WorldWideScience

Sample records for all-pm monolithic fs

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

    DEFF Research Database (Denmark)

    Turchinovich, Dmitry; Liu, Xiaomin; Lægsgaard, Jesper

    2008-01-01

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

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

    DEFF Research Database (Denmark)

    Turchinovich, Dmitry; Liu, Xiaomin; Lægsgaard, Jesper

    2008-01-01

    . 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...

  3. Mode-locked femtosecond all-normal all-PM Yb-doped fiber laser at 1060 nm

    Science.gov (United States)

    Bowen, Patrick; Singh, Harman; Runge, Antoine; Provo, Richard; Broderick, Neil G. R.

    2016-04-01

    We report an all-normal-dispersion, all-fibre, all-PM, laser operating at a central wavelength of 1060 nm. The laser is mode-locked using a nonlinear amplifying loop mirror and generates linearly polarised pulses that can be compressed to 360 fs. The laser is based on our earlier scheme operating at 1030 nm [1] and we discuss the similarities and differences between the two configurations. We also present amplification up to an output power of 1 W using a commercially built amplifier and show through numerical methods that this pulse may be recompressible to 1.65 ps.

  4. 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.

  5. 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.

  6. Monolithic Yb-fiber femtosecond laser using photonic crystal fiber

    DEFF Research Database (Denmark)

    Liu, Xiaomin; Lægsgaard, Jesper; Turchinovich, Dmitry

    2008-01-01

    We demonstrate, both experimentally and theoretically, an environmentally stable monolithic all-PM modelocked femtosecond Yb-fiber laser, with laser output pulse compressed in a spliced-on low-loss hollow-core photonic crystal fiber. Our laser provides direct fiber-end delivery of 4 nJ pulses of...

  7. Monolithic ceramics

    Science.gov (United States)

    Herbell, Thomas P.; Sanders, William A.

    1992-01-01

    A development history and current development status evaluation are presented for SiC and Si3N4 monolithic ceramics. In the absence of widely sought improvements in these materials' toughness, and associated reliability in structural applications, uses will remain restricted to components in noncritical, nonman-rated aerospace applications such as cruise missile and drone gas turbine engine components. In such high temperature engine-section components, projected costs lie below those associated with superalloy-based short-life/expendable engines. Advancements are required in processing technology for the sake of fewer and smaller microstructural flaws.

  8. 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...

  9. 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.

  10. 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.

  11. Washcoated Pd/Al2O3 monoliths for the liquid phase hydrodechlorination of dioxins

    OpenAIRE

    Cobo, Martha; Orrego, Andrés; Conesa Ferrer, Juan Antonio

    2012-01-01

    The catalytic activity and durability of 2 wt.% Pd/Al2O3 in powder and washcoated on cordierite monoliths were examined for the liquid phase hydrodechlorination (LPHDC) of polychlorinated dibenzo-p-dioxins/polychlorinated dibenzofurans (PCDD/Fs), also known as dioxins. NaOH was employed as a neutralizing agent, and 2-propanol was used as a hydrogen donor and a solvent. Fresh and spent powder and monolith samples were characterized by elemental analysis, surface area, hydrogen chemisorption, s...

  12. 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.

  13. A monolithic white laser

    Science.gov (United States)

    Fan, Fan; Turkdogan, Sunay; Liu, Zhicheng; Shelhammer, David; Ning, C. Z.

    2015-09-01

    Monolithic semiconductor lasers capable of emitting over the full visible-colour spectrum have a wide range of important applications, such as solid-state lighting, full-colour displays, visible colour communications and multi-colour fluorescence sensing. The ultimate form of such a light source would be a monolithic white laser. However, realizing such a device has been challenging because of intrinsic difficulties in achieving epitaxial growth of the mismatched materials required for different colour emission. Here, we demonstrate a monolithic multi-segment semiconductor nanosheet based on a quaternary alloy of ZnCdSSe that simultaneously lases in the red, green and blue. This is made possible by a novel nanomaterial growth strategy that enables separate control of the composition, morphology and therefore bandgaps of the segments. Our nanolaser can be dynamically tuned to emit over the full visible-colour range, covering 70% more perceptible colours than the most commonly used illuminants.

  14. 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.

  15. 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.

  16. Monolithic catalytic igniters

    Science.gov (United States)

    La Ferla, R.; Tuffias, R. H.; Jang, Q.

    1993-01-01

    Catalytic igniters offer the potential for excellent reliability and simplicity for use with the diergolic bipropellant oxygen/hydrogen as well as with the monopropellant hydrazine. State-of-the-art catalyst beds - noble metal/granular pellet carriers - currently used in hydrazine engines are limited by carrier stability, which limits the hot-fire temperature, and by poor thermal response due to the large thermal mass. Moreover, questions remain with regard to longevity and reliability of these catalysts. In this work, Ultramet investigated the feasibility of fabricating monolithic catalyst beds that overcome the limitations of current catalytic igniters via a combination of chemical vapor deposition (CVD) iridium coatings and chemical vapor infiltration (CVI) refractory ceramic foams. It was found that under all flow conditions and O2:H2 mass ratios tested, a high surface area monolithic bed outperformed a Shell 405 bed. Additionally, it was found that monolithic catalytic igniters, specifically porous ceramic foams fabricated by CVD/CVI processing, can be fabricated whose catalytic performance is better than Shell 405 and with significantly lower flow restriction, from materials that can operate at 2000 C or higher.

  17. 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

  18. 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.

  19. Monolithic freeform element

    Science.gov (United States)

    Kiontke, Sven R.

    2015-09-01

    For 10 years there has been the asphere as one of the new products to be accepted by the market. All parts of the chain design, production and measurement needed to learn how to treat the asphere and what it is helpful for. The aspheric optical element now is established and accepted as an equal optical element between other as a fast growing part of all the optical elements. Now we are focusing onto the next new element with a lot of potential, the optical freeform surface. Manufacturing results will be shown for fully tolerance optic including manufacturing, setup and optics configurations including measurement setup. The element itself is a monolith consisting of several optical surfaces that have to be aligned properly to each other. The freeform surface is measured for surface form tolerance (irregularity, slope, Zernike, PV).

  20. 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.

  1. 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

  2. 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

  3. 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

  4. UV-LED photopolymerised monoliths

    Czech Academy of Sciences Publication Activity Database

    Abele, S.; Nie, F.; Foret, František; Paull, B.; Macka, M.

    2008-01-01

    Roč. 133, č. 7 (2008), s. 864-866. ISSN 0003-2654 R&D Projects: GA AV ČR KAN400310651 Institutional research plan: CEZ:AV0Z40310501 Keywords : photopolymerisation * UV- LED * polymethacrylate monolith Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 3.761, year: 2008

  5. 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).

  6. 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).

  7. 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.

  8. 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

  9. Hydrodynamics of a Monolithic Stirrer Reactor

    OpenAIRE

    Kritzinger, H.P.

    2011-01-01

    The Monolithic Stirrer Reactor (MSR) is a novel concept for heterogeneously catalyzed reactors and is presented as an alternative device to slurry reactors. It uses a modified stirrer on which structured catalyst supports (monoliths) are fixed to form permeable blades. The monoliths consist of small square parallel channels on which a layer of catalytic material can be applied. The stirrer now has both a catalytic and a mixing function. The main advantage of this reactor type is the ease of t...

  10. Counterflow isotachophoresis in a monolithic column.

    Science.gov (United States)

    Liu, Bingwen; Cong, Yongzheng; Ivory, Cornelius F

    2014-09-01

    This study describes stationary counterflow isotachophoresis (ITP) in a poly(acrylamide-co-N,N'-methylenebisacrylamide) monolithic column as a means for improving ITP processing capacity and reducing dispersion. The flow profile in the monolith was predicted using COMSOL's Brinkman Equation application mode, which revealed that the flow profile was mainly determined by monolith permeability. As monolith permeability decreases, the flow profile changes from a parabolic shape to a plug shape. An experimental monolithic column was prepared in a fused-silica capillary using an ultraviolet-initiated polymerization method. A monolithic column made from 8% (wt.) monomer was chosen for the stationary counterflow ITP experiments. Counterflow ITP in the monolithic column showed undistorted analyte zones with significantly reduced dispersion compared to the severe dispersion observed in an open capillary. Particularly, for r-phycoerythrin focused by counterflow ITP, its zone width in the monolithic column was only one-third that observed in an open capillary. These experiments demonstrate that stationary counterflow ITP in monoliths can be a robust and practical electrofocusing method. PMID:24935025

  11. 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.

  12. 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.

  13. 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

  14. Microfluidic devices and methods including porous polymer monoliths

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-12-01

    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.

  15. 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.

  16. 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...

  17. 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.

  18. 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…

  19. Streamlining the RI/FS process

    International Nuclear Information System (INIS)

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

  20. 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.

  1. 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

  2. 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.

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

    International Nuclear Information System (INIS)

    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. (letter)

  4. 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.

  5. InterProScan検索結果: FS761866 [

    Lifescience Database Archive (English)

    Full Text Available FS761866 FS761866_3_ORF2 B34F16034975FDC2 PANTHER PTHR11129 PROTEIN FARNESYLTRANSFERASE ALPHA SUBUNIT/RA...B GERANYLGERANYL TRANSFERASE ALPHA SUBUNIT 1.2e-32 T IPR008940 unintegrated ...

  6. SeaWiFS Technical Report Series. Volume 39; SeaWiFS Calibration Topics

    Science.gov (United States)

    Hooker, Stanford B. (Editor); Firestone, Elaine R. (Editor); Barnes, Robert A.; Yeh, Eueng-nan; Eplee, Robert E.

    1996-01-01

    For Earth-observing satellite instruments, it was standard to consider each instrument band to have a spectral response that is infinitely narrow, i.e., to have a response from a single wavelength. The Sea-viewing Wide Field-of-view Sensor (SeaWiFS) bands, however, have nominal spectral bandwidths of 20 and 40nm. These bandwidths affect the SeaWiFS measurements on orbit. The effects are also linked to the manner in which the instrument was calibrated and to the spectral shape of the radiance that SeaWiFS views. Currently, SeaWiFS is calibrated such that the digital counts from each instrument band are linked to the Earth-exiting radiance at an individual center wavelength. Before launch, SeaWiFS will be recalibrated so that the digital counts from each band will be linked to the Earth-exiting radiance integrated over the spectral response of that band. In this technical memorandum, the effects of the instrument calibration and the source spectral shape on SeaWiFS measurements, including the in-band and out-of-band responses, and the center wavelengths are discussed.

  7. Quarry residuals RI/FS scoping document

    International Nuclear Information System (INIS)

    The purpose of this document is to serve as a planning tool for the implementation of the Quarry Residual Remedial Investigation/Feasibility Study (RI/FS) process and to provide direct input to revising and updating the 1988 Work Plan for the Weldon Spring Site Remedial Action Project (WSSRAP) Remedial Investigation/Feasibility Study-Environmental Impact Statement for the Weldon Spring Site (RI/FS-EIS) (Peterson et al. 1988) for this effort. The scoping process is intended to outline the tasks necessary to develop and implement activities in compliance with the Comprehensive Environmental Response, Compensation and Liability Act-National Environmental Policy Act (CERCLA-NEPA) process from detailed planning through the appropriate decision document. In addition to scoping the entire process, this document will serve as the primary tool for planning and accomplishing all activities to be developed in the Quarry Residual RI/FS Work Plan. Subsequent tasks are difficult to plan at this time. 10 refs., 5 figs., 5 tabs

  8. 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...

