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FITC Mouse Anti-Rat CD45 Antibody (OX-1)

Receptor-type tyrosine-protein phosphatase C,Leukocyte common antigen (L-CA),T200,Ptprc

价格 300.00 供应商现货 : 3-5个工作日
货号 S0B5058
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产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    Rat CD45
  • 分子别名

    Receptor-type tyrosine-protein phosphatase C; Leukocyte common antigen (L-CA); T200; Ptprc
  • 细胞定位

    Cell membrane
  • Accession

    P04157
  • 克隆号

    OX-1
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 反应种属 ?

    Rt
  • 阳性样本

    Lewis Rat splenocytes
  • 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 1.25μl per million cells in 100μl volume Rt
背景介绍
  • CD45, also known as protein tyrosine phosphatase receptor type C (PTPRC) or leukocyte common antigen, is a transmembrane glycoprotein expressed on nearly all hematopoietic cells and plays a crucial role in the regulation of T and B cell antigen receptor-mediated activation. It is a type 1 transmembrane protein tyrosine phosphatase (PTPase) that is involved in the activation, development, tolerance, and survival of T and B-lymphocytes. CD45 is essential for the initiation of T cell receptor (TCR) signaling and modulates cytokine and chemokine production and signaling. It also negatively regulates monocytic cell differentiation and FLT3 signaling in vivo. The protein is involved in the nuclear apoptosis process and is vital for chromatin condensation and DNA fragmentation. Furthermore, CD45 is implicated in the interaction between T cells and macrophages and has been studied as a therapeutic target for immune diseases, including autoimmunity and organ transplantation. Disruption of the equilibrium between protein tyrosine kinase and phosphatase activity, which includes CD45, can result in immunodeficiency, autoimmunity, or malignancy.

  • 流式分析

    • Flow cytometric analysis of Rat CD45 expression on Lewis Rat splenocytes. Lewis Rat splenocytes were stained with FITC Mouse IgG1, κ Isotype Control (Black line histogram) and SDT FITC Mouse Anti-Rat CD45 Antibody (Red line histogram) at 1.25μl/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.

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