Smad2/3(Acetyl-Lys19) Polyclonal Antibody, 50ul Metabolic enzymes tool compounds Mutations in the gene cause

Mutations in the gene cause Sjogren-Larsson syndrome

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

Elevate your research with these 48-well cell and tissue culture plates

Smad2/3(Acetyl-Lys19) Polyclonal Antibody, 50ul Metabolic enzymes tool compounds Mutations in the gene causeThe 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