Smad3(Phospho Ser208) Polyclonal Antibody, 50ul Gene Editing Mutations and deletions in NKX2-1

Mutations and deletions in NKX2-1 are associated with benign hereditary chorea

a glycine/phenylalanine-rich region

The protein encoded by this gene is an abundant integral membrane protein of cholinergic synaptic vesicles and is thought to be involved in vesicular transport

the histone acetyltransferase complex TRRAP/TIP60 as well as the chromatin remodeling SRCAP-containing complex

Smad3(Phospho Ser208) Polyclonal Antibody, 50ul Gene Editing Mutations and deletions in NKX2-1The 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