Cav3.3 Polyclonal Antibody, 20ul Protein Research Defects in this gene cause

Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency

which leads to stabilization of p53/TP53

Diseases associated with HTR1E include attention deficit-hyperactivity disorder

Transient transfection of this gene confers both NAALADase and dipetidyl peptidase IV activities to mammalian cells

Cav3.3 Polyclonal Antibody, 20ul Protein Research Defects in this gene causeThis gene encodes the pore forming alpha subunit of a voltage gated calcium channel. The encoded protein is a member of a subfamily of calcium channels referred to as is a low voltage activated, T type, calcium channel. The channel encoded by this protein is characterized by a slower activation and inactivation compared to other T type calcium channels. This protein may be involved in calcium signaling in neurons. Alternate splicing results in