Gene: GALNS
Official Full Name: galactosamine (N-acetyl)-6-sulfataseprovided by HGNC
Gene Summary: This gene encodes N-acetylgalactosamine-6-sulfatase which is a lysosomal exohydrolase required for the degradation of the glycosaminoglycans, keratan sulfate, and chondroitin 6-sulfate. Sequence alterations including point, missense and nonsense mutations, as well as those that affect splicing, result in a deficiency of this enzyme. Deficiencies of this enzyme lead to Morquio A syndrome, a lysosomal storage disorder. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03182 | GALNS Knockout cell line (HeLa) | Human | GALNS | 1:3~1:6 | Negative | Online Inquiry |
KO03183 | GALNS Knockout cell line (HCT 116) | Human | GALNS | 1:2~1:4 | Negative | Online Inquiry |
KO03184 | GALNS Knockout cell line (HEK293) | Human | GALNS | 1:3~1:6 | Negative | Online Inquiry |
KO03185 | GALNS Knockout cell line (A549) | Human | GALNS | 1:3~1:4 | Negative | Online Inquiry |
GALNS Gene Knockout Cell Lines are meticulously engineered cellular models designed to study the functional implications of the GALNS gene, which encodes the enzyme N-acetylgalactosamine-6-sulfatase. These knockout lines offer a unique platform to investigate glycosaminoglycan (GAG) metabolism, particularly relating to mucopolysaccharidosis type IVA (MPS IVA), characterized by accumulated glycosaminoglycans due to GALNS deficiency.
The key function of GALNS Gene Knockout Cell Lines lies in their ability to provide insights into the pathophysiology of MPS IVA by completely disabling the GALNS gene. This process allows researchers to observe phenotypic changes and assess the downstream effects of enzyme deficiency, facilitating a detailed understanding of the disease's mechanisms at the cellular level. These cell lines can be instrumental in drug screening, aiding in the design and testing of enzyme replacement therapies and small-molecule drugs aimed at restoring GAG metabolism.
In terms of scientific significance, the applications for GALNS Gene Knockout Cell Lines extend to both academic research and clinical settings. They serve as invaluable tools for elucidating disease mechanisms, validating therapeutic targets, and enhancing preclinical drug development, offering researchers a robust foundation to explore innovative treatments for lysosomal storage disorders.
What sets our GALNS Gene Knockout Cell Lines apart from alternatives is their unparalleled specificity and reproducibility. Developed under stringent quality control measures, our lines ensure authentic representation of the disease phenotype, minimizing variability seen in non-specific models or cells derived from patient tissues. Furthermore, the availability of these lines permits rapid and efficient functional studies, significantly advancing the timeline for research initiatives.
For researchers and clinicians focused on advancing the understanding and treatment of MPS IVA and related disorders, our GALNS Gene Knockout Cell Lines represent a critical resource. Their use not only enhances the potential for significant discoveries but also instills confidence that the findings will be reliable and translatable to clinical contexts. With years of experience in producing high-quality biological products, our company is committed to supporting the scientific community with tools that enable groundbreaking research and clinical advancements.
Please note that all services are for research use only. Not intended for any clinical use.
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