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)

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

Alternative splicing results in several additional transcript variants| some encoding d

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

The N-terminus of the encoded protein has six EGF-like modules

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.