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 | |
|---|---|
| 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 |
| Channel Type | Sodium Channel |
| Growth Properties | Adherent |
| Host Cell | HEK293 |
| Morphology | Epithelial |
| Product Format | frozen |
| Product Type | Ion Channel Expressing Cell |
| searchKeyword | SCN2A,BFIC3,BFIS3,BFNIS,EIEE11,HBA,HBSCI,NAC2,Na(v)1.2,Nav1.2,SCN2A1,SCN2A2 |
| Shipping | Dry ice |
| Species | Human |
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| Catalog | Product Name | Gene Name | Species | Morphology | Price |
|---|---|---|---|---|---|
| ACC-RI0048 | Human SCN2A Stable Cell Line-CHO | SCN2A | Human | Epithelial-like | INQUIRY |
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