Gene: SUCLA2
Official Full Name: succinate-CoA ligase ADP-forming subunit betaprovided by HGNC
Gene Summary: Succinyl-CoA synthetase (SCS) is a mitochondrial matrix enzyme that acts as a heterodimer, being composed of an invariant alpha subunit and a substrate-specific beta subunit. The protein encoded by this gene is an ATP-specific SCS beta subunit that dimerizes with the SCS alpha subunit to form SCS-A, an essential component of the tricarboxylic acid cycle. SCS-A hydrolyzes ATP to convert succinate to succinyl-CoA. Defects in this gene are a cause of myopathic mitochondrial DNA depletion syndrome. A pseudogene of this gene has been found on chromosome 6. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00285 | SUCLA2 Knockout cell line (HEK293) | Human | SUCLA2 | 1:3~1:6 | Negative | Online Inquiry |
KO33836 | SUCLA2 Knockout cell line (HeLa) | Human | SUCLA2 | 1:3~1:6 | Negative | Online Inquiry |
KO33837 | SUCLA2 Knockout cell line (HCT 116) | Human | SUCLA2 | 1:2~1:4 | Negative | Online Inquiry |
KO33838 | SUCLA2 Knockout cell line (A549) | Human | SUCLA2 | 1:3~1:4 | Negative | Online Inquiry |
SUCLA2 Gene Knockout Cell Lines are specially engineered cellular models that have had the SUCLA2 gene knocked out, a crucial component in the synthesis of mitochondrial DNA and energy metabolism. By selectively disabling this gene, researchers can effectively study its biological functions, the implications of SUCLA2 deficiency, and the metabolic pathways influenced by this gene.
The primary mechanism of action involves the disruption of the ATP synthase complex within mitochondria, impacting energy production and mitochondrial function. The resulting phenotype provides insights into mitochondrial dysfunction, which is associated with various metabolic disorders, age-related diseases, and neuromuscular conditions. These knockout cell lines serve as vital tools for investigating the biochemical pathways linked to SUCLA2, allowing for the detailed study of mechanisms governing cellular energy homeostasis.
The scientific importance of SUCLA2 Gene Knockout Cell Lines is underscored by their applications in both fundamental research and clinical settings. They provide a basis for evaluating therapeutic strategies aimed at restoring mitochondrial function or compensating for energy deficits in pathological conditions. Researchers can employ these models to assess drug efficacy, study disease mechanisms, and explore potential interventions tailored to conditions affected by mitochondrial dysregulation.
Unique selling points of these cell lines include their robustness in providing reproducible results and their compatibility with a wide array of experimental formats, including high-throughput screening and CRISPR/Cas9 applications. Compared to other cell lines or wild-type models, SUCLA2 knockout lines uniquely facilitate the study of energy metabolism at a granular level, ultimately paving the way for advancements in therapeutic approaches.
For researchers and clinicians focused on metabolic or mitochondrial diseases, these cell lines represent a critical asset. Their availability can accelerate the pace of discovery, transforming our understanding of energy metabolism and offering potential pathways to novel therapeutic strategies. At [Your Company Name], we are committed to providing high-quality, reliable biological products that empower scientists in their research pursuits, backed by our extensive expertise in cellular biology and genetic engineering.
Please note that all services are for research use only. Not intended for any clinical use.
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