COG8 anticorps (N-Term)

N° du produit ABIN5517541

L’anticorps anti-COG8 Polyclonal Lapin est utilisé pour la détection de COG8 dans des échantillons de Humain. Il a été validé pour WB.

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

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp COG8 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-COG8 anticorps

Épitope: N-Term

Fonction: COG8 Antibody - N-terminal region

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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP78473-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: 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.

Conseil sur la manipulation: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur COG8

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

Autre désignation: COG8

Sujet:

Background Information: 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.

Gene Name: component of oligomeric golgi complex 8

Alternative Symbols: DOR1, CDG2H

Protein Name: conserved oligomeric Golgi complex subunit 8

Poids moléculaire: 68 kDa

ID gène: 84342

NCBI Accession: NP_115758

UniProt: Q96MW5