RFX5 Rabbit Polyclonal Antibody, 100ul Funnels This protein may play a

This protein may play a role in neuroblast division and in the development of normal hearing

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

Mutations in this gene cause Costello syndrome

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

RFX5 Rabbit Polyclonal Antibody, 100ul Funnels This protein may play aA 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