Kir2.2 蛋白
(Potassium Inwardly-Rectifying Channel, Subfamily J, Member 12 (KCNJ12))
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].
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custom-made
KCNJ12
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
KCNJ12
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
Aliases for Kir2.2 蛋白
potassium voltage-gated channel subfamily J member 12 (KCNJ12) 蛋白ATP-sensitive inward rectifier potassium channel 12 (LOC746628) 蛋白
potassium voltage-gated channel subfamily J member 12 (Kcnj12) 蛋白
potassium inwardly-rectifying channel, subfamily J, member 12 (Kcnj12) 蛋白
hIRK 蛋白
hIRK1 蛋白
hkir2.2x 蛋白
IRK 蛋白
IRK-2 蛋白
IRK2 蛋白
kcnj12x 蛋白
KCNJN1 蛋白
Kir2.1 蛋白
Kir2.2 蛋白
KIR2.2 蛋白
Kir2.2v 蛋白
MB-IRK2 蛋白
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