OR2BB Polyclonal Antibody, 50ul Site-directed Mutagenesis Defects in this gene are

Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1)| also called X-linked congenital stationary night blindness (XLCSNB)

This transporter is the primary mechanism for uptake of intestinal bile acids by apical cells in the distal ileum

phosphatidylinositol 3-kinase and STAT transcription factors

The tandem array of 15 N-terminal exons| or variable exons| are followed by downstream C-terminal exons| or constant exons| which are shared by all genes in the cluster

OR2BB Polyclonal Antibody, 50ul Site-directed Mutagenesis 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