KCNQ2/3/4/5(Phospho Thr217/246/223/251) Polyclonal Antibody, 100ul Filtration posttranlational processing of proteins

posttranlational processing of proteins

Inactivating variants of this gene result in the recessive Lutheran null phenotype

Easy to use with high sensitivity and accuracy

which is enhanced by high levels of polyamines

Pseudogenes of this gene are located on the short arm of chromosomes 3

KCNQ2/3/4/5(Phospho Thr217/246/223/251) Polyclonal Antibody, 100ul Filtration posttranlational processing of proteinsThe 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