %/144 aa gi|91090252|ref|XP_969934.1| PREDICTED: similar to maggie CG14981-PA [Tribolium castaneum] FS905957 fufe ...

  7. EST Table: FS891321 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available /28 46 %/153 aa ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium c...86783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS891321 ftes ...

  8. EST Table: FS906679 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available /28 45 %/153 aa ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium c...86783|ref|XP_973163.1| PREDICTED: similar to jumping translocation breakpoint protein [Tribolium castaneum] FS906679 fufe ...

  9. EST Table: FS870505 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available illary renal cell carcinoma (translocation-associated), partial [Taeniopygia guttat...FS870505 E_FL_fner_42M22_R_0 11/12/09 n.h 10/09/28 47 %/119 aa ref|XP_002191904.1| PREDICTED: similar to pap

  10. EST Table: FS854342 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  11. EST Table: FS854422 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  12. EST Table: FS844298 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  13. EST Table: FS838985 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  14. EST Table: FS866192 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS867881 fner ...

  15. EST Table: FS864399 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS867881 fner ...

  16. EST Table: FS849525 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  17. EST Table: FS873923 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS867881 fner ...

  18. EST Table: FS855622 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  19. EST Table: FS872664 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS867881 fner ...

  20. EST Table: FS844278 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  1. EST Table: FS853014 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  2. EST Table: FS839319 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  3. EST Table: FS837523 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  4. EST Table: FS846813 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  5. EST Table: FS850142 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  6. EST Table: FS850190 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  7. EST Table: FS864278 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS867881 fner ...

  8. EST Table: FS856017 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  9. EST Table: FS855398 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  10. EST Table: FS869956 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS867881 fner ...

  11. EST Table: FS843420 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  12. EST Table: FS838404 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  13. EST Table: FS853964 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  14. EST Table: FS854620 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  15. EST Table: FS839447 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  16. EST Table: FS854928 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  17. EST Table: FS838609 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  18. EST Table: FS844761 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  19. EST Table: FS847901 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  20. EST Table: FS843821 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  1. EST Table: FS853642 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  2. EST Table: FS839617 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  3. EST Table: FS785047 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [Bombyx mori] 10/09/09 n.h 10/08/28 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS867881 fcaL ...

  4. EST Table: FS842898 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  5. EST Table: FS855815 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  6. EST Table: FS842116 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  7. EST Table: FS847208 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  8. EST Table: FS874113 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS867881 fner ...

  9. EST Table: FS846325 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein LOC100301494 [Bombyx mori] dbj|BAH22627.1| possible precursor of neuropeptides [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 FS904409 fner ...

  10. EST Table: FS914277 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS914277 E_FL_fufe_31M22_F_0 10/09/28 37 %/274 aa ref|XP_969699.1| PREDICTED: similar to fuzzy.../274 aa gi|91081315|ref|XP_969699.1| PREDICTED: similar to fuzzy CG13396-PA [Tribolium castaneum] CK514734 fufe ...

  11. EST Table: FS924625 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS924625 E_FL_fwgP_11B16_F_0 10/09/28 89 %/281 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/13 44

  12. EST Table: FS749979 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS749979 E_ET_caL-_20O02_F_0 10/09/28 91 %/147 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/08 50

  13. EST Table: FS755728 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS755728 E_ET_caL-_20O02_R_0 10/09/28 92 %/147 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/08 50

  14. EST Table: FS729831 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS729831 E_FL_bmmt_17C13_F_0 10/09/28 82 %/162 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/03 lo

  15. EST Table: FS904069 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS904069 E_FL_ftes_53L19_R_0 10/09/28 42 %/195 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/12 38

  16. EST Table: FS898341 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS898341 E_FL_ftes_30H06_R_0 10/09/28 44 %/208 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/12 40

  17. EST Table: FS927021 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS927021 E_FL_fwgP_18C07_F_0 10/09/28 88 %/265 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/13 47

  18. EST Table: FS740414 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS740414 E_FL_bmmt_17C13_R_0 10/09/28 95 %/239 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/07 54

  19. EST Table: FS771859 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS771859 E_FL_fcaL_23J22_F_0 10/09/28 83 %/173 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/08 n.

