产品中心 流式试剂&相关 流式抗体

所有图片(1/1)

Alexa Fluor® 647 Mouse Anti-Human CD28 Antibody (S-714-76)

T-cell-specific surface glycoprotein CD28,TP44

价格 1,350.00 供应商现货 : 3-5个工作日
货号 S0B1528
规格
数量
收藏 分享

产品介绍 评论(0)

产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD28
  • 分子别名

    T-cell-specific surface glycoprotein CD28, TP44
  • 免疫原

    Recombinant Protein
  • 细胞定位

    Cell membrane
  • Accession

    P10747
  • 克隆号

    S-714-76
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 反应种属 ?

    Hu
  • 纯化方式

    Protein G
  • 浓度

    0.2mg/ml
  • 标记

    Alexa Fluor® 647
  • 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
    FCM 5 μl per million cells in 100μl volume
背景介绍
  • CD28 (Cluster of Differentiation 28) is one of the proteins expressed on T cells that provide co-stimulatory signals required for T cell activation and survival. T cell stimulation through CD28 in addition to the T-cell receptor (TCR) can provide a potent signal for the production of various interleukins (IL-6 in particular). CD28 is the receptor for CD80 (B7.1) and CD86 (B7.2) proteins. When activated by Toll-like receptor ligands, the CD80 expression is upregulated in antigen-presenting cells (APCs). The CD86 expression on antigen-presenting cells is constitutive (expression is independent of environmental factors). It is generally reported, that CD28 is expressed on 50% of CD8+ T cells and more than 80% CD4+ T cells in human, but during the course of activation some T cells lose this molecule. In general, CD28 is a primary costimulatory molecule for T cell activation.

  • 流式分析

    • Flow cytometric analysis of Human CD28 expression on human PBMC (human peripheral blood mononuclear cell). Human PBMC were stained with Alexa Fluor® 488 Mouse Anti-Human CD3 antibody and either Alexa Fluor® 647 Mouse IgG1, κ Isotype Control (Left panel) or SDT Alexa Fluor® 647 Mouse Anti-Human CD28 Antibody (Right panel) at 1 μg/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

评论(0)