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

COG4 anticorps

COG4 Reactivité: Humain, Souris ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7252639
  • Antigène Voir toutes COG4 Anticorps
    COG4 (Component of Oligomeric Golgi Complex 4 (COG4))
    Reactivité
    • 26
    • 7
    • 5
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 23
    • 3
    Lapin
    Clonalité
    • 24
    • 2
    Polyclonal
    Conjugué
    • 19
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp COG4 est non-conjugé
    Application
    • 14
    • 8
    • 6
    • 3
    • 3
    • 3
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human COG4
    Isotype
    IgG
    Top Product
    Discover our top product COG4 Anticorps primaire
  • Indications d'application
    IHC 1:30-1:150, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.96 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    COG4 (Component of Oligomeric Golgi Complex 4 (COG4))
    Autre désignation
    COG4 (COG4 Produits)
    Synonymes
    anticorps COG4, anticorps DKFZp470I1314, anticorps CDG2J, anticorps COD1, anticorps AW554810, anticorps D8Ertd515e, anticorps zgc:136860, anticorps component of oligomeric golgi complex 4, anticorps COG4, anticorps cog4, anticorps Cog4
    Sujet
    The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two transcript variants encoding different isoforms have been found for this gene.
    UniProt
    Q9H9E3
Vous êtes ici:
Support technique