FOXF1 Polyclonal Antibody, 50ul RNA Synthesis Mutations in this gene are

Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy

The encoded protein is primarily localized to endosomal membranes and may function to facilitate albumin uptake by the renal proximal tubule

This gene encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria

also known as MYC

FOXF1 Polyclonal Antibody, 50ul RNA Synthesis Mutations in this gene areThis gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in the regulation of pulmonary genes as well as embryonic development.