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Alexa Fluor® 647 Rat Anti-Mouse CD274/B7-H1/PD-L1 Antibody (S-R072)

Alexa Fluor® 647 Rat Anti-Mouse CD274/B7-H1/PD-L1 Antibody (S-R072)

货号: S0B5429
价格: 1000
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD274/B7-H1/PD-L1
  • 分子别名

    Programmed cell death 1 ligand 1; PD-L1; PDCD1 ligand 1; Programmed death ligand 1; B7 homolog 1 (B7-H1); B7h1; Pdcd1l1; Pdcd1lg1; Pdl1
  • 细胞定位

    Endosome, Cell membrane
  • Accession

    Q9EP73
  • 克隆号

    S-R072
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2b
  • 应用

    FCM
  • 反应种属 ?

    Ms
  • 阳性样本

    BALB/c mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    50 μg/ml
  • 标记

    Alexa Fluor® 647
  • 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 Ms
背景介绍
  • PD-L1, also known as CD274 or B7-H1, is a type I transmembrane glycoprotein and a member of the B7 family. It was first identified in 1999. PD-L1 plays a crucial role in immune regulation by binding to PD-1 on T cells, inhibiting their activation and proliferation through multiple pathways, thus dampening tumor-reactive T cell responses. This protein is widely expressed in various cells, including antigen-presenting cells, activated T cells, B cells, and some non-hematopoietic cells. Its expression is often upregulated in tumor cells, contributing to immune evasion. Targeting PD-L1 has become a major strategy in cancer immunotherapy, with several antibodies developed to block its interaction with PD-1, enhancing anti-tumor immunity.

  • 流式分析

    • Flow cytometric analysis of Mouse CD274/B7-H1/PD-L1 expression on BALB/c mouse splenocytes. BALB/c mouse splenocytes were stained with either Alexa Fluor® 647 Rat IgG2b, κ Isotype Control (Black line histogram) or SDT Alexa Fluor® 647 Rat Anti-Mouse CD274/B7-H1/PD-L1 Antibody (Red line histogram) at 5 μl/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.