RFX5 Rabbit Polyclonal Antibody, 100ul Funnels PSCD family members have identical

PSCD family members have identical structural organization that consists of an N-terminal coiled-coil motif

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

which phosphorylates the carboxy-terminal domain (CTD) of the largest subunit of RNA polymerase II

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

RFX5 Rabbit Polyclonal Antibody, 100ul Funnels PSCD family members have identicalA 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