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PE-Cy7 Mouse Anti-Human CD8 Antibody (S-1036-34)

T-cell surface glycoprotein CD8 alpha chain,T-lymphocyte differentiation antigen T8/Leu-2,MAL,CD8A

价格 918.00 1-2周
货号 S0B8170
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产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD8α
  • 分子别名

    T-cell surface glycoprotein CD8 alpha chain; T-lymphocyte differentiation antigen T8/Leu-2; MAL; CD8A
  • 免疫原

    Recombinant Protein
  • 细胞定位

    Cell membrane
  • Accession

    P01732
  • 克隆号

    S-1036-34
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 反应种属 ?

    Hu
  • 阳性样本

    Human peripheral blood leukocytes
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    PE-Cy7
  • 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 5μl per million cells in 100μl volume Hu
背景介绍
  • CD8α is a crucial immune glycoprotein that plays a vital role in the immune response by serving as a co-receptor for the T-cell receptor (TCR) on cytotoxic T cells. It forms either a homodimer (α/α) or a heterodimer with CD8β (α/β) to interact with MHC class I molecules on antigen-presenting cells (APCs), facilitating the recognition of intracellular pathogens such as viruses. CD8α also recruits the LCK kinase, which initiates downstream signaling pathways essential for T-cell activation and proliferation. This molecule is critical for the function of cytotoxic T lymphocytes (CTLs) and is involved in various immune-related diseases, including immunodeficiencies and autoimmune conditions.

  • 流式分析

    • flow cytometric analysis of Human CD8α expression on human peripheral blood leukocytes. Human peripheral blood leukocytes were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 antibody and either PE-Cy7 Mouse IgG1, κ Isotype Control (Left panel) or SDT PE-Cy7 Mouse Anti-Human CD8α Antibody (Right panel) at 5 μl/test treated with True-Stain Monocyte Blocker™. Total viable cells, as determined by Fixable Viability Dye 515 (S0D0013), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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