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Human SCN4A Stable Cell Line-CHO

See other products for SCN4A
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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SCN4A
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CSC-RI0050
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Cat#
Product Name
Titer
Product Size
Species
Price
AD14308Z
>1x 10^9 vp/ml
1 x 0.2 ml
Human

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Fax: 1-631-614-7828
Email: info@creative-biogene.com

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Email: info@creative-biogene.com
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45-1 Ramsey Road, Shirley, NY 11967, USA
Tel: 1-631-626-9181
Fax: 1-631-614-7828
Email: info@creative-biogene.com

Europe
Tel: 44-207-097-1828

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