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UTRN Knockout Cell Lines

Gene: UTRN

Official Full Name: utrophinprovided by HGNC

Gene Summary: This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described; however, the full-length nature of these variants has not yet been determined. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO07173 UTRN Knockout cell line (HeLa) Human UTRN 1:3~1:6 Negative Online Inquiry
KO07174 UTRN Knockout cell line (HCT 116) Human UTRN 1:2~1:4 Negative Online Inquiry
KO07175 UTRN Knockout cell line (HEK293) Human UTRN 1:3~1:6 Negative Online Inquiry
KO07176 UTRN Knockout cell line (A549) Human UTRN 1:3~1:4 Negative Online Inquiry

Background

UTRN Gene Knockout Cell Lines are specialized cellular models engineered to lack the expression of the utrophin gene (UTRN), a protein involved in muscle function and regeneration. These knockout lines are generated through advanced CRISPR-Cas9 gene-editing technology, ensuring precise and efficient elimination of UTRN expression. The resulting cell lines serve as invaluable tools for studying the physiological roles of utrophin and its implications in various myopathies, notably Duchenne Muscular Dystrophy (DMD).

The key functions of UTRN gene knockout cell lines lie in their ability to mimic disease states that are characterized by the absence of utrophin, allowing researchers to explore underlying mechanisms of muscle degeneration and regeneration. By providing insight into utrophin's role in dystrophin-associated complexes, these models facilitate the screening of potential therapeutic interventions aimed at restoring muscle integrity and function in vulnerable populations.

The scientific importance of UTRN knockout cell lines spans both research and clinical applications. They are instrumental in drug discovery, where researchers can evaluate the efficacy of novel compounds that target muscle wasting conditions. Additionally, these cell lines contribute to understanding gene therapy approaches that aim to compensate for utrophin deficiency, thus paving the way for innovative treatment strategies for neuromuscular diseases.

Compared to traditional wild-type cell lines, UTRN gene knockout models offer significant advantages, including enhanced specificity for studying utrophin-related pathways and the ability to observe phenotypic changes in a controlled manner. Unlike primary muscle cells that are limited in availability, these engineered lines are readily accessible and can be characterized in high-throughput formats, making them ideal for large-scale screening efforts.

Investing in UTRN Gene Knockout Cell Lines is a strategic step for researchers and clinicians dedicated to combating muscle-related diseases. By adopting these advanced models, users can accelerate their research, thus contributing to the development of therapies that improve patient outcomes. Our company specializes in providing high-quality biological products, supported by a commitment to innovation and excellence, ensuring that our clients have access to the best tools for their scientific endeavors.

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

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