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.
Cytochrome c oxidase polypeptide III; Cytochrome c oxidase subunit 3; Cytochrome c oxidase subunit 3 Cytochrome c oxidase subunit III Cytochrome c oxidase sununit III Cytochrome oxidase sununit 3 mt-Co3 Co3 COIII COX3 COXIII
Cat # 15991725
100 µL
Cat # 16530132
100 µL
Cat # 15556092
100 µL
Cat # 17107923
100 µL
Cat # 16639844
100 µL
Cat # 15737961
100 µL
Cat # 17127548
400 µL
Cat # 10782774
100 µg
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