The human SCN1A gene encodes the pore-forming subunit of Nav1.1, a voltage-gated sodium channel expressed in CNS neurons and dorsal root ganglia. Mutations in SCN1A cause several types of epilepsies (generalized epilepsy with febrile seizures, severe myoclonic epilepsy in infancy) and some forms of familial hemiplegic migraine. Nav1.1 channels are therapeutic targets in seizure, stroke, and pain.
Product Information | |
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Catalog #: | ACC-RI0154 |
Gene Name | SCN1A |
Abbr | CHO-HuSCN1A |
Alias | SCN1A,EIEE6,FEB3,FEB3A,FHM3,GEFSP2,HBSCI,NAC1,Nav1.1,SCN1,SMEI |
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 | SCN1A,EIEE6,FEB3,FEB3A,FHM3,GEFSP2,HBSCI,NAC1,Nav1.1,SCN1,SMEI |
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