  9. 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...

  10. 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.

  11. 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.

  12. 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

  13. 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")

  14. Pepsin-modified chiral monolithic column for affinity capillary electrochromatography.

    Science.gov (United States)

    Hong, Tingting; Chi, Cuijie; Ji, Yibing

    2014-11-01

    Pepsin-modified affinity monolithic capillary electrochromatography, a novel microanalysis system, was developed by the covalent bonding of pepsin on silica monolith. The column was successfully applied in the chiral separation of (±)-nefopam. Furthermore, the electrochromatographic performance of the pepsin-functionalized monolith for enantiomeric analysis was evaluated in terms of protein content, pH of running buffer, sample volume, buffer concentration, applied voltage, and capillary temperature. The relative standard deviation (%RSD) values of retention time (intraday implied that the affinity monolith used in this research opens a new path of exploring particularly versatile class of enzymes to develop enzyme-modified affinity capillary monolith for enantioseparation. PMID:25146884

  15. Package Holds Five Monolithic Microwave Integrated Circuits

    Science.gov (United States)

    Mysoor, Narayan R.; Decker, D. Richard; Olson, Hilding M.

    1996-01-01

    Packages protect and hold monolithic microwave integrated circuit (MMIC) chips while providing dc and radio-frequency (RF) electrical connections for chips undergoing development. Required to be compact, lightweight, and rugged. Designed to minimize undesired resonances, reflections, losses, and impedance mismatches.

  16. Development of oxide fibrous monolith systems.

    Energy Technology Data Exchange (ETDEWEB)

    Goretta, K. C.

    1999-03-02

    Fibrous monolithic ceramics generally have a cellular structure that consists of a strong cell surrounded by a weaker boundary phase [1-5]. Fibrous monoliths (FMs) are produced from powders by conventional ceramic fabrication techniques, such as extrusion [1,2]. When properly engineered, they exhibit fail gracefully [3-5]. Several compositions of ceramics and cermets have been processed successfully in fibrous monolithic form [4]. The most thoroughly investigated fibrous monolith consists of Si{sub 3}N{sub 4} cells and a BN cell-boundary phase [3-5]. Through appropriate selection of initial powders and extrusion and hot-pressing parameters, very tough final products have been produced. The resultant high toughness is due primarily to delamination during fracture along textured platelike BN grains. The primary objectives of our program are to develop: (1) Oxide-based FMs, including new systems with improved properties; (2) FMs that can be pressureless sintered rather than hot-pressed; (3) Techniques for continuous extrusion of FM filaments, including solid freeform fabrication (SFF) for net-shape fabrication of FMs; (4) Predictive micromechanical models for FM design and performance; and (5) Ties with industrial producers and users of FMs.

  17. Chemical routes to monolithic hydroxyapatite formation

    Energy Technology Data Exchange (ETDEWEB)

    Brown, P. [Pennsylvania State Univ., University Park, PA (United States). Dept. of Materials Science and Engineering

    2002-07-01

    Of the inorganic materials used to replace hard tissues only hydroxyapatite is biologically familiar. The biocompatibility of hydroxyapatite is well documented, making it an attractive candidate for a hard tissue analog provided the needed mechanical properties can be realized. In selecting analogs of hard tissues, it is highly desirable to eliminate the need for preforms, thereby allowing implanted materials to accommodate to the shapes of defects. This can be accomplished if the implanted material hardens in vivo. When produced in monolithic form at physiological temperature, HAp may have the mechanical integrity required to emulate the functions of hard tissues and serve as substrata on which cellular functions can proceed. If HAp can be formed in vivo, the surgeon does not need to rely on preforms. Therefore, HAp formed in this manner can serve a variety of needs in medicine and dentistry. Because of these clinical advantages, this presentation addresses hydroxyapatite capable of being formed in vivo. A variety of reactions can be used to produce hydroxyapatite monoliths under conditions compatible with those in the body. Those reactions have features in common and their enumeration will be the basis for the presentation. In particular, the mechanistic path to HAp formation is similar to that of cements used in civil engineering. Calcium phosphate precursors undergo dissolution in aqueous solutions and precipitate HAp. In common with cement-like reactions, HAp monoliths produced in this way accommodate to physical dimensions of their forms (e.g. bone defects). Porosity becomes distributed throughout the monolith and the monolith does not undergo shrinkage as occurs during sintering. HAp formed in this way will be discussed in terms of multicomponent phase behavior, kinetics of the reactions, and mechanical properties that can be realized. (orig.)

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

    Directory of Open Access Journals (Sweden)

    Yunhui Wang

    2012-06-01

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

  19. 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.

  20. 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.

  1. InterProScan検索結果: FS871014 [

    Lifescience Database Archive (English)

    Full Text Available FS871014 FS871014_6_ORF2 C7B28FDD974051F4 PANTHER PTHR11774:SF6 PROTEIN FARNESYLTRANSFERAS...E BETA SUBUNIT (CAAX FARNESYLTRANSFERASE BETA SUBUNIT) (RAS PROTEINS PRENYLTRANSFERASE BETA) (FTASE-BETA) 5.1e-33 T IPR008930 unintegrated ...

  2. InterProScan検索結果: FS822432 [

    Lifescience Database Archive (English)

    Full Text Available FS822432 FS822432_4_ORF2 0F351EBBEAD6F2E2 PANTHER PTHR11129 PROTEIN FARNESYLTRANSFERASE ALPHA SUBUNIT/RA...B GERANYLGERANYL TRANSFERASE ALPHA SUBUNIT 2e-13 T IPR008940 unintegrated ...

  3. InterProScan検索結果: FS919501 [

    Lifescience Database Archive (English)

    Full Text Available FS919501 FS919501_2_ORF2 C2F2809CFEB5427D PANTHER PTHR11129 PROTEIN FARNESYLTRANSFERASE ALPHA SUBUNIT/RA...B GERANYLGERANYL TRANSFERASE ALPHA SUBUNIT 2.3e-30 T IPR008940 unintegrated ...

  4. InterProScan検索結果: FS906026 [

    Lifescience Database Archive (English)

    Full Text Available FS906026 FS906026_3_ORF2 B7A2133421BB2BC4 PANTHER PTHR11774:SF6 PROTEIN FARNESYLTRANSFERAS...E BETA SUBUNIT (CAAX FARNESYLTRANSFERASE BETA SUBUNIT) (RAS PROTEINS PRENYLTRANSFERASE BETA) (FTASE-BETA) 4.6e-99 T IPR008930 unintegrated ...

  5. 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 ...

  6. 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 ...

  7. EST Table: FS764450 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

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

  8. EST Table: FS936298 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS936298 E_FL_fwgP_45J17_F_0 11/12/09 n.h 10/09/28 57 %/169 aa ref|XP_001650437.1| hypothetical ... gi|91079384|ref|XP_971392.1| PREDICTED: similar to jitterbug ... CG30092-PD [Tribolium castaneum] FS936298 fwgP ...

  9. EST Table: FS936127 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS936127 E_FL_fwgP_45B09_F_0 10/09/28 50 %/151 aa ref|XP_001650437.1| hypothetical protein AaeL_ ... gi|91079384|ref|XP_971392.1| PREDICTED: similar to jitterbug ... CG30092-PD [Tribolium castaneum] FS936298 fwgP ...

  10. EST Table: FS907445 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS907445 E_FL_fufe_11D11_F_0 10/09/28 58 %/192 aa ref|XP_001599201.1| PREDICTED: similar to ENSA ... gi|91079384|ref|XP_971392.1| PREDICTED: similar to jitterbug ... CG30092-PD [Tribolium castaneum] FS936298 fufe ...

  11. EST Table: FS912982 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS912982 E_FL_fufe_27N15_F_0 11/12/09 n.h 10/09/28 46 %/216 aa ref|XP_001606351.1| PREDICTED: si ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS912982 fufe ...

  12. EST Table: FS917646 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917646 E_FL_fufe_41P09_F_0 10/09/28 58 %/179 aa ref|XP_001605099.1| PREDICTED: similar to GDP- ... 1090017|ref|XP_967192.1| PREDICTED: similar to GDP-fucose ... transporter, putative [Tribolium castaneum] FS8054 ...

  13. EST Table: FS786053 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS786053 E_FL_fcaL_53A02_R_0 10/09/28 51 %/186 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS783762 fcaL ...

  14. EST Table: FS896764 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS896764 E_FL_ftes_24J05_R_0 10/09/28 47 %/236 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS783762 ftes ...

  15. EST Table: FS732506 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS732506 E_FL_bmmt_26L16_F_0 10/09/28 43 %/143 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS912982 bmmt ...

  16. EST Table: FS769708 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS769708 E_FL_fcaL_53A02_F_0 10/09/28 46 %/197 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS912982 fcaL ...

  17. EST Table: FS859085 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS859085 E_FL_fner_09F06_R_0 10/09/28 51 %/200 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS783762 fner ...

  18. EST Table: FS904539 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS904539 E_FL_fufe_02E23_F_0 10/09/28 45 %/171 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS912982 fufe ...

  19. EST Table: FS910538 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS910538 E_FL_fufe_20I12_F_0 10/09/28 low homology 10/09/12 n.h 10/08/29 35 %/145 aa F33H2.6#CE3 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS912982 fufe ...

  20. EST Table: FS743819 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS743819 E_FL_bmmt_26L16_R_0 10/09/28 47 %/236 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS783762 bmmt ...

  1. EST Table: FS767218 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS767218 E_FL_fcaL_45F06_F_0 10/09/28 45 %/160 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS912982 fcaL ...

  2. EST Table: FS927322 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS927322 E_FL_fwgP_19A08_F_0 10/09/28 50 %/212 aa ref|XP_001606351.1| PREDICTED: similar to MGC6 ... .1| PREDICTED: similar to regulator of microtubule dynamics ... 1 [Tribolium castaneum] FS912982 fwgP ...

  3. EST Table: FS935056 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS935056 E_FL_fwgP_41N17_F_0 10/09/28 67 %/264 aa ref|XP_002082836.1| GD25020 [Drosophila simula ... gi|91084227|ref|XP_969046.1| PREDICTED: similar to egalitarian ... CG4051-PA [Tribolium castaneum] FS766799 fwgP ...

  4. EST Table: FS816912 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS816912 E_FL_fmgV_49O17_F_0 10/09/28 56 %/182 aa ref|XP_001812240.1| PREDICTED: similar to clas ... (differentially expressed in chondrocytes) (mdec) (sharp ) [Tribolium castaneum] 10/09/09 50 %/173 aa FBpp01 ... (differentially expressed in chondrocytes) (mdec) (sharp ) [Tribolium castaneum] FS845099 fmgV ...

  5. EST Table: FS845099 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS845099 E_FL_fner_22L02_F_0 11/12/09 GO hit GO:0005634(nucleus)|GO:0030528(transcription regula ... (differentially expressed in chondrocytes) (mdec) (sharp ) [Tribolium castaneum] 10/09/10 low homology 10/08 ... (differentially expressed in chondrocytes) (mdec) (sharp ) [Tribolium castaneum] FS845099 fner ...

  6. 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 ...

  7. EST Table: FS726766 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS726766 E_FL_bmmt_08H14_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  8. EST Table: FS731848 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS731848 E_FL_bmmt_24O05_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  9. EST Table: FS758020 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS758020 E_FL_fcaL_07A06_F_0 10/09/28 99 %/122 aa ref|NP_001136083.1| globin 1 [Bombyx mori] dbj ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 fcaL ...

