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

The encoded protein contains a carboxy-terminal leucine zipper that mediates channel formation

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

This protein participates in attenuating transcription from the mitochondrial genome

Participates in DNA repair and in chromosomal DNA replication

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