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COQ2 Knockout Cell Lines

Gene: COQ2

Official Full Name: coenzyme Q2, polyprenyltransferaseprovided by HGNC

Gene Summary: This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone), a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. This enzyme, which is part of the coenzyme Q10 pathway, catalyzes the prenylation of parahydroxybenzoate with an all-trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency, a mitochondrial encephalomyopathy, and also COQ2 nephropathy, an inherited form of mitochondriopathy with primary renal involvement. [provided by RefSeq, Oct 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO27748 COQ2 Knockout cell line (HeLa) Human COQ2 1:3~1:6 Negative Online Inquiry
KO27749 COQ2 Knockout cell line (HCT 116) Human COQ2 1:2~1:4 Negative Online Inquiry
KO27750 COQ2 Knockout cell line (HEK293) Human COQ2 1:3~1:6 Negative Online Inquiry
KO27751 COQ2 Knockout cell line (A549) Human COQ2 1:3~1:4 Negative Online Inquiry

Background

COQ2 Gene Knockout Cell Lines represent a revolutionary tool in the field of genetic research, specifically designed to facilitate the investigation of Coenzyme Q10 biosynthesis and its implications in various physiological and pathological processes. These engineered cell lines are characterized by the targeted deletion of the COQ2 gene, which plays a critical role in the synthesis of ubiquinone, a vital cofactor involved in cellular energy production. By employing CRISPR-Cas9 technology for precise gene editing, these knockout cell lines provide a reliable model for studying the downstream effects of COQ2 deficiency, including alterations in mitochondrial function and related metabolic pathways.

The primary function of COQ2 Gene Knockout Cell Lines lies in their ability to create an in vitro environment that mimics the state of coenzyme Q10 deficiency seen in numerous mitochondrial disorders and other diseases. Researchers can investigate the cellular mechanisms underlying these conditions, enabling a better understanding of the metabolic dysregulation that may contribute to diverse diseases, including neurodegenerative disorders and cardiovascular diseases. This model system is particularly valuable in the pharmaceutical development process, where it can be used to screen for compounds that restore mitochondrial function or enhance coenzyme Q10 metabolism.

One of the significant advantages of these cell lines is their specificity and reproducibility compared to traditional models, such as wild-type or transient knockdown systems. The stable knockout mutations allow for longer-term studies and reduced variability, which is crucial for obtaining robust data. Moreover, the ease of maintenance and the compatibility of these cell lines with various assays further enhance their utility for laboratories focused on metabolic research and drug discovery.

For researchers and clinicians, the value of COQ2 Gene Knockout Cell Lines extends beyond merely serving as a research tool; they represent a pathway to novel therapeutic approaches targeting mitochondrial dysfunction. With the rise of interest in personalized medicine, these cell lines can help tailor treatments to specific metabolic deficiencies, improving patient outcomes.

As leaders in genetic engineering and cell line development, our company is dedicated to providing high-quality, innovative biological products that empower researchers to unravel complex biological questions and drive discoveries that enhance human health.

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

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