ARG64570

anti-KCNQ4 antibody

anti-KCNQ4 antibody for Western blot and Human

Neuroscience antibody

Overview

Product Description Goat Polyclonal antibody recognizes KCNQ4
Tested Reactivity Hu
Tested Application WB
Specificity This antibody is expected to recognise both reported isoforms (NP_004691.2; NP_751895.1); may cross-react in Mouse;
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name KCNQ4
Antigen Species Human
Immunogen C-DKGPSDAEVVDE
Conjugation Un-conjugated
Alternate Names DFNA2; Voltage-gated potassium channel subunit Kv7.4; KQT-like 4; DFNA2A; Potassium voltage-gated channel subfamily KQT member 4; KV7.4; Potassium channel subunit alpha KvLQT4

Application Instructions

Application Suggestion
Tested Application Dilution
WB1 - 3 µg/ml
Application Note WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 9132 Human KCNQ4

Swiss-port # P56696 Human Potassium voltage-gated channel subfamily KQT member 4

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. [provided by RefSeq, Jul 2008]
Research Area Neuroscience antibody
Calculated MW 77 kDa

Images (1) Click the Picture to Zoom In

  • ARG64570 anti-KCNQ4 antibody WB image

    Western Blot: Cerebellum lysate (35 µg protein in RIPA buffer) stained with ARG64570 anti-KCNQ4 antibody at 2 µg/ml dilution.