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KCNQ4, Goat, Polyclonal Antibody, Abnova™

Goat polyclonal antibody raised against synthetic peptide of KCNQ4.

Supplier:  Abnova Corporation PAB11544

Catalog No. 89-115-168


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Description

Description

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

Sequence: C-DKGPSDAEVVDE
Specifications

Specifications

KCNQ4
Polyclonal
Unconjugated
ELISA (1:4000) Western Blot (1-3 ug/mL) The optimal working dilution should be determined by the end user.
KCNQ4
KCNQ4
A synthetic peptide corresponding to human KCNQ4.
100 μg
Primary
Human
Liquid
ELISA, Western Blot
0.5 mg/mL
Goat polyclonal antibody raised against synthetic peptide of KCNQ4.
In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
DFNA2/KV7.4
Goat
Antigen affinity purification
RUO
9132
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
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