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HLA-DRA anticorps

L’anticorps Lapin Polyclonal anti-HLA-DRA a été validé pour WB, IHC, ELISA, IF et ICC. Il convient pour détecter HLA-DRA dans des échantillons de Humain, Rat et Souris.
N° du produit ABIN6262290

Aperçu rapide pour HLA-DRA anticorps (ABIN6262290)

Antigène

Voir toutes HLA-DRA Anticorps
HLA-DRA (HLA Class II DR alpha (HLA-DRA))

Reactivité

  • 96
  • 17
  • 10
  • 9
  • 8
  • 8
  • 4
  • 3
  • 3
  • 1
Humain, Rat, Souris

Hôte

  • 61
  • 49
  • 4
  • 1
  • 1
Lapin

Clonalité

  • 66
  • 50
Polyclonal

Conjugué

  • 58
  • 12
  • 7
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp HLA-DRA est non-conjugé

Application

  • 56
  • 50
  • 38
  • 33
  • 17
  • 15
  • 13
  • 10
  • 9
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)
  • Specificité

    HLA-DRA Antibody detects endogenous levels of total HLA-DRA

     Réactivité croisée

    Humain, Souris, Rat (Rattus)

    Purification

    The antiserum was purified by peptide affinity chromatography using SulfoLinkTM Coupling Resin (Thermo Fisher Scientific).

    Immunogène

    A synthesized peptide derived from human HLA-DRA

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000 IHC 1:50-1:200, IF/ICC 1:100-1:500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Rabbit IgG in phosphate buffered saline ,  pH 7.4, 150  mM NaCl, 0.02 % sodium azide and 50 % glycerol.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20 °C.Stable for 12 months from date of receipt

    Date de péremption

    12 months
  • Antigène

    HLA-DRA (HLA Class II DR alpha (HLA-DRA))

    Autre désignation

    HLA-DRA

    Sujet

    Description: 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 accommodates 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 a 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 microenvironment has been implicated in the regulation of antigen loading into MHC II molecules, increased acidification produces increased proteolysis and efficient peptide loading.

    Gene: HLA-DRA

    Poids moléculaire

    29kDa

    ID gène

    3122

    UniProt

    P01903

    Pathways

    TCR Signaling, CXCR4-mediated Signaling Events, Human Leukocyte Antigen (HLA) in Adaptive Immune Response
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