Presku: | AAP50251 |
Size: | 100 ug |
Weight: | 29kDa |
Gene: | 4514 |
Format: | Lyophilized powder |
Target: | 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. |
Alternative names: | MTCO3 |