COG8 anticorps (N-Term)

N° du produit ABIN5517541

Détail du produit anti-COG8 anticorps

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

Épitope: N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp COG8 est non-conjugé

Application: Western Blotting (WB)

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.

Restrictions: For Research Use only

Stockage

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.

Détails sur COG8

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

Autre désignation: COG8 (COG8 Produits)

Synonymes: anticorps CDG2H, anticorps DOR1, anticorps BB235941, anticorps C87832, anticorps component of oligomeric golgi complex 8, anticorps Cog8, anticorps cog8, anticorps 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