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Pacific Blue Mouse Anti-Rat CD4 Antibody (S-R631)

Pacific Blue Mouse Anti-Rat CD4 Antibody (S-R631)

货号: S0B5127
价格: 450
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD4
  • 分子别名

    T-cell surface glycoprotein CD4; T-cell surface antigen T4/Leu-3; W3/25 antigen
  • 细胞定位

    Cell membrane
  • Accession

    P05540
  • 克隆号

    S-R631
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 应用

    FCM
  • 反应种属 ?

    Rt
  • 阳性样本

    Lewis Rat splenocytes
  • 纯化方式

    Protein G
  • 浓度

    50 μg/ml
  • 标记

    Pacific Blue
  • 性状

    Liquid
  • 缓冲体系

    PBS, 25% Glycerol, 1% BSA, 0.3% 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 推荐种属
FCM 5μl per million cells in 100μl volume Rt
背景介绍
  • CD4, also known as cluster of differentiation 4, is a glycoprotein expressed on the surface of certain immune cells, particularly helper T cells. It plays a crucial role in the immune system by acting as a co-receptor with the T cell receptor (TCR) to bind to major histocompatibility complex class II (MHC II) molecules on antigen-presenting cells, facilitating the activation and differentiation of T cells. CD4+ T cells, often referred to as helper T cells, are essential for coordinating immune responses. They secrete various cytokines to activate other immune cells like B cells, macrophages, and cytotoxic T cells, and can differentiate into subtypes such as Th1, Th2, Th17, and regulatory T cells, each with specific functions. Additionally, CD4 is significant in medical contexts like HIV infection, where the virus targets CD4+ T cells, leading to a decline in their numbers and compromising immune function.

  • 流式分析

    • Flow cytometric analysis of Rat CD4 expression on Lewis Rat splenocytes. Lewis Rat splenocytes were stained with Brilliant Violet 605™ Mouse Anti-Rat CD3 Antibody and either Pacific Blue Mouse IgG1, κ Isotype Control (Left panel) or SDT Pacific Blue Mouse Anti-Rat CD4 Antibody (Right panel) at 5μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.