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FITC Rat Anti-Mouse PD-1 (CD279) Antibody (S-R496)

Programmed cell death protein 1,Protein PD-1,mPD-1,CD279,Pd1,Pdcd1

价格 650.00 供应商现货 : 3-5个工作日
货号 S0B5648
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    PD-1 (CD279)
  • 分子别名

    Programmed cell death protein 1; Protein PD-1; mPD-1; CD279; Pd1; Pdcd1
  • 细胞定位

    Cell membrane
  • Accession

    Q02242
  • 克隆号

    S-R496
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2a
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse 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 5μl per million cells in 100μl volume Ms
背景介绍
  • Programmed cell death protein 1 (PD-1), also known as CD279, is a type I transmembrane protein and a member of the CD28 immunoglobulin superfamily, encoded by the _PDCD1_ gene. It is primarily expressed on the surface of various immune cells, including T cells, B cells, macrophages, dendritic cells, and natural killer cells. PD-1 plays a crucial role in regulating immune responses by binding to its ligands, PD-L1 (B7-H1) and PD-L2 (B7-DC), which are expressed on antigen-presenting cells and tumor cells. When PD-1 interacts with its ligands, it triggers inhibitory signals that downregulate T cell activity, preventing excessive immune responses and promoting self-tolerance. However, this pathway can also be exploited by cancer cells to evade immune surveillance, leading to tumor progression. As a result, PD-1 has become a key target in cancer immunotherapy, with several anti-PD-1 antibodies approved for treating various cancers, achieving significant and durable efficacy in some patients.

  • 流式分析

    • C57BL/6 mouse splenocytes treated overnight with 3 μg/ml Concanavalin A (Right panel) or untreated (Left panel) was stained with Brilliant Violet 421™ Rat Anti-Mouse CD3 and SDT FITC Rat Anti-Mouse PD-1 (CD279) Antibody at 5 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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