KCNH4 Rabbit Polyclonal Antibody, 100ul 3D Culture Type II hyperoxaluria is caused

Type II hyperoxaluria is caused by mutations in this gene

It has essential roles in B cell growth and differentiation

Immunohistochemistry showed that FAM3A is expressed prominently in the vascular endothelium

The protein encoded by this gene is a cyclosporine-binding protein and is mainly located within the endoplasmic reticulum

KCNH4 Rabbit Polyclonal Antibody, 100ul 3D Culture Type II hyperoxaluria is causedVoltage gated potassium (Kv) channels represent the most complex class of voltage gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release heart rate insulin secretion neuronal excitability epithelial electrolyte transport smooth muscle contraction and cell volume. This gene encodes a member of the potassium channel voltage gated subfamily H. This member is a pore forming