KCNQ3
This gene encodes a protein that controls the excitability of neurons. By joining forces with the by-products of the related KCNQ2 or KCNQ5 genes, which both produce integral membrane proteins, the encoded protein creates an M-channel. M1 muscarinic acetylcholine receptors suppress M-channel currents, while retigabine, a novel anti-convulsant medication, activates them. Epilepsy, benign neonatal type 2, or benign familial neonatal convulsions type 2 are both caused by defects in this gene.
| Full Name | Potassium voltage-gated channel subfamily Q member 3 |
| Gene ID | Human: 3786 Mouse: 110862 Rat: 29682 Monkey: 700785 |
| UniProt ID | Human: O43525 Mouse: Q8K3F6 Rat: O88944 Monkey: F7DI95 |
| Alternative Names | EBN2; BFNC2; KV7.3; potassium voltage-gated channel subfamily KQT member 3; potassium channel subunit alpha KvLQT3; potassium channel, voltage gated KQT-like subfamily Q, member 3; potassium channel, voltage-gated, subfamily Q, member 3; potassium voltage-gated channel, KQT-like subfamily, member 3; voltage-gated potassium channel subunit Kv7.3; KCNQ3; Potassium voltage-gated channel subfamily Q member 3 |
Product List
Loading...
mProX™ Human KCNQ3 Stable Cell Line
[CAT#: S01YF-1123-KX32]
- Product Category:
- Membrane Protein Stable Cell Lines
- Target Protein: KCNQ3 Target Family: Kv7 Target Protein Species: Human Host Cell Type: CHO-K1; HEK293
Can't find the products you're looking for? Optimize our parameters for better results.
Filter By Tag
Note: All of our products are for Research Use Only (RUO). NOT intended for diagnostic, therapeutic or clinical use. We DO NOT offer patients any direct products or services. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.
