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PE-Cy7 Mouse Anti-Human CD80 Antibody (S-3119)

T-lymphocyte activation antigen CD80,Activation B7-1 antigen,BB1,CTLA-4 counter-receptor B7.1 (B7),CD28LG,CD28LG1,LAB7

价格 900.00 供应商现货 : 3-5个工作日
货号 S0B8720
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产品规格
  • 宿主来源

    Mouse
  • 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); CD28LG; CD28LG1; LAB7
  • 细胞定位

    Cell membrane
  • Accession

    P33681
  • 克隆号

    S-3119
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 反应种属 ?

    Hu
  • 阳性样本

    Raji
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    PE-Cy7
  • 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
  • CD80, also known as B7-1, is a co-stimulatory molecule expressed on antigen-presenting cells (APCs) such as dendritic cells, macrophages, and B cells. It plays a crucial role in the immune response by interacting with CD28 on T cells to provide a necessary co-stimulatory signal for T cell activation. Additionally, CD80 can bind to CTLA-4, an inhibitory receptor on T cells, which serves as a negative regulatory mechanism to control the extent of the immune response. This dual functionality highlights the importance of CD80 in both initiating and modulating immune reactions, making it a key target in immunotherapy research for conditions such as cancer and autoimmune diseases.

  • 流式分析

    • Flow cytometric analysis of Human CD80 expression on Raji cells. Cells from the Raji (Human Burkitt's lymphoma B lymphocyte, right) or 293T (Human embryonic kidney epithelial cell, left) was stained with either PE/Cy7 Mouse IgG1, κ Isotype Control (black line histogram) or SDT PE/Cy7 Mouse Anti-Human CD80 antibody (red line histogram) at 5μl/test treated with True-Stain Monocyte Blocker™, cells without incubation with primary antibody and secondary antibody (blue line histogram) was used as unlabeled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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