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Glucosylceramidase anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement Glucosylceramidase dans WB. Il présente une réactivité envers Humain, Souris, Boeuf (Vache), Chien, Cobaye, Cheval, Porc, Lapin et Rat.
N° du produit ABIN5514399

Aperçu rapide pour Glucosylceramidase anticorps (N-Term) (ABIN5514399)

Antigène

Glucosylceramidase (GLCM)

Reactivité

Humain, Souris, Boeuf (Vache), Chien, Cobaye, Cheval, Porc, Lapin, Rat

Hôte

  • 5
  • 1
Lapin

Clonalité

  • 5
  • 1
Polyclonal

Conjugué

  • 4
  • 1
  • 1
Cet anticorp Glucosylceramidase est non-conjugé

Application

  • 6
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Épitope

    • 4
    • 4
    N-Term

    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

    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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