KCNQ4 Polyclonal Antibody | G-AB-03217

KCNQ4 Polyclonal Antibody | G-AB-03217 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Cancer, Neuroscience

Synonyms: 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

Reactivity: Human, Mouse

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: NP_004691

Clonality: Polyclonal

Immunogen: Synthetic peptide of human KCNQ4

Clone #:

Conjugation: Unconjugated

Swissprot: P56696

Santa Cruz: sc-12442/sc-20882/sc-50417

Calculated MW: 77 kDa

Observed MW:

Concentration: 0.9 mg/mL

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Application: WB, IHC, ELISA

Dilution: WB 1:200-1:1000, IHC 1:50-1:200

Storage: Store at -20°C. Avoid freeze / thaw cycles.

KCNQ4 Polyclonal Antibody DataSheet