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COG7 anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-COG7 a été validé pour WB. Il convient pour détecter COG7 dans des échantillons de Humain et Souris.
N° du produit ABIN1537568

Aperçu rapide pour COG7 anticorps (C-Term) (ABIN1537568)

Antigène

Voir toutes COG7 Anticorps
COG7 (Component of Oligomeric Golgi Complex 7 (COG7))

Reactivité

  • 16
  • 8
  • 1
Humain, Souris

Hôte

  • 13
  • 2
  • 1
Lapin

Clonalité

  • 14
  • 2
Polyclonal

Conjugué

  • 11
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp COG7 est non-conjugé

Application

  • 15
  • 12
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB)

Clone

RB37109
  • Épitope

    • 7
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 725-753, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This COG7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 725-753 amino acids from the C-terminal region of human COG7.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Stockage commentaire

    COG7 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • Antigène

    COG7 (Component of Oligomeric Golgi Complex 7 (COG7))

    Autre désignation

    COG7

    Sujet

    The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.

    Poids moléculaire

    86344

    ID gène

    91949

    NCBI Accession

    NP_705831

    UniProt

    P83436
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