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| 23054 |
A Novel Rapid and Highly Sensitive Cell Based System for the Detection and Characterization of HIV
AIDS, the disease caused by the virus HIV, represents a devastating global pandemic. According to a United Nations report in 2010, HIV has killed nearly 30 million people worldwide, with over 2.5 million additional infections each year. Detecting HIV particles is critical not only to patient diagnosis, but also for basic and clinical research, the source of future therapies. Unfortunately, current methods are severely lacking. Phenotypic testing can take over a month to complete and only reports a single time point. Another system widely used for research employs cell lines that express CD4 and co-receptors at abnormally high levels, rendering results of questionable physiological relevance. Patients, physicians, and researchers alike would benefit greatly from a new method of detecting and characterizing HIV; one that is rapid, sensitive, adaptable, and most importantly, physiologically accurate.
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| 22893 |
String Matching in Hardware using the FM-Index
UC Researchers have developed a Field-Programmable-Gate-Array (FPGA) based hardware implementation that utilizes the FM-Index for exact pattern matching for string searching. This method of FM-Index string matching has a higher effective throughput than brute force due to the higher number of character comparisons per cycle performed by the FM-Index. Further, the speed of this method is in the order of two orders of magnitude greater than Bowtie software tools and ten to seventy times faster than the traditional method using FHAST.
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| 22861 |
A Novel Reporter System that Detects DNA Mutations in Pluripotent Stem Cells
DNA mutation events (gene rearrangements, base-pair substitutions) cause genomic instability, and can lead to cell death or cancer. These events also potentially lead to gene dysfunction and genetic disorders. DNA mutation events have many possible causes, such as inherited mutations in genes involved in genomic integrity, or exposure to environmental toxins. Human stem cell technology, in which stem cells can be differentiated into any cell type in the body, has the great potential to advance the discovery of therapeutics for unmet medical needs. However, recent reports indicate increased DNA mutation frequency in stem cells, which limits their potential use for discovery or therapeutic purposes. Therefore, technologies that enable the detection of the different types of DNA mutations would advance the characterization and selection of human stem cell lines for discovery or therapeutic purposes, and help characterize the mutagenic potential of environmental toxins.
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| 21322 |
Methods and Implementations for Storing Sparse Vectors
This invention consists of a set of methods and algorithms to compress the information contained in large vectors of binary or integer variables. These vectors occur in a variety of applications where objects are represented by spectral fingerprints, which by nature tend to be large and sparse. By leveraging the power law distributions often observed in these spaces, researchers at UCI have developed new lossless compression methods using integer entropy coding. In contrast to current compression systems requiring 1024 bits to store each molecule, the UCI methods can achieve lossless compression to a mere 300-400 bits.
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| 21082 |
Plasmid Expressing Recombinant RILP-GST Protein
Researchers at the University of California, Irvine have developed a plasmid that expresses recombinant GST-RILP protein. RILP is a Rab7 effector protein and therefore selectively binds the GTP-bound form of Rab7.
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| 20874 |
Crop Improvement And Production Of Value-Added Compound Using The Rice Beta-Glucanase Genes, Gns2-Gns9
Patent rights to a group of novel rice beta-glucanase genes and the corresponding beta-glucanase enzymes are available for non-exclusive licensing. The genes, and the gene promoters, are useful in a variety of transgenic monocot plants for achieving increased plant resistance to fungal infection, improved growth characteristics, biomass conversion and high levels of expression of heterologous protein in various tissues obtained from the plants.
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| 20472 |
Vectors for Antibody Expression
Recombinant antibodies have a wide variety of uses as research tools, therapeutics and diagnostics. Vectors utilized for the cloning and expression of antibody variable (V) regions make the expression of whole recombinant antibodies possible. In addition, expression of recombinant antibodies in a variety of cell types would provide greater utility to recombinant antibody technology.
