NDUFB9 anticorps

N° du produit ABIN7268815

Cet anticorps Lapin Monoclonal détecte spécifiquement NDUFB9 dans WB et IHC. Il présente une réactivité envers Humain.

Aperçu rapide pour NDUFB9 anticorps (ABIN7268815)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp NDUFB9 est non-conjugé

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

Détail du produit anti-NDUFB9 anticorps

Fonction: NDUFB9 Rabbit mAb

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Monoclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant protein of Human NDUFB9.

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

Agent conservateur: Sodium azide

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

Stock: -20 °C

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

Détails sur NDUFB9

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

Autre désignation: NDUFB9

Sujet: 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

Poids moléculaire: 21kDa

ID gène: 4715

UniProt: Q9Y6M9

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