  10. EST Table: FS728770 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS728770 E_FL_bmmt_14C18_F_0 10/09/28 100 %/153 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  11. EST Table: FS731569 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS731569 E_FL_bmmt_24B10_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  12. EST Table: FS728623 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS728623 E_FL_bmmt_13M04_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  13. EST Table: FS732973 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS732973 E_FL_bmmt_20A14_F_0 10/09/28 100 %/169 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  14. EST Table: FS730824 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS730824 E_FL_bmmt_19P19_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  15. EST Table: FS727444 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS727444 E_FL_bmmt_10G04_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  16. EST Table: FS732505 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS732505 E_FL_bmmt_26L14_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  17. EST Table: FS727897 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS727897 E_FL_bmmt_11L01_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 bmmt ...

  18. EST Table: FS758602 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS758602 E_FL_fcaL_08M16_F_0 10/09/28 100 %/173 aa ref|NP_001136083.1| globin 1 [Bombyx mori] db ... f|XP_974703.1| PREDICTED: similar to hemoglobin C1 polymer ... [Tribolium castaneum] FS798513 fcaL ...

  19. 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 ...

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. EST Table: FS908703 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available gnl|Amel|GB12094-PF 10/09/10 84 %/119 aa gi|255522795|ref|NP_001157310.1| longitudinals lacking isoform 1 [Tribolium castaneum] FS908703 fufe ... ...FS908703 E_FL_fufe_15A03_F_0 11/12/09 GO hit GO:0005515(protein binding) 10/09/28 8

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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 ... i|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia -inducible factor 1 alpha [Tribolium castaneum] FS9 ...

  10. 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 ... i|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia -inducible factor 1 alpha [Tribolium castaneum] FS7 ...

  11. EST Table: FS877412 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

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

  12. EST Table: 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 ...

  13. 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 ...

  14. 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.

  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. 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.

  17. 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

  18. Characterization of SOI monolithic detector system

    International Nuclear Information System (INIS)

    A monolithic active pixel sensor for charged particle tracking was developed. This research is performed within the framework of an R and D project called TRAPPISTe (Tracking Particles for Physics Instrumentation in SOI Technology) whose aim is to evaluate the feasibility of developing a Monolithic Active Pixel Sensor (MAPS) with Silicon-on-Insulator (SOI) technology. Two chips were fabricated: TRAPPISTe-1 and TRAPPISTe-2. TRAPPISTe-1 was produced at the WINFAB facility at the Université catholique de Louvain (UCL), Belgium, in a 2μm fully depleted (FD-SOI) CMOS process. TRAPPISTe-2 was fabricated with the LAPIS 0.2μm FD-SOI CMOS process. The electrical characterization on single transistor test structures and of the electronic readout for the TRAPPISTe series of monolithic pixel detectors was carried out. The behavior of the prototypes’ electronics as a function of the back voltage was studied. Results showed that both readout circuits exhibited sensitivity to the back voltage. Despite this unwanted secondary effect, the responses of TRAPPISTe-2 amplifiers can be improved by a variation in the circuit parameters

  19. Performance of monolithic concrete waste forms

    International Nuclear Information System (INIS)

    Liquid wastes can be made into concrete or cement waste form that can be poured into a concrete vault forming a monolith. The waste isolation performance of monolithic concrete waste forms or vaults is generally dominated by the influence of cracks through the structure. In relation to water flow rate and crack spacing, monolithic concrete vaults have three general regions of performance. At extremely low flow rates, release is strictly diffusionally limited. In most situations, flow rates will not be low enough to ensure diffusional release. At slightly greater flow rates (the magnitude of which is dependent upon the diffusion coefficients and crack spacing), release is controlled by the flow rate of water through cracks in the structure with release rate approximately proportional to Darcy flow. In this region, release is not sensitive to block size and the vault behaves as an equivalent porous medium from a mass transport perspective. At higher flow rates, release rate is controlled by diffusion out of intact blocks of waste form. In this situation the release rate is very sensitive to block size (crack spacing) but independent of flow. (author)

  20. 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

  1. Sub-100-fs Yb:CALGO nonlinear regenerative amplifier

    OpenAIRE

    pouysegur, julien; Delaigue, Martin; Zaouter, Yoann; Hönninger, Clemens; Mottay, Eric; Jaffrès, Anaël; Loiseau, Pascal; Viana, Bruno; Georges, Patrick; Druon, Frédéric

    2013-01-01

    We report on the first diode-pumped Yb∶CaGdAlO 4 regenerative amplifier in the sub-100-fs regime. It generates pulses at a central wavelength of 1047 nm with up to 24 μJ energy (after compression) at a repetition rate of 50 kHz. The measured pulse duration is 97 fs, with a spectral bandwidth of 19 nm. We describe in detail how non-linear effects are optimally used to compensate gain narrowing in order to overcome the 100 fs barrier. Many industrial applications, such as athermal microma-chini...

  2. 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.

  3. Components for monolithic fiber chirped pulse amplification laser systems

    Science.gov (United States)

    Swan, Michael Craig

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

  4. Nanoparticle modified monolithic materials for phosphopeptide enrichment

    Czech Academy of Sciences Publication Activity Database

    Křenková, Jana; Foret, František

    Caparica : Proteomass Scientific Society, 2014 - (Lodeiro, C.; Capelo, J.; Santos, H.; Oliveira, E.; Nunez-Glez, C.; Araújo, J.; Lodeiro, A.). s. 31 ISBN 978-989-98793-9-3. [Caparica Christmas Conference on Sample Treatment 2014 /1./. 08.12.2014-10.12.2014, Caparica - Almada] R&D Projects: GA ČR(CZ) GA14-06319S Grant ostatní: GA AV ČR(CZ) M200311201 Institutional support: RVO:68081715 Keywords : nanoparticles * monolith * phsophopeptides Subject RIV: CB - Analytical Chemistry, Separation

  5. 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.

  6. Monolithic fabrication of millimeter-scale machines

    International Nuclear Information System (INIS)

    Silicon-based MEMS techniques dominate sub-millimeter scale manufacturing, while a myriad of conventional methods exist to produce larger machines measured in centimeters and beyond. So-called mesoscale devices, existing between these length scales, remain difficult to manufacture. We present a versatile fabrication process, loosely based on printed circuit board manufacturing techniques, for creating monolithic, topologically complex, three-dimensional machines in parallel at the millimeter to centimeter scales. The fabrication of a 90 mg flapping wing robotic insect demonstrates the sophistication attainable by these techniques, which are expected to support device manufacturing on an industrial scale. (paper)

  7. Thiol-ene-based monolithic microreactors

    Czech Academy of Sciences Publication Activity Database

    Novotný, Jakub; Lafleur, J. P.; Kutter, J. P.

    Brno : Institute of Analytical Chemistry AS CR, 2014 - (Foret, F.; Křenková, J.; Drobníková, I.; Guttman, A.; Klepárník, K.), s. 53-55 ISBN 978-80-904959-2-0. [CECE 2014. International Interdisciplinary Meeting on Bioanalysis /11./. Brno (CZ), 20.10.2014-22.10.2014] Institutional support: RVO:68081715 Keywords : thiol-ene * monolith * enzyme immobilization Subject RIV: CB - Analytical Chemistry, Separation http://www.ce-ce.org/CECE2014/CECE%202014%20proceedings_full.pdf

  8. 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.

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. 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- ...

  14. 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.

  15. 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

  16. 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.

  17. 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.

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

    DEFF Research Database (Denmark)

    Pryds, Nini; Clemens, Frank; Menon, Mohan; Nielsen, Pernille Hedemark; Brodersen, Karen; Bjørk, Rasmus; Bahl, Christian Robert Haffenden; Engelbrecht, Kurt; Nielsen, Kaspar Kirstein; Smith, Anders

    2011-01-01

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

  19. 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 ...

  20. 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 ...

  1. EST Table: FS902354 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS902354 E_FL_ftes_47C16_R_0 11/12/09 n.h 10/09/28 31 %/102 aa ref|XP_973013.1| PREDICTED: simil ... ar to chromosome 15 open reading ... frame 26 [Tribolium castaneum] gb|EFA10210.1| hypo ... 973013.1| PREDICTED: similar to chromosome 15 open reading ... frame 26 [Tribolium castaneum] FS902354 ftes ...

  2. EST Table: FS805424 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS805424 E_FL_fmgV_17O11_F_0 11/12/09 n.h 10/09/28 59 %/128 aa ref|XP_001605099.1| PREDICTED: si ... milar to GDP-fucose ... transporter, putative [Nasonia vitripennis] 10/09/ ... 1090017|ref|XP_967192.1| PREDICTED: similar to GDP-fucose ... transporter, putative [Tribolium castaneum] FS8054 ...

  3. EST Table: FS786414 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS786414 E_FL_fcaL_18C22_R_0 10/09/28 62 %/206 aa ref|XP_973797.1| PREDICTED: similar to NADH-ub ... subunit, mitochondrial precursor (Complex I-75kD) (CI -75kD) [Tribolium castaneum] gb|EFA09221.1| hypothe ... subunit, mitochondrial precursor (Complex I-75kD) (CI -75kD) [Tribolium castaneum] FS873341 fcaL ...

  4. EST Table: FS741663 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS741663 E_FL_bmmt_20K24_R_0 10/09/28 56 %/248 aa ref|XP_973797.1| PREDICTED: similar to NADH-ub ... subunit, mitochondrial precursor (Complex I-75kD) (CI -75kD) [Tribolium castaneum] gb|EFA09221.1| hypothe ... subunit, mitochondrial precursor (Complex I-75kD) (CI -75kD) [Tribolium castaneum] FS873341 bmmt ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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 ...

  10. EST Table: FS920857 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS920857 E_FL_fufe_51L23_F_0 10/09/28 49 %/210 aa ref|XP_001657166.1| lupus ... la ribonucleoprotein ... [Aedes aegypti] gb|EAT45048.1| lupus ... la ribonucleoprotein [Aedes aegypti] 10/09/13 50 % ... gi|91082895|ref|XP_972070.1| PREDICTED: similar to lupus ... la ribonucleoprotein [Tribolium castaneum] FS79082 ...

  11. EST Table: FS822271 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS822271 E_FL_fmgV_11P16_R_0 11/12/09 n.h 10/09/28 75 %/112 aa ref|XP_001656149.1| fetal 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 ...

  12. EST Table: FS730102 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS730102 E_FL_bmmt_17O20_F_0 10/09/28 75 %/142 aa ref|NP_726360.3| egalitarian ... [Drosophila melan ... ogaster] gb|AAF47054.4| egalitarian ... [Drosophila melanogaster] 10/09/03 75 %/142 aa FBp ... gi|91084227|ref|XP_969046.1| PREDICTED: similar to egalitarian ... CG4051-PA [Tribolium castaneum] FS766799 bmmt ...

  13. EST Table: FS760443 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS760443 E_FL_fcaL_14G03_F_0 10/09/28 66 %/220 aa ref|NP_726360.3| egalitarian ... [Drosophila melan ... ogaster] gb|AAF47054.4| egalitarian ... [Drosophila melanogaster] 10/09/08 66 %/220 aa FBp ... gi|91084227|ref|XP_969046.1| PREDICTED: similar to egalitarian ... CG4051-PA [Tribolium castaneum] FS766799 fcaL ...

