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)

and also a C-terminal domain which resembles enoyl-CoA-isomerase

ATG16L2 may play a role in autophagy

This gene encodes a member of the apolipoprotein B mRNA-editing enzyme catalytic polypeptide 3 family of proteins

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

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