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Pacific Blue Mouse Anti-Human MICA Antibody (S-2794)

MHC class I polypeptide-related sequence A,MIC-A,PERB11.1

价格 600.00 1-2周
货号 S0B80690
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产品介绍 评论(0)

产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    MICA
  • 分子别名

    MHC class I polypeptide-related sequence A; MIC-A; PERB11.1
  • 细胞定位

    Cytoplasm, Cell membrane, Endoplasmic reticulum
  • Accession

    Q29983
  • 克隆号

    S-2794
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1,k
  • 同型对照

    S0B1542
  • 反应种属 ?

    Hu
  • 阳性样本

    HeLa
  • 纯化方式

    Protein G
  • 浓度

    0.2 mg/ml
  • 标记

    Pacific Blue
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.09% sodium azide

  • 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 Hu
背景介绍
  • MICA (MHC class I polypeptide-related sequence A) and MICB (MHC class I polypeptide-related sequence B) are stress-inducible proteins that belong to the MHC class I family but do not bind to β2-microglobulin or present peptides. They are encoded by genes located within the HLA class I region of chromosome 6. MICA and MICB are expressed on the cell membrane in response to cellular stress or cancer transformation. These proteins act as ligands for the NKG2D receptor, which is expressed on most natural killer (NK) cells, CD8 αβ T cells, and γδ T cells. The binding of MICA/B to NKG2D can activate these immune cells, leading to cytotoxic responses against stressed or transformed cells. MICA and MICB are highly polymorphic, with over 106 alleles reported for MICA and 25 for MICB. This polymorphism may affect their affinity for NKG2D and, consequently, the activation thresholds of NK and T cells.

  • 流式分析

    • Flow cytometric analysis of Human MICA expression on HeLa cells. Cells from the HeLa (Human cervix adenocarcinoma epithelial cells) were stained with either Pacific Blue Mouse IgG1, κ Isotype Control (black line histogram) or SDT Pacific Blue Mouse Anti-Human MICA Antibody (red line histogram) at 5 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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