The human SCN2A gene encodes the pore-forming subunit of Nav1.2, a voltage-gated sodium channel expressed in CNS neurons. SCN2A mutations are associated with benign familial neonatal-infantile seizures. Nav1.2 channels are therapeutic targets in seizure, stroke, and pain.
Product Information | |
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Catalog #: | ACC-RI0157 |
Gene Name | SCN2A |
Abbr | HEK293-HuSCN2A |
Alias | SCN2A,BFIC3,BFIS3,BFNIS,EIEE11,HBA,HBSCI,NAC2,Na(v)1.2,Nav1.2,SCN2A1,SCN2A2 |
Growth Properties | Adherent |
Host Cell | HEK293 |
Morphology | Epithelial |
Shipping | Dry ice |
Product Type | Ion Channel Expressing Cell |
Channel Type | Sodium Channel |
Species | Human |
Product Format | frozen |
searchKeyword | SCN2A,BFIC3,BFIS3,BFNIS,EIEE11,HBA,HBSCI,NAC2,Na(v)1.2,Nav1.2,SCN2A1,SCN2A2 |
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