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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
UbcH5b (His tag, C-terminus)
- 供应商:
艾美捷科技有限公司
- 规格:
100ug
【产品形式】:艾美捷为您提供的UbcH5b (His标签, C-terminus)形式为20mM Tris-Cl, pH7.5, 1mM DTT
【背景资料】:UbcH5b, also known as UBE2D2, is a member of the ubiquitin E2 conjugating enzyme family, essential components of the ubiquitin cascade. The selectivity of the ubiquitin cascade for a particular substrate protein relies on the interaction between the E2 conjugating enzyme (of which a cell contains relatively few) and an ubiquitin E3 ligase, of which over 600 have been identified to date. The specific E2-E3 pair required for ubiquitination of a particular substrate protein in vivo may also control the type of ubiquitin modification (mono-, multi-, poly-ubiquitin), the exact substrate lysine residue(s) to be modified and, in the case of polyubiquitination, the chain length and lysine linkage type. UbcH5b is associated with the signal-induced conjugation and subsequent degradation of IκBα in the presence of the SCF complexes (Skp/Cul/F-Box) and with Hdm2 mediated p53 ubiquitination. In vitro UbcH5b acts as a promiscuous E2 and is able to interact with a range of different E3 enzymes and participate in polyubiquitin chain synthesis. Recombinant human UbcH5b protein expressed with a C-terminal His-tag. Protein has utility in ubiquitination reactions, polyubiquitin chain synthesis, identification of substrate specific E2-E3 pairs and determination of E2 polyubiquitin linkage specificity.
英国Viva Bioscience公司是一家研发、生产并销售蛋白降解相关产品的公司。其产品主要用于细胞自噬、泛素化和蛋白酶体研究(也覆盖其他蛋白降解相关的产品),其产品价格合理、质量可靠且具有创新性。目前VIVA Bioscience提供逾460种产品,涉及细胞自噬、蛋白泛素化和讲解相关的所有试剂盒、蛋白、底物以及多种抑制剂、激活剂等全系列产品。作为多家进口品牌的中国区域总代理,艾美捷科技与Viva Bioscience一道为中国科研工作者们提供更好、更新的自噬、泛素化和蛋白酶体等研究工具。
点击UbcH5b (His标签, C-terminus)查看更详细产品说明,更多应用、储存、价格、货期等信息请致电垂询Viva Bioscience中国区域授权总代理艾美捷科技有限公司。
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文献和实验Hepatitis C Virus RNA-Dependent RNA Polymerase (NS5B Polymerase)
The hepatitis C virus (HCV) chronically infects approx 4 million patients in the United States alone, and constitutes a major cause of chronic liver disease and hepatocellular carcinoma (1 –3 ). Current antiviral therapies for chronic
Preparation and Handling of Hepatitis C Viral Proteins NS3 and NS5B for Structural Studies
protease and the NS5B RNA-dependent RNA polymerase are the most popular targets from a drug-discovery perspective. A number of active-site inhibitors of the NS3 protease as well as allosteric inhibitors of the NS5B polymerase are being developed
to measure the interaction between hepatitis C virus NS5B polymerase (wild type and/or mutants) and a small-molecule inhibitor. Viral polymerase proteins are captured on a Ni2+ -nitrilotriacetic acid sensor surface while the small-�molecule inhibitors
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