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PE-Cy7 Rat Anti-Mouse CD4 Antibody (S-R382)

PE-Cy7 Rat Anti-Mouse CD4 Antibody (S-R382)

货号: S0B5517
价格: 600
规格: 25T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD4
  • 分子别名

    T-cell surface glycoprotein CD4; T-cell differentiation antigen L3T4; T-cell surface antigen T4/Leu-3
  • 细胞定位

    Cell membrane
  • Accession

    P06332
  • 克隆号

    S-R382
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2b,k
  • 应用

    FCM
  • 反应种属 ?

    Ms
  • 阳性样本

    BALB/c mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    0.2mg/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
稀释度
应用 稀释度 推荐种属
FCM 1.25μl per million cells in 100μl volume Ms
背景介绍
  • CD4 is a glycoprotein that functions as a co-receptor for the T-cell receptor (TCR) and is primarily expressed on the surface of helper T cells, monocytes, macrophages, and dendritic cells. It is a member of the immunoglobulin superfamily, consisting of four immunoglobulin domains (D1 to D4) that interact with MHC class II molecules on antigen-presenting cells. This interaction, mediated by the D1 domain of CD4, ensures that T cells recognize antigens presented by MHC II. The cytoplasmic tail of CD4 contains motifs that recruit the tyrosine kinase Lck, which amplifies T cell activation signals. Additionally, CD4 is crucial in the immune response, as it helps activate CD4+ T helper cells, which in turn stimulate other immune cells to combat infections. However, CD4 is also the primary receptor for HIV, allowing the virus to enter host T cells and cause immunodeficiency.

  • 流式分析

    • Flow cytometric analysis of Mouse CD4 expression on BALB/c mouse splenocytes. BALB/c mouse splenocytes were stained with Brilliant Violet 421™ Rat Anti-Mouse CD3 Antibody and either PE-Cy7 Rat IgG2b, κ Isotype Control (Left panel) or SDT Percp-Cy5.5 Rat Anti-Mouse CD4 Antibody (Right panel) at 1.25 μl/test treated with True-Stain Monocyte Blocker™. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.