Gene: KCNJ6
Official Full Name: potassium inwardly rectifying channel subfamily J member 6provided by HGNC
Gene Summary: This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA15134 | KCNJ6 Knockout cell line (AC16) | Human | KCNJ6 | 1:3-1:4 | negative | Online Inquiry |
| KOA30578 | KCNJ6 Knockout cell line (BEAS-2B) | Human | KCNJ6 | 1:3~1:4 | negative | Online Inquiry |
| KOA46004 | KCNJ6 Knockout cell line (U-2932) | Human | KCNJ6 | 1:2-1:4 | negative | Online Inquiry |
| KOA61390 | KCNJ6 Knockout cell line (TPC-1) | Human | KCNJ6 | 1:5-1:8 | negative | Online Inquiry |
| KOA76818 | KCNJ6 Knockout cell line (NCM460) | Human | KCNJ6 | 1:2~1:3 | negative | Online Inquiry |
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