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FIGURE: 1 / 4
Immunogen sequence: YHSSLAPTPQ LGGHWPPTGI TPLNPL
Highest antigen sequence identity to the following orthologs: Mouse - 81%, Rat - 85%.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Co3; Cytochrome c oxidase polypeptide III; Cytochrome c oxidase subunit 3
Gene Aliases: COIII; COX3; COXIII; MT-CO3; MTCO3
UniProt ID: (Human) P00414
Entrez Gene ID: (Human) 4514
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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