产品中心 流式试剂&相关 流式抗体

所有图片(1/1)

Biotin Mouse Anti-Human FcεRIα Antibody (AER-37)

FceRIa,FceRI-a,FceRI-alpha,FceRI alpha,high affinity IgE receptor

价格 1,200.00 供应商现货 : 3-5个工作日
货号 S0B8059
规格
数量
收藏 分享

产品介绍 评论(0)

产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    FcεRIα
  • 分子别名

    FceRIa, FceRI-a, FceRI-alpha, FceRI alpha, high affinity IgE receptor
  • 细胞定位

    Cell membrane
  • Accession

    P12319
  • 克隆号

    AER-37
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG2a,k
  • 反应种属 ?

    Hu
  • 阳性样本

    Human PBMC
  • 纯化方式

    Protein A
  • 浓度

    0.2 mg/ml
  • 标记

    Biotin
  • 性状

    Liquid
  • 缓冲体系

    PBS pH7.4, 0.03% 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 Hu
背景介绍
  • FcεRIα is a single-pass transmembrane glycoprotein of the immunoglobulin superfamily that forms the ligand-binding backbone of the tetrameric high-affinity IgE receptor (FcεRI) expressed on mast cells and basophils; its extracellular region folds into two Ig-like domains that clamp the Fc portion of IgE with picomolar affinity, positioning the constant heavy-chain ε2-3 interface for optimal recognition, while a short cytoplasmic tail lacks signaling motifs but critically nucleates the entire receptor complex by juxtamembrane interactions with the four-helix FcεRIβ subunit and the disulfide-linked FcRγ homodimer, thereby dictating the architecture of the transmembrane three-helix bundle that propagates ITAM-based phosphorylation cascades upon IgE/allergen crosslinking and drives immediate degranulation, cytokine release and the clinical manifestations of type I hypersensitivity.

  • 流式分析

    • Flow cytometric analysis of Human FcεRIα expression on Human PBMC. Human PBMC (peripheral blood mononuclear cells) were stained with Brilliant Violet 421™ Mouse Anti-Human CD14 Antibody and either Biotin Mouse IgG2b, κ Isotype Control (Left panel) or Biotin Mouse Anti-Human FcεRIα Antibody (Right panel) at 5 μl/test followed by Sav-PE. Total viable cells, as determined by Fixable Viability Dye 515 (S0D0013), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

评论(0)