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IgA anticorps (Middle Region)

Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN635180
  • Antigène Voir toutes IgA Anticorps
    IgA
    Épitope
    Middle Region
    Reactivité
    Humain
    Hôte
    • 1
    Lapin
    Clonalité
    • 1
    Polyclonal
    Conjugué
    • 1
    Cet anticorp IgA est non-conjugé
    Application
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Specificité
    PIGA antibody was raised against the middle region of PIGA
    Purification
    Affinity purified
    Immunogène
    PIGA antibody was raised using the middle region of PIGA corresponding to a region with amino acids SVKSLCEGLEKAIFQLKSGTLPAPENIHNIVKTFYTWRNVAERTEKVYDR
  • Indications d'application
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    Commentaires

    PIGA Blocking Peptide, catalog no. 33R-8916, is also available for use as a blocking control in assays to test for specificity of this PIGA antibody

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of PIGA antibody in PBS
    Concentration
    Lot specific
    Buffer
    PBS
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Antigène
    IgA
    Abstract
    IgA Produits
    Synonymes
    anticorps MB-1, anticorps IG-alpha, anticorps IGA, anticorps IgA, anticorps Igh-2, anticorps CD79a molecule, anticorps immunoglobulin heavy constant alpha, anticorps CD79A, anticorps Igha
    Classe de substances
    Antibody
    Sujet
    PIGA is a protein required for synthesis of N-acetylglucosaminyl phosphatidylinositol (GlcNAc-PI), the first intermediate in the biosynthetic pathway of GPI anchor. The GPI anchor is a glycolipid found on many blood cells and which serves to anchor proteins to the cell surface. Paroxysmal nocturnal hemoglobinuria, an acquired hematologic disorder, has been shown to result from mutations in this gene.
    Poids moléculaire
    19 kDa (MW of target protein)
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