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CSGALNACT2 Knockout Cell Lines

Gene: CSGALNACT2

Official Full Name: chondroitin sulfate N-acetylgalactosaminyltransferase 2provided by HGNC

Gene Summary: This gene encodes a member of the chondroitin N-acetylgalactosaminyltransferase family. The encoded protein is involved in elongation during chondroitin sulfate synthesis. Alternative splicing of this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome X. [provided by RefSeq, Feb 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO18514 CSGALNACT2 Knockout cell line (HeLa) Human CSGALNACT2 1:3~1:6 Negative Online Inquiry
KO18515 CSGALNACT2 Knockout cell line (HCT 116) Human CSGALNACT2 1:2~1:4 Negative Online Inquiry
KO18516 CSGALNACT2 Knockout cell line (HEK293) Human CSGALNACT2 1:3~1:6 Negative Online Inquiry
KO18517 CSGALNACT2 Knockout cell line (A549) Human CSGALNACT2 1:3~1:4 Negative Online Inquiry

Background

CSGALNACT2 Gene Knockout Cell Lines are genetically engineered cell lines wherein the CSGALNACT2 gene has been systematically disrupted, rendering it non-functional. This gene encodes the enzyme CSGALNACT2, which is responsible for catalyzing the addition of specific sugar groups to glycosaminoglycans, a crucial step in the biosynthesis of glycoproteins and proteoglycans. By creating knockout models, researchers can investigate the phenotypic consequences of CSGALNACT2 deficiency, providing vital insights into its role in cell signaling, development, and disease.

The mechanism underlying these cell lines involves CRISPR-Cas9 technology, a precise method for inducing site-specific double-strand breaks in DNA, followed by repair processes that lead to gene disruption. This allows for the creation of knockout cell lines with high efficiency and specificity. The CSGALNACT2 knockout models are invaluable for elucidating the pathway dynamics related to glycosylation, studying the molecular biology of various conditions such as cancer, obesity, and developmental disorders.

The scientific importance of these cell lines extends to both research and clinical settings, facilitating the exploration of therapeutic targets and biomarkers linked to glycosylation changes. In drug development, understanding the role of CSGALNACT2 may unlock novel strategies for intervention in glycan-related diseases.

A key advantage of our CSGALNACT2 Gene Knockout Cell Lines lies in the precision of gene editing, alongside robust validation of gene knockout efficiency. Unlike traditional methods that may have off-target effects or incomplete gene knockout, our cell lines promise high specificity and reproducibility for experimental designs.

For researchers and clinicians, these cell lines offer an unprecedented opportunity to investigate the biological implications of glycosylation alterations, making them a valuable resource for advancing knowledge in multiple fields of biomedicine. Our commitment to high-quality genetic products and a deep understanding of molecular biology underscores our expertise in delivering pioneering solutions for scientific research.

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

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