COX6B1 anticorps

N° du produit ABIN7880571

L’anticorps anti-COX6B1 Polyclonal Lapin est utilisé pour la détection de COX6B1 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, IF, IHC (p) et FACS.

Aperçu rapide pour COX6B1 anticorps (ABIN7880571)

Antigène: COX6B1 (Cytochrome C Oxidase Subunit VIb Polypeptide 1 (Ubiquitous) (COX6B1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp COX6B1 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Détail du produit anti-COX6B1 anticorps

Fonction: COX6B1 Antibody / Cytochrome c oxidase subunit 6B1

Purification: Antigen affinity purified

Immunogène: Amio acids TKIKNYKTAPFDSRF were used as the immunogen for the COX6B1 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the COX6B1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the COX6B1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur COX6B1

Antigène: COX6B1 (Cytochrome C Oxidase Subunit VIb Polypeptide 1 (Ubiquitous) (COX6B1))

Autre désignation: COX6B1

Sujet: Cytochrome c oxidase subunit 6B1 is an enzyme that in humans is encoded by the COX6B1 gene. Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. This nuclear gene encodes subunit VIb. Mutations in this gene are associated with severe infantile encephalomyopathy. Three pseudogenes COX6BP-1, COX6BP-2 and COX6BP-3 have been found on chromosomes 7, 17 and 22q13.1-13.2, respectively.

UniProt: P14854