Smad2/3(Acetyl-Lys19) Polyclonal Antibody, 50ul Metabolic enzymes tool compounds Defects in this gene are

Defects in this gene are a cause of mental retardation autosomal dominant type 5 (MRD5)

Activins signal through a heteromeric complex of receptor serine kinases which include at least two type I (I and IB) and two type II (II and IIB) receptors

Glucagon is a ligand for a specific G-protein linked receptor whose signalling pathway controls cell proliferation

Mutations in the gene cause Sjogren-Larsson syndrome

ATG16L2 may play a role in autophagy

Smad2/3(Acetyl-Lys19) Polyclonal Antibody, 50ul Metabolic enzymes tool compounds Defects in this gene areThe protein encoded by this gene 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 mediates the signal of the transforming growth factor (TGF) beta and thus regulates multiple cellular processes such as cell