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ST8SIA1 Knockout Cell Lines

Gene: ST8SIA1

Official Full Name: ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1provided by HGNC

Gene Summary: Gangliosides are membrane-bound glycosphingolipids containing sialic acid. Ganglioside GD3 is known to be important for cell adhesion and growth of cultured malignant cells. The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to GM3 to produce gangliosides GD3 and GT3. The encoded protein may be found in the Golgi apparatus and is a member of glycosyltransferase family 29. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2015]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35437 ST8SIA1 Knockout cell line (A549) Human ST8SIA1 1:3~1:4 Negative Online Inquiry

Background

ST8SIA1 Gene Knockout Cell Lines are advanced biological tools specifically engineered to disrupt the ST8SIA1 gene, which encodes an enzyme involved in the biosynthesis of specific gangliosides crucial for cellular signaling pathways. By utilizing CRISPR-Cas9 technology, these cell lines effectively serve as models for studying the functional roles of ST8SIA1 in both normal physiological processes and various pathologies, including neurodegenerative diseases and cancers.

The primary mechanism underlying ST8SIA1 Gene Knockout Cell Lines involves homologous recombination, leading to a precise deletion of the ST8SIA1 gene. As a result, these cell lines exhibit a significant reduction or complete absence of the enzyme's activity, providing researchers with a powerful platform to elucidate the multifaceted roles of ST8SIA1 in cell differentiation, proliferation, and apoptosis. Scientists can further examine the downstream effects on ganglioside composition, thus better understanding various disease mechanisms associated with altered glycosylation patterns.

The scientific importance of these knockout cell lines is underscored by their wide range of applications in both basic and translational research settings. They can facilitate the identification of therapeutic targets and potential biomarkers, enabling the development of novel interventions for conditions such as Alzheimer’s disease and certain types of cancers where aberrant glycosylation is implicated.

Compared to other alternatives, ST8SIA1 Gene Knockout Cell Lines offer unparalleled specificity and reliability, as they provide a consistent genetic background to assess the direct effects of the ST8SIA1 disruption. This specificity allows for more accurate interpretations of experimental results, significantly enhancing research reproducibility. Their ease of use in standard culture conditions makes them accessible for laboratories of varying scales, from academic research facilities to clinical diagnostic centers.

In conclusion, the ST8SIA1 Gene Knockout Cell Lines are invaluable resources for researchers and clinicians alike, delivering precise genetic modifications that enhance the understanding of complex biological systems. Our company specializes in high-quality genetic tools, and we are committed to supporting the advancement of scientific research by providing innovative solutions tailored to the needs of the research community.

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

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