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- W2013804913 abstract "By functional coexpression screening of a rat cDNA library in Xenopus oocytes, we have cloned a protein (KCRF: K Channel Regulatory Factor) that reduces currents of several K+ channels: G protein-activated GIRK1/4 (Kir3.1/Kir3.4), inward rectifier IRK1 (Kir2.1), and voltage-dependent KV1.1/KVβ1.1. KCRF did not modulate two other K+ channels: ROMK1 (Kir1.1) and GIRK1/2 (Kir3.1/Kir3.2) and the voltage-dependent L-type Ca2+ channels. Western blot analysis showed that KCRF is ubiquitous in rat tissues. Biochemical and electrophysiological experiments revealed that coexpression of KCRF causes a decrease in the level of expression of IRK1 and KV1.1/KVβ1.1 proteins in the oocytes." @default.
- W2013804913 created "2016-06-24" @default.
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- W2013804913 date "2000-08-01" @default.
- W2013804913 modified "2023-09-25" @default.
- W2013804913 title "Expression Cloning of KCRF, a Potassium Channel Regulatory Factor" @default.
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- W2013804913 doi "https://doi.org/10.1006/bbrc.2000.3240" @default.
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