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| 20237 |
Method of Producing Novel Unmarked Recombinant Vaccine Vector for Tuberculosis
Mycobacterium tuberculosis is a disease that infects millions of people each year; in addition, the related bacterium, Mycobacterium bovis, infects domesticated animals, resulting in substantial economic losses. Currently, humans are administered Bacille Calmette-Guerin (BCG) vaccine to prevent tuberculosis. However, BCG vaccines have variable efficacy - on average about 50%. Recombinant BCG vaccines have been developed that express a key antigen of M. tuberculosis and are more potent than BCG. However, these recombinant BCG vaccines contain antibiotic resistance markers; regulatory authorities want vaccines to be free of such antibiotic resistance markers to diminish their dissemination to other pathogens in the environment. Unmarked vaccine vectors (i.e. those lacking an antibiotic resistance marker) have been produced by various means, but these methods have resulted in low levels of expression of recombinant proteins. Preferably, unmarked strains would not only express large amounts of the recombinant proteins, but express them from genes integrated into the chromosome because such constructs tend to be more stable than when the genes are expressed from a plasmid. Due to safety, potency, regulatory, and stability issues, there is a need for a better vaccine that can prevent and treat tuberculosis in humans and animals.
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| 19653 |
Novel Recombinant Adenovirus Vectors for Tissue-Specific Gene Expression in Heart
Targeted gene delivery to somatic tissues has importance in both genetic research and therapeutics. One of the most effective gene delivery vectors known is the recombinant human adenoviruses, which possess high infectivity with respect to a broad range of tissue types. The low selectivity (as to tissue type) is a disadvantage of these vectors limiting their usefulness as an in vivo therapeutic. Vectors which combine high infectivity with tissue- specific expression are needed.
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| 18327 |
Transcriptional Activation Factors (cjun, Ap-2, Sp1, Ctf/nf-1)
Eukaryotic promoters are regulated by a combination of sequence-specific DNA-binding proteins, general transcription initiation factors, and associated accessory factors. The sequence-specific transcription factors can be divided into several classes on the basis of the activation domains they posess. This disclosure relates to several Human cDNA clones and/or expression vectors encoding c-jun, AP2, SP1, and CTF/NF1 TAF genes. Reference; B.D. Dynlacht, et al., Isolation of Coactivators Associated with the TATA-Binding Protein That Mediate Transcriptional Activation. 1991. Cell 66:563-76
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| 18326 |
In Vitro Translation Vectors/drosophila Tafs
In Drosophila and human cells, the TATA binding protein (TBP) of the transcription factor IID (TFIID) complex is tightly associated with multiple subunits termed TBP-associated factors (TAFs) that are essential for mediating regulation of RNA polymerase II transcription. This diclosure makes available various cDNA expression clones encoding dTAFs 250, 150, 110, 80,60,40,30, and 30B (in vitro translation vectors) from Drosophila. References; C.P. Verrijzer, et al., Drosophila TAFII150: similarity to Yeast Gene TSM-1 and Specific Binding to Core Promoter DNA. 1994. Science 264:933-41 T. Hoey, et al., Molecular Cloning and Functional Analysis of Drosophila TAF110 Reveal Properties Expected of Coactivators. 1993. Cell 72; 247-60
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| 18317 |
Compositions And Methods For Plant Pathogen Resistance
Researchers at the University of California at Berkeley have identified a plant resistance gene family, the members of which encode plant resistance polypeptides having P-Loop and LRR structural motifs. This resistance gene class includes Prf, RPS2, RPM1, N, and L6 and represents a large fraction of known plant disease resistance genes. The invention further involves transgenic plants and transformed host cells that express these DNAs and exhibit enhanced disease resistance to plant pathogens. For example, when expressed in transgenic plants, Prf confers Fenthion sensitivity and resistance to a wide variety of phytopathogens, including not only Pseudomonas syringae, but also unrelated pathogens such as Xanthomonas campestris.
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| 17515 |
Radio Antenna With Improved Support System
Radio antennas must maintain their paraboloid shape and directional positioning in order to work properly. However wind can load the antenna dish and cause it to lose its shape and position. To address this situation, researchers at UC Berkeley have developed a support system that strengthens antenna dishes and provides several structural enhancements. The support system consists of reinforcements that enable firm radial and torsional support as well as an optimal amount of axial flexibility and support. This design allows for a large open area so that azimuth and elevation-bearing systems can be positioned near to the reflector vertex. This positioning enables lower loads and less structural requirements for the pedestal and drives.
