COG8 Antikörper (N-Term)

Produktnummer ABIN5517541

Der Kaninchen Polyklonal anti-COG8 Antikörper wird verwendet zum Nachweis von COG8 in Proben von Human. Er wurde validiert für WB.

Kurzübersicht für COG8 Antikörper (N-Term) (ABIN5517541)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser COG8 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-COG8 Antikörper

Bindungsspezifität: N-Term

Verwendungszweck: COG8 Antibody - N-terminal region

Sequenz: MATAATIPSV ATATAAALGE VEDEGLLASL FRDRFPEAQW RERPDVGRYL

Aufreinigung: Affinity purified

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

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Kommentare:

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: prevent freeze-thaw cycles

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu COG8

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

Andere Bezeichnung: COG8

Hintergrund:

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

Molekulargewicht: 68 kDa

Gen-ID: 84342

NCBI Accession: NP_115758

UniProt: Q96MW5