O4A47 Polyclonal Antibody, 20ul Microplate Mixer Retinitis pigmentosa is an inherited

Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities

subcellular location:Seems to be excluded from nucleoli

Drosophila

This mitochondrial protein initiates the degradation of 1

Gene Ontology (GO) annotations related to this gene include serine-type endopeptidase inhibitor activity

O4A47 Polyclonal Antibody, 20ul Microplate Mixer Retinitis pigmentosa is an inheritedOlfactory 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