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ELK Biotechnology

ES6013

KCNQ2/3/4/5 (phospho Thr217/246/223/251) Rabbit Polyclonal Antibody

KCNQ2/3/4/5 (phospho Thr217/246/223/251) Rabbit Polyclonal Antibody

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KCNQ2/3/4/5 (phospho Thr217/246/223/251) Rabbit Polyclonal Antibody

Overview

Product name: KCNQ2/3/4/5 (phospho Thr217/246/223/251) rabbit pAb
Alternative Names: KCNQ2; Potassium voltage-gated channel subfamily KQT member 2; KQT-like 2; Neuroblastoma-specific potassium channel subunit alpha KvLQT2; Voltage-gated potassium channel subunit Kv7.2; KCNQ3; Potassium voltage-gated channel subfamily KQT me
Applications: WB;IHC;IF;ELISA
Recommended Dilutions: Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. Not yet tested in other applications.
Immunogen: The antiserum was produced against synthesized peptide derived from human Kv7.3/KCNQ3 around the phosphorylation site of Thr246. AA range:191-240
Storage: Rabbit
Storage: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
GeneID（Human）: 3785/3786/9132/56479
Human Swiss-Prot No: O43526/O43525/P56696/Q9NR82
Cellular localization: Cell membrane ; Multi-pass membrane protein .
Background: 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],
Species Reactivity: Human;Mouse;Rat
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