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PE Mouse Anti-Human CD3 Antibody (OKT3)

PE Mouse Anti-Human CD3 Antibody (OKT3)

货号: S0B0180
价格: 845
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD3
  • 分子别名

    T-cell surface antigen T3/Leu-4 epsilon chain, CD3e, T3E
  • 细胞定位

    Cell membrane
  • Accession

    P07766
  • 克隆号

    OKT3
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG2a,k
  • 应用

    FCM
  • 反应种属 ?

    Hu
  • 纯化方式

    Protein G
  • 浓度

    20μg/ml
  • 标记

    PE
  • 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 5 μl per million cells in 100μl volume
背景介绍
  • CD3 (cluster of differentiation 3) is a protein complex and T cell co-receptor that is involved in activating both the cytotoxic T cell (CD8+ naive T cells) and T helper cells (CD4+ naive T cells). It is composed of four distinct chains. In mammals, the complex contains a CD3γ chain, a CD3δ chain, and two CD3ε chains. These chains associate with the T-cell receptor (TCR) and the CD3-zeta (ζ-chain) to generate an activation signal in T lymphocytes. The TCR, CD3-zeta, and the other CD3 molecules together constitute the TCR complex. The CD3–T cell receptor (TCR) complex plays a central role in the T-cell-mediated immunoresponse as it is involved in the recognition of antigens and subsequent signal transduction and activation of immunocompetent T lymphocytes. Because CD3 is required for T cell activation, drugs (often monoclonal antibodies) that target it are being investigated as immunosuppressant therapies (e.g., otelixizumab, teplizumab) for type 1 diabetes and other autoimmune diseases.

  • 流式分析

    • Flow cytometric analysis of CD3 expression on Jurkat. Cells from the Jurkat (Human T cell leukemia T lymphocyte, Right) or Ramos (Human Burkitt's lymphoma B lymphocyte, Left) was stained with Phycoerythrin Mouse IgG2a, κ Isotype Control (Black line histogram) and SDT PE Mouse Anti-Human CD3 antibody (Red line histogram) at 0.1 μg/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