Smad3 mouse Monoclonal Antibody(4C9), 50ul Molecular Biologyn Mutations in this gene cause

Mutations in this gene cause autosomal dominant nocturnal frontal lobe epilepsy type 4

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Does not oxidize spermidine

in addition to an F-box| this protein contains 10 tandem leucine-rich repeats

Smad3 mouse Monoclonal Antibody(4C9), 50ul Molecular Biologyn Mutations in this 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 functions as a transcriptional modulator activated by transforming growth factor beta and is thought to play a role in the regulation of