EDC4 Polyclonal Antibody, 20ul Mammalian Expression 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)

This enzyme binds bile acid with high affinity

KIR proteins are thought to play an important role in regulation of the immune response

Contains 2 Kazal-like domains

Part of a complex consisting of DCP1A

EDC4 Polyclonal Antibody, 20ul Mammalian Expression Defects in this gene areIn the process of mRNA degradation, seems to play a role in mRNA decapping. Component of a complex containing DCP2 and DCP1A which functions in decapping of ARE containing mRNAs. Promotes complex formation between DCP1A and DCP2. Enhances the Catalytic activity of DCP2 (in vitro).,PTM: Phosphorylated upon DNA damage, probably by ATM or ATR.,Belongs to the WD repeat EDC4 family.,Contains 4 WD repeats.,subunit: Part of a decapping complex consisting of