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GAA anticorps

GAA Reactivité: Humain WB Hôte: Lapin Monoclonal unconjugated
N° du produit ABIN7267404
  • Antigène Voir toutes GAA Anticorps
    GAA (Glucosidase, Alpha, Acid (GAA))
    Reactivité
    • 47
    • 22
    • 21
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 47
    • 4
    Lapin
    Clonalité
    • 48
    • 3
    Monoclonal
    Conjugué
    • 26
    • 5
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GAA est non-conjugé
    Application
    • 47
    • 19
    • 15
    • 13
    • 13
    • 8
    • 7
    • 5
    • 3
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Fonction
    GAA Rabbit mAb
     Réactivité croisée
    Humain, Souris, Rat
    Attributs du produit
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human GAA.
    Isotype
    IgG
    Top Product
    Discover our top product GAA Anticorps primaire
  • Indications d'application
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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 -20°C. Avoid freeze / thaw cycles.
  • Antigène
    GAA (Glucosidase, Alpha, Acid (GAA))
    Autre désignation
    GAA (GAA Produits)
    Synonymes
    anticorps LYAG, anticorps E430018M07Rik, anticorps glucosidase alpha, acid, anticorps glucosidase, alpha, acid, anticorps transmembrane and coiled-coil domain family 1, anticorps glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II), anticorps GAA, anticorps Gaa, anticorps TMCC1, anticorps gaa
    Sujet
    This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in multiple transcript variants.,GAA, LYAG, glucosidase alpha, acid,Cancer,Signal Transduction,Endocrine & Metabolism,GAA
    Poids moléculaire
    120,100,75kDa
    ID gène
    2548
    UniProt
    P10253
    Pathways
    Cellular Glucan Metabolic Process
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