NR0B2 Polyclonal Antibody, 50ul Variant Libraries Mutations in this gene are

Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10)

The encoded protein may represent an important signaling intermediate between neuropeptide-activated receptors or neurotransmitters that increase calcium flux and the downstream signals that regulate neuronal activity

which promotes survival of pancreatic beta-cells

Sterol-C4-mehtyl oxidase-like protein was isolated based on its similarity to the yeast ERG25 protein

The concentrative nucleoside transporter (CNT) family comprises three members: CNT1

NR0B2 Polyclonal Antibody, 50ul Variant Libraries Mutations in this gene areThe protein encoded by this gene is an unusual orphan receptor that contains a putative ligand binding domain but lacks a conventional DNA binding domain. The gene product is a member of the nuclear hormone receptor family, a group of transcription factors regulated by small hydrophobic hormones, a subset of which do not have known ligands and are referred to as orphan nuclear receptors. The protein has been shown to interact with retinoid and thyroid