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UGT8 Knockout Cell Lines

Gene: UGT8

Official Full Name: UDP glycosyltransferase 8provided by HGNC

Gene Summary: The protein encoded by this gene belongs to the UDP-glycosyltransferase family. It catalyzes the transfer of galactose to ceramide, a key enzymatic step in the biosynthesis of galactocerebrosides, which are abundant sphingolipids of the myelin membrane of the central and peripheral nervous systems. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO34848 UGT8 Knockout cell line (HeLa) Human UGT8 1:3~1:6 Negative Online Inquiry
KO34849 UGT8 Knockout cell line (HCT 116) Human UGT8 1:2~1:4 Negative Online Inquiry
KO34850 UGT8 Knockout cell line (HEK293) Human UGT8 1:3~1:6 Negative Online Inquiry

Background

UGT8 Gene Knockout Cell Lines are specialized cell lines in which the uridine diphosphate-glucuronosyltransferase 8 (UGT8) gene has been inactivated through targeted gene editing techniques such as CRISPR-Cas9. UGT8 plays a critical role in the biosynthesis of plasmalogens, a class of phospholipids associated with cellular membrane integrity and functionality. By knocking out this gene, researchers gain invaluable insights into the physiological consequences of UGT8 deficiency, as well as the impacts on myelination and neurodegenerative diseases.

These knockout cell lines work by providing a model system that mimics the genetic and biochemical environment of UGT8-deficient conditions. The cells can be utilized to study the mechanistic pathways involved in lipid metabolism, cell signaling, and the development of pathologies associated with myelin sheath disorders, including Krabbe disease and multiple sclerosis. This research is crucial for developing therapeutic strategies that target these conditions.

The scientific importance of UGT8 gene knockout cell lines lies in their versatility for both in vitro and drug discovery applications. By facilitating high-throughput screenings and functional assays, researchers can efficiently identify compounds that may restore UGT8 function or compensate for its loss. Unlike traditional models that may exhibit heterogeneity or incomplete penetrance of genetic modifications, these cell lines provide a uniform and reproducible platform for experimental validation.

One of the standout advantages of utilizing UGT8 gene knockout cell lines is their specificity in simulating human disease mechanisms. Compared to alternative models, such as animal models or non-specific cell lines, these knockout lines offer a more streamlined and ethically sound approach for studying human-related pathologies.

For researchers and clinicians seeking to unravel the complexities associated with UGT8 dysfunction, our UGT8 Gene Knockout Cell Lines represent a powerful tool that can enhance the understanding of critical biological processes and facilitate the development of targeted treatments. As a leader in providing innovative biological products, our company is committed to advancing research with high-quality, well-characterized cell lines that empower scientific discovery.

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

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