Gene: ACADSB
Official Full Name: acyl-CoA dehydrogenase short/branched chainprovided by HGNC
Gene Summary: Short/branched chain acyl-CoA dehydrogenase(ACADSB) is a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. Substrate specificity is the primary characteristic used to define members of this gene family. The ACADSB gene product has the greatest activity towards the short branched chain acyl-CoA derivative, (S)-2-methylbutyryl-CoA, but also reacts significantly with other 2-methyl branched chain substrates and with short straight chain acyl-CoAs. The cDNA encodes for a mitochondrial precursor protein which is cleaved upon mitochondrial import and predicted to yield a mature peptide of approximately 43.7-KDa. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO39139 | ACADSB Knockout cell line (HeLa) | Human | ACADSB | 1:3~1:6 | Negative | Online Inquiry |
KO39140 | ACADSB Knockout cell line (HCT 116) | Human | ACADSB | 1:2~1:4 | Negative | Online Inquiry |
KO39141 | ACADSB Knockout cell line (HEK293) | Human | ACADSB | 1:3~1:6 | Negative | Online Inquiry |
KO39142 | ACADSB Knockout cell line (A549) | Human | ACADSB | 1:3~1:4 | Negative | Online Inquiry |
ACADSB Gene Knockout Cell Lines are genetically engineered cellular models designed to functionally eliminate the ACADSB gene, which encodes the short-chain acyl-CoA dehydrogenase. This gene plays a crucial role in the metabolism of fatty acids, particularly those with a short chain length. By creating a knockout model, researchers can effectively study the downstream effects of ACADSB deficiency, providing invaluable insights into metabolic disorders, particularly those related to mitochondrial function and fatty acid oxidation.
The mechanism by which these knockout cell lines operate involves the use of advanced gene-editing techniques, such as CRISPR/Cas9, to create a targeted disruption of the ACADSB gene. This allows for the observation of phenotypic changes and biochemical pathways that are altered in the absence of functional ACADSB protein. Such models are essential for elucidating the pathophysiology of conditions associated with fatty acid oxidation disorders, thus facilitating the search for therapeutic interventions.
In terms of scientific significance, ACADSB Gene Knockout Cell Lines have broad applications in both research and clinical settings. They serve as powerful tools for studying metabolic pathways, drug discovery, and testing the efficacy of potential treatments for related metabolic disorders. The availability of these sophisticated models allows for high-throughput screening and can accelerate the transition from bench to bedside in the development of new therapeutic options.
What sets our ACADSB Gene Knockout Cell Lines apart from alternatives is their robust validation and characterization. Unlike other models that may produce variable results or exhibit low fidelity to human physiology, our cell lines have been rigorously tested for consistency and specificity, ensuring that researchers receive reliable and reproducible data. This is vital for generating high-quality scientific publications and advancing clinical understanding.
For researchers and clinicians alike, the ACADSB Gene Knockout Cell Lines represent an invaluable asset in the quest for more effective metabolic disorder treatments. They provide a unique opportunity to investigate the roles of fatty acid metabolism in disease and hold great potential for future therapeutic breakthroughs.
Our company is dedicated to advancing scientific research by providing high-quality biological products that meet the rigorous demands of modern research and clinical applications. Through our expertise in genetic engineering, we ensure that our products, such as the ACADSB Gene Knockout Cell Lines, are at the forefront of innovation, facilitating cutting-edge discoveries and breakthroughs in the life sciences.
Please note that all services are for research use only. Not intended for any clinical use.
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