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For research use only.

Verified Samples Verified Samples in WB: Human fetal brain, Mouse brain
Verified Samples in IHC: Human liver cancer, Human brain
Dilution WB 1:200-1:1000,  IHC 1:50-1:200
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse
Applications WB,  IHC
Clonality Polyclonal
Immunogen Synthetic peptide of human KCNQ4
Abbre KCNQ4
Synonyms DFNA 2,  DFNA2,  KCNQ 4,  KCNQ4,  KQT like 4,  KQT-like 4,  KV7.4,  Kcnq4,  Potassium channel KQT like 4,  Potassium channel subunit alpha KvLQT4,  Potassium voltag,  Potassium voltage gated channel KQT like protein 4,  Potassium voltage gated channel KQT like subfamily member 4
Swissprot
Calculated MW 77 kDa
Cellular Localization Basal cell membrane. Situated at the basal membrane of cochlear outer hair cells.
Concentration 0.9 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Neuroscience
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background The protein encoded by this gene forms a potassium channel that is thought to play a critical role in the regulation of neuronal excitability, particularly in sensory cells of the cochlea. The current generated by this channel is inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. The encoded protein can form a homomultimeric potassium channel or possibly a heteromultimeric channel in association with the protein encoded by the KCNQ3 gene. Defects in this gene are a cause of nonsyndromic sensorineural deafness type 2 (DFNA2), an autosomal dominant form of progressive hearing loss. Two transcript variants encoding different isoforms have been found for this gene.
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Unconjugated

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