CBP Polyclonal Antibody, 50ul[BT-AP01269] Capsule Filter Mutations in this gene are

Mutations in this gene are the cause of certain genetically-related cataract disorders

such as hypotension

and plays a role in pre-mRNA splicing

and it associates maximally with the nucleotide-free states of these GTPases

may be associated with split-hand/split-foot malformation

CBP Polyclonal Antibody, 50ul[BT-AP01269] Capsule Filter Mutations in this gene areCREBBP is ubiquitously expressed and is involved in the transcriptional coactivation of many different transcription factors. First isolated as a nuclear protein that binds to cAMP response element binding protein (CREB), CREBBP is now known to play critical roles in embryonic development, growth control, and homeostasis by coupling chromatin remodeling to transcription factor recognition. CREB binding protein has intrinsic histone acetyltransferase