Gene: NDUFAF6
Official Full Name: NADH:ubiquinone oxidoreductase complex assembly factor 6provided by HGNC
Gene Summary: This gene encodes a protein that localizes to mitochondria and contains a predicted phytoene synthase domain. The encoded protein plays an important role in the assembly of complex I (NADH-ubiquinone oxidoreductase) of the mitochondrial respiratory chain through regulation of subunit ND1 biogenesis. Mutations in this gene are associated with complex I enzymatic deficiency. [provided by RefSeq, Nov 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO26351 | NDUFAF6 Knockout cell line (HeLa) | Human | NDUFAF6 | 1:3~1:6 | Negative | Online Inquiry |
KO26352 | NDUFAF6 Knockout cell line (HCT 116) | Human | NDUFAF6 | 1:2~1:4 | Negative | Online Inquiry |
KO26353 | NDUFAF6 Knockout cell line (HEK293) | Human | NDUFAF6 | 1:3~1:6 | Negative | Online Inquiry |
KO26354 | NDUFAF6 Knockout cell line (A549) | Human | NDUFAF6 | 1:3~1:4 | Negative | Online Inquiry |
NDUFAF6 Gene Knockout Cell Lines are genetically modified cell lines specifically designed to lack functional NDUFAF6, a crucial gene involved in mitochondrial complex I assembly and function. These cell lines serve as invaluable tools for studying the impact of NDUFAF6 deficiency on cellular metabolism, mitochondrial stability, and overall cell health. By creating a targeted disruption of the NDUFAF6 gene, researchers can investigate the downstream effects on oxidative phosphorylation and energy production, facilitating an understanding of mitochondrial diseases and metabolic disorders.
The mechanism of action relies on the CRISPR-Cas9 gene-editing technology that precisely excises portions of the NDUFAF6 gene, ensuring a loss of function. This knockout model enables comprehensive assessments of mitochondrial dynamics, bioenergetics, and the associated cellular pathways, allowing researchers to explore the molecular underpinnings of diseases linked to mitochondrial dysfunction, such as neurodegenerative diseases, muscle disorders, and metabolic syndromes.
The scientific importance of the NDUFAF6 Gene Knockout Cell Lines cannot be overstated, as they provide a standardized model for preclinical studies, enhancing the understanding of mitochondrial biology and paving the way for novel therapeutic strategies. In a clinical research context, these cell lines can be utilized to screen potential drug candidates that target mitochondrial dysfunction, ultimately contributing to the development of effective therapeutic interventions.
Compared to other cellular models, the NDUFAF6 knockout lines offer a unique advantage by providing a clear, focused mechanism to study mitochondrial disease pathways. This clarity enhances experimental design, allowing for more reliable and reproducible results. Moreover, the knockout cells represent an essential step towards understanding broader mitochondrial physiology.
For researchers and clinicians focused on mitochondrial research or related metabolic studies, the NDUFAF6 Gene Knockout Cell Lines are indispensable. They not only expedite the research process by providing an already established model but also substantially enrich the potential for translational research aimed at improving patient outcomes.
Our company, recognized for its commitment to advancing biological sciences, offers this innovative product backed by extensive expertise in genetic engineering and cell model development. We strive to empower the research community with high-quality tools that further the boundaries of scientific discovery.
Please note that all services are for research use only. Not intended for any clinical use.
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