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Human SCN4A Stable Cell Line-CHO

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Cat.No.
CSC-RI0162
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.
Growth Properties
Adherent
Morphology
Epithelial-like
Host Cell
CHO-K1
Ship
Dry ice
Gene Information
Official Symbol
SCN4A
Synonyms
SCN4A; HOKPP2; HYKPP; HYPP; NAC1A; Na(V)1.4; Nav1.4; SkM1; sodium channel, voltage-gated, type IV, alpha subunit; skeletal muscle voltage-dependent sodium channel type IV alpha subunit; sodium channel protein skeletal muscle subunit alpha; sodium channel protein type 4 subunit alpha; sodium channel protein type IV subunit alpha; voltage-gated sodium channel subunit alpha Nav1.4
Gene ID
MIM
UniProt ID
P35499
Chromosome Location
17q23.3
Pathway
Axon guidance, organism-specific biosystem; Developmental Biology, organism-specific biosystem; Interaction between L1 and Ankyrins, organism-specific biosystem; L1CAM interactions, organism-specific biosystem;
Function
voltage-gated sodium channel activity;

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