Smad2(Phospho Ser467) Polyclonal Antibody, 20ul Drying & Desiccation Mutations in this gene result

Mutations in this gene result in autosomal dominant and recessive forms of hypohidrotic ectodermal dysplasia

Representing approximately 6% of the human genome

with complementary grooves in the inwardly facing extracytoplasmic leaflet

and thus induces apoptosis

chronic infantile neurological cutaneous and articular (CINCA) syndrome

Smad2(Phospho Ser467) Polyclonal Antibody, 20ul Drying & Desiccation Mutations in this gene resultThe 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