  14. EST Table: FS760916 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS760916 E_FL_fcaL_15N11_F_0 10/09/28 65 %/226 aa ref|NP_726360.3| egalitarian ... [Drosophila melan ... ogaster] gb|AAF47054.4| egalitarian ... [Drosophila melanogaster] 10/09/08 65 %/226 aa FBp ... gi|91084227|ref|XP_969046.1| PREDICTED: similar to egalitarian ... CG4051-PA [Tribolium castaneum] FS766799 fcaL ...

  15. EST Table: FS766799 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS766799 E_FL_fcaL_44A12_F_0 11/12/09 n.h 10/09/28 64 %/225 aa ref|NP_726360.3| egalitarian ... [Dro ... sophila melanogaster] gb|AAF47054.4| egalitarian ... [Drosophila melanogaster] 10/09/08 64 %/225 aa FBp ... gi|91084227|ref|XP_969046.1| PREDICTED: similar to egalitarian ... CG4051-PA [Tribolium castaneum] FS766799 fcaL ...

  16. EST Table: FS934100 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS934100 E_FL_fwgP_39A22_F_0 10/09/28 98 %/215 aa ref|NP_001037177.1| protein star ... [Bombyx mori] ... gb|AAL51081.1|AF455272_1 Star ... [Bombyx mori] 10/09/13 30 %/183 aa FBpp0143162|Der ... A 10/09/10 32 %/200 aa gi|270014292|gb|EFA10740.1| star ... [Tribolium castaneum] FS906952 fwgP ...

  17. EST Table: FS915854 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915854 E_FL_fufe_36J04_F_0 10/09/28 98 %/236 aa ref|NP_001037177.1| protein star ... [Bombyx mori] ... gb|AAL51081.1|AF455272_1 Star ... [Bombyx mori] 10/09/12 31 %/197 aa FBpp0143162|Der ... A 10/09/10 31 %/214 aa gi|270014292|gb|EFA10740.1| star ... [Tribolium castaneum] FS906952 fufe ...

  18. EST Table: FS855782 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS855782 E_FL_fner_52O24_F_0 10/09/28 98 %/189 aa ref|NP_001037177.1| protein star ... [Bombyx mori] ... gb|AAL51081.1|AF455272_1 Star ... [Bombyx mori] 10/09/11 low homology 10/08/29 n.h 1 ... A 10/09/10 31 %/169 aa gi|270014292|gb|EFA10740.1| star ... [Tribolium castaneum] FS906952 fner ...

  19. EST Table: FS853803 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS853803 E_FL_fner_47G07_F_0 10/09/28 99 %/206 aa ref|NP_001037177.1| protein star ... [Bombyx mori] ... gb|AAL51081.1|AF455272_1 Star ... [Bombyx mori] 10/09/11 31 %/167 aa FBpp0143162|Der ... A 10/09/10 32 %/186 aa gi|270014292|gb|EFA10740.1| star ... [Tribolium castaneum] FS906952 fner ...

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. EST Table: FS840960 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

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

  7. EST Table: 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 ...

  8. 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 ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. EST Table: FS767137 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available mology 10/09/10 n.h 10/09/10 32 %/152 aa gi|91083365|ref|XP_966462.1| PREDICTED: escargot [Tribolium castaneum] FS841374 fcaL ... ...FS767137 E_FL_fcaL_45B05_F_0 10/09/28 n.h 10/09/08 n.h 10/08/28 n.h 10/09/10 low ho

  14. 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- ...

  15. 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- ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. EST Table: FS913906 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS913906 E_FL_fufe_30K16_F_0 11/12/09 GO hit GO:0006355(regulation of transcription, DNA-depende ... 40 %/332 aa ref|XP_967427.2| PREDICTED: similar to hypoxia -inducible factor 1 alpha [Tribolium castaneum] 10/ ... i|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia -inducible factor 1 alpha [Tribolium castaneum] FS9 ...

  20. EST Table: FS764096 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS764096 E_FL_fcaL_35M01_F_0 11/12/09 GO hit GO:0004871(signal transducer activity)|GO:0007165(s ... 48 %/117 aa ref|XP_967427.2| PREDICTED: similar to hypoxia -inducible factor 1 alpha [Tribolium castaneum] 10/ ... i|189237669|ref|XP_967427.2| PREDICTED: similar to hypoxia -inducible factor 1 alpha [Tribolium castaneum] FS7 ...

  1. 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 ...

  2. 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 ...

  3. EST Table: FS892940 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

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

  4. EST Table: 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 ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. EST Table: FS903628 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

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

  13. EST Table: 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 ...

  14. Calibration of SeaWiFS. II. Vicarious techniques

    International Nuclear Information System (INIS)

    We present an overview of the vicarious calibration of the Sea-Viewing Wide Field-of-View Sensor (SeaWiFS). This program has three components: the calibration of the near-infrared bands so that the atmospheric correction algorithm retrieves the optical properties of maritime aerosols in the open ocean; the calibration of the visible bands against in-water measurements from the Marine Optical Buoy (MOBY); and a calibration-verification program that uses comparisons between SeaWiFS retrievals and globally distributed in situ measurements of water-leaving radiances. This paper describes the procedures as implemented for the third reprocessing of the SeaWiFS global mission data set. The uncertainty in the near-infrared vicarious gain is 0.9%. The uncertainties in the visible-band vicarious gains are 0.3%, corresponding to uncertainties in the water-leaving radiance of approximately 3%. The means of the SeaWiFS/in situ matchup ratios for water-leaving radiances are typically within 5% of unity in Case 1 waters, while chlorophyll a ratios are within 1% of unity. SeaWiFS is the first ocean-color mission to use an extensive and ongoing prelaunch and postlaunch calibration program, and the matching results demonstrate the benefits of a comprehensive approach

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

    Institute of Scientific and Technical Information of China (English)

    YANG; Qiang; CHEN; YingRu; LIU; YaoRu

    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.

  16. 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.

  17. 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.

  18. Present status of the MONOLITH project

    International Nuclear Information System (INIS)

    MONOLITH is a proposed massive (34 kt) magnetized tracking calorimeter at the Gran Sasso laboratory in Italy, optimized for the detection of atmospheric muon neutrinos. The main goal is to establish (or reject) the neutrino oscillation hypothesis through an explicit observation of the full first oscillation swing. The Δm2 sensitivity range for this measurement comfortably covers the complete Super-Kamiokande allowed region. Other measurements include studies of matter effects, the NC up/down ratio, ν bar / ν ratio, the study of cosmic ray muons in the multi-TeV range, and auxiliary measurements from the CERN to Gran Sasso neutrino beam. Depending on approval, data taking with the part of the detector could start towards the end of 2004

  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. 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.)

  1. 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.

  2. 400W Yb:YAG Innoslab fs-Amplifier.

    Science.gov (United States)

    Russbueldt, P; Mans, T; Rotarius, G; Weitenberg, J; Hoffmann, H D; Poprawe, R

    2009-07-20

    The Innoslab design, already established for neodymium doped laser crystals, was applied to ytterbium doped laser materials. Recent progresses in brightness of high power diode lasers facilitate efficient pumping of quasi-three-level laser materials. Innoslab amplifiers are compared to competing thin-disk and fiber fs-amplifiers. A compact diode-pumped Yb:YAG Innoslab fs-oscillator-amplifier system, scalable to the kilowatt range, was realized. Numerical simulations result in conditions for high efficiency and beam quality. Nearly transform and diffraction limited 680 fs pulses at 400 W average output power and 76 MHz repetition rate without using CPA technology have been achieved at room temperature so far. PMID:19654625

  3. Calibration of SeaWiFS. I. Direct techniques

    International Nuclear Information System (INIS)

    We present an overview of the calibration of the Sea-viewing Wide Field-of-View Sensor (SeaWiFS) from its performance verification at the manufacturer's facility in the completion of its third year of on-orbit measurements. These calibration procedures have three principal parts: a prelaunch radiometric calibration that is traceable to the National Institute of Standards and Technology; the Transfer-to-Orbit Experiment, a set of measurements that determine changes in the instrument's calibration from its manufacture to the start of on-orbit operations; and measurements of the sun and the moon to determine radiometric changes on orbit. To our knowledge, SeaWiFS is the only instrument that uses routine lunar measurements to determine changes in its radiometric sensitivity. On the basis of these methods, the overall uncertainty in the SeaWiFS top-of-the-atmosphere radiances is estimated to be 4-5%. We also show the results of comparison campaigns with aircraft- and ground-based measurements, plus the results of an experiment, called the Southern Ocean Band 8 Gain Study. These results are used to check the calibration of the SeaWiFS bands. To date, they have not been used to change the instrument's prelaunch calibration coefficients. In addition to these procedures, SeaWiFS is a vicariously calibrated instrument for ocean-color measurements. In the vicarious calibration of the SeaWiFS visible bands, the calibration coefficients are modified to force agreement with surface truth measurements from the Marine Optical Buoy, which is moored off the Hawaiian Island of Lanai. This vicarious calibration is described in a companion paper

  4. Nanoparticle-modified monolithic pipette tips for phosphopeptide enrichment

    OpenAIRE

    Křenková, J. (Jana); Foret, F. (František)

    2013-01-01

    We have developed monolithic materials modified by either iron oxide or hydroxyapatite nanoparticles within polypropylene pipette tips. The developed materials were used for selective and efficient enrichment of phosphopeptides.

  5. 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.

  6. 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...

  7. Hierarchical Porous Polystyrene Monoliths from PolyHIPE.

    Science.gov (United States)

    Yang, Xinjia; Tan, Liangxiao; Xia, Lingling; Wood, Colin D; Tan, Bien

    2015-09-01

    Hierarchical porous polystyrene monoliths (HCP-PolyHIPE) are obtained by hypercrosslinking poly(styrene-divinylbenzene) monoliths prepared by polymerization of high internal phase emulsions (PolyHIPEs). The hypercrosslinking is achieved using an approach known as knitting which employs formaldehyde dimethyl acetal (FDA) as an external crosslinker. Scanning electron microscopy (SEM) confirms that the macroporous structure in the original monolith is retained during the knitting process. By increasing the amount of divinylbenzene (DVB) in PolyHIPE, the BET surface area and pore volume of the HCP-PolyHIPE decrease, while the micropore size increases. BET surface areas of 196-595 m(2) g(-1) are obtained. The presence of micropores, mesopores, and macropores is confirmed from the pore size distribution. With a hierarchical porous structure, the monoliths reveal comparable gas sorption properties and potential applications in oil spill clean-up. PMID:26178423

  8. 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.

