The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.
Protein Aliases: Co3; COIII; COX3; COXIII; Cytochrome c oxidase polypeptide III; Cytochrome c oxidase subunit 3; Cytochrome c oxidase subunit III; Cytochrome c oxidase sununit III; Cytochrome oxidase sununit 3; mt-Co3
Gene Aliases: COIII; COXIII; MT-CO3; MTCO3
UniProt ID: (Mouse) P00416
Entrez Gene ID: (Mouse) 17710