BCL3 Polyclonal Antibody, 100ul Cell Biology Mutations in this gene cause

Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness

also known as autosomal dominant speech and language disorder with orofacial dyspraxia

ETS family members have a highly conserved 85-amino acid ETS domain that binds purine-rich DNA sequences

6-bisphosphate

BCL3 Polyclonal Antibody, 100ul Cell Biology Mutations in this gene causeThis gene is a proto oncogene candidate. It is identified by its translocation into the immunoglobulin alpha locus in some cases of B cell leukemia. The protein encoded by this gene contains seven ankyrin repeats, which are most closely related to those found in I kappa B proteins. This protein functions as a transcriptional co activator that activates through its association with NF kappa B homodimers. The expression of this gene can be induced by NF