KCNQ2 蛋白
(Potassium Voltage-Gated Channel, KQT-Like Subfamily, Member 2 (KCNQ2))
The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
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custom-made
KCNQ2
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
KCNQ2
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 KCNQ2 蛋白
potassium voltage-gated channel subfamily Q member 2 (KCNQ2) 蛋白potassium voltage-gated channel, subfamily Q, member 2 (Kcnq2) 蛋白
potassium voltage-gated channel subfamily Q member 2 (Kcnq2) 蛋白
potassium voltage-gated channel subfamily KQT member 2 (LOC100537363) 蛋白
potassium voltage-gated channel, KQT-like subfamily, member 2a (kcnq2a) 蛋白
BFNC 蛋白
BFNS1 蛋白
EBN 蛋白
EBN1 蛋白
EIEE7 蛋白
ENB1 蛋白
HNSPC 蛋白
KCNA11 蛋白
KQT2 蛋白
KV7.2 蛋白
KVEBN1 蛋白
mKQT2.3 蛋白
mKQT2.4 蛋白
Nmf134 蛋白
zgc:171872 蛋白
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