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Catalog Number | orb1730631 |
---|---|
Category | Antibodies |
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 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 KCNQ2 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. |
Species/Host | Rabbit |
Clonality | Polyclonal |
Tested applications | ELISA, IHC |
Reactivity | Human, Mouse, Rat |
Isotype | Rabbit IgG |
Immunogen | The antiserum was produced against synthesized peptide derived from human Kv7.3/KCNQ3 around the phosphorylation site of Thr246. AA range:191-240 |
Dilution range | IHC: 1/50-1/100; ELISA: 1/10000 |
Conjugation | Unconjugated |
Entrez | 3785, 9132, 3786, 56479 |
UniProt ID | P56696, O43526, O43525, Q9NR82 |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Buffer/Preservatives | Liquid in PBS containing 50% glycerol, 0.5% rAlbumin and 0.02% sodium azide, pH 7.3. |
Alternative names | KCNQ2; Potassium voltage-gated channel subfamily K Read more... |
Note | For research use only |
Expiration Date | 12 months from date of receipt. |
ELISA, IHC-P | |
Human, Mouse, Rat | |
Rabbit | |
Polyclonal | |
Unconjugated |
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