Gene: ATPAF2
Official Full Name: ATP synthase mitochondrial F1 complex assembly factor 2provided by HGNC
Gene Summary: This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith-Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO23417 | ATPAF2 Knockout cell line (HeLa) | Human | ATPAF2 | 1:3~1:6 | Negative | Online Inquiry |
KO23418 | ATPAF2 Knockout cell line (HCT 116) | Human | ATPAF2 | 1:2~1:4 | Negative | Online Inquiry |
KO23419 | ATPAF2 Knockout cell line (HEK293) | Human | ATPAF2 | 1:3~1:6 | Negative | Online Inquiry |
KO23420 | ATPAF2 Knockout cell line (A549) | Human | ATPAF2 | 1:3~1:4 | Negative | Online Inquiry |
ATPAF2 Gene Knockout Cell Lines are genetically engineered cellular models that have had the ATPAF2 gene, known for its role in mitochondrial function and cellular energy metabolism, selectively inactivated. This knockout approach allows researchers to study the downstream effects on metabolic processes, mitochondrial dynamics, and overall cellular physiology, making it an invaluable tool in the field of cellular and molecular biology.
The ATPAF2 gene is integral in ATP synthesis within the mitochondria, and knocking it out elucidates the role of this gene in energy production and homeostasis. The resulting cell lines demonstrate significant changes in ATP levels, reactive oxygen species (ROS) generation, and alterations in mitochondrial morphology. By employing these knockout models, scientists can investigate not only the gene's direct impact on energy metabolism but also its broader implications in conditions such as cancer metabolism, neurodegenerative diseases, and metabolic syndromes.
The scientific importance of ATPAF2 Gene Knockout Cell Lines extends to various applications, including drug discovery, genetic research, and the development of novel therapies targeting metabolic dysfunctions. These models are essential for studies aiming to delineate the pathways of energy regulation and the consequences of mitochondrial dysfunction, which is pivotal in many disease states.
One of the primary advantages of utilizing ATPAF2 knockout cell lines is their specificity. Compared to similar models, these lines offer a unique perspective on ATP synthesis pathways, resulting in more targeted and reliable experimental outcomes. Furthermore, they enable high-throughput screening of compounds that may restore mitochondrial function or compensate for the loss of ATPAF2 activity.
For researchers and clinicians invested in understanding mitochondrial biology and its linkage to metabolic diseases, ATPAF2 Gene Knockout Cell Lines provide a critical resource. These models facilitate innovative research, which could lead to breakthroughs in therapeutic strategies aimed at managing conditions associated with mitochondrial dysfunction.
Our company specializes in the development of high-quality genetic models and provides a wide array of tools for advancing research in cellular and molecular biology. With our expertise, we ensure that every product, including the ATPAF2 Gene Knockout Cell Lines, meets rigorous scientific standards to support your research endeavors effectively.
Please note that all services are for research use only. Not intended for any clinical use.
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