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IgA Antikörper (Middle Region)

Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN635180
  • Target Alle IgA Antikörper anzeigen
    IgA
    Bindungsspezifität
    Middle Region
    Reaktivität
    Human
    Wirt
    • 1
    Kaninchen
    Klonalität
    • 1
    Polyklonal
    Konjugat
    • 1
    Dieser IgA Antikörper ist unkonjugiert
    Applikation
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Spezifität
    PIGA antibody was raised against the middle region of PIGA
    Aufreinigung
    Affinity purified
    Immunogen
    PIGA antibody was raised using the middle region of PIGA corresponding to a region with amino acids SVKSLCEGLEKAIFQLKSGTLPAPENIHNIVKTFYTWRNVAERTEKVYDR
  • Applikationshinweise
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    Kommentare

    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

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of PIGA antibody in PBS
    Konzentration
    Lot specific
    Buffer
    PBS
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target
    IgA
    Abstract
    IgA Produkte
    Synonyme
    MB-1 antikoerper, IG-alpha antikoerper, IGA antikoerper, IgA antikoerper, Igh-2 antikoerper, CD79a molecule antikoerper, immunoglobulin heavy constant alpha antikoerper, CD79A antikoerper, Igha antikoerper
    Substanzklasse
    Antibody
    Hintergrund
    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.
    Molekulargewicht
    19 kDa (MW of target protein)
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