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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 |
| Channel Subgroup | Inwardly rectifying (Kir) |
| Channel Type | Potassium Channel |
| Growth Properties | Adherent |
| Host Cell | HEK293 |
| Morphology | Epithelial |
| Product Format | frozen |
| Product Type | Ion Channel Expressing Cell |
| searchKeyword | KCNJ1,Kir1.1,ROMK1,ROMK,KIR1.1 |
| Shipping | Dry ice |
| Species | Human |
Our products are only for research use. Not intended for any clinical or diagnostic use.
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