The human SCN8A gene encodes the pore-forming subunit of Nav1.6, a voltage-gated sodium channel expressed in central and peripheral nervous systems. Mutations in the mouse ortholog cause ataxia and other movement disorders. Nav1.6 channels are therapeutic targets in multiple sclerosis and seizure.
Product Information | |
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Catalog #: | ACC-RI0168 |
Gene Name | SCN8A |
Abbr | CHO-HuSCN8A |
Alias | SCN8A,CerIII,NaCh6,Nav1.6,PN4,MED,CIAT,CERIII,EIEE13,FLJ33996 |
Growth Properties | Adherent |
Host Cell | CHO |
Morphology | Epithelial-like |
Shipping | Dry ice |
Product Type | Ion Channel Expressing Cell |
Channel Type | Sodium Channel |
Species | Human |
Product Format | frozen |
searchKeyword | SCN8A,CerIII,NaCh6,Nav1.6,PN4,MED,CIAT,CERIII,EIEE13,FLJ33996 |
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