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Description
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]
Specifications
Specifications
| Antigen | KCNJ12 |
| Applications | Immunohistochemistry (PFA fixed) |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Rabbit polyclonal antibody raised against recombinant KCNJ12. |
| Dilution | Immunohistochemistry (1:200-1:500) The optimal working dilution should be determined by the end user. |
| Formulation | In PBS, pH 7.2, (40% glycerol, 0.02% sodium azide) |
| Gene | KCNJ12 |
| Gene Alias | FLJ14167/IRK2/KCNJN1/Kir2.2/Kir2.2v/hIRK/hIRK1/hkir2.2x/kcnj12x |
| Gene Symbols | KCNJ12 |
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