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GUSB Knockout Cell Lines

Gene: GUSB

Official Full Name: glucuronidase betaprovided by HGNC

Gene Summary: This gene encodes a hydrolase that degrades glycosaminoglycans, including heparan sulfate, dermatan sulfate, and chondroitin-4,6-sulfate. The enzyme forms a homotetramer that is localized to the lysosome. Mutations in this gene result in mucopolysaccharidosis type VII. Alternative splicing results in multiple transcript variants. There are many pseudogenes of this locus in the human genome.[provided by RefSeq, May 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO37448 GUSB Knockout cell line (HeLa) Human GUSB 1:3~1:6 Negative Online Inquiry
KO37449 GUSB Knockout cell line (HCT 116) Human GUSB 1:2~1:4 Negative Online Inquiry
KO37450 GUSB Knockout cell line (HEK293) Human GUSB 1:3~1:6 Negative Online Inquiry
KO37451 GUSB Knockout cell line (A549) Human GUSB 1:3~1:4 Negative Online Inquiry

Background

GUSB Gene Knockout Cell Lines are genetically modified cell lines that have had the glucuronidase (GUSB) gene selectively disrupted, rendering them invaluable tools for studying the function of GUSB and the metabolic pathways influenced by this enzyme. The GUSB gene encodes for an enzyme that plays a critical role in the hydrolysis of glucuronides, which are important molecules involved in the detoxification processes within cells.

These cell lines operate through the principle of gene knockout, where specific genetic sequences are silenced using techniques such as CRISPR-Cas9 or other gene editing methods. By removing the GUSB gene, researchers can investigate the physiological effects of its absence, enabling the elucidation of pathways involved in glucuronidation and its implications in various diseases, particularly lysosomal storage disorders.

The scientific importance of GUSB Gene Knockout Cell Lines lies in their utility for both basic and applied research. They can be employed to model human diseases in vitro, allowing researchers to uncover the underlying mechanisms of pathologies related to GUSB deficiency, such as mucopolysaccharidosis type VII (MPS VII). In clinical settings, these cell lines provide an experimental framework for evaluating therapeutic interventions or potential gene therapies, enhancing the translational impact of research.

Compared to alternative models, such as wild-type cell lines or non-specific knockout models, GUSB Gene Knockout Cell Lines offer a precise and targeted approach to studying the effects of glucuronidase deficiency. They provide a consistent and reproducible platform for experimentation, facilitating more accurate and reliable data collection.

The value of these cell lines to researchers and clinicians is profound, as they bridge the gap between basic research and clinical understanding, guiding the development of novel therapies and improving patient outcomes. Our company prides itself on delivering high-quality genetic tools and cell lines that are meticulously validated and characterized, ensuring that researchers have access to reliable resources that advance their scientific endeavors.

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

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