購物車
幫助
021-54845833/15800441009
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Background: |
This gene encodes a protein that functions in the regulation of neuronal excitability. The encoded protein forms an M-channel by associating with the products of the related KCNQ2 or KCNQ5 genes, which both encode integral membrane proteins. M-channel currents are inhibited by M1 muscarinic acetylcholine receptors and are activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). Alternative splicing of this gene results in multiple transcript variants. |
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Applications: |
ELISA, IHC |
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Name of antibody: |
KCNQ3 |
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Immunogen: |
Synthetic peptide of human KCNQ3 |
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Full name: |
potassium channel, voltage gated KQT-like subfamily Q, member 3 |
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Synonyms: |
EBN2; BFNC2; KV7.3 |
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SwissProt: |
O43525 |
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ELISA Recommended dilution: |
2000-5000 |
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IHC positive control: |
Human tonsil |
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IHC Recommend dilution: |
25-100 |