  20. EST Table: FS939144 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS939144 E_FL_fwgP_54A24_F_0 10/09/28 89 %/280 aa ref|NP_001036933.1| molting fluid... carboxypeptidase A [Bombyx mori] dbj|BAD60916.1| molting fluid carboxypeptidase A [Bombyx mori] 10/09/13 45

  1. EST Table: FS914333 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS914333 E_FL_fufe_31P15_F_0 10/09/28 83 %/247 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/12 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  2. EST Table: FS930900 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS930900 E_FL_fwgP_29J02_F_0 10/09/28 78 %/193 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/13 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  3. EST Table: FS908726 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS908726 E_FL_fufe_15B10_F_0 10/09/28 80 %/287 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/12 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  4. EST Table: FS917537 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917537 E_FL_fufe_41K08_F_0 10/09/28 81 %/259 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/12 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  5. EST Table: FS912099 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS912099 E_FL_fufe_25D20_F_0 10/09/28 81 %/269 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/12 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  6. EST Table: FS910501 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS910501 E_FL_fufe_20G17_F_0 10/09/28 79 %/271 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/12 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  7. EST Table: FS914344 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS914344 E_FL_fufe_32A04_F_0 10/09/28 84 %/252 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/12 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  8. EST Table: FS846798 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS846798 E_FL_fner_27I16_F_0 10/09/28 76 %/176 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/10 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  9. EST Table: FS805988 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS805988 E_FL_fmgV_19H04_F_0 10/09/28 80 %/200 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/09 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  10. EST Table: FS914324 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS914324 E_FL_fufe_31P03_F_0 10/09/28 79 %/263 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/12 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  11. EST Table: FS925836 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS925836 E_FL_fwgP_14J18_F_0 10/09/28 80 %/229 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/13 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  12. EST Table: FS854196 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS854196 E_FL_fner_48H18_F_0 10/09/28 81 %/211 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/11 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  13. EST Table: FS764459 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS764459 E_FL_fcaL_36N24_F_0 10/09/28 80 %/221 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/08 low homology 10/08/28 n.h 10/09/10 40 %/150 aa AG

  14. EST Table: FS759057 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS759057 E_FL_fcaL_10C12_F_0 10/09/28 78 %/214 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/08 low homology 10/08/28 n.h 10/09/10 41 %/150 aa AG

  15. EST Table: FS764592 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS764592 E_FL_fcaL_37E11_F_0 10/09/28 81 %/229 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/08 low homology 10/08/28 n.h 10/09/10 42 %/150 aa AG

  16. EST Table: FS918053 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918053 E_FL_fufe_43C23_F_0 10/09/28 83 %/247 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/12 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  17. EST Table: FS840757 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS840757 E_FL_fner_10H07_F_0 10/09/28 81 %/160 aa ref|NP_001040506.1| bmp-2 protein... [Bombyx mori] gb|ABF60228.1| bmp-2 [Bombyx mori] 10/09/10 low homology 10/08/29 n.h 10/09/10 42 %/150 aa AG

  18. EST Table: FS928371 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS928371 E_FL_fwgP_22B11_F_0 10/09/28 87 %/119 aa ref|XP_975463.1| PREDICTED: similar to rasputin...066-PA 10/09/10 87 %/119 aa gi|91076984|ref|XP_975463.1| PREDICTED: similar to rasputin CG9412-PB [Tribolium castaneum] CK541017 fwgP ...

  19. EST Table: FS891235 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS891235 E_FL_ftes_02B20_R_0 11/12/09 GO hit GO:0003779(actin binding)|GO:0007010(cytoskeleton organization...)|GO:0015629(actin cytoskeleton)|GO:0030036(actin cytoskeleton organization) 10/09/2

  20. 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 ...

  1. 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

  2. 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 ...

