| 产品详情 |
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| Antigenic Specificity | KCNQ3 |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | mouse |
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| Isotype | n/a |
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| Format | peptide affinity purified |
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| Size | 80 µl, 400 µl |
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| Concentration | n/a |
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| Applications | WB. RUO |
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| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
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| Description | 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 one of two related proteins encoded by the KCNQ2 and KCNQ5 genes, 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 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). This KCNQ3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 651-679 amino acids from the C-terminal region of human KCNQ3. |
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| Immunogen | Human KCNQ3. |
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| Other Names | KCNQ3; Potassium voltage-gated channel subfamily KQT member 3; KQT-like 3; Potassium channel subunit alpha KvLQT3; Voltage-gated potassium channel subunit Kv7.3; potassium voltage-gated channel, KQT-like subfamily, member 3; BFNC2; EBN2; KV7.3; potassium channel, voltage-gated, subfamily Q, member 3; potassium voltage-gated channel KQT-like protein 3 |
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| Gene, Accession # | KCNQ3, SwissProt: O43525 |
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| Catalog # | abx028226 |
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| Price | |
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| Order / More Info | KCNQ3 Antibody from ABBEXA |
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| Product Specific References | n/a |
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