Olfactory receptor 9Q2 Polyclonal Antibody, 100ul Lysosome Defects in this gene are

Defects in this gene are a cause of Duane-radial ray syndrome (DRRS)

where it catalyzes the transfer of galactose from UDP-galactose to substrates containing a terminal beta-linked galactose moiety

The amino acid sequence of this isozyme is 92% identical to that of rat homolog

suggesting that this gene may have a role in the p53-dependent growth regulatory pathway

The N-terminal portion is transported to the nucleus where it homodimerizes to form the active kinase which promotes the condensation of chromatin during apoptosis

Olfactory receptor 9Q2 Polyclonal Antibody, 100ul Lysosome Defects in this gene areOlfactory 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