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AGA anticorps

AGA Reactivité: Humain, Souris WB, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6294189
  • Antigène Voir toutes AGA Anticorps
    AGA (Aspartylglucosaminidase (AGA))
    Reactivité
    • 20
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Humain, Souris
    Hôte
    • 20
    • 1
    Lapin
    Clonalité
    • 21
    Polyclonal
    Conjugué
    • 10
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp AGA est non-conjugé
    Application
    • 11
    • 7
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human AGA
    Isotype
    IgG
    Top Product
    Discover our top product AGA Anticorps primaire
  • Indications d'application
    WB 1:500 - 1:1000
    IF 1:50 - 1:100
    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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 -20C. Avoid freeze / thaw cycles.
  • Antigène
    AGA (Aspartylglucosaminidase (AGA))
    Autre désignation
    AGA (AGA Produits)
    Synonymes
    anticorps AGU, anticorps ASRG, anticorps GA, anticorps AW060726, anticorps aspartylglucosaminidase, anticorps AGA, anticorps Aga
    Sujet
    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.
    Poids moléculaire
    37.208 kDa
    ID gène
    175
    UniProt
    P20933
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