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CPT2 Knockout Cell Lines

Gene: CPT2

Official Full Name: carnitine palmitoyltransferase 2provided by HGNC

Gene Summary: The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO20920 CPT2 Knockout cell line (HeLa) Human CPT2 1:3~1:6 Negative Online Inquiry
KO20921 CPT2 Knockout cell line (HCT 116) Human CPT2 1:2~1:4 Negative Online Inquiry
KO20922 CPT2 Knockout cell line (HEK293) Human CPT2 1:3~1:6 Negative Online Inquiry
KO20923 CPT2 Knockout cell line (A549) Human CPT2 1:3~1:4 Negative Online Inquiry

Background

CPT2 Gene Knockout Cell Lines are specifically engineered cellular models that have had the CPT2 gene (carnitine palmitoyltransferase 2) deactivated through precise genetic modification techniques, such as CRISPR-Cas9. This gene plays a critical role in the oxidation of long-chain fatty acids within mitochondria, impacting metabolic pathways and energy production. By utilizing these knockout cell lines, researchers can investigate the functional consequences of CPT2 deficiency, examining not only fatty acid metabolism but also exploring implications on broader metabolic disorders, including obesity, diabetes, and cardiovascular diseases.

The key mechanism underlying the functionality of CPT2 Gene Knockout Cell Lines lies in their ability to mimic certain pathological conditions attributed to flawed fatty acid metabolism, enabling scientists to explore related biochemical pathways in a controlled laboratory setting. Researchers can study alterations in metabolic profiles, enzyme activity, and cellular responses to nutrient availability, which are essential for understanding diverse health implications.

In terms of scientific importance, these cell lines represent a valuable resource for research focused on mitochondrial dysfunction and its associated diseases. They are instrumental in developing therapeutic strategies and drug candidates aimed at correcting or compensating for CPT2-related metabolic abnormalities.

The unique selling points of CPT2 Gene Knockout Cell Lines include their high specificity and reliability for studies requiring precise genetic backgrounds, ensuring reproducibility and robustness in experimental results. Unlike alternative models, these cell lines offer a more nuanced insight into the metabolic pathways directly impacted by CPT2 deletions, facilitating advanced research into targeted treatments and metabolic therapies.

For researchers and clinicians dedicated to understanding metabolic pathways and their implications in disease, CPT2 Gene Knockout Cell Lines provide an invaluable platform. The insights gained through utilizing these models can significantly enhance the development of innovative approaches to mitigate metabolic disorders.

Our company is dedicated to advancing genetic tools and cellular models, ensuring that researchers have access to high-quality, reliable products that empower their scientific endeavors and contribute to meaningful breakthroughs in health and medicine.

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

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