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Glucosylceramidase anticorps (N-Term)

GLCM Reactivité: Souris, Porc, Lapin, Boeuf (Vache), Rat, Chien, Cobaye, Cheval, Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5514399
  • Antigène Tous les produits Glucosylceramidase (GLCM)
    Glucosylceramidase (GLCM)
    Épitope
    N-Term
    Reactivité
    Souris, Porc, Lapin, Boeuf (Vache), Rat, Chien, Cobaye, Cheval, Humain
    Hôte
    Lapin
    Clonalité
    Polyclonal
    Application
    Western Blotting (WB)
    Séquence
    FSSPSREECP KPLSRVSIMA GSLTGLLLLQ AVSWASGARP CIPKSFGYSS
    Homologie
    Cow: 75%, Dog: 75%, Guinea Pig: 75%, Horse: 75%, Human: 100%, Mouse: 75%, Pig: 79%, Rabbit: 75%, Rat: 75%
    Attributs du produit
    This is a rabbit polyclonal antibody against GLCM. It was validated on Western Blot.
    Purification
    Affinity purified
    Immunogène
    The immunogen is a synthetic peptide directed towards the N-terminal region of Human GLCM
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Antigène
    Glucosylceramidase (GLCM)
    Autre désignation
    GLCM (GLCM Produits)
    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.

    Alias Symbols: GBA, GC, GLUC,

    Protein Interaction Partner: NUDCD1, UBC, ITCH, ATP6V1B1, SNCA, FBXO6, TCP1, CBL, NEDD4, PARK2, HSP90AA1, HSPA4, PSAP,

    Protein Size: 536
    ID gène
    2629
    NCBI Accession
    XP_006711333
    UniProt
    P04062
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