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.
Human Kv1.1 Potassium Channel Cell Line
For pricing information, detailed technical sheets, or to speak with one of our experts, please contact us at 1.877.CRIVER.1 (1.877.274.8371) or by using our online form.
Can't find what you are looking for? Contact us. We are always developing new cell lines and can work with you on custom projects.