NDUFV2 Antikörper

Produktnummer ABIN5704011

Dieser Anti-NDUFV2 Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von NDUFV2 in WB, ELISA, IHC, IF und IP. Geeignet für Human, Maus und Ratte.

Kurzübersicht für NDUFV2 Antikörper (ABIN5704011)

Target: NDUFV2 (NADH Dehydrogenase (Ubiquinone) Flavoprotein 2, 24kDa (NDUFV2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NDUFV2 Antikörper ist unkonjugiert

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

Produktdetails anti-NDUFV2 Antikörper

Verwendungszweck: NDUFV2 antibody

Immunogen: NADH dehydrogenase (ubiquinone) flavoprotein 2, 24kDa

Isotyp: IgG

Anwendungsinformationen

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

Kommentare:

mouse heart tissue were subjected to SDS PAGE followed by western blot with FNab05636(NDUFV2 antibody) at dilution of 1:400

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: PBS with 0.02 % sodium azide and 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.

Handhabung: Avoid repeated freeze / thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: -20°C for 12 months

Haltbarkeit: 12 months

Details zu NDUFV2

Target: NDUFV2 (NADH Dehydrogenase (Ubiquinone) Flavoprotein 2, 24kDa (NDUFV2))

Andere Bezeichnung: NDUFV2

Hintergrund:

Synonyms: NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial (NDUFV2)|NADH-ubiquinone oxidoreductase 24 kDa subunit|NDUFV2

Background: The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes the 24 kDa subunit of complex I, and is involved in electron transfer. Mutations in this gene are implicated in Parkinson's disease, bipolar disorder, schizophrenia, and have been found in one case of early onset hypertrophic cardiomyopathy and encephalopathy. A non-transcribed pseudogene of this locus is found on chromosome 19.

Molekulargewicht: 24 kDa

Gen-ID: 4729

UniProt: P19404