KCNQ2

gene product
BFNC, EBN, EBN1, ENB1, HNSPC, KCNA11, Kv7.2
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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antibodies-online
130 antibodies
Novus Biologicals
3 antibodies
Invitrogen Antibodies
2 antibodies
LifeSpan BioSciences, Inc.
44 antibodies
Abnova Corporation
3 antibodies
Atlas Antibodies
2 antibodies
GeneTex
4 antibodies
Aviva Systems Biology
6 antibodies
OriGene
6 antibodies
Rockland Immunochemicals, Inc.
1 antibody
Biorbyt
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Boster Biological Technology
2 antibodies
Cell Signaling Technology, Inc
1 antibody
NovoPro Bioscience Inc.
1 antibody
Creative Biolabs
3 antibodies
Creative Diagnostics
2 antibodies
MyBioSource
3 antibodies
NSJ Bioreagents
1 antibody
ProSci
1 antibody
Acris Antibodies GmbH
3 antibodies
Antibodies Incorporated
2 antibodies
St John's Laboratory
3 antibodies
United States Biological
1 antibody
Abbkine Scientific Co.Ltd.
2 antibodies
Sigma-Aldrich
5 antibodies
Abgent
2 antibodies
EMD Millipore
1 antibody
UC Davis/NIH NeuroMab Facility
2 antibodies