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Invivo anti-Mouse CD45.2 Recombinant mAb

Ly-5.2,LCA

价格 700.00 供应商现货 : 3-5个工作日
货号 S0B7073
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD45.2
  • 分子别名

    Ly-5.2; LCA
  • 细胞定位

    Cell membrane
  • Accession

    P06800
  • 克隆号

    104.2
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    Mouse IgG2a, κ
  • 同型对照

    Invivo mouse IgG2a isotype control
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse splenocytes
  • 纯化方式

    Protein A
  • 浓度

    5 mg/ml
  • 纯度

    >95%(Determined by SDS-PAGE)
  • 内毒素含量

    <1EU/mg
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS pH7.4, containing no preservative

  • 储存条件

    2 to 8 °C for 2 weeks under sterile conditions;
    -20 °C for 3 months under sterile conditions;
    -80 °C for 24 months under sterile conditions.
    Please avoid repeated freeze-thaw cycles.

  • 应用

    in vivo blocking

    in vitro blocking

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 1:250 Ms
背景介绍
  • The CD45.2 protein is a receptor-type protein tyrosine phosphatase predominantly expressed on the surface of all nucleated hematopoietic cells in mice. It serves as a key genetic marker for distinguishing hematopoietic cell subsets in mice. As a common isoform of the CD45 antigen, CD45.2 participates in the transduction of T-cell and B-cell receptor signals by regulating the activity of Src family kinases. It plays a critical role in lymphocyte development, activation, and the establishment of immune tolerance. The allelic variation of its encoding gene, Ptprc, determines the difference between CD45.1 and CD45.2. This distinction is widely utilized in experimental research, such as hematopoietic stem cell transplantation and immune cell lineage tracing, making it a classic molecular marker for the identification of mouse models in immunological studies.

  • 流式分析

    • Flow cytometric analysis of C57BL/6 mouse splenocytes labelling mouse CD45.2 antibody at 1/250 dilution (2 μg) / (right panel) compared with a Mouse IgG2a, κ Isotype Control / (left panel). Goat Anti-Mouse IgG Alexa Fluor® 488 was used as the secondary antibody. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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