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Human KCNA1 Stable Cell Line-CHO

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Cat.No.
CSC-RI0026
Background
Kv1.1 is a voltage-gated, delayed rectifier, potassium channel. It is expressed in the brain, heart, retina, skeletal muscle and pancreatic islets and is primarily involved with maintaining the resting membrane potential and modulating electrical excitability in neurons and muscle cells. Mutations of this ion channel have been linked to episodic ataxia, an autosomal dominant human disorder that produces persistent myokymia (successive, involuntary, small muscle contractions or tics that affect a bundle of muscles).
Growth Properties
Adherent
Morphology
Epithelial-like
Host Cell
CHO-K1
Ship
Dry ice
Gene Information
Official Symbol
KCNA1
Synonyms
KCNA1; potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia); AEMK; potassium voltage-gated channel subfamily A member 1; HUK1; Kv1.1; MBK1; RBK1; voltage-gated K(+) channel HuKI; voltage-gated potassium channel HBK1; voltage-gated potassium channel subunit Kv1.1; EA1; MK1; HBK1; KV1.1; MGC126782; MGC138385;
Gene ID
MIM
UniProt ID
Q09470
Chromosome Location
12p13
Pathway
Neuronal System, organism-specific biosystem; Potassium Channels, organism-specific biosystem; Voltage gated Potassium channels, organism-specific biosystem;
Function
delayed rectifier potassium channel activity; potassium channel activity; potassium ion transmembrane transporter activity; voltage-gated ion channel activity;

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