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

Defects in this gene can result in three different disorders

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

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

Type I and II receptors form a stable complex after ligand binding

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