NDUFA2 Antikörper

Produktnummer ABIN7264183

Produktdetails anti-NDUFA2 Antikörper

Target: NDUFA2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 2, 8kDa (NDUFA2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NDUFA2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human NDUFA2 (NP_002479.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000 IHC 1:50-1:100 IF 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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: Store at -20°C. Avoid freeze / thaw cycles.

Details zu NDUFA2

Target: NDUFA2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 2, 8kDa (NDUFA2))

Andere Bezeichnung: NDUFA2 (NDUFA2 Produkte)

Synonyme: NDUFA2 antikoerper, b8 antikoerper, cd14 antikoerper, cib8 antikoerper, AV000592 antikoerper, B8 antikoerper, C1-B8 antikoerper, CI-B8 antikoerper, CD14 antikoerper, CIB8 antikoerper, NADH:ubiquinone oxidoreductase subunit A2 antikoerper, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 antikoerper, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2, 8kDa antikoerper, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 antikoerper, Ndufa2 antikoerper, NDUFA2 antikoerper, ndufa2 antikoerper

Hintergrund: The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants.

Molekulargewicht:

Observed_MW: 11 kDa

Calculated_MW: 8 kDa/10 kDa

Gen-ID: 4695

UniProt: O43678