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)

The protein (calponin 2) encoded by CNN2

It mediates posttranslational endoproteolytic processing for several integrin alpha subunits and is thought to process prorenin| pro-membrane type-1 matrix metalloproteinase and HIV-1 glycoprotein gp160

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

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