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Human KCNJ1 Stable Cell Line-HEK293

Kir1.1 is an inwardly rectifying potassium channel expessed in kidney, skeletal muscle, liver, pancreas, spleen, and the central nervous system. Mutations in Kir1.1 are responsible for Bartter"s syndrome (renal salt loss) and hereditary hypertension with hyperkalemia. Kir1.1 has therapeutic potential in treatment of hypertension.

Product Information
Catalog #:  ACC-RI0114
Gene Name KCNJ1
Abbr HEK293-HuKCNJ1
Alias KCNJ1,Kir1.1,ROMK1,ROMK,KIR1.1
Growth Properties Adherent
Host Cell HEK293
Morphology Epithelial
Shipping Dry ice
Product Type Ion Channel Expressing Cell
Channel Type Potassium Channel
Channel Subgroup Inwardly rectifying (Kir)
Species Human
Product Format frozen
searchKeyword KCNJ1,Kir1.1,ROMK1,ROMK,KIR1.1
Our products are only for research use. Not intended for any clinical or diagnostic use.

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