NR0B2 Polyclonal Antibody, 50ul Variant Libraries more recent studies in different

more recent studies in different populations have been unable to replicate this association

that fuses PDGFRB to that of the translocation

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

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

NR0B2 Polyclonal Antibody, 50ul Variant Libraries more recent studies in differentThe 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