Date published: 2026-5-25

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ACSL Substrates

Santa Cruz Biotechnology now offers a broad range of ACSL Substrates for use in various applications. ACSL substrates are specialized compounds that serve as the starting materials for acyl-CoA synthetase long-chain (ACSL) enzymes, which are pivotal in the metabolism of long-chain fatty acids. These enzymes catalyze the conversion of free fatty acids into acyl-CoA, an essential step for their incorporation into complex lipids, energy production via β-oxidation, and signaling pathways. In scientific research, ACSL substrates are crucial for studying lipid metabolism, energy homeostasis, and the role of fatty acid activation in various biological processes. Researchers utilize these substrates to investigate how different fatty acids are metabolized within cells, how they contribute to the synthesis of vital cellular components, and how disruptions in these pathways may lead to metabolic disorders. By providing a consistent and high-purity source of ACSL substrates, Santa Cruz Biotechnology enables precise experimental conditions, ensuring reproducibility and reliability in research outcomes. These substrates are also essential for developing and validating assays that measure ACSL activity, helping scientists understand the nuances of lipid metabolism and the impact of genetic or pharmacological interventions on these critical pathways. By offering a comprehensive selection of ACSL substrates, Santa Cruz Biotechnology supports the scientific community in advancing research on lipid biochemistry, metabolic regulation, and the intricate mechanisms underlying fatty acid metabolism. View detailed information on our available ACSL Substrates by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Hydroxydecanoate sodium salt

71186-53-3sc-200992
sc-200992A
100 mg
500 mg
$89.00
$339.00
7
(1)

5-Hydroxydecanoate sodium salt serves as a versatile acyl chain modifier, exhibiting unique interactions with lipid membranes. Its hydroxyl group enhances hydrogen bonding, promoting distinct solubility profiles in various solvents. This compound participates in specific enzymatic pathways, influencing lipid biosynthesis and degradation. Its kinetic behavior is characterized by rapid incorporation into metabolic cycles, allowing for nuanced studies of fatty acid metabolism and cellular energy dynamics.