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AGA Antikörper

AGA Reaktivität: Human, Maus WB, IF Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN6294189
  • Target Alle AGA Antikörper anzeigen
    AGA (Aspartylglucosaminidase (AGA))
    Reaktivität
    • 20
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Human, Maus
    Wirt
    • 20
    • 1
    Kaninchen
    Klonalität
    • 21
    Polyklonal
    Konjugat
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser AGA Antikörper ist unkonjugiert
    Applikation
    • 11
    • 7
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein of human AGA
    Isotyp
    IgG
    Top Product
    Discover our top product AGA Primärantikörper
  • Applikationshinweise
    WB 1:500 - 1:1000
    IF 1:50 - 1:100
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20C. Avoid freeze / thaw cycles.
  • Target
    AGA (Aspartylglucosaminidase (AGA))
    Andere Bezeichnung
    AGA (AGA Produkte)
    Synonyme
    AGU antikoerper, ASRG antikoerper, GA antikoerper, AW060726 antikoerper, aspartylglucosaminidase antikoerper, AGA antikoerper, Aga antikoerper
    Hintergrund
    This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. This enzyme is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. Mutations in this gene are associated with the lysosomal storage disease aspartylglycosaminuria that results in progressive neurodegeneration. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is subject to proteolytic processing.
    Molekulargewicht
    37.208 kDa
    Gen-ID
    175
    UniProt
    P20933
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