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Human KCNA1 Stable Cell Line-HEK293

The human KCNA1 gene encodes the pore-forming subunit of Kv1.1, a voltage-gated potassium channel. Mutations in KCNA1 cause several congenital disorders including episodic ataxia type 1, neuromyotonia, and autosomal dominant hypomagnesia. Kv1.1 channels expressed in neurons are therapeutic targets in multiple sclerosis, stroke and seizure.

Product Information
Catalog #:  ACC-RI0121
Gene Name KCNA1
Abbr HEK293-HuKCNA1
Alias KCNA1,AEMK,HUK1,Kv1.1,MBK1,RBK1,EA1,MK1,HBK1,KV1.1,MGC126782,MGC138385
Growth Properties Adherent
Host Cell HEK293
Morphology Epithelial
Shipping Dry ice
Product Type Ion Channel Expressing Cell
Channel Type Potassium Channel
Channel Subgroup Voltage-gated (Kv)
Species Human
Product Format frozen
searchKeyword KCNA1,AEMK,HUK1,Kv1.1,MBK1,RBK1,EA1,MK1,HBK1,KV1.1,MGC126782,MGC138385

Related Products

Catalog Product Name Gene Name Species Morphology Price
ACC-RI0026 Human KCNA1 Stable Cell Line-CHO KCNA1 Human Epithelial-like INQUIRY
Our products are only for research use. Not intended for any clinical or diagnostic use.

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