  9. EST Table: FS895931 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS895931 E_FL_ftes_20D04_R_0 10/09/28 48 %/263 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 48 %/263 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 ftes ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...68 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 41 %/309 aa gnl|Ame

  10. EST Table: FS804514 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS804514 E_FL_fmgV_15G04_F_0 10/09/28 46 %/124 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 46 %/124 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fmgV ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...27 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 38 %/134 aa gnl|Ame

  11. EST Table: FS844460 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS844460 E_FL_fner_20N15_F_0 10/09/28 50 %/102 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 50 %/102 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fner ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...27 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 40 %/109 aa gnl|Ame

  12. EST Table: FS773374 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS773374 E_FL_fcaL_01E22_R_0 10/09/28 46 %/259 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 46 %/259 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 fcaL ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...48 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 41 %/265 aa gnl|Ame

  13. EST Table: FS788376 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS788376 E_FL_fcaL_24G15_R_0 10/09/28 50 %/137 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 50 %/137 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 fcaL ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...38 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 58 %/116 aa gnl|Ame

  14. EST Table: FS756160 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS756160 E_FL_fcaL_01E22_F_0 10/09/28 45 %/124 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 45 %/124 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fcaL ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...27 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 37 %/134 aa gnl|Ame

  15. EST Table: FS918452 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918452 E_FL_fufe_44G17_F_0 10/09/28 46 %/244 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 46 %/244 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fufe ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...93 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 40 %/253 aa gnl|Ame

  16. EST Table: FS772104 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS772104 E_FL_fcaL_24G15_F_0 10/09/28 50 %/114 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 50 %/114 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fcaL ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...42 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 38 %/125 aa gnl|Ame

  17. EST Table: FS892889 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS892889 E_FL_ftes_09I06_R_0 10/09/28 48 %/279 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 48 %/279 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 ftes ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...04 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 44 %/295 aa gnl|Ame

  18. EST Table: FS787334 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS787334 E_FL_fcaL_21B10_R_0 10/09/28 47 %/229 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 47 %/229 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 fcaL ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...28 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 41 %/235 aa gnl|Ame

  19. EST Table: FS881026 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS881026 E_FL_ftes_20D04_F_0 10/09/28 48 %/142 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 48 %/142 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 ftes ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...64 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 40 %/146 aa gnl|Ame

  20. EST Table: FS909077 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909077 E_FL_fufe_16C10_F_0 10/09/28 45 %/224 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 45 %/224 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fufe ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...55 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 39 %/236 aa gnl|Ame

  1. EST Table: FS783759 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS783759 E_FL_fcaL_45F03_R_0 10/09/28 49 %/292 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 49 %/292 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 fcaL ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...91 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 44 %/298 aa gnl|Ame

  2. EST Table: FS771043 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS771043 E_FL_fcaL_21B10_F_0 10/09/28 50 %/102 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 50 %/102 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fcaL ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...27 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 40 %/109 aa gnl|Ame

  3. EST Table: FS877343 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS877343 E_FL_ftes_09I06_F_0 10/09/28 48 %/136 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 48 %/136 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 ftes ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...64 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 40 %/146 aa gnl|Ame

  4. EST Table: FS915025 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915025 E_FL_fufe_34A03_F_0 10/09/28 41 %/189 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 41 %/189 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS937283 fufe ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...64 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 36 %/200 aa gnl|Ame

  5. EST Table: FS863113 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS863113 E_FL_fner_20N15_R_0 10/09/28 48 %/243 aa ref|XP_975194.1| PREDICTED: similar to something...l|GB19080-PA 10/09/10 48 %/243 aa gi|91081571|ref|XP_975194.1| PREDICTED: similar to something about silencing protein 10 [Tribolium castaneum] FS823506 fner ... ... about silencing protein 10 [Tribolium castaneum] gb|EFA01562.1| hypothetical protein TcasGA2...43 aa AGAP002960-PA Protein|2R:30130647:30132122:-1|gene:AGAP002960 10/09/10 44 %/249 aa gnl|Ame

  6. EST Table: FS844060 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS844060 E_FL_fner_19L13_F_0 10/09/28 34 %/181 aa ref|NP_001086875.1| RMI1, RecQ mediated genome ... sp|Q6DDH2.1|RMI1_XENLA RecName: Full=RecQ-mediated genome ... instability protein 1 gb|AAH77592.1| MGC83955 prot ... 08958.1| PREDICTED: similar to RMI1, RecQ mediated genome ... instability 1, homolog [Tribolium castaneum] FS765 ...

  7. EST Table: FS912677 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS912677 E_FL_fufe_26P02_F_0 10/09/28 34 %/181 aa ref|NP_001086875.1| RMI1, RecQ mediated genome ... sp|Q6DDH2.1|RMI1_XENLA RecName: Full=RecQ-mediated genome ... instability protein 1 gb|AAH77592.1| MGC83955 prot ... 08958.1| PREDICTED: similar to RMI1, RecQ mediated genome ... instability 1, homolog [Tribolium castaneum] FS765 ...

  8. 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 ...

  9. 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.

  10. 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 ...

  11. EST Table: FS920735 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

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

  12. 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 ...

  13. EST Table: FS844986 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS844986 E_FL_fner_22F20_F_0 10/09/28 100 %/124 aa ref|NP_001037584.1| ferritin [Bombyx mori...43 %/125 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fner ... ...age protein [Bombyx mandarina] 10/09/10 44 %/118 aa FBpp0225182|DvirGJ10765-PA 10/0

  14. EST Table: FS753697 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS753697 E_ET_caL-_13L15_R_0 10/09/28 100 %/117 aa ref|NP_001037584.1| ferritin [Bombyx mori...XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS902032 caL- ... ...age protein [Bombyx mandarina] 10/09/08 39 %/118 aa FBpp0225182|DvirGJ10765-PA 10/0

  15. EST Table: FS838114 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS838114 E_FL_fner_03A05_F_0 10/09/28 100 %/124 aa ref|NP_001037584.1| ferritin [Bombyx mori...43 %/125 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fner ... ...age protein [Bombyx mandarina] 10/09/10 44 %/118 aa FBpp0225182|DvirGJ10765-PA 10/0

  16. EST Table: FS846115 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS846115 E_FL_fner_25J21_F_0 10/09/28 100 %/125 aa ref|NP_001037584.1| ferritin [Bombyx mori...43 %/125 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fner ... ...age protein [Bombyx mandarina] 10/09/10 44 %/118 aa FBpp0225182|DvirGJ10765-PA 10/0

  17. EST Table: FS729170 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS729170 E_FL_bmmt_15E09_F_0 10/09/28 100 %/122 aa ref|NP_001037584.1| ferritin [Bombyx mori...43 %/125 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 bmmt ... ...age protein [Bombyx mandarina] 10/09/03 44 %/118 aa FBpp0225182|DvirGJ10765-PA 10/0

  18. EST Table: FS772899 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS772899 E_FL_fcaL_26N24_F_0 10/09/28 100 %/112 aa ref|NP_001037584.1| ferritin [Bombyx mori...42 %/119 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fcaL ... ...age protein [Bombyx mandarina] 10/09/08 42 %/111 aa FBpp0225182|DvirGJ10765-PA 10/0

  19. EST Table: FS760534 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS760534 E_FL_fcaL_14K23_F_0 10/09/28 99 %/119 aa ref|NP_001037584.1| ferritin [Bombyx mori...3 %/125 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fcaL ... ...age protein [Bombyx mandarina] 10/09/08 44 %/118 aa FBpp0225182|DvirGJ10765-PA 10/08

  20. EST Table: FS750521 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS750521 E_ET_caL-_01M02_R_0 10/09/28 100 %/116 aa ref|NP_001037584.1| ferritin [Bombyx mori...XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS902032 caL- ... ...age protein [Bombyx mandarina] 10/09/08 39 %/117 aa FBpp0225182|DvirGJ10765-PA 10/0

  1. EST Table: FS895596 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS895596 E_FL_ftes_18N24_R_0 10/09/28 99 %/112 aa ref|NP_001037584.1| ferritin [Bombyx mori...P_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS902032 ftes ... ...age protein [Bombyx mandarina] 10/09/12 40 %/104 aa FBpp0225182|DvirGJ10765-PA 10/08

  2. EST Table: FS843493 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS843493 E_FL_fner_18C18_F_0 10/09/28 100 %/125 aa ref|NP_001037584.1| ferritin [Bombyx mori...43 %/125 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fner ... ...age protein [Bombyx mandarina] 10/09/10 44 %/118 aa FBpp0225182|DvirGJ10765-PA 10/0

  3. EST Table: FS846994 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS846994 E_FL_fner_28B11_F_0 10/09/28 99 %/134 aa ref|NP_001037584.1| ferritin [Bombyx mori...2 %/133 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fner ... ...age protein [Bombyx mandarina] 10/09/10 44 %/118 aa FBpp0225182|DvirGJ10765-PA 10/08

  4. EST Table: FS930244 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS930244 E_FL_fwgP_27J02_F_0 10/09/28 99 %/115 aa ref|NP_001037584.1| ferritin [Bombyx mori...444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fwgP ... ...age protein [Bombyx mandarina] 10/09/13 41 %/121 aa FBpp0225182|DvirGJ10765-PA 10/08

  5. EST Table: FS748226 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS748226 E_ET_caL-_13L15_F_0 10/09/28 100 %/116 aa ref|NP_001037584.1| ferritin [Bombyx mori...XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 caL- ... ...age protein [Bombyx mandarina] 10/09/08 39 %/117 aa FBpp0225182|DvirGJ10765-PA 10/0

  6. EST Table: FS803091 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS803091 E_FL_fmgV_11H01_F_0 10/09/28 97 %/130 aa ref|NP_001037584.1| ferritin [Bombyx mori...2 %/133 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fmgV ... ...age protein [Bombyx mandarina] 10/09/09 44 %/118 aa FBpp0225182|DvirGJ10765-PA 10/08

  7. EST Table: FS901683 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS901683 E_FL_ftes_44F09_R_0 10/09/28 80 %/132 aa ref|NP_001037584.1| ferritin [Bombyx mori...a gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS902032 ftes ... ...age protein [Bombyx mandarina] 10/09/12 37 %/132 aa FBpp0172483|DmojGI23266-PA 10/08

  8. EST Table: FS847049 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ] gb|ABF51339.1| ferritin isoform 1 [Bombyx mori] gb|ABG76018.1| iron storage protein [Bombyx mori] gb|ABG76019.1| iron stor...FS847049 E_FL_fner_28E03_F_0 10/09/28 100 %/112 aa ref|NP_001037584.1| ferritin [Bombyx mori...42 %/119 aa gi|91077444|ref|XP_966312.1| PREDICTED: similar to putative ferritin 2 isoform 1 [Tribolium castaneum] FS916237 fner ... ...age protein [Bombyx mandarina] 10/09/10 42 %/111 aa FBpp0225182|DvirGJ10765-PA 10/0

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. 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 ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. EST Table: FS909692 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS909692 E_FL_fufe_18A05_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 ...

  18. 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 ...

  19. 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 ...

  20. 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.

  1. 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...

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

    OpenAIRE

    Bartłomiej Gaweł; Kamila Gaweł; Gisle Øye

    2010-01-01

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

  3. 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.

  4. Microwaves integrated circuits: hybrids and monolithics - fabrication technology

    International Nuclear Information System (INIS)

    Several types of microwave integrated circuits are presented together with comments about technologies and fabrication processes; advantages and disadvantages in their utilization are analysed. Basic structures, propagation modes, materials used and major steps in the construction of hybrid thin film and monolithic microwave integrated circuits are described. Important technological applications are revised and main activities of the microelectronics lab. of the University of Sao Paulo (Brazil) in the field of hybrid and monolithic microwave integrated circuits are summarized. (C.L.B.)

  5. Extended Leach Testing of Simulated LAW Cast Stone Monoliths

    International Nuclear Information System (INIS)

    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. 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

  7. EST Table: FS804892 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available PREDICTED: similar to neutral sphingomyelinase (n-smase) activation associated factor fan [Nasonia vitripenn...0 68 %/254 aa gi|91082881|ref|XP_971631.1| PREDICTED: similar to neutral sphingomyelinase (n-smase) activation associated factor fan [Tribolium castaneum] FS804892 fmgV ...

  8. 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 ...

