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HIV-1 p66 pol

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  • $50 - 1800
  • prospecbio
  • HIV-127
  • 以色列
  • 2025年07月12日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      大量

    • 英文名

      HIV-1 p66 pol Recombinant

    • 保质期

      1年

    • 供应商

      上海沪震实业有限公司

    • 保存条件

      -20°C

    • 规格

      2μg/10μg/100μg

    HIV-1 p66 pol

    CATALOGUE NUMBER

    HIV-127

    INTRODUCTION

    Human immunodeficiency virus (HIV) is a retrovirusthat can lead to a condition in which the immune systembegins to fail, leading to opportunistic infections. HIV primarily infects vital cells in the humanimmune systemsuch as helper T cells(specifically CD4+ T cells), macrophagesand dendritic cells. HIV infection leads to low levels of CD4+ T cells through three main mechanisms: firstly, direct viral killing of infected cells; secondly, increased rates of apoptosisin infected cells; and thirdly, killing of infected CD4+ T cells by CD8 cytotoxic lymphocytesthat recognize infected cells. When CD4+ T cell numbers decline below a critical level, cell-mediated immunityis lost, and the body becomes progressively more susceptible to opportunistic infections. HIV was classified as a member of the genus Lentivirus, part of the family of Retroviridae. Lentiviruses have many common morphologies and biological properties. Many species are infected by lentiviruses, which are characteristically responsible for long-duration illnesses with a long incubation period. Lentiviruses are transmitted as single-stranded, positive-sense, enveloped RNA viruses. Upon entry of the target cell, the viral RNA genomeis converted to double-stranded DNAby a virally encoded reverse transcriptasethat is present in the virus particle. This viral DNA is then integrated into the cellular DNA by a virally encoded integraseso that the genome can be transcribed. Once the virus has infected the cell, two pathways are possible: either the virus becomes latentand the infected cell continues to function, or the virus becomes active and replicates, and a large number of virus particles are liberated that can then infect other cells.

    DESCRIPTION

    HIV-1 p66 Recombinant- is a 71kDa protein derived from pol gene. The HIV-1 p66 is glycosylated with N-linked sugars and produced using baculovirus vectors in insect cells.

    SOURCE

    Baculovirus Insect Cells.

    PHYSICAL APPEARANCE

    Sterile filtered colorless clear solution.

    FORMULATION

    The protein solution contains 30mM Tris pH-7, 0.15M NaCl and 0.2mM EDTA.

    PURITY

    Greater than 90.0% as determined by HPLC analysis & SDS-PAGE.

    STABILITY

    Recombinant HIV-1 p66 although stable at 4°C for 3 weeks, should be stored below -18°C. 
    For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). 
    Please avoid freeze-thaw cycles.

    APPLICATIONS

    HIV-1 p66 pol antigen is suitable for ELISA and Western blots, excellent antigen for early detection of HIV seroconvertors with minimal specificity problems.

    USAGE

    ProSpec's products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.

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    图标文献和实验
    相关实验
    • Effective Pol III-Expressed Long Hairpin RNAs Targeted to Multiple Unique Sites of HIV-1

      mutable viruses such as HIV-1. A combinatorial approach is therefore required for long-term inhibition of gene expression. RNA Pol III-driven long hairpin RNA (lhRNA) duplexes can be cleaved several times by Dicer, yielding multiple functional siRNAs

    • HIV测定结果的判定方法

      以上阴性对照的OD值>0.1,应重复实验。)。样品OD值<临界值者为HIV抗体阴性。 (4)、正常情况下,阳性对照孔的OD值≥0.80(若1孔阳性对照的OD值<0.8应舍弃,若有2孔或2孔以上阳性对照的OD值<0.8,应重复实验。样品OD值≥临界值者为HIV抗体阳性。 3、HIV测定(蛋白印迹法)结果的判定方法 根据卫生部1990(2)号文件的规定,蛋白印迹法的判断标准为: (1)、阳性:至少有一条env(gp160,gp120,gp41)带和一条pol(p65,p51,p32)带

    • Assays for the Evaluation of HIV-1 Integrase Inhibitors

      into the nucleus and integrated in the host chromosome. The only viral enzyme required for HIV-1 integration is integrase (IN), a protein of 32 kDa encoded by the 3′-end of the pol gene. The enzyme is produced by protease-mediated cleavage of the gag-pol precursor

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