Gene: ATP5F1D
Official Full Name: ATP synthase F1 subunit deltaprovided by HGNC
Gene Summary: This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the delta subunit of the catalytic core. Alternatively spliced transcript variants encoding the same isoform have been identified. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00413 | ATP5F1D Knockout cell line (HeLa) | Human | ATP5F1D | 1:3~1:6 | Negative | Online Inquiry |
KO19582 | ATP5F1D Knockout cell line (HCT 116) | Human | ATP5F1D | 1:2~1:4 | Negative | Online Inquiry |
KO19583 | ATP5F1D Knockout cell line (HEK293) | Human | ATP5F1D | 1:3~1:6 | Negative | Online Inquiry |
KO19584 | ATP5F1D Knockout cell line (A549) | Human | ATP5F1D | 1:3~1:4 | Negative | Online Inquiry |
ATP5F1D Gene Knockout Cell Lines are genetically engineered cellular models designed to investigate the role of the ATP5F1D gene, which encodes a critical component of the mitochondrial ATP synthase complex. By employing CRISPR/Cas9 gene-editing technology, these cell lines exhibit a complete knockout of the ATP5F1D gene, allowing researchers to explore the functional implications of this gene’s absence in cellular metabolism and energy production.
The primary function of ATP5F1D is to provide a structural role within the ATP synthase complex, essential for ATP generation during oxidative phosphorylation. The knockout of this gene disrupts ATP synthesis, leading to a cascade of metabolic changes that researchers can study in contexts such as mitochondrial dysfunction, cellular stress responses, and apoptosis. By utilizing these cell lines, scientists can gain insights into diseases associated with mitochondrial dysfunction, including neurodegenerative diseases and metabolic disorders, thus enhancing our understanding of cellular bioenergetics.
The scientific importance of ATP5F1D Gene Knockout Cell Lines extends to both research and clinical applications. In research settings, these models serve as invaluable tools for drug discovery, enabling the screening of compounds that can modulate mitochondrial function. Clinicians and biotechnologists can also leverage these models to develop novel therapeutic strategies aimed at mitochondrial-related diseases.
A significant advantage of our ATP5F1D Gene Knockout Cell Lines over alternatives lies in their high fidelity and reproducibility. Unlike traditional methods that may produce heterogeneous cell populations, our engineered lines provide a consistent background for experimental designs. Additionally, our expert team offers comprehensive support, including experimental consultation and troubleshooting, ensuring users can maximize the potential of these models.
In conclusion, ATP5F1D Gene Knockout Cell Lines represent a cutting-edge resource for researchers and clinicians alike, providing potent tools to unravel mitochondrial function and its implications in health and disease. With our robust expertise in cellular engineering and commitment to advancing scientific discovery, we are poised to support your research endeavors with high-quality biological products.
Please note that all services are for research use only. Not intended for any clinical use.
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