  3. EST Table: FS838457 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 10/09/10 56 %/160 aa gnl|Amel|GB17380-PA 10/09/10 59 %/150 aa gi|189235487|ref|XP_968396.2| PREDICTED: similar to failed axon connections protein [Tribolium castaneum] FS937483 fner ...

  4. EST Table: FS898353 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 29 50 %/248 aa C28H8.11a#CE01822#WBGene00016201#tryptophan 2, 3- dioxygenase#status:Confirmed#UniProt:Q09474...FS898353 E_FL_ftes_30H20_R_0 11/12/09 GO hit GO:0004833(tryptophan 2,3-dioxygenase

  5. EST Table: FS795745 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 29 51 %/290 aa C28H8.11a#CE01822#WBGene00016201#tryptophan 2, 3- dioxygenase#status:Confirmed#UniProt:Q09474...FS795745 E_FL_ffbm_19C09_F_0 11/12/09 GO hit GO:0004833(tryptophan 2,3-dioxygenase

  6. EST Table: FS906524 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS906524 E_FL_fufe_08G24_F_0 10/09/28 98 %/275 aa ref|NP_001037666.1| telomerase re...verse transcriptase [Bombyx mori] gb|ABC95023.1| telomerase reverse transcriptase [Bombyx mori] gb|ABF56516.1| telomerase

  7. EST Table: FS904468 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS904468 E_FL_fufe_02B14_F_0 10/09/28 99 %/289 aa ref|NP_001037666.1| telomerase re...verse transcriptase [Bombyx mori] gb|ABC95023.1| telomerase reverse transcriptase [Bombyx mori] gb|ABF56516.1| telomerase

  8. EST Table: FS914954 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS914954 E_FL_fufe_33M18_F_0 10/09/28 97 %/294 aa ref|NP_001037666.1| telomerase re...verse transcriptase [Bombyx mori] gb|ABC95023.1| telomerase reverse transcriptase [Bombyx mori] gb|ABF56516.1| telomerase

  9. EST Table: FS908974 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS908974 E_FL_fufe_15N13_F_0 10/09/28 99 %/299 aa ref|NP_001037666.1| telomerase re...verse transcriptase [Bombyx mori] gb|ABC95023.1| telomerase reverse transcriptase [Bombyx mori] gb|ABF56516.1| telomerase

  10. EST Table: FS882164 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS882164 E_FL_ftes_23H19_F_0 10/09/28 98 %/202 aa ref|NP_001037666.1| telomerase re...verse transcriptase [Bombyx mori] gb|ABC95023.1| telomerase reverse transcriptase [Bombyx mori] gb|ABF56516.1| telomerase

  11. EST Table: FS896540 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS896540 E_FL_ftes_23H19_R_0 10/09/28 97 %/175 aa ref|NP_001037666.1| telomerase re...verse transcriptase [Bombyx mori] gb|ABC95023.1| telomerase reverse transcriptase [Bombyx mori] gb|ABF56516.1| telomerase

  12. EST Table: FS876589 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS876589 E_FL_ftes_07E06_F_0 10/09/28 100 %/223 aa ref|NP_001037666.1| telomerase r...everse transcriptase [Bombyx mori] gb|ABC95023.1| telomerase reverse transcriptase [Bombyx mori] gb|ABF56516.1| telomerase

  13. EST Table: FS768412 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ytosis)|GO:0016192(vesicle-mediated transport) 10/09/28 80 %/292 aa ref|NP_001164155.1| Ras opposite [Tribol... 10/09/10 75 %/289 aa gnl|Amel|GB12540-PA 10/09/10 80 %/292 aa gi|282392023|ref|NP_001164155.1| Ras opposite [Tribolium castaneum] FS768412 fcaL ...

