Anti-MHC Class II抗体[CVS20] (ab23206)

概述

  • 产品名称Anti-MHC Class II抗体[CVS20]
    参阅全部 MHC Class II 一抗
  • 描述
    小鼠单克隆抗体[CVS20] to MHC Class II
  • 特异性This antibody reacts with Equine MHC Class II antigen. Reacts with all B cells and 95% T cells.
  • 经测试应用适用于: Flow Cyt, IHC-Fr, WBmore details
  • 种属反应性
    与反应: Horse, Cow, Dog, Human
  • 免疫原

    Tissue/ cell preparation of 3132 cells (Horse)

性能

  • 形式Liquid
  • 存放说明Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
  • 存储溶液Preservative: 0.09% Sodium Azide
    Constituents: Tissue culture supernatant, 5-10% Foetal calf serum, 0.2M Tris HCl. pH 7.4
  • 纯度Tissue culture supernatant
  • 克隆单克隆
  • 克隆编号CVS20
  • 骨髓瘤x63-Ag8.653
  • 同种型IgG1
  • 研究领域

应用

Our Abpromise guarantee covers the use of ab23206 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

应用 Ab评论 说明
Flow Cyt
IHC-Fr
WB
  • 应用说明Flow Cyt: 1/50 - 1/100. Use 10µl of the suggested working dilution to label 106 cells in 100µl.
    IHC-Fr: Use at an assay dependent dilution.

    Not tested in other applications.
    Optimal dilutions/concentrations should be determined by the end user.
  • 靶标

    • 功能Binds peptides derived from antigens that access the endocytic route of antigen presenting cells (APC) and presents them on the cell surface for recognition by the CD4 T-cells. The peptide binding cleft accomodates peptides of 10-30 residues. The peptides presented by MHC class II molecules are generated mostly by degradation of proteins that access the endocytic route, where they are processed by lysosomal proteases and other hydrolases. Exogenous antigens that have been endocytosed by the APC are thus readily available for presentation via MHC II molecules, and for this reason this antigen presentation pathway is usually referred to as exogenous. As membrane proteins on their way to degradation in lysosomes as part of their normal turn-over are also contained in the endosomal/lysosomal compartments, exogenous antigens must compete with those derived from endogenous components. Autophagy is also a source of endogenous peptides, autophagosomes constitutively fuse with MHC class II loading compartments. In addition to APCs, other cells of the gastrointestinal tract, such as epithelial cells, express MHC class II molecules and CD74 and act as APCs, which is an unusual trait of the GI tract. To produce a MHC class II molecule that presents an antigen, three MHC class II molecules (heterodimers of an alpha and a beta chain) associate with a CD74 trimer in the ER to form an heterononamer. Soon after the entry of this complex into the endosomal/lysosomal system where antigen processing occurs, CD74 undergoes a sequential degradation by various proteases, including CTSS and CTSL, leaving a small fragment termed CLIP (class-II-associated invariant chain peptide). The removal of CLIP is facilitated by HLA-DM via direct binding to the alpha-beta-CLIP complex so that CLIP is released. HLA-DM stabilizes MHC class II molecules until primary high affinity antigenic peptides are bound. The MHC II molecule bound to a peptide is then transported to the cell membrane surface. In B cells, the interaction between HLA-DM and MHC class II molecules is regulated by HLA-DO. Primary dendritic cells (DCs) also to express HLA-DO. Lysosomal miroenvironment has been implicated in the regulation of antigen loading into MHC II molecules, increased acidification produces increased proteolysis and efficient peptide loading.
    • 序列相似性Belongs to the MHC class II family.
      Contains 1 Ig-like C1-type (immunoglobulin-like) domain.
    • 细胞定位Cell membrane. Endoplasmic reticulum membrane. Golgi apparatus > trans-Golgi network membrane. Endosome membrane. Lysosome membrane. The MHC class II complex transits through a number of intracellular compartments in the endocytic pathway until it reaches the cell membrane for antigen presentation.
    • Information by UniProt
    • 数据库链接
    • 别名
      • D6S221E antibody
      • DMA antibody
      • DMB antibody
      • DP beta 1 antibody
      • DP beta 1 chain antibody
      • DP(W4) beta chain antibody
      • DPB 1 antibody
      • DPB1 antibody
      • DPB1_HUMAN antibody
      • DRB antibody
      • H2Ea antibody
      • HLA class II histocompatibility antigen antibody
      • HLA class II histocompatibility antigen DM beta chain antibody
      • HLA class II histocompatibility antigen, DP beta 1 chain antibody
      • HLA class II histocompatibility antigen, DP(W4) beta chain antibody
      • HLA DMB antibody
      • HLA DP1A antibody
      • HLA DPB1 antibody
      • HLA SB alpha chain antibody
      • HLA-A antibody
      • HLA-A histocompatibility type antibody
      • HLA-DP antibody
      • HLA-DP histocompatibility type, beta-1 subunit antibody
      • HLA-DP1B antibody
      • HLA-DPB antibody
      • HLA-DPB1 antibody
      • HLADM antibody
      • HLADP1B antibody
      • HLASB antibody
      • HLASB histocompatibility type antibody
      • Human MHC class II HLA SB alpha antibody
      • LA class II histocompatibility antigen DP alpha 1 chain antibody
      • Major histocompatibility complex class II antibody
      • Major histocompatibility complex class II DP alpha 1 antibody
      • Major histocompatibility complex class II DP beta 1 antibody
      • Major histocompatibility complex, class I, A antibody
      • MHC class II antigen DMB antibody
      • MHC class II antigen DPB1 antibody
      • MHC class II DP3 alpha antibody
      • MHC class II DPA1 antibody
      • MHC class II HLA-DP-beta-1 antibody
      • MHC DPB1 antibody
      • MHC HLA DPB1 antibody
      • PLT1 antibody
      • Primed lymphocyte test 1 antibody
      • RING6 antibody
      • RING7 antibody
      see all

    Anti-MHC Class II antibody [CVS20] 图像

    • ab23206 staining MHC Class II in equine peripheral blood lymphocytes by Flow Cytometric analysis.

    Anti-MHC Class II antibody [CVS20] (ab23206)参考文献

    ab23206 has not yet been referenced specifically in any publications.

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