O13A1 Polyclonal Antibody, 50ul Hepatocytes A mutation in this gene

A mutation in this gene is the cause of autosomal dominant distal hereditary motor neuropathy type 2C

It is a predominantly cytoplasmic protein and is expressed in a variety of human cell lines

Mutations in this gene have been associated with neurodegenerative diseases and several cancers

CD1D encodes a divergent member of the CD1 family of transmembrane glycoproteins

Cytochrome c oxidase

O13A1 Polyclonal Antibody, 50ul Hepatocytes A mutation in this geneOlfactory 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