CCDC115 Antikörper (AA 1-180) (PE)

Produktnummer ABIN7980904

Der Kaninchen Polyklonal anti-CCDC115 Antikörper wird verwendet zum Nachweis von CCDC115 in Proben von Human. Er wurde validiert für FACS.

Kurzübersicht für CCDC115 Antikörper (AA 1-180) (PE) (ABIN7980904)

Target: CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCDC115 Antikörper ist konjugiert mit PE

Applikation: Flow Cytometry (FACS)

Produktdetails anti-CCDC115 Antikörper (PE)

Bindungsspezifität: AA 1-180

Verwendungszweck: Anti-CCDC115 Antibody PE Conjugated

Kreuzreaktivität (Details): No cross-reactivity with other proteins

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human CCDC115 recombinant protein (Position: M1-A180).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Flow Cytometry, Optimal dilutions should be determined by end users.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Haltbarkeit: 12 months

Details zu CCDC115

Target: CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))

Andere Bezeichnung: CCDC115

Hintergrund:

Background: Coiled-coil domain containing 115 is a protein that in humans is encoded by the CCDC115 gene. The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans.

Gene Full Name: vacuolar ATPase assembly factor VMA22

Gen-ID: 84317

UniProt: Q96NT0