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ACADL Knockout Cell Lines

Gene: ACADL

Official Full Name: acyl-CoA dehydrogenase long chainprovided by HGNC

Gene Summary: The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03772 ACADL Knockout cell line (HeLa) Human ACADL 1:3~1:6 Negative Online Inquiry
KO03773 ACADL Knockout cell line (HEK293) Human ACADL 1:3~1:6 Negative Online Inquiry

Background

ACADL Gene Knockout Cell Lines are genetically engineered human cell models specifically designed to facilitate comprehensive studies on the acyl-CoA dehydrogenase family, particularly the long-chain acyl-CoA dehydrogenase (ACADL) gene. These cell lines are valuable tools for investigating the role of ACADL in fatty acid metabolism and its implications in metabolic disorders. By employing CRISPR-Cas9 gene editing techniques, the ACADL gene has been accurately knocked out, enabling researchers to observe the resultant metabolic changes and elucidate the pathways affected by its absence.

The primary function of ACADL Gene Knockout Cell Lines is to enable the study of long-chain fatty acid oxidation processes. The absence of the ACADL gene disrupts fatty acid metabolism, leading to altered energy production pathways and providing insight into various metabolic pathways. These cell lines serve as instrumental models for exploring the implications of ACADL deficiency, such as the potential development of cardiomyopathy, fatty liver disease, and disorders related to energy metabolism imbalances.

The scientific importance of these cell lines extends to both research and clinical applications. They provide an effective platform for elucidating the biological effects of ACADL dysfunction in disease models, which can lead to the identification of novel therapeutic targets. The ability to study the functional implications of ACADL knockout in a controlled environment enhances our understanding of similar metabolic syndromes and paves the way for innovative treatment strategies.

One of the unique selling points of ACADL Gene Knockout Cell Lines compared to other metabolic disorder models is their specificity and fidelity in representing the human cellular context, which often cannot be replicated using animal models. Researchers benefit from the direct applicability of findings to human health conditions, thus bridging the gap between laboratory research and clinical relevance more effectively than non-human models.

The value of this product to researchers and clinicians lies in its potential to accelerate the discovery of novel biomarkers and therapeutics related to metabolic health. Given the increasing prevalence of metabolic disorders globally, the insights gained from using ACADL Gene Knockout Cell Lines may significantly contribute to advancing medical knowledge and enhancing patient care.

Our company is dedicated to providing high-quality, meticulously characterized biological products that empower researchers to push the frontiers of scientific discovery. With our expertise in genetic engineering and a commitment to advancing cellular models, we are positioned to support the ongoing advancements in metabolic research and beyond.

Please note that all services are for research use only. Not intended for any clinical use.

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