Gene: ATP5F1B
Official Full Name: ATP synthase F1 subunit betaprovided 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 beta subunit of the catalytic core. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO19589 | ATP5F1B Knockout cell line (HeLa) | Human | ATP5F1B | 1:3~1:6 | Negative | Online Inquiry |
KO19590 | ATP5F1B Knockout cell line (HCT 116) | Human | ATP5F1B | 1:2~1:4 | Negative | Online Inquiry |
KO19591 | ATP5F1B Knockout cell line (HEK293) | Human | ATP5F1B | 1:3~1:6 | Negative | Online Inquiry |
KO19592 | ATP5F1B Knockout cell line (A549) | Human | ATP5F1B | 1:3~1:4 | Negative | Online Inquiry |
ATP5F1B Gene Knockout Cell Lines are engineered cellular systems created to study the functional implications of the ATP5F1B gene, part of the ATP synthase complex essential for ATP production in mitochondria. These knockout cell lines feature targeted disruptions of the ATP5F1B gene, providing researchers with a powerful model to investigate the gene’s role in cellular metabolism, energy production, and the associated pathways implicated in various health conditions.
The key mechanisms of these knockout cell lines involve the loss of ATP5F1B protein expression, which directly affects ATP synthesis, leading to disruptions in cellular energy balance and increased production of reactive oxygen species (ROS). Researchers can observe the consequent physiological changes, including altered metabolic profiles, increased apoptosis rates, and adaptations in mitochondrial dynamics. This insight is invaluable for understanding diseases such as cancer, neurodegenerative disorders, and metabolic syndromes where mitochondrial dysfunction is a critical feature.
The scientific importance of ATP5F1B Gene Knockout Cell Lines lies in their applicability in both basic and applied research settings. They serve as model systems for drug testing, gene therapy evaluations, and can aid in deciphering complex molecular interactions within the mitochondrial systems. Their relevance to ongoing research in mitochondrial pathophysiology positions them as critical tools for discovering novel therapeutic strategies.
Compared to alternatives such as wild-type cell lines or non-specific gene knockouts, these targeted cell lines offer greater specificity and control over experimental conditions. This precision allows for clearer interpretation of results and enhanced reproducibility, reducing variability often seen with less specific models.
For researchers and clinicians alike, the ATP5F1B Gene Knockout Cell Lines provide not only a robust tool for elucidating gene function but also pave the way for advancements in regenerative medicine and therapeutic developments targeting mitochondrial dysfunction. Our company specializes in providing high-quality biologically relevant models, and our expertise ensures that you receive a product backed by rigorous validation and cutting-edge technology. We are committed to supporting your research endeavors with reliable, innovative solutions that drive scientific discovery forward.
Please note that all services are for research use only. Not intended for any clinical use.
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