  9. EST Table: FS920310 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

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

  10. EST Table: 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 ...

  11. 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

  12. EST Table: FS853720 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS853720 E_FL_fner_47C14_F_0 10/09/28 43 %/253 aa ref|XP_001866947.1| thyroid ... receptor interacti ... ng protein [Culex quinquefasciatus] gb|EDS44216.1| thyroid ... receptor interacting protein [Culex quinquefasciat ...

  13. EST Table: FS804950 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS804950 E_FL_fmgV_16J14_F_0 10/09/28 56 %/204 aa ref|XP_001850215.1| atlastin [Cul...ex quinquefasciatus] gb|EDS31585.1| atlastin [Culex quinquefasciatus] 10/09/09 56 %/199 aa FBpp0240107|DwilG

  14. EST Table: FS804817 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS804817 E_FL_fmgV_16D19_F_0 10/09/28 91 %/129 aa ref|NP_001036916.1| G protein alpha subunit Go ... 9 71 %/129 aa C26C6.2#CE05311#WBGene00001648#locus:goa -1#guanine nucleotide-binding protein#status:Confir ...

  15. EST Table: FS746795 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS746795 E_ET_caL-_07B08_F_0 11/12/09 GO hit GO:0004871(signal transducer activity)|GO:0005525(G ... 8 90 %/104 aa C26C6.2#CE05311#WBGene00001648#locus:goa -1#guanine nucleotide-binding protein#status:Confir ...

  16. EST Table: FS761027 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS761027 E_FL_fcaL_16D07_F_0 10/09/28 88 %/100 aa ref|NP_001036916.1| G protein alpha subunit Go ... 8 71 %/100 aa C26C6.2#CE05311#WBGene00001648#locus:goa -1#guanine nucleotide-binding protein#status:Confir ...

  17. EST Table: FS850345 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS850345 E_FL_fner_37J10_F_0 10/09/28 92 %/144 aa ref|NP_001036916.1| G protein alpha subunit Go ... 9 71 %/144 aa C26C6.2#CE05311#WBGene00001648#locus:goa -1#guanine nucleotide-binding protein#status:Confir ...

  18. EST Table: FS939452 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS939452 E_FL_fwgP_54P16_F_0 10/09/28 92 %/150 aa ref|NP_001036916.1| G protein alpha subunit Go ... 9 72 %/150 aa C26C6.2#CE05311#WBGene00001648#locus:goa -1#guanine nucleotide-binding protein#status:Confir ...

  19. EST Table: FS931777 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS931777 E_FL_fwgP_32D23_F_0 10/09/28 93 %/186 aa ref|NP_001036916.1| G protein alpha subunit Go ... 9 75 %/186 aa C26C6.2#CE05311#WBGene00001648#locus:goa -1#guanine nucleotide-binding protein#status:Confir ...

  20. EST Table: FS751863 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS751863 E_ET_caL-_07B08_R_0 10/09/28 100 %/104 aa gb|ADB25316.1| guanine nucleotide-binding pro ... 8 90 %/104 aa C26C6.2#CE05311#WBGene00001648#locus:goa -1#guanine nucleotide-binding protein#status:Confir ...

  1. 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 ...

  2. 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/repe...rfusion inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  3. 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/repe...rfusion inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  4. 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/repe...rfusion inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  5. 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/repe...rfusion inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  6. 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/repe...rfusion inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  7. 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 [

  8. 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/repe...rfusion inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  9. 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/repe...rfusion inducible protein [Bombyx mori] gb|ABD36179.1| ischemia/reperfusion inducible protein [Bombyx mori

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. 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 ...

  14. 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

  15. 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 ...

  16. 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 ...

  17. EST Table: FS935487 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS935487 E_FL_fwgP_43C09_F_0 10/09/28 45 %/248 aa ref|XP_001660682.1| filamin, putative [Aedes a ... gi|91079384|ref|XP_971392.1| PREDICTED: similar to jitterbug ... CG30092-PD [Tribolium castaneum] BY917108 fwgP ...

  18. 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 ...

  19. 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 ...

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. 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 ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. 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 ...

  18. 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 ...

  19. 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 ...

  20. 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 ...

  1. 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 ...

  2. 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 ...

  3. 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 ...

  4. 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 ...

  5. 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 ...

  6. 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 ...

  7. 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 ...

  8. 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 ...

  9. 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 ...

  10. 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 ...

  11. 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 ...

  12. 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 ...

  13. 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 ...

  14. 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 ...

  15. 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 ...

  16. 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 ...

  17. 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 ...

  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: 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

  20. 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

  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. 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

  16. EST Table: FS898541 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS898541 E_FL_ftes_31D05_R_0 11/12/09 GO hit GO:0004114(3',5'-cyclic-nucleotide phosphodiesteras ... 38 %/165 aa C32E12.2#CE45035#WBGene00016328#locus:pde-5 #cyclic nucleotide phosphodiesterase#status:Partial ...

  17. EST Table: FS902705 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS902705 E_FL_ftes_48H24_R_0 10/09/28 68 %/169 aa emb|CAY54163.1| unnamed protein product [Helic ... 39 %/179 aa C32E12.2#CE45035#WBGene00016328#locus:pde-5 #cyclic nucleotide phosphodiesterase#status:Partial ...

  18. EST Table: FS765754 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS765754 E_FL_fcaL_40N11_F_0 10/09/28 39 %/201 aa ref|XP_002431371.1| GPI transamidase component ... PIG -U, putative [Pediculus humanus corporis] gb|EEB186 ... 33.1| GPI transamidase component PIG -U, putative [Pediculus humanus corporis] 10/09/08 ...

  19. EST Table: FS817044 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS817044 E_FL_fmgV_50E16_F_0 10/09/28 39 %/201 aa ref|XP_002431371.1| GPI transamidase component ... PIG -U, putative [Pediculus humanus corporis] gb|EEB186 ... 33.1| GPI transamidase component PIG -U, putative [Pediculus humanus corporis] 10/09/09 ...

  20. EST Table: FS839595 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS839595 E_FL_fner_07C07_F_0 10/09/28 32 %/104 aa ref|XP_002430196.1| GPI transamidase component ... PIG -S, putative [Pediculus humanus corporis] gb|EEB174 ... 58.1| GPI transamidase component PIG -S, putative [Pediculus humanus corporis] 10/09/10 ...

  1. Dispersive waves in fs cascaded second-harmonic generation

    DEFF Research Database (Denmark)

    Bache, Morten; Bang, Ole; Krolikowski, Wieslaw;

    2009-01-01

    Dispersive waves are observed in simulations of cascaded (phase-mismatched) second-harmonic generation. When generating ultra-short fs compressed near-IR solitons the dispersive waves are strongly red-shifted, depending on the soliton wavelength. Semi-analytical calculations predict the wavelengths....

  2. EST Table: FS917013 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917013 E_FL_fufe_40A18_F_0 10/09/28 53 %/189 aa gb|ADD18996.1| putative L-carnitine ... dehydratas ... 43 %/189 aa C24A3.4#CE40019#WBGene00016034#E. coli L-carnitine ... dehydratase#status:Partially_confirmed#UniProt:Q18 ...

  3. EST Table: FS750822 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS750822 E_ET_caL-_03E11_R_0 10/09/28 50 %/156 aa ref|XP_974629.1| PREDICTED: similar to alpha m ... 35 %/124 aa C24A3.4#CE40019#WBGene00016034#E. coli L-carnitine ... dehydratase#status:Partially_confirmed#UniProt:Q18 ...

  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: FS918927 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918927 E_FL_fufe_45N12_F_0 11/12/09 GO hit GO:0004497(monooxygenase activity)|GO:0005506(iron ... d pteridine as one donor, and incorporation of one atom ... of oxygen)|GO:0055114(oxidation reduction) 10/09/2 ...

  7. EST Table: FS922952 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922952 E_FL_fwgP_06C06_F_0 11/12/09 GO hit GO:0004497(monooxygenase activity)|GO:0005506(iron ... d pteridine as one donor, and incorporation of one atom ... of oxygen)|GO:0055114(oxidation reduction) 10/09/2 ...

  8. 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 ...

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. 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

  16. EST Table: FS892293 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ombyx mori] dbj|BAE53372.1| antibacterial peptide [Bombyx mori] dbj|BAF51564.1| gloverin2 [Bombyx mori] 10/09/12 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS866683 ftes ...

  17. EST Table: FS898270 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ombyx mori] dbj|BAE53372.1| antibacterial peptide [Bombyx mori] dbj|BAF51564.1| gloverin2 [Bombyx mori] 10/09/12 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS866683 ftes ...

  18. EST Table: FS798943 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ombyx mori] dbj|BAE53373.1| antibacterial peptide [Bombyx mori] dbj|BAF63528.1| gloverin4 [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 FS798027 ffbm ...

  19. EST Table: FS899154 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ombyx mori] dbj|BAE53372.1| antibacterial peptide [Bombyx mori] dbj|BAF51564.1| gloverin2 [Bombyx mori] 10/09/12 n.h 10/08/29 n.h 10/09/10 n.h 10/09/10 n.h 10/09/10 n.h FS866683 ftes ...

  20. EST Table: FS796949 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ombyx mori] dbj|BAE53372.1| antibacterial peptide [Bombyx mori] dbj|BAF51564.1| gloverin2 [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 FS917189 ffbm ...

  1. EST Table: FS797895 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available ombyx mori] dbj|BAE53373.1| antibacterial peptide [Bombyx mori] dbj|BAF63528.1| gloverin4 [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 FS798027 ffbm ...

  2. 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

  3. 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

  4. 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/

  5. EST Table: FS772198 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS772198 E_FL_fcaL_24L09_F_0 10/09/28 80 %/191 aa ref|XP_001655629.1| starch ... branching enzyme ii ... [Aedes aegypti] gb|EAT36211.1| starch ... branching enzyme ii [Aedes aegypti] 10/09/08 78 %/ ...

  6. EST Table: FS911397 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS911397 E_FL_fufe_23B20_F_0 10/09/28 60 %/232 aa ref|XP_395304.2| PREDICTED: similar to TatD DN ... /29 32 %/229 aa CD4.2#CE16950#WBGene00000795#locus:crn - 2#status:Confirmed#UniProt:O44160#protein_id:AAB8 ...

  7. 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 ...

  8. EST Table: FS840482 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS840482 E_FL_fner_09K17_F_0 10/09/28 low homology 10/09/10 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  9. EST Table: FS906714 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS906714 E_FL_fufe_09A08_F_0 10/09/28 low homology 10/09/12 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  10. EST Table: FS816318 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS816318 E_FL_fmgV_48E11_F_0 10/09/28 low homology 10/09/09 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  11. EST Table: FS727495 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS727495 E_FL_bmmt_10I12_F_0 10/09/28 low homology 10/09/03 low homology 10/08/28 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  12. EST Table: FS769764 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS769764 E_FL_fcaL_53D03_F_0 10/09/28 low homology 10/09/08 low homology 10/08/28 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  13. EST Table: FS915720 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915720 E_FL_fufe_36C24_F_0 10/09/28 low homology 10/09/12 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  14. EST Table: FS835316 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS835316 E_FL_fmgV_48E11_R_0 10/09/28 low homology 10/09/10 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  15. EST Table: FS899621 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS899621 E_FL_ftes_35G18_R_0 10/09/28 low homology 10/09/12 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  16. EST Table: FS920114 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS920114 E_FL_fufe_49G13_F_0 10/09/28 low homology 10/09/13 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  17. EST Table: FS917360 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS917360 E_FL_fufe_41C07_F_0 10/09/28 low homology 10/09/12 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  18. EST Table: FS907544 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS907544 E_FL_fufe_11I07_F_0 10/09/28 low homology 10/09/12 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  19. EST Table: FS847057 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS847057 E_FL_fner_28E13_F_0 10/09/28 91 %/100 aa ref|NP_001116812.1| tubulointerstitial nephrit ... is antigen [Bombyx mori] gb|ABB71105.1| TIN -ag-RP [Bombyx mori] 10/09/10 low homology 10/08/29 ...

