Olfactory receptor 8I2 Polyclonal Antibody, 100ul Peptide Synthesis Mutations in the gene cause

Mutations in the gene cause Sjogren-Larsson syndrome

This family of proteins interact with

including an invariant arg-phe-pro motif

Mutations in this gene cause arginine:glycine amidinotransferase deficiency| an inborn error of creatine synthesis characterized by mental retardation| language impairment| and behavioral disorders

and host defense against pathogens

Olfactory receptor 8I2 Polyclonal Antibody, 100ul Peptide Synthesis Mutations in the gene causeOlfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G protein coupled receptors (GPCR) arising from single coding exon genes. Olfactory receptors share a 7 transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein mediated