KCNH6 Polyclonal Antibody, 100ul Glassware Sets and also familial hypertrophic cardiomyopathy

and also familial hypertrophic cardiomyopathy

Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency

This protein is preferentially expressed in human intestinal intraepithelial lymphocytes (IEL)

Allelic variations in this gene are associated with heparin cofactor II deficiency

This gene belongs to a family of putative cation channels that are specific to spermatozoa and localize to the flagellum

KCNH6 Polyclonal Antibody, 100ul Glassware Sets and also familial hypertrophic cardiomyopathyVoltage 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