Human KCNQ4 blocking peptide (CDBP1678)

Synthetic Human KCNQ4 blocking peptide for Apuri, BL, ELISA Datasheet

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Product Overview
Blocking/Immunizing peptide for anti-KCNQ4 antibody
Target
KCNQ4
Nature
Synthetic
Species Reactivity
Human
Tag/Conjugate
Unconjugated
Application Notes
For in vitro research use only. Not intended for any diagnostic or therapeutic purpose. Not for human or animal consumption.
Format
Lyophilized powder
Size
100 μg
Storage
Shipped at ambient temperature, store at -20°C.
UniProt ID
Antigen 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, Jul 2008]
Function
potassium channel activity; voltage-gated ion channel activity; voltage-gated potassium channel activity;
Synonyms
KCNQ4; potassium voltage-gated channel, KQT-like subfamily, member 4; DFNA2; potassium voltage-gated channel subfamily KQT member 4; Kv7.4; potassium channel KQT-like 4; potassium channel subunit alpha KvLQT4; KV7.4; DFNA2A;

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