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Alexa Fluor® 647 anti-human CD

152 (CTLA-4)
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  • ¥2747.80
  • BioLegend
  • 349920
  • 美国
  • 2025年12月21日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体名

      Alexa Fluor® 647 anti-human CD152 (CTLA-4)

    • 抗体英文名

      Alexa Fluor® 647 anti-human CD152 (CTLA-4)

    • 供应商

      上海善然生物科技有限公司

    • 库存

      现货

    • 保存条件

      冷藏

    • 规格

      100tests

    Clone

    L3D10

    Regulatory Status RUO

    Other Names Cytotoxic T-Lymphocyte Antigen 4

    Isotype Mouse IgG1, κ

    Description CD152, also known as Cytotoxic T-Lymphocyte Antigen 4 (CTLA-4), is a 33 kD member of the

    immunoglobulin superfamily. It is transiently expressed on activated T cells. CTLA4 is

    expressed on the surface of helper T cells and transmits an inhibitory signal to T cells.

    Regulatory T cells express high levels of CTLA-4. CTLA-4 (CD152) is similar to CD28 in amino

    acid sequence, structure, and genomic organization. Whereas CD28 delivers a costimulatory

    signal in T cell activation, CTLA-4 negatively regulates cell-mediated immune responses

    through interaction with CD80 (B7-1) and CD86 (B7-2) present on antigen presenting cells

    (APC). CTLA-4 is thought to play a role in the induction and maintenance of immunological

    tolerance as well as the development of protective immunity and thymocyte regulation.

    Mutations in the CTLA-4 gene have been associated with various autoimmune diseases, such

    as systemic lupus erythematosus, insulin-dependent diabetes mellitus, and other autoimmune

    diseases. A transcript of the CTLA-4 gene that may represent a native soluble form of CTLA-4

    (sCTLA-4) showed that eleven of twenty patients with autoimmune thyroid disease (ATD) had

    a high concentration of sCTLA-4, whereas only 1 of 30 apparently healthy volunteers

    contained measurable levels. sCTLA-4 immunoreactivity was inhibited by its binding to B7.1,

    suggesting that sCTLA-4 is a functional receptor. sCTLA4 also plays a role in the initial

    immune response to infection of immune cells by HIV, along with the CD-1 pathway and

    others.

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