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KCNJ12


Official Full Name
potassium inwardly rectifying channel subfamily J member 12
Organism
Homo sapiens
Gene ID
3768
Background
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]
Synonyms
IRK2; hIRK; IRK-2; hIRK1; KCNJN1; Kir2.2; kcnj12x; hkir2.2x

Cat.No. Product Name Price
SHH323215 shRNA set against Human KCNJ12 (NM_021012.4) Inquiry
SHH323219 shRNA set against Mouse KCNJ12 (NM_010603.6) Inquiry
SHH323223 shRNA set against Rat KCNJ12 (NM_053981.2) Inquiry
SHL189642 shRNA set against Human KCNJ12(NM_021012.4) Inquiry
SHL189696 shRNA set against Rat Kcnj12(NM_053981.2) Inquiry
Cat.No. Product Name Price
CDFR013686 Rat Kcnj12 cDNA Clone(NM_053981.2) Inquiry
MiUTR1H-05135 KCNJ12 miRNA 3'UTR clone Inquiry
MiUTR1R-02819 KCNJ12 miRNA 3'UTR clone Inquiry
CDCR306454 Human KCNJ12 ORF Clone(NM_021012.4) Inquiry
CDCR380719 Rat Kcnj12 ORF Clone(NM_053981.2) Inquiry
CDCS415237 Human KCNJ12 ORF Clone (BC027982) Inquiry
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