Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

VPS13B anticorps

VPS13B Reactivité: Souris, Rat IF, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7076176
  • Antigène Tous les produits VPS13B
    VPS13B (Vacuolar Protein Sorting 13 Homolog B (Yeast) (VPS13B))
    Reactivité
    • 6
    • 5
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    Souris, Rat
    Hôte
    • 10
    • 1
    Lapin
    Clonalité
    • 10
    • 1
    Polyclonal
    Conjugué
    • 7
    • 2
    • 1
    • 1
    Cet anticorp VPS13B est non-conjugé
    Application
    • 7
    • 5
    • 2
    • 1
    • 1
    • 1
    Immunofluorescence (IF), Immunohistochemistry (IHC)
     Réactivité croisée
    Rat
    Purification
    Affinity purification
    Immunogène
    Recombinant protein corresponding to Mouse VPS13B/CHS1
  • Indications d'application
    IHC/IF (M,R) 1:1000-1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    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
  • Antigène
    VPS13B (Vacuolar Protein Sorting 13 Homolog B (Yeast) (VPS13B))
    Autre désignation
    VPS13B/CHS1 (VPS13B Produits)
    Synonymes
    anticorps 1810042B05Rik, anticorps 2310042E16Rik, anticorps 4732488H20, anticorps C330002D13Rik, anticorps C87206, anticorps Coh1, anticorps D230005K13, anticorps mKIAA0532, anticorps mKIAA5032, anticorps CHS1, anticorps COH1, anticorps Cohh1, anticorps vacuolar protein sorting 13 homolog B, anticorps vacuolar protein sorting 13B, anticorps VPS13B, anticorps Vps13b
    Sujet
    This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene.
    ID gène
    666173
    NCBI Accession
    NP_796125
    UniProt
    Q80TY5
Vous êtes ici: