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COG8 anticorps (N-Term)

L’anticorps Lapin Polyclonal anti-COG8 a été validé pour WB. Il convient pour détecter COG8 dans des échantillons de Humain.
N° du produit ABIN5517541

Aperçu rapide pour COG8 anticorps (N-Term) (ABIN5517541)

Antigène

Voir toutes COG8 Anticorps
COG8 (Component of Oligomeric Golgi Complex 8 (COG8))

Reactivité

  • 9
  • 1
  • 1
Humain

Hôte

  • 6
  • 2
  • 1
Lapin

Clonalité

  • 9
Polyclonal

Conjugué

  • 6
  • 1
  • 1
  • 1
Cet anticorp COG8 est non-conjugé

Application

  • 5
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 4
    • 2
    • 1
    N-Term

    Séquence

    MATAATIPSV ATATAAALGE VEDEGLLASL FRDRFPEAQW RERPDVGRYL

    Purification

    Affinity purified

    Immunogène

    The immunogen is a synthetic peptide directed towards the N terminal region of human COG8
  • 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

    COG8 (Component of Oligomeric Golgi Complex 8 (COG8))

    Autre désignation

    COG8

    Sujet

    This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance.

    Alias Symbols: DOR1, CDG2H

    Protein Size: 612

    ID gène

    84342

    NCBI Accession

    NM_032382, NP_115758

    UniProt

    Q96MW5
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