Gene: ACSL1
Official Full Name: acyl-CoA synthetase long chain family member 1provided by HGNC
Gene Summary: The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00918 | ACSL1 Knockout cell line(Hep G2) | Human | ACSL1 | 1:2~1:4 | Negative | Online Inquiry |
KO20035 | ACSL1 Knockout cell line (HeLa) | Human | ACSL1 | 1:3~1:6 | Negative | Online Inquiry |
KO20036 | ACSL1 Knockout cell line (HCT 116) | Human | ACSL1 | 1:2~1:4 | Negative | Online Inquiry |
KO20037 | ACSL1 Knockout cell line (HEK293) | Human | ACSL1 | 1:3~1:6 | Negative | Online Inquiry |
KO20038 | ACSL1 Knockout cell line (A549) | Human | ACSL1 | 1:3~1:4 | Negative | Online Inquiry |
ACSL1 Gene Knockout Cell Lines are specialized biological reagents designed to facilitate the study of acyl-CoA synthetase long-chain family member 1 (ACSL1) gene functions through the elimination of its expression. These cell lines are created using advanced CRISPR-Cas9 gene editing technology, which allows for precise and efficient ablation of the ACSL1 gene. By knocking out this critical gene, researchers can explore its role in fatty acid metabolism, energy homeostasis, and various associated metabolic disorders.
The key function of these cell lines is to provide a controlled system for investigating the physiological impacts of ACSL1 deficiency. This is particularly valuable in deciphering its involvement in cellular processes such as lipid synthesis, signaling pathways, and cell proliferation. The underlying mechanism hinges on the absence of the ACSL1 enzyme, which plays a crucial role in converting long-chain fatty acids into acyl-CoA derivatives. This metabolic disruption can lead to various downstream effects, enabling researchers to map out the gene's contributions to health and disease.
Scientifically, ACSL1 Gene Knockout Cell Lines are instrumental for researchers in metabolic diseases, cancer, and cardiovascular studies. Their utility extends beyond basic research; these cell lines can also facilitate drug screening and the study of therapeutic interventions targeting metabolic pathways. Unique selling points include their high specificity and reliability as research tools, as well as their potential for reproducible results in experimental assays, which are often challenges with alternative methods such as pharmacological inhibition.
For researchers and clinicians alike, these knockout cell lines offer invaluable insights which could shape future therapeutic strategies and enhance our understanding of metabolic diseases. The ability to study gene function in a controlled environment promotes greater clarity in how ACSL1 engages with other cellular mechanisms, ultimately paving the way for innovative treatment options.
With a commitment to advancing research and development, our company leverages extensive experience in genetic engineering and cell line production, ensuring that our ACSL1 Gene Knockout Cell Lines meet the highest standards of quality and consistency, equipping scientific communities with essential tools for groundbreaking discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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