  14. EST Table: FS830202 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS830202 E_FL_fmgV_34C08_R_0 10/09/28 94 %/274 aa ref|NP_001040163.1| ischemia/reperfusion... inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  15. EST Table: FS916028 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS916028 E_FL_fufe_37B11_F_0 10/09/28 88 %/153 aa ref|NP_001040163.1| ischemia/reperfusion... inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  16. EST Table: FS906495 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS906495 E_FL_fufe_08F15_F_0 10/09/28 87 %/189 aa ref|NP_001040163.1| ischemia/reperfusion... inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  17. EST Table: FS811216 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS811216 E_FL_fmgV_34C08_F_0 10/09/28 87 %/135 aa ref|NP_001040163.1| ischemia/reperfusion... inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  18. EST Table: FS897929 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS897929 E_FL_ftes_29A02_R_0 10/09/28 98 %/262 aa ref|NP_001040163.1| ischemia/reperfusion... inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  19. EST Table: FS859767 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS859767 E_FL_fner_11E17_R_0 10/09/28 96 %/209 aa ref|NP_001040163.1| ischemia/reperfusion... inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  20. EST Table: FS911194 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS911194 E_FL_fufe_22H22_F_0 10/09/28 89 %/176 aa ref|NP_001040163.1| ischemia/reperfusion... inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  1. EST Table: FS898521 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS898521 E_FL_ftes_31C04_R_0 11/12/09 n.h 10/09/28 99 %/234 aa ref|NP_001040163.1| ischemia/reperfusion... inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [

  2. EST Table: FS747747 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS747747 E_ET_caL-_11D03_F_0 10/09/28 44 %/103 aa ref|XP_002435218.1| charged multi...vesicular body protein, putative [Ixodes scapularis] gb|EEC08042.1| charged multivesicular body protein, put

  3. EST Table: FS767534 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS767534 E_FL_fcaL_46E16_F_0 10/09/28 78 %/181 aa ref|XP_001653066.1| charged multi...vesicular body protein 2a [Aedes aegypti] gb|EAT47555.1| charged multivesicular body protein 2a [Aedes aegyp

  4. EST Table: FS752978 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS752978 E_ET_caL-_11D03_R_0 11/12/09 n.h 10/09/28 44 %/103 aa ref|XP_002435218.1| charge...d multivesicular body protein, putative [Ixodes scapularis] gb|EEC08042.1| charged multivesicular body

  5. EST Table: FS911565 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 0/09/10 78 %/161 aa gnl|Amel|GB19218-PA 10/09/10 83 %/161 aa gi|189241909|ref|XP_970822.2| PREDICTED: similar to Darkener of apricot CG33553-PG [Tribolium castaneum] FS918661 fufe ...

  6. EST Table: FS779323 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available /09/10 79 %/201 aa gnl|Amel|GB19218-PA 10/09/10 75 %/196 aa gi|189241909|ref|XP_970822.2| PREDICTED: similar to Darkener of apricot CG33553-PG [Tribolium castaneum] FS779323 fcaL ...

  7. EST Table: FS791410 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 0/09/10 75 %/133 aa gnl|Amel|GB19218-PA 10/09/10 81 %/133 aa gi|189241909|ref|XP_970822.2| PREDICTED: similar to Darkener of apricot CG33553-PG [Tribolium castaneum] FS918661 ffbm ...

  8. EST Table: FS936163 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 0/09/10 77 %/159 aa gnl|Amel|GB19218-PA 10/09/10 83 %/159 aa gi|189241909|ref|XP_970822.2| PREDICTED: similar to Darkener of apricot CG33553-PG [Tribolium castaneum] FS918661 fwgP ...

