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FITC Mouse Anti-Human CD154 Antibody (S-R579)

CD40 ligand,CD40-L,T-cell antigen Gp39,TNF-related activation protein (TRAP),Tumor necrosis factor ligand superfamily member 5,CD40L,TNFSF5,TRAP,CD40LG

价格 840.00 供应商现货 : 3-5个工作日
货号 S0B8327
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产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD154
  • 分子别名

    CD40 ligand; CD40-L; T-cell antigen Gp39; TNF-related activation protein (TRAP); Tumor necrosis factor ligand superfamily member 5; CD40L; TNFSF5; TRAP; CD40LG
  • 细胞定位

    Cell membrane
  • Accession

    P29965
  • 克隆号

    S-R579
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 反应种属 ?

    Hu
  • 阳性样本

    PMA and Ionomycin treated human PBMC
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    FITC
  • 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 Hu
背景介绍
  • CD154, also known as CD40 ligand (CD40L) or gp39, is a type II transmembrane protein belonging to the tumor necrosis factor (TNF) superfamily. It is primarily expressed on activated CD4+ T cells and can also be found on other immune cells such as CD8+ T cells, natural killer cells, platelets, dendritic cells, and endothelial cells. CD154 can form a trimeric structure and is crucial for humoral and cellular immunity. Its interaction with CD40, its classical receptor, is essential for B cell activation, proliferation, isotype switching, and germinal center formation. This interaction also plays a significant role in T cell priming and cell-mediated immune responses. In addition to CD40, CD154 can bind to several integrins, including αIIbβ3, α5β1, and αMβ2, which are involved in various inflammatory and immune processes. Abnormal expression of CD154 has been implicated in several autoimmune diseases, such as systemic lupus erythematosus (SLE), where it contributes to the overproduction of autoantibodies and inflammation.

  • 流式分析

    • Human PBMC (human peripheral blood mononuclear cells) treated 6 hours with 50 ng/ml PMA and 500 ng/ml Ionomycin was stained with PE Mouse Anti-Human CD8a and either FITC Mouse IgG1, κ Isotype Control (Left panel) or SDT FITC Mouse Anti-Human CD154 Antibody (Right panel) at 5 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software

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