OR6M1 Polyclonal Antibody, 20ul Reservoirs hereditary angioedema and Smith-Lemli-Opitz syndrome

hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11

subcellular location:Localized to plasma membrane coated pits

This protein participates in attenuating transcription from the mitochondrial genome

Claudin 4 encoded by this intronless gene (CLDN4) belongs to the claudin family

OR6M1 Polyclonal Antibody, 20ul Reservoirs hereditary angioedema and Smith-Lemli-Opitz syndromeOlfactory 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