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COCH Knockout Cell Lines

Gene: COCH

Official Full Name: cochlinprovided by HGNC

Gene Summary: The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94% and 79% amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated. [provided by RefSeq, Oct 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03023 COCH Knockout cell line (HeLa) Human COCH 1:3~1:6 Negative Online Inquiry
KO03024 COCH Knockout cell line (HCT 116) Human COCH 1:2~1:4 Negative Online Inquiry
KO03025 COCH Knockout cell line (HEK293) Human COCH 1:3~1:6 Negative Online Inquiry
KO03026 COCH Knockout cell line (A549) Human COCH 1:3~1:4 Negative Online Inquiry

Background

COCH Gene Knockout Cell Lines are genetically modified cell lines designed to facilitate the study of the Cochlin gene's role in various biological processes and disease mechanisms. The COCH gene encodes the Cochlin protein, which is implicated in hearing and balance disorders, particularly in otological conditions and otosclerosis. By effectively knocking out the COCH gene, these cell lines provide researchers with a powerful tool to elucidate the functional pathways associated with Cochlin deficiency and its physiological repercussions.

The primary mechanism of these cell lines involves the targeted disruption of the COCH gene using CRISPR/Cas9 technology, which allows for specific editing of genomic sequences. This knockout approach yields a cellular model that can mimic disease phenotypes and contribute to a deeper understanding of the Cochlin protein's roles in tissues, particularly in the inner ear. Researchers can utilize these models to investigate the molecular and cellular ramifications of Cochlin absence, paving the way for potential therapeutic interventions.

The scientific importance of COCH Gene Knockout Cell Lines lies in their applicability in both research and clinical settings. They serve as invaluable resources for studying hereditary hearing loss, aiding in the identification of new targets for gene therapy approaches, and facilitating drug discovery efforts aimed at restoring hearing function. Their specific advantage over traditional knockout models is the precision and efficiency of the CRISPR system, which minimizes off-target effects and improves reproducibility of results.

For researchers and clinicians focused on auditory health and gene therapy, the COCH Gene Knockout Cell Lines represent a significant advancement. By providing a reliable system for studying Cochlin's role in health and disease, these cell lines empower users to make groundbreaking discoveries that could lead to improved patient outcomes.

Our company specializes in the development and provision of cutting-edge genetic tools, offering a portfolio of high-quality knockout cell lines that are rigorously validated for scientific research. With a commitment to excellence and innovation, we support researchers in unlocking the mysteries of genetic functions and their applications in modern medicine.

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

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