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FITC 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

货号: S0B1645

Datasheet COA
  • 价格: ¥650
  • 规格:
  • 数量:
斯达特大包装询价 大包装询价

产品介绍 评论(0)

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
  • 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
  • 应用

    FCM
  • 反应种属 ?

    Hu
  • 阳性样本

    Human PBMC
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    FITC
  • 性状

    Liquid
  • 缓冲体系

    PBS, 25% Glycerol, 1% BSA, 0.3% Proclin 300
  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied.
稀释度
应用 稀释度 推荐种属
FCM 5 μl per million cells in 100μl volume Hu
背景介绍
  • CD127, also known as the interleukin-7 receptor alpha chain (IL-7Rα) or simply the IL-7 receptor, is a transmembrane glycoprotein primarily expressed on the surface of T cells, B cells, natural killer (NK) cells, as well as certain hematopoietic stem cells and progenitor cells. Upon binding to IL-7, CD127 activates a series of signaling pathways, including the JAK-STAT cascade, which subsequently promotes the growth and differentiation of lymphocytes. This interaction is particularly crucial during the development of T and B cells within the thymus and bone marrow, as it aids in their progression from early progenitor stages to maturity. Furthermore, the expression level of CD127 serves as an indicator for assessing lymphocyte function and status.

  • 流式分析

    • Multiparameter flow cytometric analysis of Human CD127 expression on human peripheral blood mononuclear cell populations. Human peripheral blood mononuclear cells were stained with Brilliant Violet 421™ Mouse Anti-Human CD3 antibody and either FITC Mouse IgG1, κ Isotype Control (Left panel) or SDT FITC Mouse Anti-Human CD127 antibody (Right panel) at 1 μg/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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