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PE Rabbit Anti-Human CD80 Antibody (S-288-177)

PE Rabbit Anti-Human CD80 Antibody (S-288-177)

货号: S0B1540
价格: 845
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    CD80
  • 分子别名

    T-lymphocyte activation antigen CD80, Activation B7-1 antigen, BB1, CTLA-4 counter-receptor B7.1 (B7)
  • 免疫原

    Recombinant Protein
  • 细胞定位

    Membrane
  • Accession

    P33681
  • 克隆号

    S-288-177
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 应用

    FCM
  • 反应种属 ?

    Hu
  • 纯化方式

    Protein A
  • 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
  • CD80 (B7-1) is a cell surface glycoprotein that belongs to the B7 family of immune regulatory molecules. It is primarily expressed on antigen-presenting cells, such as dendritic cells, macrophages, and activated B cells. CD80 functions as a costimulatory molecule that interacts with CD28 and CTLA-4 receptors expressed on T cells. This interaction plays a crucial role in the regulation of T cell activation and immune responses. Specifically, CD80 binding to CD28 on T cells provides a costimulatory signal that enhances T cell proliferation, cytokine production, and survival. This interaction promotes the development of effective immune responses against pathogens. However, CD80 also binds to CTLA-4, which has higher affinity for CD80 compared to CD28. The CD80-CTLA-4 interaction inhibits T cell activation and proliferation, thus preventing excessive or autoreactive immune responses.

  • 流式分析

    • Flow cytometric analysis of Human CD80 expression on Raji. Cells from the Raji (Human Burkitt's lymphoma B lymphocyte, Right) or 293T (Human embryonic kidney epithelial cell, Left) was stained with Phycoerythrin Rabbit IgG Isotype Control (Black line histogram) and SDT PE Rabbit Anti-Human CD80 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