CACNB3 Polyclonal Antibody, 20ul Site-directed Mutagenesis Defects in this gene are

Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC)

in addition to the MAPKK pathways

inactivate RHO family proteins by stimulating their hydrolysis of GTP

Mutations in CYC1 may cause mitochondrial complex III deficiency

CACNB3 Polyclonal Antibody, 20ul Site-directed Mutagenesis Defects in this gene areThis 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.