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 | |
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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 |
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