Gene: ATP5F1C
Official Full Name: ATP synthase F1 subunit gammaprovided 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 gamma subunit of the catalytic core. Alternatively spliced transcript variants encoding different isoforms have been identified. This gene also has a pseudogene on chromosome 14. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO19585 | ATP5F1C Knockout cell line (HeLa) | Human | ATP5F1C | 1:3~1:6 | Negative | Online Inquiry |
KO19586 | ATP5F1C Knockout cell line (HCT 116) | Human | ATP5F1C | 1:2~1:4 | Negative | Online Inquiry |
KO19587 | ATP5F1C Knockout cell line (HEK293) | Human | ATP5F1C | 1:3~1:6 | Negative | Online Inquiry |
KO19588 | ATP5F1C Knockout cell line (A549) | Human | ATP5F1C | 1:3~1:4 | Negative | Online Inquiry |
ATP5F1C Gene Knockout Cell Lines are a vital tool for researchers studying mitochondrial function, energy production, and associated metabolic disorders. These cell lines have been genetically engineered to lack the ATP5F1C gene, which encodes a crucial subunit of ATP synthase, an enzyme responsible for synthesizing adenosine triphosphate (ATP) during oxidative phosphorylation. By eliminating this key component, researchers can investigate the functional consequences of impaired ATP synthesis, providing insights into cellular metabolism and the pathogenesis of mitochondrial diseases.
The primary function of ATP5F1C Gene Knockout Cell Lines is to model conditions of mitochondrial dysfunction. The absence of the ATP5F1C protein disrupts the assembly of ATP synthase, leading to reduced ATP production and an accumulation of metabolic intermediates. This altered metabolic state can be mimicked in laboratory settings, allowing scientists to explore the cellular responses to energy depletion, investigate compensatory mechanisms, and screen for potential therapeutic compounds that may restore mitochondrial function.
In terms of scientific importance, these cell lines are invaluable for unveiling the molecular underpinnings of diseases such as Leigh syndrome and other mitochondrial disorders. Their applications extend across various research fields, including neurobiology, cardiovascular health, and cancer biology, where metabolic shifts are implicated in disease progression.
Compared to conventional cell lines, ATP5F1C Gene Knockout Cell Lines provide a more accurate model of mitochondrial dysfunction. This specificity enables targeted experimentation that can lead to significant discoveries about disease mechanisms or treatment strategies that may not be feasible using alternative models.
For researchers and clinicians focused on mitochondrial health and disease, ATP5F1C Gene Knockout Cell Lines represent an essential resource for advancing knowledge and developing innovative therapeutic approaches. At [Your Company Name], we are committed to producing high-quality biological products that empower scientific research and contribute to breakthroughs in health and medicine.
Please note that all services are for research use only. Not intended for any clinical use.
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