RFX5 Rabbit Polyclonal Antibody, 100ul Funnels This gene encodes a putative

This gene encodes a putative 39S subunit protein and belongs to the L47P ribosomal protein family

and is concentrated at the leading edge of migratory cells

It is expressed in tissues involved in absorption and secretion and may contribute to the etiology of diabetes and other metabolic disorders

and two most abundant spliced variants encode the somatic form and the testicular form

is a 482 amino acid protein that localizes to the lysosomal membrane and belongs to the CCZ1 family

RFX5 Rabbit Polyclonal Antibody, 100ul Funnels This gene encodes a putativeA lack of MHC II expression results in a severe immunodeficiency syndrome called MHC II deficiency or the bare lymphocyte syndrome (BLS; MIM 209920). At least 4 complementation groups have been identified in B cell lines established from patients with BLS. The molecular defects in complementation groups B C and D all lead to a deficiency in RFX a nuclear protein complex that binds to the X box of MHC II promoters. The lack of RFX binding activity in