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| 17509 |
Radio Antenna With Improved Low Noise Amplification
Solid-state amplifiers used on radio antennas reach their lowest noise temperature when cooled to well below room temperature. To achieve the low temperature, the amplifier is placed in a refrigerated vacuum dewar. However, the glass seal on the dewar through which the transmission line passes significantly reflects input waves ? especially at the highest frequencies. To minimize this reflection, researchers at UC Berkeley have developed a design enhancement on the vacuum dewar of radio antennas. In addition to the design modification, the Berkeley team has identified materials that minimize the amount of loss on the input line. These design features have been shown to reduce the maximum reflection from -10 dB to -16.5 dB.
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| 17508 |
Radio Antenna With Reduced Interference
The performance of radio antennas can be degraded from interference caused by thermal radiation as well as signals traveling along the ground and reflected by the ground. To minimize these sources of interference, researchers at UC Berkeley have developed design enhancements for radio antennas. These refinements minimize thermal background noise as well as low radio frequency interference, and they don?t intercept radiation along the symmetry axis of the antenna, or any rays that reach the feed (detector).
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| 17507 |
Radio Antenna With Improved Feed System
Log-periodic antennas are capable of transmitting and receiving signals across a large bandwidth. However, their bandwidth range can be too large for the entire signal to be simultaneously digitized. To address this issue, researchers at UC Berkeley have developed an innovative feed for broadband antennas. This feed converts the broadband radio signals such that they can be more readily digitized and processed.
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| 17501 |
Radio Antenna Image Processing Improvements
The image processing of synthetic aperture radar (SAR) can be used to capture extremely high-resolution images. Corner turners are the signal-processing devices used to perform these data-intensive operations. Current corner turners require huge amounts of memory and consequently are expensive. An alternative corner turner based on custom, programmable chips has been proposed, but it is also expensive. To address this issue, researchers at UC Berkeley have developed a novel design for a corner turner that doesn?t rely on memory to perform the voluminous transpose operations. In comparison to the alternative approaches, this highly efficient Berkeley corner turn is less expensive.
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| 17420 |
Radio Antenna With Improved Connection System
The latest log-periodic antenna designs enable devices such as amplifiers and cryogenic electronics to be placed near the antenna without interrupting the signal. However, the antenna feeds and connections can still cause undesired ohmic losses, high receiver noise temperatures, spillover, and the excitation of unwanted frequency modes. To address these issues, researchers at UC Berkeley have developed a novel system of connections and feeds that minimizes unwanted effects. This efficient design enables shorter transmission lines while allowing for cryogenic electronics to be attached. The resulting antenna reduces ohmic losses, spillover and receiver noise temperature, and it eliminates the excitation of unwanted frequency modes. The Berkeley team has developed two versions of this antenna. The first version is easy to fabricate but produces an elliptical polarization. The second version is a modification of the first and provides greater polarization purity (circular polarization).
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| 17268 |
Fluorescence Resonance Energy Transfer (fret)-based Sensor Of Rangtp-importin B Interaction
Scientists at the University of California Berkeley have designed FRET sensor of a complex of Ran-GTP-importin b that is a fluorescent protein construct consisting of Importin b-domain (IBB) of importin a flanked by fluorescent proteins (donor and acceptor) capable of FRET. The sensor functions as an indirect sensor of Ran-GTP through its Ran-GTP sensitive specific interaction with importin b. See: P. Kalab, Weis, K., and Heald, R. (2002), Visualization of a Ran-GTP Gradient in Interphase and Mitotic Xenopus Egg Extracts. Science, March 29, 2002, Vol. 295, 2452-2456. The small guanosine triphosphate Ran is loaded with guanosine tripohosphate (GTP) by the chromatin bound guanine nucleotide exchange factor RCC1 and releases import cargoes in the nucleus during interphase. In mitosis, Ran-GTP promotes spindle assembly around the chromosomes by locally discharging cargoes that regulate microtubule dynamics and organization. We used fluorescence energy transfer-based biosensors to visualize gradients of Ran-GTP and liberated cargoes around chromosomes in mitotic Xenopus egg extacts. Both gradients were required to assemble and maintain spindle structure. During interphase, Ran-GTP was highly enriched in the nucleoplasm, and a steep concentration difference between nuclear and cytoplasmic Ran-GTP was established, providing evidence for a Ran-GTP gradient surrounding chromosomes throughout the cell cycle.
