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Human SCN4A Stable Cell Line-CHO

Cat.No.
CSC-RI0162
Human SCN4A Stable Cell Line-CHO
Abbr
CHO-HuSCN4A
Alias
SCN4A,HOKPP2,HYKPP,HYPP,NAC1A,Na(V)1.4,Nav1.4,SkM1
Growth Properties
Adherent
Host Cell
CHO-K1
Morphology
Epithelial-like
Shipping
Dry ice
Species
Human
Background
The human SCN4A gene encodes the pore-forming subunit of Nav1.1, a voltage-gated sodium channel expressed in skeletal muscle. SCN4A mutations cause paramyotonia congenita and hypokalemic periodic paralysis. Nav1.4 are therapeutic targets in myotonia.

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