NDUFA2 anticorps

N° du produit ABIN7264183

Détail du produit anti-NDUFA2 anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NDUFA2 est non-conjugé

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

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

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

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000 IHC 1:50-1:100 IF 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 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 NDUFA2

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

Autre désignation: NDUFA2 (NDUFA2 Produits)

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

Sujet: 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.

Poids moléculaire:

Observed_MW: 11 kDa

Calculated_MW: 8 kDa/10 kDa

ID gène: 4695

UniProt: O43678