  9. EST Table: FS824424 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS824424 E_FL_fmgV_17P08_R_0 10/09/28 31 %/260 aa ref|XP_001868268.1| thymus-specif...ic serine protease [Culex quinquefasciatus] gb|EDS26459.1| thymus-specific serine protease [Culex quinquefas

  10. EST Table: FS835826 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS835826 E_FL_fmgV_49K21_R_0 10/09/28 32 %/274 aa ref|XP_001868268.1| thymus-specif...ic serine protease [Culex quinquefasciatus] gb|EDS26459.1| thymus-specific serine protease [Culex quinquefas

  11. EST Table: FS824164 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS824164 E_FL_fmgV_17D09_R_0 10/09/28 32 %/284 aa ref|XP_001868268.1| thymus-specif...ic serine protease [Culex quinquefasciatus] gb|EDS26459.1| thymus-specific serine protease [Culex quinquefas

  12. EST Table: FS816912 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available milar to class b basic helix-loop-helix protein (bhlhb) (differentially expressed in chondrocytes) (mdec) (sharp...asic helix-loop-helix protein (bhlhb) (differentially expressed in chondrocytes) (mdec) (sharp) [Tribolium castaneum] FS845099 fmgV ...

  13. EST Table: FS845099 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available PREDICTED: similar to class b basic helix-loop-helix protein (bhlhb) (differentially expressed in chondrocytes) (mdec) (sharp...lar to class b basic helix-loop-helix protein (bhlhb) (differentially expressed in chondrocytes) (mdec) (sharp) [Tribolium castaneum] FS845099 fner ...

  14. EST Table: FS903743 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available inc ion binding) 10/09/28 30 %/147 aa gb|EFA01352.1| grauzone [Tribolium castaneum] 10/09/12 low homology 10...mel|GB16690-PA 10/09/10 30 %/147 aa gi|270004904|gb|EFA01352.1| grauzone [Tribolium castaneum] FS903743 ftes ...

  15. EST Table: FS764096 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available cription) 10/09/28 48 %/117 aa ref|XP_967427.2| PREDICTED: similar to hypoxia-inducible factor 1 alpha [Trib...|GB16786-PA 10/09/10 48 %/117 aa gi|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia-inducible factor 1 alpha [Tribolium castaneum] FS764096 fcaL ...

  16. EST Table: FS798461 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available 10 low homology 10/09/10 low homology 10/09/10 44 %/145 aa gi|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia-inducible factor 1 alpha [Tribolium castaneum] FS913906 ffbm ...

  17. EST Table: FS913906 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available , DNA-dependent)|GO:0007165(signal transduction) 10/09/28 40 %/332 aa ref|XP_967427.2| PREDICTED: similar to hypoxia...40 %/332 aa gi|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia-inducible factor 1 alpha [Tribolium castaneum] FS913906 fufe ...

  18. EST Table: FS907005 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS907005 E_FL_fufe_09O11_F_0 10/09/28 51 %/189 aa ref|XP_967427.2| PREDICTED: similar to hypoxia...002942 10/09/10 51 %/196 aa gnl|Amel|GB16786-PA 10/09/10 51 %/189 aa gi|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia

  19. EST Table: FS754028 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS754028 E_ET_caL-_14O17_R_0 10/09/28 63 %/215 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/08 63 %/215 aa FBpp0265803|DyakGE20793-PA 10

  20. EST Table: FS915956 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915956 E_FL_fufe_36N21_F_0 10/09/28 63 %/130 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/12 63 %/130 aa FBpp0265803|DyakGE20793-PA 10

  1. EST Table: FS925667 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS925667 E_FL_fwgP_14C05_F_0 10/09/28 68 %/193 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/13 68 %/193 aa FBpp0265803|DyakGE20793-PA 10

  2. EST Table: FS868205 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS868205 E_FL_fner_36C20_R_0 10/09/28 65 %/215 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/11 65 %/215 aa FBpp0265803|DyakGE20793-PA 10

  3. EST Table: FS913726 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS913726 E_FL_fufe_30C09_F_0 10/09/28 67 %/192 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/12 67 %/192 aa FBpp0265803|DyakGE20793-PA 10

  4. EST Table: FS915398 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915398 E_FL_fufe_35C18_F_0 10/09/28 63 %/130 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/12 63 %/130 aa FBpp0265803|DyakGE20793-PA 10

  5. EST Table: FS827460 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS827460 E_FL_fmgV_26H01_R_0 10/09/28 64 %/210 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/10 64 %/210 aa FBpp0265803|DyakGE20793-PA 10