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| 17267 |
Fluorescence Resonance Energy Transfer (fret)-based Direct Sensor Of Rangtp
Scientists at the University of California Berkeley have designed FRET-based sensor of Ran-GTP that is a fluorescent protein construct consisting of Ran binding domain flanked by fluorescent proteins (donor and acceptor) capable of FRET. The sensor functions as: 1) a direct sensor of Ran-GTP, and 2) an indirect sensor of Ran-GTP-binding proteins such as importin-b family proteins. See: P. Kalab, Weis, K., and Heald, R. (2002), Visualization of a Ran-GTP Gradient in Interphase and Mitotic Xenopus Egg Extracts. Science, March 29, 2002, Vol. 295, 2452-2456. The small guanosine triphosphate Ran is loaded with guanosine tripohosphate (GTP) by the chromatin bound guanine nucleotide exchange factor RCC1 and releases import cargoes in the nucleus during interphase. In mitosis, Ran-GTP promotes spindle assembly around the chromosomes by locally discharging cargoes that regulate microtubule dynamics and organization. We used fluorescence energy transfer-based biosensors to visualize gradients of Ran-GTP and liberated cargoes around chromosomes in mitotic Xenopus egg extacts. Both gradients were required to assemble and maintain spindle structure. During interphase, Ran-GTP was highly enriched in the nucleoplasm, and a steep concentration difference between nuclear and cytoplasmic Ran-GTP was established, providing evidence for a Ran-GTP gradient surrounding chromosomes throughout the cell cycle.
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| 17235 |
Reagents To Study The Structure And Function Of The Prototype Map Kinase Scaffold Protein, Ste5
This invention makes available plasmids designed to express derivatives of Saccharomyces cerevisiae Ste5 protein tagged with an N-terminal in-frame (His)6 tract and a c-Myc epitope recognized by the monoclonal antibody, 9E10, and /or fused in-frame at either its N- or C-terminus to the Aequoria victoria Green Fluorescent Protein (GFP), or mutant derivatives of Ste5 in these contexts. References: Hasson et al. 1994. Mol. Cell Biol. 14:1054-65 Inouye et al. 1997. Science 278:103-6 Inouye et al. 1997. Genetics 147:479-92 Sette et al. 2000. Mol Biol. Cell 11:4033-49 Bardwell et al. 2001. J. Biol. Chem. 276:10374-86 Kunzler et al. 2001. Genetics 157:1089-105
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| 17216 |
Phage Dna From Listeria Monocytogenes
Listeria monocytogenes is a non-spore-forming, opportunistic Gram-positive pathogen, responsible for severe infections in both animals and humans. Recurrent outbreaks of Listeriosis have emphasized the need for better understanding of the molecular pathogenicity mechanisms and the interaction of the organism and specific bacteriophages. Investigators at University of California, Berkeley have made an integration vector carrying the integrase and attachment site of phage A118. References: Loessner et al. 2000. Mol. Microbiology 35:324-40. Fleming et al. 1985. New Eng. J. Med. 312:404-7
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| 17139 |
Recombinant Murine Cytomegalovirus Rvm78, And Its Related Reagents
Human cytomegalovirus (HCMV) is a ubiquitous herpesvirus infecting more than 75% of the U.S population. It is a leading cause of birth defects in newborns, a major cause of morbidity and mortality in immunocompromised individuals, such as transplant recipients and patients with AIDS, and even in healthy adults, this virus causes a life-long subclinical infection that may be associated with the development of atherosclerosis. Study of murine cytomegalovirus (MCMV) serves as a model for understanding of HCMV- associated diseases. The reagents covered in this invention include (1) MCMV mutant (RvM78) that contained a mutation at viral open reading frame M78, (2) an expression plasmid construct (pM78-FLAG) that contains M78 coding sequence driven by an eukaryotic expression cassette, and (3) a mouse 3T3 cell line that contains pM78-Flag and expresses M78 protein. References: Zhan et al. 2000 Virology 266:264-74. Zhan et al. 2000 J. Virology 74:7411-21
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| 17138 |
Murine H60 Gene (plasmid) For Minor Histocompatibility Antigen
Minor histocompatibility (H) antigens elicit T cell responses and thereby cause chronic graft rejection and graft-vs.-host disease among MHC identical individuals. Although numerous independent H loci exist in mice of a given MHC haplotype, certain H antigens dominate the immune response and are thus of considerable conceptual and therapeutic importance. The H60 gene was isolated as a cDNA clone from the mouse strain BALB.B. This gene contains an antigenic peptide that elicits a strong cytotoxic T cell response when C57BL/6 mice are immunized with BALB.B spleen cells. References: Malarkannan et al. 1998. J Immunol. 161:3501-9. Karttunen et al. 1992. PNAS 89:6020-4.
