KCNQ2/3/4/5(Phospho Thr217/246/223/251) Polyclonal Antibody, 20ul Modification Enzymes This member is a delayed

This member is a delayed rectifier potassium channel and its activity is modulated by some other family members

a rare salt wasting disease resulting from target organ unresponsiveness to mineralocorticoids

This receptor may play a role in smooth muscle contraction

Alternative splicing in the 5' UTR results in multiple transcr

The protein directly targets mitochondria and causes apoptotic changes

KCNQ2/3/4/5(Phospho Thr217/246/223/251) Polyclonal Antibody, 20ul Modification Enzymes This member is a delayedThe M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti convulsant drug. Defects in this