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PE Rat Anti-Mouse CD5 Antibody (53-7.3)

T-cell surface glycoprotein CD5,Lymphocyte antigen 1 (Ly-1,Lyt-1),Ly-1,Cd5

价格 300.00 供应商现货 : 3-5个工作日
货号 S0B8160
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD5
  • 分子别名

    T-cell surface glycoprotein CD5; Lymphocyte antigen 1 (Ly-1; Lyt-1); Ly-1; Cd5
  • 细胞定位

    Cell membrane
  • Accession

    P13379
  • 克隆号

    53-7.3
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2a,k
  • 反应种属 ?

    Ms
  • 阳性样本

    BALB/c mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    PE
  • 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 Ms
背景介绍
  • CD5, also known as T-cell surface glycoprotein CD5 or Leu-1, is a type I transmembrane glycoprotein expressed on the surface of T cells, thymocytes, and a subset of B cells called B-1a cells. It belongs to the scavenger receptor superfamily and has a molecular mass of approximately 67 kDa. CD5 plays a crucial role in modulating immune responses by regulating the activation of T cells and B cells. In T cells, CD5 expression is upregulated upon activation and helps to fine-tune T cell receptor (TCR) signaling, promoting cell survival and non-responsiveness. In B cells, particularly B-1a cells, CD5 helps to prevent overactivation by dampening signals from the B cell receptor (BCR), ensuring that these cells only respond to strong stimuli. The exact ligand for CD5 remains unclear, but it is suggested that it may interact homophilically or with CD72 on B cells.

  • 流式分析

    • Flow cytometric analysis of Mouse CD5 expression on BALB/c mouse splenocytes. BALB/c mouse splenocytes were stained with Brilliant Violet 421™ Rat Anti-Mouse CD3 Antibody and either PE Rat IgG2a, κ Isotype Control (Left panel) or PE Rat Anti-Mouse CD5 Antibody (Right panel) at 5 μl/test. 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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