Smad2 Polyclonal Antibody, 50ul[BT-AP08378] DNA Fragments subunit:Interacts with CLK1

subunit:Interacts with CLK1

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

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

Phosphorylation of the receptor attenuates signaling (Matteson et al

HLA-G is expressed on fetal derived placental cells

Smad2 Polyclonal Antibody, 50ul[BT-AP08378] DNA Fragments subunit:Interacts with CLK1Mothers 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