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HEXB Knockout Cell Lines

Gene: HEXB

Official Full Name: hexosaminidase subunit betaprovided by HGNC

Gene Summary: Hexosaminidase B is the beta subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Beta subunit gene mutations lead to Sandhoff disease (GM2-gangliosidosis type II). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO17127 HEXB Knockout cell line (HeLa) Human HEXB 1:3~1:6 Negative Online Inquiry
KO17128 HEXB Knockout cell line (HCT 116) Human HEXB 1:2~1:4 Negative Online Inquiry
KO17129 HEXB Knockout cell line (HEK293) Human HEXB 1:3~1:6 Negative Online Inquiry
KO39184 HEXB Knockout cell line (A549) Human HEXB 1:3~1:4 Negative Online Inquiry

Background

HEXB Gene Knockout Cell Lines are specifically engineered cellular models in which the HEXB gene, responsible for encoding the enzyme β-hexosaminidase B, has been inactivated through directed mutagenesis. This innovative product allows researchers to delineate the biological role of HEXB, particularly in the context of lysosomal storage disorders such as Sandhoff disease. The knockout mechanism results in the absence of this critical enzyme, enabling detailed functional analyses of cellular processes that rely on glycosphingolipid metabolism and the implications of lysosomal dysfunction.

These cell lines serve as vital tools for investigating the biochemical pathways impacted by HEXB deficiency, facilitating studies on substrate accumulation, cellular autophagy, and the downstream effects on neuronal health and development. Their utility extends into both academic and clinical research, allowing scientists to explore therapeutic interventions and the molecular basis of disease progression.

The specific advantages of using HEXB Gene Knockout Cell Lines include the reliability of results owing to their precise gene targeting, which eliminates off-target effects commonly associated with other gene-editing techniques. Furthermore, they offer enhanced reproducibility and consistency in experimental setups, essential for high-quality research data. These cell lines stand out among alternatives because they are already fully characterized and validated, thus saving researchers time in model development and providing an immediate platform for experimental use.

As such, HEXB Gene Knockout Cell Lines are invaluable for both fundamental bioscience researchers and clinical laboratory settings. They facilitate the path towards discovering new therapeutic agents and enhance our understanding of lysosomal diseases, ultimately providing insights that could lead to effective treatments.

This product exemplifies our company's dedication to advancing biological research through innovative tools, rooted in rigorous scientific validation and an understanding of user needs. Our expertise in developing reliable and effective biological products ensures that researchers and clinicians have access to high-quality resources to drive their work forward.

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

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