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USH1C Knockout Cell Lines

Gene: USH1C

Official Full Name: USH1 protein network component harmoninprovided by HGNC

Gene Summary: This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO32309 USH1C Knockout cell line (HeLa) Human USH1C 1:3~1:6 Negative Online Inquiry
KO32310 USH1C Knockout cell line (HCT 116) Human USH1C 1:2~1:4 Negative Online Inquiry
KO32311 USH1C Knockout cell line (HEK293) Human USH1C 1:3~1:6 Negative Online Inquiry
KO32312 USH1C Knockout cell line (A549) Human USH1C 1:3~1:4 Negative Online Inquiry

Background

USH1C Gene Knockout Cell Lines are genetically engineered cellular models that have had the USH1C gene disrupted, enabling researchers to explore the function and implications of this gene in various biological contexts. These cell lines serve as invaluable tools for studying Usher syndrome, a leading cause of combined deafness and blindness, by allowing for the investigation of cellular pathways and mechanisms associated with the loss of USH1C function.

The primary function of the USH1C gene is to encode harmonin, a scaffolding protein critical for the development and maintenance of sensory organs, particularly in the inner ear and retina. The knockout of this gene provides insight into the specific cellular alterations and pathological changes that accompany the dysfunction of harmonin, elucidating how mutations or loss of this protein lead to the clinical manifestations of Usher syndrome. Researchers can utilize these cell lines to analyze signal transduction pathways, gene expression profiles, and cellular responses to potential therapeutic agents.

Scientifically, the USH1C Gene Knockout Cell Lines hold great significance in advancing our understanding of hereditary hearing and vision loss, thereby facilitating the discovery of novel therapeutic interventions. In clinical settings, they offer a platform for drug screening and validation, allowing for the assessment of compounds that could restore function or mitigate dysfunction associated with USH1C loss.

Compared to alternative models, such as primary cell cultures or traditional knockout mice, these cell lines provide a consistent and reproducible experimental system that is easier to manipulate and scale. This streamlining of research methodologies reduces variability and enhances the reproducibility of results, making them a practical choice for both academic and industrial applications.

For researchers and clinicians focusing on genetic hearing and vision impairments, USH1C Gene Knockout Cell Lines are invaluable assets. They not only accelerate the pace of discovery but also open new avenues for the development of targeted therapies. Our company specializes in providing high-quality, rigorously validated biological products designed to support cutting-edge research in genetics and molecular biology, ensuring that scientists have the tools they need to make meaningful progress in their fields.

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

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