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

Type II hyperoxaluria is caused by mutations in this gene

The protein encoded by this gene plays a crucial role in B-cell development

CCT7 encodes a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT)

These proteins contain conserved cysteine residues at fixed positions| and are distantly related to MIP-1alpha| a member of the CC-chemokine family

Immunohistochemistry showed that FAM3A is expressed prominently in the vascular endothelium

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