  20. EST Table: FS843600 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS843600 E_FL_fner_18H08_F_0 10/09/28 low homology 10/09/10 low homology 10/08/29 46 %/101 aa DY ... 3.1#CE15745#WBGene00006574#locus:tin - 13#status:Confirmed#UniProt:O45319#protein_id:CAB ...

  1. EST Table: FS846743 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS846743 E_FL_fner_27G07_F_0 10/09/28 91 %/103 aa ref|NP_001116812.1| tubulointerstitial nephrit ... is antigen [Bombyx mori] gb|ABB71105.1| TIN -ag-RP [Bombyx mori] 10/09/10 low homology 10/08/29 ...

  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: FS728946 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS728946 E_FL_bmmt_14K14_F_0 10/09/28 81 %/101 aa ref|NP_001166191.1| cactus ... [Bombyx mori] dbj|B ... AI67121.1| Cactus ... [Bombyx mori] 10/09/03 n.h 10/08/28 n.h 10/09/10 n ...

  6. EST Table: FS850063 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS850063 E_FL_fner_36M09_F_0 10/09/28 90 %/130 aa ref|NP_001166191.1| cactus ... [Bombyx mori] dbj|B ... AI67121.1| Cactus ... [Bombyx mori] 10/09/11 n.h 10/08/29 n.h 10/09/10 n ...

  7. EST Table: FS832352 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS832352 E_FL_fmgV_40B23_R_0 10/09/28 41 %/248 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/10 low homology 10/08/29 n. ...

  8. EST Table: FS758813 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS758813 E_FL_fcaL_09G17_F_0 10/09/28 41 %/259 aa ref|NP_001121786.1| alpha-esterase 3 [Bombyx m ... ori] gb|ACD80423.1| carboxylesterase CarE -14 [Bombyx mori] 10/09/08 low homology 10/08/28 n. ...

  9. EST Table: FS829080 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS829080 E_FL_fmgV_30P15_R_0 10/09/28 39 %/278 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/10 low homology 10/08/29 n. ...

  10. EST Table: FS816178 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS816178 E_FL_fmgV_47O10_F_0 10/09/28 58 %/211 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/09 42 %/208 aa FBpp0239503| ...

  11. EST Table: FS808440 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS808440 E_FL_fmgV_26F15_F_0 10/09/28 60 %/251 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/09 42 %/251 aa FBpp0081074| ...

  12. EST Table: FS825585 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS825585 E_FL_fmgV_21D02_R_0 10/09/28 41 %/223 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/10 low homology 10/08/29 n. ...

  13. EST Table: FS822704 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS822704 E_FL_fmgV_13C14_R_0 11/12/09 n.h 10/09/28 42 %/190 aa ref|NP_001116501.1| alpha-esteras ... rm 1 [Bombyx mori] gb|ACB12411.1| carboxylesterase CarE -8 variant 1 [Bombyx mori] 10/09/10 low homology 10 ...

  14. EST Table: FS826338 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS826338 E_FL_fmgV_23E21_R_0 10/09/28 44 %/189 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/10 30 %/182 aa FBpp0159923| ...

  15. EST Table: FS803358 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS803358 E_FL_fmgV_12C18_F_0 10/09/28 53 %/142 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/09 38 %/134 aa FBpp0239503| ...

  16. EST Table: FS810728 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS810728 E_FL_fmgV_32M03_F_0 10/09/28 55 %/234 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/09 42 %/210 aa FBpp0239503| ...

  17. EST Table: FS828659 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS828659 E_FL_fmgV_29M22_R_0 10/09/28 99 %/282 aa ref|NP_001116814.1| alpha-esterase 40 [Bombyx ... mori] gb|ACB12414.1| carboxylesterase CarE -10 [Bombyx mori] 10/09/10 low homology 10/08/29 lo ...

  18. EST Table: FS803632 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS803632 E_FL_fmgV_12O23_F_0 10/09/28 91 %/116 aa ref|NP_001166806.1| alpha-esterase 19 isoform ... 2 [Bombyx mori] gb|ACB12412.1| carboxylesterase CarE -8 variant 2 [Bombyx mori] 10/09/09 n.h 10/08/29 n. ...

  19. EST Table: FS816380 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS816380 E_FL_fmgV_48H05_F_0 10/09/28 92 %/136 aa ref|NP_001166806.1| alpha-esterase 19 isoform ... 2 [Bombyx mori] gb|ACB12412.1| carboxylesterase CarE -8 variant 2 [Bombyx mori] 10/09/09 38 %/121 aa FBp ...

  20. EST Table: FS833842 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS833842 E_FL_fmgV_44C23_R_0 10/09/28 97 %/271 aa ref|NP_001116814.1| alpha-esterase 40 [Bombyx ... mori] gb|ACB12414.1| carboxylesterase CarE -10 [Bombyx mori] 10/09/10 low homology 10/08/29 lo ...

  1. EST Table: FS831899 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS831899 E_FL_fmgV_38N18_R_0 10/09/28 41 %/223 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/10 low homology 10/08/29 n. ...

  2. EST Table: FS829564 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS829564 E_FL_fmgV_32F08_R_0 10/09/28 42 %/251 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/10 30 %/227 aa FBpp0154663| ...

  3. EST Table: FS822343 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS822343 E_FL_fmgV_12C18_R_0 10/09/28 43 %/218 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/10 31 %/207 aa FBpp0154663| ...

  4. EST Table: FS826552 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS826552 E_FL_fmgV_23O13_R_0 10/09/28 46 %/252 aa ref|NP_001121785.1| alpha-esterase 49 [Bombyx ... mori] gb|ACD80422.1| carboxylesterase CarE -13 [Bombyx mori] 10/09/10 low homology 10/08/29 n. ...

  5. EST Table: FS810575 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS810575 E_FL_fmgV_32F08_F_0 10/09/28 57 %/199 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/09 39 %/189 aa FBpp0261886| ...

  6. EST Table: FS777809 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS777809 E_FL_fcaL_15K03_R_0 10/09/28 99 %/268 aa ref|NP_001116814.1| alpha-esterase 40 [Bombyx ... mori] gb|ACB12414.1| carboxylesterase CarE -10 [Bombyx mori] 10/09/08 low homology 10/08/28 lo ...

  7. EST Table: FS830824 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS830824 E_FL_fmgV_35O13_R_0 10/09/28 41 %/223 aa ref|NP_001116815.1| carboxylesterase CarE -11 [ ... Bombyx mori] gb|ACB12415.1| carboxylesterase CarE -11 [Bombyx mori] 10/09/10 low homology 10/08/29 n. ...

  8. 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

  9. EST Table: FS915693 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS915693 E_FL_fufe_36B16_F_0 11/12/09 GO hit GO:0000166(nucleotide binding)|GO:0004812(aminoacyl ... thetase#status:Confirmed#UniProt:Q9U1R2#protein_id:CAE ... 17953.1 10/09/10 73 %/281 aa AGAP003315-PA Protein ...

  10. EST Table: FS888238 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS888238 E_FL_ftes_41K16_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane)|G ...

  11. EST Table: FS765139 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS765139 E_FL_fcaL_38P12_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane)|G ...

  12. EST Table: FS750807 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS750807 E_ET_caL-_03D18_R_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane) 1 ...

  13. EST Table: FS750562 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS750562 E_ET_caL-_01O20_R_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane) 1 ...

  14. EST Table: FS760564 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS760564 E_FL_fcaL_14M09_F_0 11/12/09 GO hit GO:0003824(catalytic activity)|GO:0005524(ATP bindi ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane) 1 ...

  15. EST Table: FS745612 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS745612 E_ET_caL-_01O20_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane) 1 ...

  16. EST Table: FS902051 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS902051 E_FL_ftes_46A17_R_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane) 1 ...

  17. EST Table: FS766316 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS766316 E_FL_fcaL_42J04_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane)|G ...

  18. EST Table: FS865228 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS865228 E_FL_fner_27J16_R_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane) 1 ...

  19. EST Table: FS749652 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS749652 E_ET_caL-_19L13_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane) 1 ...

  20. EST Table: FS751737 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS751737 E_ET_caL-_06K18_R_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane)|G ...

  1. EST Table: FS851582 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS851582 E_FL_fner_41B16_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane)|G ...

  2. EST Table: FS812589 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS812589 E_FL_fmgV_37P19_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane) 1 ...

  3. EST Table: FS769167 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS769167 E_FL_fcaL_51F10_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane)|G ...

  4. EST Table: FS886043 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS886043 E_FL_ftes_34P15_F_0 11/12/09 GO hit GO:0005524(ATP binding)|GO:0006754(ATP biosynthetic ... ase activity, coupled to transmembrane movement of ions , phosphorylative mechanism)|GO:0016020(membrane)|G ...

  5. EST Table: FS928778 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS928778 E_FL_fwgP_23E08_F_0 10/09/28 53 %/233 aa ref|XP_001605588.1| PREDICTED: similar to rap5 ... 0 %/116 aa Y18D10A.17#CE21413#WBGene00012484#locus:car - 1#status:Confirmed#UniProt:Q9XW17#protein_id:CAA2 ...

  6. EST Table: FS931520 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS931520 E_FL_fwgP_31H14_F_0 10/09/28 53 %/233 aa ref|XP_001605588.1| PREDICTED: similar to rap5 ... 0 %/116 aa Y18D10A.17#CE21413#WBGene00012484#locus:car - 1#status:Confirmed#UniProt:Q9XW17#protein_id:CAA2 ...

  7. EST Table: FS887642 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS887642 E_FL_ftes_39O11_F_0 10/09/28 52 %/212 aa ref|XP_001605588.1| PREDICTED: similar to rap5 ... 0 %/116 aa Y18D10A.17#CE21413#WBGene00012484#locus:car - 1#status:Confirmed#UniProt:Q9XW17#protein_id:CAA2 ...

  8. EST Table: FS869548 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS869548 E_FL_fner_40B05_R_0 10/09/28 88 %/238 aa ref|NP_001040121.1| endothelial-monocyte activ ... 58 %/160 aa F58B3.5c#CE44546#WBGene00003415#locus:mars - 1#status:Confirmed#UniProt:D3YT56#protein_id:CBK1 ...

  9. EST Table: FS851222 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS851222 E_FL_fner_40B05_F_0 10/09/28 75 %/241 aa ref|NP_001040121.1| endothelial-monocyte activ ... 64 %/107 aa F58B3.5c#CE44546#WBGene00003415#locus:mars - 1#status:Confirmed#UniProt:D3YT56#protein_id:CBK1 ...

  10. EST Table: FS853917 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS853917 E_FL_fner_47L09_F_0 10/09/28 75 %/241 aa ref|NP_001040121.1| endothelial-monocyte activ ... 64 %/107 aa F58B3.5c#CE44546#WBGene00003415#locus:mars - 1#status:Confirmed#UniProt:D3YT56#protein_id:CBK1 ...

