NDUFB9 Antikörper

Produktnummer ABIN7268815

Dieses Kaninchen Monoklonal-Antikörper erkennt spezifisch NDUFB9 in WB und IHC. Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für NDUFB9 Antikörper (ABIN7268815)

Target: NDUFB9 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 9, 22kDa (NDUFB9))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser NDUFB9 Antikörper ist unkonjugiert

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

Produktdetails anti-NDUFB9 Antikörper

Verwendungszweck: NDUFB9 Rabbit mAb

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Monoclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of Human NDUFB9.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,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 NDUFB9

Target: NDUFB9 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 9, 22kDa (NDUFB9))

Andere Bezeichnung: NDUFB9

Hintergrund: The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants.,NDUFB9,B22,CI-B22,LYRM3,UQOR22,Endocrine & Metabolism,Mitochondrial metabolism,Oxidative phosphorylation,Neuroscience,Neurodegenerative Diseases,NDUFB9

Molekulargewicht: 21kDa

Gen-ID: 4715

UniProt: Q9Y6M9

Pathways: Sensory Perception of Sound, SARS-CoV-2 Protein Interaktom