GPR82 Polyclonal Antibody, 100ul Enzymes A mutation in this gene

A mutation in this gene was associated with Birk-Barel mental retardation dysmorphism syndrome

and contiguous with the luteinizing hormone beta subunit gene

Reduce hands-on time

FOXO1 belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain

This gene encodes a protein containing a lines-like domain

GPR82 Polyclonal Antibody, 100ul Enzymes A mutation in this geneProbable G protein coupled receptor 82 encoded by GPR82 is an orphan G protein coupled receptor of unknown function. Probable G protein coupled receptor 82 is a member of a family of proteins that contain seven transmembrane domains and transduce extracellular signals through heterotrimeric G proteins.