Smad3 Polyclonal Antibody, 100ul[BT-AP08392] Pathway and Network Analysis This gene encodes a member

This gene encodes a member of the lysophospholipid acyltransferase family

Mutations in this gene have been associated with KBG syndrome| which is characterized by macrodontia| distinctive craniofacial features| short stature| skeletal anomalies| global developmental delay| seizures and intellectual disability

PAK proteins| a family of serine/threonine p21-activating kinases| include PAK1| PAK2| PAK3 and PAK4

and it has a potential role in renovascular hypertension which has known correlations to renal failure

Experience secure and efficient centrifugation with our 1

Smad3 Polyclonal Antibody, 100ul[BT-AP08392] Pathway and Network Analysis This gene encodes a memberThe protein encoded by SMAD3 belongs to the SMAD, a family of proteins similar to the gene products of the Drosophila gene mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein functions as a transcriptional modulator activated by transforming growth factor beta and is thought to play a role in the regulation of