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SensoLyte® 490 HIV Protease Assay Kit

FRET 适用: Human Immunodeficiency Virus (HIV) Fluorometric
产品编号 ABIN1882480
发货至: 中国
  • 抗原 See all HIV products
    HIV (Human Immunodeficiency Virus (HIV))
    适用
    • 1
    • 1
    • 1
    Human Immunodeficiency Virus (HIV)
    检测方法
    Fluorometric
    应用范围
    Fluorescence Resonance Energy Transfer Microscopy (FRET)
    品牌
    SensoLyte®
    产品特性
    The SensoLyte® 490 HIV Protease Assay Kit uses an optimized FRET peptide substrate for a continuous measurement of HIV protease activities. This FRET-based fluorogenic substrate is derived from a natural processing site for HIV-1 PR. Incubation of the recombinant HIV-1 PR with this substrate results in specific cleavage and a time-dependent increase in fluorescence intensity that is linearly related to the extent of substrate hydrolysis. Because of its simplicity and precision in the determination of reaction rates required for kinetic analysis, this kit offers many advantages over the commonly used HPLC or electrophoresis-based assays for peptide substrate hydrolysis by retroviral PRs.
  • 说明

    FRET-based Assay Kit

    限制
    仅限研究用
  • 注意事项
    Protect Components A and B from light.
    储存条件
    -20 °C
  • Hallengärd, Haller, Petersson, Boberg, Maltais, Isaguliants, Wahren, Bråve: "Increased expression and immunogenicity of HIV-1 protease following inactivation of the enzymatic activity." in: Vaccine, Vol. 29, Issue 4, pp. 839-48, (2011) (PubMed).

    Frick, Ginzburg, Lam: "A method to simultaneously monitor hepatitis C virus NS3 helicase and protease activities." in: Methods in molecular biology (Clifton, N.J.), Vol. 587, pp. 223-33, (2010) (PubMed).

    Yu, Kabashima, Tang, Shibata, Kitazato, Kobayashi, Lee, Kai: "Selective and facile assay of human immunodeficiency virus protease activity by a novel fluorogenic reaction." in: Analytical biochemistry, Vol. 397, Issue 2, pp. 197-201, (2010) (PubMed).

  • 抗原
    HIV (Human Immunodeficiency Virus (HIV))
    Abstract
    HIV 产品
    物质类
    Virus, Virus
    背景
    HIV protease (PR) is identified as an important drug-screening target for the design of selective acquired immunodeficiency syndrome (AIDS) therapeutics.
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