NKAP Polyclonal Antibody, 20ul Cell Biology It encodes a heparin-binding protein

It encodes a heparin-binding protein

Defects in ACTA2 cause aortic aneurysm familial thoracic type 6

This gene encodes a member of the epidermal growth factor receptor (EGFR) family of receptor tyrosine kinases

Defects in HSPB1 are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

The product of MED13 is proposed to form a sub-complex with MED12

NKAP Polyclonal Antibody, 20ul Cell Biology It encodes a heparin-binding proteinThis gene encodes a protein that is involved in the activation of the ubiquitous transcription factor NF kappaB. This protein is associated with the the histone deacetylase HDAC3 and with the Notch corepressor complex, and it thereby acts as a transcriptional repressor of Notch target genes. It is also required for alphabeta T cell development. A related pseudogene has been identified on chromosome X, while a related and intronless retrocopy, which