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NDUFS7 Knockout Cell Lines

Gene: NDUFS7

Official Full Name: NADH:ubiquinone oxidoreductase core subunit S7provided by HGNC

Gene Summary: This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO36413 NDUFS7 Knockout cell line (HeLa) Human NDUFS7 1:3~1:6 Negative Online Inquiry
KO36414 NDUFS7 Knockout cell line (HCT 116) Human NDUFS7 1:2~1:4 Negative Online Inquiry
KO36415 NDUFS7 Knockout cell line (HEK293) Human NDUFS7 1:3~1:6 Negative Online Inquiry
KO36416 NDUFS7 Knockout cell line (A549) Human NDUFS7 1:3~1:4 Negative Online Inquiry

Background

NDUFS7 Gene Knockout Cell Lines are sophisticated cellular models engineered to lack the NDUFS7 gene, a crucial component of the mitochondrial electron transport chain, specifically involved in Complex I function. By eliminating the expression of this gene, these cell lines serve as invaluable tools for studying mitochondrial dysfunction, bioenergetics, and the pathological mechanisms underlying various diseases, including neurodegenerative disorders and metabolic syndromes.

These cell lines function by facilitating the detailed exploration of the consequences of NDUFS7 deficiency, allowing researchers to investigate the resulting impacts on cellular respiration, ATP production, and reactive oxygen species generation. The specific knockout of the NDUFS7 gene leads to a measurable reduction in oxidative phosphorylation efficiency, thus providing insights into the compensatory mechanisms cells may employ in response to low energy states. Researchers can utilize these models to unravel complex signaling pathways involved in mitochondrial health, cellular metabolism, and the aging process.

In the context of scientific research, NDUFS7 Gene Knockout Cell Lines hold significant importance. They are vital for drug discovery, therapeutic target validation, and the investigation of mitochondrial diseases, allowing for a better understanding of disease mechanisms and identification of potential intervention strategies. These cell lines are also applicable in preclinical studies where the interaction between drug candidates and mitochondrial functions can be assessed.

Compared to other available models, our NDUFS7 Gene Knockout Cell Lines are rigorously characterized and validated for consistency and functionality, ensuring that researchers obtain reliable and reproducible results. They are easy to culture and manipulate, offering flexibility for various downstream applications, including CRISPR gene editing, metabolic assays, and high-throughput screening.

For researchers and clinicians, investing in NDUFS7 Gene Knockout Cell Lines translates to enhanced understanding and exploration of mitochondrial biology, making significant contributions to the field of regenerative medicine and disease research. By utilizing these specialized cell lines, users can advance their projects with the confidence that they are backed by our company’s commitment to providing high-quality, scientifically accurate biological products supported by extensive expertise in genetic engineering and cell biology.

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

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