ATP6 Rabbit mAb

Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in mitochondrial ATP synthesis coupled proton transport. Located in mitochondrion. Is expressed in several structures, including alimentary system, brain, heart, integumental system, and sensory organ. Human ortholog(s) of this gene implicated in Leber hereditary optic neuropathy, NARP syndrome, Parkinson's disease, multiple sclerosis, and systemic lupus erythematosus. Orthologous to human MT-ATP6 (mitochondrially encoded ATP synthase membrane subunit 6). Synonyma: ATP6