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KCNJ6
Potassium inwardly rectifying channel subfamily J member 6BIR1, GIRK2, hiGIRK2, KATP2, KCNJ7, Kir3.2
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]
Top validated antibodies |
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| Novus Biologicals |  NB100-74575 |
3 references | Polyclonal |
WB
EL
ICC
IHC
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| Proteintech Group | 21647-1-AP |
4 references | Polyclonal |
WB
EL
IHC
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| GeneTex | GTX54832 |
Polyclonal |
WB
ICC
IP
IHC
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| NovoPro Bioscience Inc. | 119212 |
Polyclonal |
WB
EL
IHC
FC
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| antibodies-online | ABIN2840507 |
Polyclonal |
WB
IHC
FC
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