Gene: NDUFS8
Official Full Name: NADH:ubiquinone oxidoreductase core subunit S8provided by HGNC
Gene Summary: This gene encodes a subunit of mitochondrial NADH:ubiquinone oxidoreductase, or Complex I, a multimeric enzyme of the respiratory chain responsible for NADH oxidation, ubiquinone reduction, and the ejection of protons from mitochondria. The encoded protein is involved in the binding of two of the six to eight iron-sulfur clusters of Complex I and, as such, is required in the electron transfer process. Mutations in this gene have been associated with Leigh syndrome. [provided by RefSeq, Mar 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36409 | NDUFS8 Knockout cell line (HeLa) | Human | NDUFS8 | 1:3~1:6 | Negative | Online Inquiry |
KO36410 | NDUFS8 Knockout cell line (HCT 116) | Human | NDUFS8 | 1:2~1:4 | Negative | Online Inquiry |
KO36411 | NDUFS8 Knockout cell line (HEK293) | Human | NDUFS8 | 1:3~1:6 | Negative | Online Inquiry |
KO36412 | NDUFS8 Knockout cell line (A549) | Human | NDUFS8 | 1:3~1:4 | Negative | Online Inquiry |
NDUFS8 Gene Knockout Cell Lines are specifically engineered cellular models that have had the NDUFS8 gene, a critical component of the mitochondrial respiratory chain complex I, disrupted or excised. This gene plays a pivotal role in mitochondrial bioenergetics, as it encodes an essential subunit that aids in electron transfer during oxidative phosphorylation. By effectively creating a cellular context in which the NDUFS8 function is abolished, these knockout cell lines provide researchers with a unique opportunity to study the biochemical and cellular consequences of impaired mitochondrial function.
The primary mechanism of action in NDUFS8 knockout models involves the alteration of mitochondrial energy metabolism, leading to observable phenotypes such as reduced ATP production, increased reactive oxygen species (ROS), and a switch to anaerobic metabolic pathways. Researchers can utilize these cell lines to elucidate the pathophysiology associated with mitochondrial disorders and contribute valuable insights into diseases, including neurodegenerative conditions, metabolic syndromes, and cancer.
From a scientific perspective, these cell lines hold significant importance in research and potential clinical applications. They offer a reliable model for drug screening and the development of therapeutic interventions aimed at restoring mitochondrial function. Furthermore, they serve as a platform for genetic studies, enabling high-throughput screening for compounds that may reverse or mitigate the effects of mitochondrial dysfunction.
What sets NDUFS8 Gene Knockout Cell Lines apart from traditional models is not only their specificity but also the ability to generate reproducible results reflective of real-world physiological conditions. This specificity allows researchers to target pathways with precision, enhancing the predictive validity of experimental outcomes.
With their unique advantages, these knockout cell lines become invaluable tools for researchers and clinicians aiming to deepen understanding and treatment of mitochondrial-related diseases. Our company prides itself on delivering high-quality biological products, backed by cutting-edge technology and comprehensive expertise in genetic engineering. We remain committed to supporting the scientific community by providing tools that facilitate groundbreaking research and therapeutic innovation.
Please note that all services are for research use only. Not intended for any clinical use.
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