  6. EST Table: FS908509 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS908509 E_FL_fufe_14G14_F_0 10/09/28 69 %/175 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/12 69 %/175 aa FBpp0265803|DyakGE20793-PA 10

  7. EST Table: FS757922 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS757922 E_FL_fcaL_06L10_F_0 10/09/28 70 %/134 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/08 70 %/134 aa FBpp0265803|DyakGE20793-PA 10

  8. EST Table: FS725073 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS725073 E_FL_bmmt_03J18_F_0 10/09/28 42 %/178 aa ref|XP_002093691.1| GE20623 [Dros...ophila yakuba] gb|EDW93403.1| GE20623 [Drosophila yakuba] 10/09/03 42 %/178 aa FBpp0265633|DyakGE20623-PA 10

  9. EST Table: FS865889 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS865889 E_FL_fner_29H21_R_0 10/09/28 33 %/136 aa ref|XP_002094233.1| GE20311 [Dros...ophila yakuba] gb|EDW93945.1| GE20311 [Drosophila yakuba] 10/09/11 33 %/136 aa FBpp0265321|DyakGE20311-PA 10

  10. EST Table: FS733322 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS733322 E_FL_bmmt_21A19_F_0 10/09/28 43 %/193 aa ref|XP_002093691.1| GE20623 [Dros...ophila yakuba] gb|EDW93403.1| GE20623 [Drosophila yakuba] 10/09/03 43 %/193 aa FBpp0265633|DyakGE20623-PA 10

  11. EST Table: FS761851 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS761851 E_FL_fcaL_28M14_F_0 10/09/28 70 %/168 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/08 70 %/168 aa FBpp0265803|DyakGE20793-PA 10

  12. EST Table: FS759853 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS759853 E_FL_fcaL_12J07_F_0 10/09/28 67 %/146 aa ref|XP_002090121.1| GE20538 [Dros...ophila yakuba] gb|EDW89833.1| GE20538 [Drosophila yakuba] 10/09/08 67 %/146 aa FBpp0265548|DyakGE20538-PA 10

  13. EST Table: FS751073 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS751073 E_ET_caL-_04B22_R_0 10/09/28 62 %/210 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/08 62 %/210 aa FBpp0265803|DyakGE20793-PA 10

  14. EST Table: FS740394 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS740394 E_FL_bmmt_17B15_R_0 10/09/28 63 %/135 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/07 63 %/135 aa FBpp0265803|DyakGE20793-PA 10

  15. EST Table: FS808471 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS808471 E_FL_fmgV_26H01_F_0 10/09/28 70 %/160 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/09 70 %/160 aa FBpp0265803|DyakGE20793-PA 10

  16. EST Table: FS756618 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS756618 E_FL_fcaL_02L02_F_0 10/09/28 70 %/134 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/08 70 %/134 aa FBpp0265803|DyakGE20793-PA 10

  17. EST Table: FS918670 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918670 E_FL_fufe_45B04_F_0 10/09/28 64 %/208 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/13 64 %/208 aa FBpp0265803|DyakGE20793-PA 10

  18. EST Table: FS778790 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS778790 E_FL_fcaL_28M14_R_0 10/09/28 64 %/210 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/08 64 %/210 aa FBpp0265803|DyakGE20793-PA 10

  19. EST Table: FS896075 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS896075 E_FL_ftes_20M05_R_0 10/09/28 51 %/102 aa ref|XP_002093585.1| GE20674 [Dros...ophila yakuba] gb|EDW93297.1| GE20674 [Drosophila yakuba] 10/09/12 51 %/102 aa FBpp0265684|DyakGE20674-PA 10

  20. EST Table: FS738963 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS738963 E_FL_bmmt_13B13_R_0 10/09/28 60 %/120 aa ref|XP_002093380.1| GE20793 [Dros...ophila yakuba] gb|EDW93092.1| GE20793 [Drosophila yakuba] 10/09/07 60 %/120 aa FBpp0265803|DyakGE20793-PA 10