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NDUFS3 Knockout Cell Lines

Gene: NDUFS3

Official Full Name: NADH:ubiquinone oxidoreductase core subunit S3provided by HGNC

Gene Summary: This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.[provided by RefSeq, Apr 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO36421 NDUFS3 Knockout cell line (HeLa) Human NDUFS3 1:3~1:6 Negative Online Inquiry
KO36422 NDUFS3 Knockout cell line (HCT 116) Human NDUFS3 1:2~1:4 Negative Online Inquiry
KO36423 NDUFS3 Knockout cell line (HEK293) Human NDUFS3 1:3~1:6 Negative Online Inquiry

Background

NDUFS3 Gene Knockout Cell Lines are specialized cellular models designed to facilitate the study of mitochondrial respiratory chain dysfunction. The NDUFS3 gene encodes a crucial component of the NADH-ubiquinone oxidoreductase complex I, which is responsible for initiating oxidative phosphorylation in mitochondria. By creating knockout variants of this gene, researchers can investigate the biochemical pathways affected by its absence, providing insights into mitochondrial diseases and respiratory chain deficiencies.

These cell lines operate through a targeted gene editing mechanism, usually employing CRISPR-Cas9 technology or other gene-editing strategies that result in the specific inactivation of the NDUFS3 gene. The resultant knockout cells exhibit a range of phenotypic alterations, such as impaired ATP synthesis, altered reactive oxygen species (ROS) production, and disruptions in cellular metabolism. Such changes serve as a reliable model for studying the pathophysiological roles associated with mitochondrial dysfunction, including neurodegenerative diseases, metabolic disorders, and aging processes.

The scientific importance of NDUFS3 Gene Knockout Cell Lines is underscored by their applications in research settings focused on mitochondrial biology and pharmacological testing. They provide a platform for screening drug candidates aimed at restoring mitochondrial function or mitigating the effects of mitochondrial diseases. Furthermore, these cell lines enable detailed proteomic and genomic analyses that can unveil therapeutic targets.

Compared to existing alternatives, NDUFS3 Gene Knockout Cell Lines offer specificity and reproducibility without the confounding factors often seen in heterogeneous primary cell cultures. Their well-characterized nature ensures high experimental fidelity and facilitates comparison across studies. This makes them highly valuable to researchers and clinicians alike who are exploring innovative solutions to combat mitochondrial dysfunction.

By choosing NDUFS3 Gene Knockout Cell Lines, researchers can leverage state-of-the-art monoclonal cell technology backed by our company’s extensive expertise in cellular models and gene editing. Our commitment to quality and scientific integrity ensures that each product is designed to meet rigorous standards, equipping users with the tools necessary for groundbreaking discoveries in mitochondrial research and beyond.

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

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