This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KCNJ12-20-RE | 20 (40 μL) | 200 μL |  |
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| KCNJ12-20-OR | 20 (40 μL) | 200 μL |  |
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| KCNJ12-20-GO | 20 (40 μL) | 200 μL |  |
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| KCNJ12-20-GR | 20 (40 μL) | 200 μL |  |
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| KCNJ12-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
Gene Symbol : KCNJ12
Gene Name : Potassium voltage-gated channel subfamily J member 12
Chromosome : CHR 17: 213,763,86-214,198,69
Locus : 17p11.2
Alt. Genes : CFM1
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