您现在的位置: 首页   -  产品中心   -  免疫学   -   抗体
Pacific Blue Rabbit Anti-Human CD4 Antibody (S-R163)

Pacific Blue Rabbit Anti-Human CD4 Antibody (S-R163)

货号: S0B5529
价格: 999
规格: 25T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    CD4
  • 分子别名

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

    Cell membrane, Endoplasmic reticulum
  • Accession

    P01730
  • 克隆号

    S-R163
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 应用

    FCM
  • 反应种属 ?

    Hu
  • 阳性样本

    human peripheral blood cells
  • 纯化方式

    Protein A
  • 浓度

    0.2 mg/ml
  • 标记

    Pacific Blue
  • 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, -20 °C as supplied

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
  • CD4 is a glycoprotein found on the surface of certain immune cells, such as helper T cells, monocytes, macrophages, and dendritic cells. It is a monomeric type I transmembrane molecule composed of four immunoglobulin-like domains (D1 to D4) and encoded by a single gene. As a co-receptor for the T-cell receptor (TCR), CD4 plays a crucial role in the immune response by binding to the MHC class II molecules on antigen-presenting cells, which helps T cells recognize and respond to foreign antigens. The interaction between CD4 and MHC class II molecules also activates downstream signaling pathways, leading to the activation of transcription factors and promoting T cell activation. Additionally, CD4 is significant in HIV infection, as the virus binds to CD4 to enter host cells.

  • 流式分析

    • Flow cytometric analysis of Human CD4 expression on human peripheral blood lymphocytes. Human peripheral blood lymphocytes were stained with Alexa Fluor® 647 Mouse Anti-Human CD3 antibody and either Pacific Blue™ Rabbit IgG Isotype Control (Left panel) or SDT Pacific Blue™ Rabbit Anti-Human CD4 Antibody (Right panel) at 5 μl/test. Fluorescent histograms were gated events with lymphocytes. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.