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NDUFB5 Knockout Cell Lines

Gene: NDUFB5

Official Full Name: NADH:ubiquinone oxidoreductase subunit B5provided by HGNC

Gene Summary: The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO05212 NDUFB5 Knockout cell line (HeLa) Human NDUFB5 1:3~1:6 Negative Online Inquiry
KO05213 NDUFB5 Knockout cell line (HCT 116) Human NDUFB5 1:2~1:4 Negative Online Inquiry
KO05214 NDUFB5 Knockout cell line (HEK293) Human NDUFB5 1:3~1:6 Negative Online Inquiry
KO05215 NDUFB5 Knockout cell line (A549) Human NDUFB5 1:3~1:4 Negative Online Inquiry

Background

NDUFB5 Gene Knockout Cell Lines are advanced cellular models designed for the functional analysis of the NDUFB5 gene, which encodes a critical subunit of the mitochondrial NADH dehydrogenase complex I. By utilizing CRISPR-Cas9 gene editing technology, these cell lines have been meticulously engineered to knock out the NDUFB5 gene, providing researchers with a powerful tool to study its role in cellular energy metabolism, mitochondrial dysfunction, and related pathophysiological conditions.

The primary mechanism by which NDUFB5 gene knockout cell lines function involves the disruption of complex I activity within the mitochondrial electron transport chain. This leads to significant changes in ATP production, increased reactive oxygen species (ROS) generation, and alterations in metabolic profiles. Such mechanistic insights are invaluable, especially in the realms of neurodegenerative diseases, metabolic disorders, and cancer research, where mitochondrial dysfunction plays a pivotal role.

The scientific importance of these cell lines is underscored by their wide-ranging applications in both research and clinical settings. They can be employed in drug screening assays to evaluate compounds that may restore mitochondrial function or mitigate the effects of NDUFB5 deficiency. Additionally, these cell lines serve as a platform for elucidating the molecular pathways that contribute to diseases associated with mitochondrial impairment, offering the potential for the development of novel therapeutic strategies.

Compared to traditional models, the NDUFB5 gene knockout cell lines offer several unique advantages: the precision and efficiency of CRISPR technology ensure a complete gene disruption, while the ability to easily propagate and modify these cell lines allows for real-time experimentation and validation of results. Moreover, they provide a reproducible model for consistent findings across studies, which is crucial for translational research efforts.

For researchers and clinicians striving to deepen their understanding of mitochondrial biology and its implications in human health, these cell lines stand out as an essential resource. They not only streamline the discovery process but also empower scientists to uncover new therapeutic avenues targeting mitochondrial dysfunction.

Our company is committed to advancing biological research through innovative cell models and cutting-edge editing techniques, ensuring that our products meet the highest standards of scientific excellence and support the ongoing quest for knowledge in the life sciences.

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

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