ATP5G3 Polyclonal Antibody, 100ul In vitro Transcription and murine studies suggest a

and murine studies suggest a role in tumor-associated tissue remodeling

A germline mutation of VHL is the basis of familial inheritance of VHL syndrome

This gene is located on a region of chromosome 17q21

The encoded protein may be involved in a wide range of biological processes including inflammation

ATP5G3 Polyclonal Antibody, 100ul In vitro Transcription and murine studies suggest aATP5G3 (ATP synthase, H+ transporting, mitochondrial Fo complex subunit C3) encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi subunit complexes: the soluble catalytic core, F1, and the membrane spanning component, Fo, comprising the proton channel.