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| 17135 |
Reporter Plasmid To Quantitate Filamentous-response-element (fre)-dependent Transcription
To assay transcription from promoters under the control of Filamentous Response Elements (FREs) which comprise binding sites for the transcription factors Ste7 and Tec1, investigators at UCB constructed a plasmid (YEpU-FTyZ) in which expression of the E. coli lacZ gene is driven by the FRE of the transposon Ty1. Reference; Cook et al. 1997 Nature 390:85-8.
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| 17128 |
Radio Antenna With Improved Broadband Performance
Log-periodic antennas provide the frequency independent performance that is necessary for applications in which large portions of the electromagnetic spectrum are scanned. However, the high frequency limit of these antennas is restricted because their amplifiers must be located far from the feed vertex so that they don?t interfere with radiation patterns ? and this in turn requires a long transmission line that results in unacceptable performance degradation. To address these issues, researchers at UC Berkeley have developed a non-planar log-periodic antenna that improves performance through several design refinements that include the ability to place an amplifier within the antenna. Small microwave telescopes that incorporate these design improvements can achieve unprecedented A/T over multi-octave bandwidths. In comparison to previous log-periodic antennas, this Berkeley design improves the gain, polarization purity, and transmission line losses. The antenna is capable of concurrent transmission or reception of two orthogonal polarization modes, and it includes elements that decrease the amount of cross-polarization coupling that occurs between the arms of the antenna. Moreover, this design also allows for the attachment of cryogenic electronics to enhance signal sensitivity and the performance of low noise amplifiers.
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| 17023 |
Dominant Negative Nur77 Gene Inhibitor Of Apoptosis
Apoptosis is a phenomenon observed during development of many cell types in many organisms. It is an internal, programmed cell death characterized by DNA fragmentation into nucleosome-size pieces. Anti-CD3-induced apoptosis in T-cell hybridomas and immature thymocytes requires new gene transcription and may be related to negative selection during T-cell development. Using subtractive hybridization, we isolated a complementary DNA clone encoding the orphan steroid receptor Nur77 (refs 7-9). It shows different patterns of messenger RNA induction between apoptotic and stimulated T cells. We report here the use of gel shift analysis to demonstrate that the Nur77 protein is present at high levels in apoptotic T-cell hybridomas and apoptotic thymocytes, but not in growing T cells or stimulated splenocytes. A Nur77 dominant negative protected T-cell hybridomas from activation-induced apoptosis. Hence Nur77 is necessary for induced apoptosis in T-cell hybridomas. Reference: Woronicz, J, et al., 1994 Nature 367:277-81
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| 16883 |
Plasmids For The Expression Of Transgenic Protein In T Cells
Plasmid vectors (pV-alpha-11-GH and pLCRc) have been developed for the expression of transgenic proteins in immature and mature T cells. Research using these vectors has been published: Diaz et al. Immunity 1:207 (1994) Ortiz et al. EMBO J. 16:5037 (1997) Kabra et al. J. Immunol. 162:2766 (1999)
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