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SGSH Knockout Cell Lines

Gene: SGSH

Official Full Name: N-sulfoglucosamine sulfohydrolaseprovided by HGNC

Gene Summary: This gene encodes the enzyme sulfamidase; one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with the lysosomal storage disease mucopolysaccaridosis IIIA, also known as Sanfilippo syndrome A, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined. [provided by RefSeq, Jun 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35447 SGSH Knockout cell line (HeLa) Human SGSH 1:3~1:6 Negative Online Inquiry
KO35448 SGSH Knockout cell line (HCT 116) Human SGSH 1:2~1:4 Negative Online Inquiry
KO35449 SGSH Knockout cell line (HEK293) Human SGSH 1:3~1:6 Negative Online Inquiry
KO35450 SGSH Knockout cell line (A549) Human SGSH 1:3~1:4 Negative Online Inquiry

Background

SGSH Gene Knockout Cell Lines represent a significant advancement in genetic research, specifically designed to facilitate the study of the sulfatase-modifying factor 1 (SGSH) gene, which is crucial for the proper metabolism of glycosaminoglycans. These knockout cell lines have been genetically modified to disable the SGSH gene, enabling researchers to investigate the effects of gene loss on cell function, metabolism, and disease development, particularly in conditions like Mucopolysaccharidosis type IIIA (MPS IIIA).

The primary function of SGSH Gene Knockout Cell Lines lies in their ability to model human diseases caused by deficits in the SGSH protein. By eliminating the SGSH gene, these cell lines allow for the examination of resultant phenotypic changes, cellular pathways, and molecular mechanisms underlying the pathophysiology of MPS IIIA and related disorders. Researchers can utilize these cell lines to screen therapeutic compounds, unravel pathways that lead to disease manifestation, and explore potential gene therapy approaches.

These cell lines hold considerable scientific importance and applicability in both research and clinical settings. They serve as valuable tools for drug discovery, biomarker identification, and the development of gene therapies, providing insights into therapeutic targets and biological processes affected by SGSH dysfunction. Furthermore, the ability to model genetic mutations closely replicates the in vivo conditions found in human patients, enhancing the translatability of research findings to clinical applications.

One of the standout advantages of our SGSH Gene Knockout Cell Lines is the high specificity and reliability of the gene knockout, achieved through advanced CRISPR-Cas9 editing technology. Compared to traditional models, these lines reduce off-target effects and provide a more accurate representation of gene function and cellular behavior. Additionally, they are available in various cell types, allowing researchers flexibility in their choice of platform depending on their experimental needs.

Our SGSH Gene Knockout Cell Lines offer essential resources to researchers and clinicians dedicated to understanding and treating genetic disorders. The ability to delve deeper into the genetic basis of disease equips scientists with the tools needed to drive innovation in therapies and improve patient outcomes. Backed by our company’s cutting-edge technology and commitment to advancing genetic research, we provide researchers with reliable products that empower them in their quest for scientific breakthroughs.

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

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