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KCNQ4 Knockout Cell Lines

Gene: KCNQ4

Official Full Name: potassium voltage-gated channel subfamily Q member 4provided by HGNC

Gene Summary: 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]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO33563 KCNQ4 Knockout cell line (HCT 116) Human KCNQ4 1:2~1:4 Negative Online Inquiry
KO33564 KCNQ4 Knockout cell line (HEK293) Human KCNQ4 1:3~1:6 Negative Online Inquiry

Background

KCNQ4 Gene Knockout Cell Lines are genetically engineered cellular models specifically designed to study the role of the KCNQ4 gene, which encodes a potassium ion channel critically involved in auditory function and neuronal signaling. These knockout cell lines are created through targeted gene disruption techniques, such as CRISPR-Cas9, allowing for the examination of the KCNQ4 gene's expression, function, and associated pathophysiology, particularly in relation to auditory disorders and other neurological conditions.

The primary function of these cell lines is to provide researchers with a controlled experimental environment in which the loss of KCNQ4 function can be analyzed. This enables the investigation of ionic currents regulated by potassium channels, examining how alterations in these currents can affect cellular excitability and signal propagation. Furthermore, the KCNQ4 gene knockout cell lines serve as a valuable tool for drug discovery, facilitating the testing of pharmacological compounds that may modulate KCNQ4 activity or compensate for its loss.

Scientifically, the KCNQ4 gene is implicated in various hereditary hearing loss syndromes, making these cell lines a crucial resource for understanding the underlying mechanisms of auditory neuropathies. In clinical research, they can aid in the identification of potential therapeutic targets and the development of gene therapies aimed at ameliorating auditory deficits.

What sets KCNQ4 Gene Knockout Cell Lines apart from alternative models is the specificity and reliability of their genetic modification, ensuring robust and reproducible results. They provide precise insights into KCNQ4-related pathophysiology that traditional models may not offer, enhancing the translational potential of research findings to clinical applications.

For researchers and clinicians alike, these knockout cell lines represent a cornerstone for advancing our understanding of KCNQ4's biological significance, ultimately leading to innovative treatments for hearing impairment and related disorders. Our company specializes in developing high-quality biological products that empower scientific research, leveraging cutting-edge technologies and methodologies to support the pursuit of breakthroughs in health and medicine.

Please note that all services are for research use only. Not intended for any clinical use.

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