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KCNJ8 抗体

(Potassium Inwardly-Rectifying Channel, Subfamily J, Member 8 (KCNJ8))
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins. Defects in this gene may be a cause of J-wave syndromes and sudden infant death syndrome (SIDS). [provided by RefSeq, May 2012].

Popular KCNJ8 抗体

Latest Publications for our KCNJ8 抗体

Wang, Hall, Kujawa, Li, Zhang, OMeara, Ichinose, Wang: "Methylglyoxal triggers human aortic endothelial cell dysfunction via modulation of the KATP/MAPK pathway." in: American journal of physiology. Cell physiology, Vol. 317, Issue 1, pp. C68-C81, (2019) (PubMed).

Aliases for KCNJ8 抗体

potassium voltage-gated channel subfamily J member 8 (KCNJ8) 抗体
potassium channel, inwardly rectifying subfamily J, member 8 (kcnj8) 抗体
potassium inwardly-rectifying channel, subfamily J, member 8 (Kcnj8) 抗体
potassium voltage-gated channel subfamily J member 8 (Kcnj8) 抗体
potassium inwardly-rectifying channel, subfamily J, member 8 (kcnj8) 抗体
potassium channel, inwardly rectifying subfamily J, member 8 S homeolog (kcnj8.S) 抗体
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