Smad2 Polyclonal Antibody, 50ul[BT-AP08378] DNA Fragments Defects in this gene are

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

Defects in this gene are a cause of the Cincinnati type of acrofacial dysostosis

Belongs to the glycosyl hydrolase 70 family

HLA-G is expressed on fetal derived placental cells

This protein thus is thought to function as a regulator of signal transduction by protein kinase cascade in brain and pancreatic beta-cells

Smad2 Polyclonal Antibody, 50ul[BT-AP08378] DNA Fragments Defects in this gene areMothers against decapentaplegic homolog 2 encoded by SMAD2 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