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Alexa Fluor® 647 Rat Anti-Mouse CD226 Antibody (S-R625)

Alexa Fluor® 647 Rat Anti-Mouse CD226 Antibody (S-R625)

货号: S0B5017
价格: 2800
规格: 100T
介绍: -
其他: -
产品规格
  • 宿主来源

    Rat
  • 抗原名称

    Mouse CD226
  • 分子别名

    CD226 antigen; Platelet and T-cell activation antigen 1; Pta1
  • 细胞定位

    Cell membrane
  • Accession

    Q8K4F0
  • 克隆号

    S-R625
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG2b,k
  • 应用

    FCM
  • 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

    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
  • CD226 (also known as DNAM-1) is a member of the immunoglobulin superfamily and is expressed on the surface of T cells, natural killer (NK) cells, monocytes, and macrophages. It enhances the activation, proliferation, and cytotoxic functions of T cells and NK cells by binding to its ligands CD155 and CD112 and activating downstream signaling pathways such as PI3K-AKT and VAV-1-ERK. CD226 plays a crucial role in anti-tumor immunity, with its high expression associated with better responses to immune checkpoint blockade therapies. However, its function can be inhibited by TIGIT, which competes with CD226 for binding to CD155, thereby dampening immune activation. CD226 is also involved in regulating the function of regulatory T cells (Tregs), and its absence in Tregs can exacerbate inflammatory diseases. Thus, CD226 holds potential not only in cancer immunotherapy but also in the study of autoimmune diseases.

  • 流式分析

    • Flow cytometric analysis of Mouse CD226 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with FITC Rat Anti-Mouse CD8α Antibody (S0B1534) at 5μl/test and either Alexa Fluor® 647 Rat IgG2b, κ Isotype Control (Left panel) or SDT Alexa Fluor® 647 Rat Anti-Mouse CD226 Antibody (Right panel) at 5μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.