TypeProteinGeneDiseasesCatalogueAvailable
Eag-relatedKv11.2KCNH6 GI-19727          
Eag-relatedKv11.3KCNH7 GI-19728          
Eag-relatedKv12.1KCNH8 GI-19728
Inwardly rectifyingKir1.1KCNJ1Bartter syndromeGI-19739          
Inwardly rectifyingKir2.1KCNJ2Atrial fibrillation, Andersen syndromeGI-19740          
Inwardly rectifyingKir3.1KCNJ3 
Inwardly rectifyingKir2.3KCNJ4 
Inwardly rectifyingKir3.4KCNJ5 
Inwardly rectifyingKir3.2KCNJ6, KCNJ7Implication in Down’s syndrome
Inwardly rectifyingKir6.1KCNJ8Impaired coronary vasomotility
Inwardly rectifyingKir3.3KCNJ9 
Inwardly rectifyingKir4.1, Kir1.2KCNJ10General seizure susceptibility
Inwardly rectifyingKir6.2KCNJ11Inherited diabetes mellitus type II
Inwardly rectifyingKir2.2KCNJ12Smith-Magenis syndrome gene regionGI-19741          
Inwardly rectifyingKir7.1, Kir1.4KCNJ13Snowflake vitreoretinal degeneration    
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Potassium Channels 
ORDERING: Browse through our ChanClone™ collection. Check individual subfamilies to find your relevant target. Once identified, please use the catalogue number to place a quotation. Also let us know if you are interested in corresponding polymorphic variants or mutated ion channel alleles. We are happy to share our knowledge and hope our ChanClone™ catalogue will be of benefit.