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KCNQ2

The potassium channel M, which slowly activates and deactivates, is essential for controlling the excitability of neurons. The protein produced by this gene and a similar protein expressed by the KCNQ3 gene, both of which are essential membrane proteins, come together to create the M channel. M1 muscarinic acetylcholine receptors inhibit M channel currents, while retigabine, a novel anti-convulsant medication, activates them. Benign neonatal type 1 epilepsy, also known as benign familial neonatal convulsions type 1, is brought on by errors in this gene.

Full Name Potassium voltage-gated channel subfamily Q member 2
Gene ID Human: 3785
Mouse: 16536
Rat: 170848
Monkey: 719614
UniProt ID Human: O43526
Mouse: Q9Z351
Rat: O88943
Monkey: F7ASD7
Alternative Names EBN; BFNC; DEE7; EBN1; ENB1; HNSPC; KV7.2; KCNA11; potassium voltage-gated channel subfamily KQT member 2; neuroblastoma-specific potassium channel subunit alpha KvLQT2; potassium channel, voltage gated KQT-like subfamily Q, member 2; voltage-gated potassium channel subunit Kv7.2; KCNQ2; Potassium voltage-gated channel subfamily Q member 2

Product List

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Product Category:
Membrane Protein Stable Cell Lines
Target Protein: KCNQ2/KCNQ3 Target Family: Voltage Gated Potassium Channel Target Protein Species: Human
Product Category:
Membrane Protein Stable Cell Lines
Target Protein: KCNQ2/KCNQ4 Target Family: Voltage Gated Potassium Channel Target Protein Species: Human
Product Category:
Membrane Protein Stable Cell Lines
Target Protein: KCNQ2 Target Family: Kv7 Target Protein Species: Human Host Cell Type: CHO-K1; HEK293
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