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Alexa Fluor® 647 Mouse Anti-Human CD28 Antibody (15E8)

Alexa Fluor® 647 Mouse Anti-Human CD28 Antibody (15E8)

货号: S0B0122
价格: 650
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD28
  • 分子别名

    TP44
  • 细胞定位

    Membrane
  • Accession

    P10747
  • 克隆号

    15E8
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 应用

    FCM
  • 反应种属 ?

    Hu
  • 纯化方式

    Protein G
  • 浓度

    20μg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 0.1% BSA, 0.01% 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
FCM 5μl 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 Jurkat. Cells from the Jurkat (Human T cell leukemia T lymphocyte, Right) or THP-1 (Human monocytic leukemia monocyte, Left) was stained with Alexa Fluor® 647 Mouse IgG1, κ Isotype Control (Black line histogram) and SDT Alexa Fluor® 647 Mouse Anti-Human CD28 Antibody (15E8) (Red line histogram) at 5μl/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.
  • 实验方案