Smad3 Polyclonal Antibody, 20ul[BT-AP14309] Adeno-associated Virus Packaging Defects in this gene are

Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

The activity of this ubiquitin ligase has been implicated in the development of certain forms of Parkinson's disease| the regulation of the cellular response to hypoxia and induction of apoptosis

The human engrailed homologs 1 and 2 encode homeodomain-containing proteins and have been implicated in the control of pattern formation during development of the central nervous system

Alpha-CPs play important roles in post-transcriptional activities and have different cellular distributions

and NF-kappa-B

Smad3 Polyclonal Antibody, 20ul[BT-AP14309] Adeno-associated Virus Packaging Defects in this gene areThe 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