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GBA anticorps

GBA Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6571743
  • Antigène Voir toutes GBA Anticorps
    GBA (Glucosidase, Beta, Acid (GBA))
    Reactivité
    • 53
    • 29
    • 16
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 64
    • 10
    Lapin
    Clonalité
    • 57
    • 17
    Polyclonal
    Conjugué
    • 33
    • 15
    • 9
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Cet anticorp GBA est non-conjugé
    Application
    • 53
    • 26
    • 25
    • 8
    • 8
    • 7
    • 5
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human GBA (NP_000148.2).
    Isotype
    IgG
    Top Product
    Discover our top product GBA Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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 -20°C. Avoid freeze / thaw cycles.
  • Antigène
    GBA (Glucosidase, Beta, Acid (GBA))
    Autre désignation
    GBA (GBA Produits)
    Synonymes
    anticorps GBA1, anticorps GCB, anticorps GLUC, anticorps BETA-GLUCOSIDASE, anticorps T12J13.8, anticorps T12J13_8, anticorps beta glucosidase 25, anticorps PSPTO3318, anticorps PSPTO4290, anticorps GC, anticorps GCase, anticorps betaGC, anticorps glucosylceramidase beta, anticorps beta glucosidase 25, anticorps beta-glucosidase, anticorps Beta-glucosidase, anticorps glucosidase, beta, acid, anticorps glucosylceramidase, anticorps bglX-2, anticorps GBA, anticorps BGLU25, anticorps PSPTO_3318, anticorps bglX, anticorps bglA4, anticorps Gba, anticorps LOC100399524, anticorps bglA.2, anticorps bglX-2
    Sujet
    This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.
    Poids moléculaire

    Observed_MW: 60kDa

    Calculated_MW: 29kDa/50kDa/54kDa/57kDa/59kDa

    ID gène
    2629
    UniProt
    P04062
    Pathways
    Cellular Glucan Metabolic Process
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