Kir2.2 抗体
(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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Latest Publications for our Kir2.2 抗体
: "Inward rectifier potassium currents in mammalian skeletal muscle fibres." in: The Journal of physiology, Vol. 593, Issue 5, pp. 1213-38, (2015) (PubMed).: "Cortactin is required for N-cadherin regulation of Kv1.5 channel function." in: The Journal of biological chemistry, Vol. 286, Issue 23, pp. 20478-89, (2011) (PubMed).
: "Regulation of cardiac inward rectifier potassium current (I(K1)) by synapse-associated protein-97." in: The Journal of biological chemistry, Vol. 285, Issue 36, pp. 28000-9, (2010) (PubMed).
Aliases for Kir2.2 抗体
potassium voltage-gated channel subfamily J member 12 (KCNJ12) 抗体ATP-sensitive inward rectifier potassium channel 12 (LOC746628) 抗体
potassium voltage-gated channel subfamily J member 12 (Kcnj12) 抗体
potassium inwardly-rectifying channel, subfamily J, member 12 (Kcnj12) 抗体
hIRK 抗体
hIRK1 抗体
hkir2.2x 抗体
IRK 抗体
IRK-2 抗体
IRK2 抗体
kcnj12x 抗体
KCNJN1 抗体
Kir2.1 抗体
Kir2.2 抗体
KIR2.2 抗体
Kir2.2v 抗体
MB-IRK2 抗体
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