您现在的位置: 首页   -  产品中心   -  免疫学   -   抗体
Alexa Fluor® 647 Mouse Anti-Mouse CD244.2 Antibody (S-R736)

Alexa Fluor® 647 Mouse Anti-Mouse CD244.2 Antibody (S-R736)

货号: S0B5283
价格: 300
规格: 20T
介绍: -
其他: -
产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    CD244.2
  • 分子别名

    Natural killer cell receptor 2B4; NK cell type I receptor protein 2B4 (NKR2B4); Non-MHC restricted killing associated; SLAM family member 4 (SLAMF4); Signaling lymphocytic activation molecule 4; 2b4; Nmrk; Cd244
  • 细胞定位

    Cell membrane
  • Accession

    Q07763
  • 克隆号

    S-R736
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,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

    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
  • CD244.2 protein, also known as natural killer cell receptor 2B4 isoform 2 precursor, is a type-I transmembrane protein belonging to the signaling lymphocytic activation molecule (SLAM) family. It is encoded by the CD244 gene and primarily expressed in various immune cells such as NK cells, T cells, monocytes, eosinophils, myeloid-derived suppressor cells, and dendritic cells. This protein mainly binds to its ligand CD48, another SLAM family member, to transmit stimulatory or inhibitory signals and regulate immune responses, including NK cell-mediated cytotoxicity, leukocyte activation, and cytokine production. CD244.2 plays a crucial role in the immune system and has potential as a therapeutic target in cancer and other immune-related diseases.

  • 流式分析

    • Flow cytometric analysis of Mouse CD244.2 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with FITC Rat Anti-Mouse CD49b Antibody and either Mouse IgG1, κ Isotype Control (Left panel) or SDT Alexa Fluor® 647 Mouse Anti-Mouse CD244.2 Antibody (Right panel) at 5 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.