GeneBio Systems
KCNQ4 Polyclonal Antibody
KCNQ4 Polyclonal Antibody
SKU:E-AB-16544
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Size: 200μL
Storage: Store at -20℃ 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.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: KCNQ4
Target Synonym: DFNA 2;DFNA2;KCNQ 4;Kcnq4;KCNQ4;KQT like 4;KQT-like 4;KV7.4;Potassium channel KQT like 4;Potassium channel subunit alpha KvLQT4;Potassium voltage gated channel KQT like protein 4;Potassium voltage gated channel KQT like subfamily member 4;Potassium voltage gated channel subfamily KQT member 4;Potassium voltage-gated channel subfamily KQT member 4;Voltage gated potassium channel subunit Kv7.4;Voltage-gated potassium channel subunit Kv7.4
Research Areas: Cancer;Neuroscience
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P56696
Accession:
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.
Concentration: 0.9 mg/mL
Immunogen: Synthetic peptide of human KCNQ4
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:200-1:1000;IHC 1:50-1:200
Calculated MW: 77kDa
ObservedMW:
