KCNQ2/3/4/5(Phospho Thr217/246/223/251) Polyclonal Antibody, 20ul Modification Enzymes a rare salt wasting disease

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

Alternative splicing in the 5' UTR results in multiple transcr

This gene belongs to the protein kinase superfamily

This receptor may play a role in smooth muscle contraction

NUP160 is 1 of up to 60 proteins that make up the 120-MD nuclear pore complex

KCNQ2/3/4/5(Phospho Thr217/246/223/251) Polyclonal Antibody, 20ul Modification Enzymes a rare salt wasting diseaseThe 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