NR0B2 Polyclonal Antibody, 50ul Variant Libraries An important paralog of PGRMC2

An important paralog of PGRMC2 is PGRMC1

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

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

The protein encoded by this gene is the receptor for colony stimulating factor 1| a cytokine which controls the production| differentiation| and function of macrophages

NR0B2 Polyclonal Antibody, 50ul Variant Libraries An important paralog of PGRMC2The 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