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Invivo anti-Mouse I-A/I-E Recombinant mAb

H-2 class II histocompatibility antigen,I-A beta chain,H2-Eb1

价格 1,000.00 供应商现货 : 3-5个工作日
货号 S0B7082
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    I-A/I-E
  • 分子别名

    H-2 class II histocompatibility antigen, I-A beta chain; H2-Eb1
  • 细胞定位

    Membrane
  • Accession

    P18468, Q3U060
  • 克隆号

    M5/114.15.2
  • 抗体类型

    Rat mAb
  • 抗体同种型

    Rat IgG2b,k
  • 同型对照

    Invivo rat IgG2b isotype control, anti-keyhole limpet hemocyanin
  • 反应种属 ?

    Ms
  • 阳性样本

    C57BL/6 mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    5 mg/ml
  • 纯度

    >95% (Determined by SDS-PAGE)
  • 内毒素含量

    <1EU/mg
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS pH7.4, containing no preservative

  • 储存条件

    2 to 8 °C for 2 weeks under sterile conditions;
    -20 °C for 3 months under sterile conditions;
    -80 °C for 24 months under sterile conditions.
    Please avoid repeated freeze-thaw cycles.

  • 应用

    in vivo MHC II blockade

    Functional assays

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 1:500 Ms
背景介绍
  • I-A/I-E proteins are part of the Major Histocompatibility Complex (MHC) class II molecules, which are heterodimeric transmembrane glycoproteins expressed on antigen-presenting cells such as dendritic cells, macrophages, and B cells. These proteins are encoded by four genes located in the mouse MHC and are composed of α and β subunits. The I-A and I-E molecules are highly polymorphic and can form hybrid molecules in heterozygous individuals, contributing to the diversity of antigen presentation. They play a crucial role in presenting peptide antigens to CD4+ helper T cells, initiating adaptive immune responses. Additionally, MHC class II molecules can trigger intracellular signaling pathways in antigen-presenting cells, influencing their proliferation, maturation, and apoptosis.

  • 流式分析

    • Flow cytometric analysis of C57BL/6 mouse splenocytes labeled with mouse I-A/I-E antibody at 1/500 dilution (1 μg) / (right panel) compared with a Rat IgG2b, κ Isotype Control / (left panel). Goat Anti-Rat IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD19 - Brilliant Violet 421™ antibody separately. Total viable cells, as determined by Fixable Viability Dye 662 (S0B88806), were used for analysis. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.

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