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Human SCN4A Stable Cell Line-CHO
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.
| Product Information | |
|---|---|
| Catalog #: | ACC-RI0162 |
| Gene Name: | SCN4A |
| Abbr | CHO-HuSCN4A |
| Alias | SCN4A,HOKPP2,HYKPP,HYPP,NAC1A,Na(V)1.4,Nav1.4,SkM1 |
| Channel Type | Sodium Channel |
| Growth Properties | Adherent |
| Host Cell | CHO-K1 |
| Morphology | Epithelial-like |
| Product Format | frozen |
| Product Type | Ion Channel Expressing Cell |
| searchKeyword | SCN4A,HOKPP2,HYKPP,HYPP,NAC1A,Na(V)1.4,Nav1.4,SkM1 |
| Shipping | Dry ice |
| Species | Human |
Related Products
| Catalog | Product Name | Gene Name | Species | Morphology | Price |
|---|---|---|---|---|---|
| ACC-RI0050 | Human SCN4A Stable Cell Line-HEK293 | SCN4A | Human | Epithelial | INQUIRY |
Our products are only for research use. Not intended for any clinical or diagnostic use.
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