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FITC Rat anti-Mouse CD8α Antibody (2.43)

T-cell surface glycoprotein CD8 alpha chain,T-cell surface glycoprotein Lyt-2,Lyt-2,Lyt2

价格 380.00 供应商现货 : 3-5个工作日
货号 S0B5120
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Rat
  • 抗原名称

    mouse CD8α
  • 分子别名

    T-cell surface glycoprotein CD8 alpha chain; T-cell surface glycoprotein Lyt-2; Lyt-2; Lyt2
  • 细胞定位

    Cell membrane
  • Accession

    P01731
  • 克隆号

    2.43
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2b,k
  • 反应种属 ?

    Ms
  • 阳性样本

    BALB/c mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    0.1 mg/ml
  • 标记

    FITC
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.3% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied.

  • 应用

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 2μl per million cells in 100μl volume Ms
背景介绍
  • CD8A, also known as CD8 or T-cell surface glycoprotein CD8 alpha chain, is a crucial integral membrane glycoprotein predominantly found on cytotoxic T lymphocytes. It functions as a coreceptor, aiding the T-cell receptor (TCR) in recognizing antigens presented by antigen-presenting cells (APCs) in the context of MHC class I molecules. This interaction is vital for the activation of cytotoxic T-lymphocytes (CTLs), which can then identify and eliminate infected or tumor cells. CD8A can exist as a homodimer of two alpha chains or as a heterodimer with a beta chain, both forms sharing significant homology to immunoglobulin variable light chains. The protein is also involved in intracellular signaling pathways, leading to lymphokine production, motility, adhesion, and activation of CTLs. Additionally, CD8A has been implicated in various diseases and is classified as a disease-related gene.

  • 流式分析

    • Flow cytometric analysis of Mouse CD8α expression on BALB/c mouse splenocytes. BALB/c mouse splenocytes were stained with Brilliant Violet 421™ Rat Anti-Mouse CD3 Antibody and either FITC Rat IgG2b, κ Isotype Control (Left panel) or SDT FITC Rat anti-Mouse CD8α Antibody (Right panel) at 2μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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