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POMT1 Knockout Cell Lines

Gene: POMT1

Official Full Name: protein O-mannosyltransferase 1provided by HGNC

Gene Summary: The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO31704 POMT1 Knockout cell line (HeLa) Human POMT1 1:3~1:6 Negative Online Inquiry
KO31705 POMT1 Knockout cell line (HCT 116) Human POMT1 1:2~1:4 Negative Online Inquiry
KO31706 POMT1 Knockout cell line (HEK293) Human POMT1 1:3~1:6 Negative Online Inquiry
KO31707 POMT1 Knockout cell line (A549) Human POMT1 1:3~1:4 Negative Online Inquiry

Background

POMT1 Gene Knockout Cell Lines are genetically engineered cell lines designed to specifically disrupt the POMT1 gene, which is crucial for the proper glycosylation of proteins. Glycosylation is a fundamental post-translational modification that affects protein stability, activity, and cellular localization. The knockout of the POMT1 gene leads to defects in O-mannosylation, which can significantly impact cellular function, making these cell lines an invaluable tool for studying the molecular mechanisms underlying glycosylation disorders, particularly those affecting muscle and neuronal tissues.

The primary mechanisms of POMT1 gene knockout involve the use of CRISPR/Cas9 technology, which allows precise editing of the genome. This results in a complete loss of POMT1 expression, thus enabling researchers to investigate the resulting phenotypic changes in cellular models. This insight is particularly vital for understanding associated pathologies, including congenital muscular dystrophies and dystroglycanopathies. The utilization of these knockout cell lines paves the way for exploratory studies into therapeutic interventions, gene functions, and the impact of glycosylation alterations on cell signaling pathways and disease progression.

In research settings, POMT1 Gene Knockout Cell Lines represent a critical advancement over traditional models, offering enhanced specificity and reproducibility in experiments assessing glycosylation and its effects. Compared to wild-type cell lines, the knockout variants enable targeted investigations, providing clearer insights into gene function and the development of novel therapeutic strategies. These cell lines also facilitate high-throughput screening of potential therapeutic compounds aimed at restoring normal glycosylation patterns.

For researchers and clinicians engaged in genetic studies or drug development centered around glycosylation disorders, POMT1 Gene Knockout Cell Lines are essential for elucidating the underlying biology and advancing toward effective treatments. Our company prides itself on its expertise in producing high-quality genetic models, ensuring that researchers have access to the most reliable and cutting-edge tools to drive their scientific inquiries. As leaders in biological product development, we are committed to supporting the research community with innovative solutions tailored to their needs.

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

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