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Human SCN1A Stable Cell Line-CHO

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
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

Related Products

Catalog Product Name Gene Name Species Morphology Price
ACC-RI0047 Human SCN1A Stable Cell Line-HEK293 SCN1A Human Epithelial INQUIRY
Our products are only for research use. Not intended for any clinical or diagnostic use.

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