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KCNQ3


Official Full Name
potassium voltage-gated channel subfamily Q member 3
Organism
Homo sapiens
Gene ID
3786
Background
This gene encodes a protein that functions in the regulation of neuronal excitability. The encoded protein forms an M-channel by associating with the products of the related KCNQ2 or KCNQ5 genes, which both encode integral membrane proteins. M-channel currents are inhibited by M1 muscarinic acetylcholine receptors and are activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014]
Synonyms
EBN2; BFNC2; KV7.3

Cat.No. Product Name Price
SHL192182 shRNA set against Rat Kcnq3(NM_031597.3) Inquiry
SHH323667 shRNA set against Human KCNQ3 (NM_004519.3) Inquiry
SHH323671 shRNA set against Mouse KCNQ3 (NM_152923.2) Inquiry
SHH323675 shRNA set against Rat KCNQ3 (NM_031597.3) Inquiry
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CDFL006477 Mouse Kcnq3 cDNA Clone(NM_152923.2) Inquiry
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CDCB184216 Rabbit KCNQ3 ORF clone (XM_008255917.1) Inquiry
CDCL123321 Human KCNQ3 ORF clone (NM_001204824.1) Inquiry
CDCR270035 Mouse Kcnq3 ORF Clone(NM_152923.2) Inquiry
CDCR379616 Rat Kcnq3 ORF Clone(NM_031597.3) Inquiry
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CC-735 KCNQ3 Easy KO Kit Inquiry
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