Mouse monoclonal antibody [S26A-23] to KCNQ2The 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]
Immunogen
Fusion protein amino acids 1-59 of human KCNQ2, accession number O43526
Key Feature
Clonality
Monoclonal
Isotype
IgG1
Clone Number
S26A-23
Host Species
Mouse
Tested Applications
IHCIHC-FIPWB
We recommend a working dilution of 1-10ug/mL (WB), 0.1-1.0ug/mL (Perox) (IHC/ICC), 1.0-10ug/mL (IF).:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml (Please refer to the vial label for the specific concentration)
Purification
Protein G
Target Information
Gene Synonyms
KCNQ2 KV7.2 ENB1 voltage gated potassium channel subunit Kv7.2 KQT like2 BFNC KCNA11 KVEBN1. KvLQT2 HNSPC KQT like 2 EBN1
Target
KCNQ2
Molecular Weight(MW)
95kDa (note)
Application
Application
IHC analysis of KCNQ2 in human hippocampal tissues using
Application
IHC analysis of KCNQ2 in frozen sections of mouse brain using
Application Notes
We recommend a working dilution of 1-10ug/mL (WB), 0.1-1.0ug/mL (Perox) (IHC/ICC), 1.0-10ug/mL (IF).:
Additional Information
Form
Liquid
Storage Instructions
Aliquot and store at -20 C. Avoid repeated freeze-thaw cycles.