BCL6B Polyclonal Antibody, 50ul RNA Synthesis Mutations in this gene cause

Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome

BMPs are involved in endochondral bone formation and embryogenesis

Expressed by B-lymphocytes

cell metabolism

A pseudogene has been identified on chromosome 22

BCL6B Polyclonal Antibody, 50ul RNA Synthesis Mutations in this gene causeActs as a sequence specific transcriptional repressor in association with BCL6. May function in a narrow stage or be related to some events in the early B cell development.,Contains 1 BTB (POZ) domain.,Contains 5 C2H2 type zinc fingers.,subunit: Associates with BCL6 through the BTB domain.,tissue specificity: Ubiquitously expressed with higher expression found in heart and placenta.,