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Alexa Fluor® 488 Mouse Anti-Human CD127 Antibody (S-R462)

Interleukin-7 receptor subunit alpha,IL-7 receptor subunit alpha,IL-7R subunit alpha,IL-7R-alpha,IL-7RA,CDw127,IL7R

价格 1,293.00 供应商现货 : 3-5个工作日
货号 S0B5689
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产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD127
  • 分子别名

    Interleukin-7 receptor subunit alpha; IL-7 receptor subunit alpha; IL-7R subunit alpha; IL-7R-alpha; IL-7RA; CDw127; IL7R
  • 细胞定位

    Cell membrane
  • Accession

    P16871
  • 克隆号

    S-R462
  • 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 lymphocytes
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    Alexa Fluor® 488
  • 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
  • CD127, also known as the interleukin-7 receptor alpha (IL7R-α), is a type I cytokine receptor encoded by the IL7R gene in humans. It is a subunit of the functional interleukin-7 receptor and thymic stromal lymphopoietin (TSLP) receptors. CD127 is expressed on the surface of hematopoietic cells, particularly lymphoid lineage cells, and plays a crucial role in the development, survival, and function of T cells. It is involved in signaling pathways that promote cell survival and proliferation through the activation of JAK1, JAK3, STAT5, and the PI3K-AKT pathway. Additionally, CD127 exists in both membrane-bound and soluble forms, with the soluble form (sCD127) potentially having antagonistic or agonistic effects on IL-7 activity depending on the context.

  • 流式分析

    • Flow cytometric analysis of Human CD127 expression on human peripheral blood lymphocytes. Human peripheral blood lymphocytes were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 antibody and either Alexa Fluor®488 Mouse IgG1, κ Isotype Control (Left panel) or SDT Alexa Fluor®488 Mouse Anti-Human CD127 antibody (Right panel) at 5 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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