  11. EST Table: FS910600 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS910600 E_FL_fufe_20L12_F_0 10/09/28 78 %/287 aa ref|NP_001040121.1| endothelial-monocyte activ ... 59 %/149 aa F58B3.5c#CE44546#WBGene00003415#locus:mars - 1#status:Confirmed#UniProt:D3YT56#protein_id:CBK1 ...

  12. EST Table: FS918507 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS918507 E_FL_fufe_44J10_F_0 10/09/28 79 %/296 aa ref|NP_001040121.1| endothelial-monocyte activ ... 57 %/160 aa F58B3.5c#CE44546#WBGene00003415#locus:mars - 1#status:Confirmed#UniProt:D3YT56#protein_id:CBK1 ...

  13. EST Table: FS790451 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available |255522795|ref|NP_001157310.1| longitudinals lacking isoform 1 [Tribolium castaneum] FS908703 ffbm ... ...|gene:AGAP005245 10/09/10 82 %/119 aa gnl|Amel|GB12094-PF 10/09/10 84 %/119 aa gi

  14. EST Table: FS854150 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS854150 E_FL_fner_48F18_F_0 10/09/28 76 %/142 aa gb|AAV91017.1| hemolymph ... proteinase 19 [Manduc ... i|189239809|ref|XP_970870.2| PREDICTED: similar to hemolymph ... proteinase 19 [Tribolium castaneum] DC548890 fner ...

  15. EST Table: FS850053 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS850053 E_FL_fner_36L23_F_0 10/09/28 50 %/205 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/11 n.h 10/08/29 n.h 10 ...

  16. EST Table: FS741228 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS741228 E_FL_bmmt_19H11_R_0 10/09/28 40 %/146 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/07 n.h 10/08/28 n.h 10 ...

  17. EST Table: FS847527 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS847527 E_FL_fner_29J22_F_0 10/09/28 98 %/188 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/10 n.h 10/08/29 n.h 10 ...

  18. EST Table: FS905056 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS905056 E_FL_fufe_03N22_F_0 10/09/28 39 %/197 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/12 n.h 10/08/29 n.h 10 ...

  19. EST Table: FS795834 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS795834 E_FL_ffbm_19G08_F_0 10/09/28 98 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  20. EST Table: FS795560 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS795560 E_FL_ffbm_18K07_F_0 10/09/28 98 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  1. EST Table: FS796261 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS796261 E_FL_ffbm_20L11_F_0 10/09/28 97 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  2. EST Table: FS792589 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS792589 E_FL_ffbm_10B23_F_0 10/09/28 54 %/237 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  3. EST Table: FS851187 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS851187 E_FL_fner_39P15_F_0 11/12/09 GO hit GO:0005576(extracellular region) 10/09/28 51 %/210 ... aa ref|NP_001119728.1| hemolymph ... protein [Bombyx mori] dbj|BAA02093.1| hemolymph ... pr ...

  4. EST Table: FS857193 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS857193 E_FL_fner_03O03_R_0 10/09/28 98 %/226 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/11 n.h 10/08/29 n.h 10 ...

  5. EST Table: FS796765 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS796765 E_FL_ffbm_22C23_F_0 10/09/28 32 %/247 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  6. EST Table: FS793009 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS793009 E_FL_ffbm_11F09_F_0 10/09/28 97 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  7. EST Table: FS730639 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS730639 E_FL_bmmt_19H11_F_0 10/09/28 39 %/178 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/03 n.h 10/08/28 n.h 10 ...

  8. EST Table: FS799343 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS799343 E_FL_ffbm_29P10_F_0 10/09/28 98 %/215 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  9. EST Table: FS844781 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS844781 E_FL_fner_21L24_F_0 10/09/28 34 %/143 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/10 n.h 10/08/29 n.h 10 ...

  10. EST Table: FS795182 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS795182 E_FL_ffbm_17J03_F_0 10/09/28 98 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  11. EST Table: FS921475 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS921475 E_FL_fwgP_01M19_F_0 10/09/28 39 %/197 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10 ...

  12. EST Table: FS867952 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS867952 E_FL_fner_35H06_R_0 10/09/28 32 %/113 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/11 n.h 10/08/29 n.h 10 ...

  13. EST Table: FS838432 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS838432 E_FL_fner_03O03_F_0 10/09/28 98 %/184 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/10 n.h 10/08/29 n.h 10 ...

  14. EST Table: FS793238 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS793238 E_FL_ffbm_11P15_F_0 10/09/28 98 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  15. EST Table: FS794815 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS794815 E_FL_ffbm_16I08_F_0 10/09/28 98 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  16. EST Table: FS868395 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS868395 E_FL_fner_36L23_R_0 11/12/09 GO hit GO:0005576(extracellular region) 10/09/28 56 %/224 ... aa ref|NP_001119728.1| hemolymph ... protein [Bombyx mori] dbj|BAA02093.1| hemolymph ... pr ...

  17. EST Table: FS739869 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS739869 E_FL_bmmt_15J22_R_0 10/09/28 33 %/109 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/07 n.h 10/08/28 n.h 10 ...

  18. EST Table: FS796800 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS796800 E_FL_ffbm_22E10_F_0 10/09/28 98 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  19. EST Table: FS868095 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS868095 E_FL_fner_35N18_R_0 11/12/09 GO hit GO:0005576(extracellular region) 10/09/28 33 %/114 ... aa ref|NP_001119728.1| hemolymph ... protein [Bombyx mori] dbj|BAA02093.1| hemolymph ... pr ...

  20. EST Table: FS865938 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS865938 E_FL_fner_29J22_R_0 11/12/09 GO hit GO:0005576(extracellular region) 10/09/28 98 %/225 ... aa ref|NP_001119728.1| hemolymph ... protein [Bombyx mori] dbj|BAA02093.1| hemolymph ... pr ...

  1. EST Table: FS922759 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS922759 E_FL_fwgP_05J08_F_0 10/09/28 38 %/206 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/13 n.h 10/08/29 n.h 10 ...

  2. EST Table: FS791687 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS791687 E_FL_ffbm_07H15_F_0 11/12/09 GO hit GO:0005576(extracellular region) 10/09/28 98 %/262 ... aa ref|NP_001119728.1| hemolymph ... protein [Bombyx mori] dbj|BAA02093.1| hemolymph ... pr ...

  3. EST Table: FS939534 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS939534 cesb0088 10/09/28 65 %/185 aa gb|AAV91017.1| hemolymph ... proteinase 19 [Manduca sexta] 10 ... i|189239809|ref|XP_970870.2| PREDICTED: similar to hemolymph ... proteinase 19 [Tribolium castaneum] DC548890 cesb ...

  4. EST Table: FS789790 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS789790 E_FL_ffbm_01L24_F_0 10/09/28 98 %/262 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/09 n.h 10/08/29 n.h 10 ...

  5. EST Table: FS869514 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS869514 E_FL_fner_39P15_R_0 10/09/28 54 %/237 aa ref|NP_001119728.1| hemolymph ... protein [Bombyx ... mori] dbj|BAA02093.1| hemolymph ... protein [Bombyx mori] 10/09/11 n.h 10/08/29 n.h 10 ...

  6. EST Table: FS874457 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/11 49 %/188 aa FBpp0149335|DgriGH15429-PA 10/08/29 low homology 10/0...FS874457 E_FL_ftes_01A06_F_0 10/09/28 57 %/166 aa gb|AAN39695.1| ATP synthase-like

  7. EST Table: FS890668 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 50 %/191 aa FBpp0274195|DpseGA20881-PA 10/08/29 low homology 10/0...FS890668 E_FL_ftes_53C11_F_0 10/09/28 56 %/172 aa gb|AAN39695.1| ATP synthase-like

  8. EST Table: FS903947 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 52 %/205 aa FBpp0127866|DanaGF24674-PA 10/08/29 low homology 10/0...FS903947 E_FL_ftes_53C11_R_0 10/09/28 55 %/208 aa gb|AAN39695.1| ATP synthase-like

  9. EST Table: FS875675 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/11 50 %/201 aa FBpp0274195|DpseGA20881-PA 10/08/29 low homology 10/0...FS875675 E_FL_ftes_04J04_F_0 10/09/28 56 %/182 aa gb|AAN39695.1| ATP synthase-like

  10. EST Table: FS891852 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 49 %/229 aa FBpp0274195|DpseGA20881-PA 10/08/29 low homology 10/0...FS891852 E_FL_ftes_04J04_R_0 10/09/28 55 %/208 aa gb|AAN39695.1| ATP synthase-like

  11. EST Table: FS928348 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS928348 E_FL_fwgP_22A11_F_0 10/09/28 74 %/212 aa gb|AAQ12887.1| Z9-desaturase SFWG5A [Choristoneura paralle...la] gb|AAQ12888.1| Z9-desaturase SFWG5B [Choristoneura parallela] 10/09/13 52 %/214

  12. EST Table: FS890946 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 47 %/233 aa FBpp0180399|DperGL16292-PA 10/08/29 low homology 10/0...FS890946 E_FL_ftes_01A06_R_0 10/09/28 55 %/203 aa gb|AAN39695.1| ATP synthase-like

  13. EST Table: FS886342 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 40 %/193 aa FBpp0149335|DgriGH15429-PA 10/08/29 n.h 10/09/10 41 %...FS886342 E_FL_ftes_35N22_F_0 10/09/28 58 %/129 aa gb|AAN39695.1| ATP synthase-like

  14. EST Table: FS889111 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 49 %/171 aa FBpp0149335|DgriGH15429-PA 10/08/29 n.h 10/09/10 50 %...FS889111 E_FL_ftes_44I23_F_0 10/09/28 59 %/149 aa gb|AAN39695.1| ATP synthase-like

  15. EST Table: FS902675 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 52 %/205 aa FBpp0127866|DanaGF24674-PA 10/08/29 low homology 10/0...FS902675 E_FL_ftes_48G04_R_0 10/09/28 55 %/208 aa gb|AAN39695.1| ATP synthase-like

  16. EST Table: FS891415 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 52 %/205 aa FBpp0127866|DanaGF24674-PA 10/08/29 low homology 10/0...FS891415 E_FL_ftes_02N09_R_0 10/09/28 55 %/208 aa gb|AAN39695.1| ATP synthase-like

  17. EST Table: FS894399 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 49 %/229 aa FBpp0274195|DpseGA20881-PA 10/08/29 low homology 10/0...FS894399 E_FL_ftes_14O11_R_0 10/09/28 55 %/208 aa gb|AAN39695.1| ATP synthase-like

  18. EST Table: FS924668 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available FS924668 E_FL_fwgP_11D20_F_0 10/09/28 73 %/252 aa gb|AAQ12887.1| Z9-desaturase SFWG5A [Choristoneura paralle...la] gb|AAQ12888.1| Z9-desaturase SFWG5B [Choristoneura parallela] 10/09/13 52 %/255

  19. EST Table: FS879230 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/11 50 %/182 aa FBpp0149335|DgriGH15429-PA 10/08/29 n.h 10/09/10 51 %...FS879230 E_FL_ftes_14O11_F_0 10/09/28 58 %/160 aa gb|AAN39695.1| ATP synthase-like

  20. EST Table: FS898330 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available protein [Choristoneura parallela] 10/09/12 49 %/229 aa FBpp0274195|DpseGA20881-PA 10/08/29 low homology 10/0...FS898330 E_FL_ftes_30G18_R_0 10/09/28 55 %/208 aa gb|AAN39695.1| ATP synthase-like