CACNB3 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in CYC1 may cause

Mutations in CYC1 may cause mitochondrial complex III deficiency

This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis

The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell

Antiapoptotic protein BCL2-associated athanogene 4 (BAG4/SODD) and adaptor proteins TRADD and TRAF2 have been shown to interact with this receptor

in addition to the MAPKK pathways

CACNB3 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in CYC1 may causeThis gene encodes a regulatory beta subunit of the voltage dependent calcium channel. Beta subunits are composed of five domains, which contribute to the regulation of surface expression and gating of calcium channels and may also play a role in the regulation of transcription factors and calcium transport.