Date published: 2026-6-3

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ASM Substrates

Santa Cruz Biotechnology now offers a broad range of ASM Substrates for use in various applications. ASM substrates are integral tools in scientific research, particularly in the study of sphingolipid metabolism and the role of acid sphingomyelinase (ASM) in cellular processes. ASM is an enzyme responsible for the hydrolysis of sphingomyelin into ceramide and phosphorylcholine, a reaction that plays a crucial role in regulating cell membrane composition, signal transduction, and apoptosis. By utilizing ASM substrates, researchers can investigate the activity of this enzyme under various experimental conditions, allowing for a deeper understanding of how sphingolipid metabolism impacts cell function and homeostasis. These substrates are essential in enzymatic assays designed to measure ASM activity, providing insights into the regulation of ceramide production and its downstream effects on cellular signaling pathways. ASM substrates are also used in studies exploring the role of ceramide in mediating stress responses, inflammation, and programmed cell death, as well as in the context of neurodegenerative diseases where altered sphingolipid metabolism is often implicated. Additionally, these substrates enable researchers to dissect the biochemical pathways involved in the turnover of sphingomyelin in cell membranes, contributing to a broader understanding of lipid metabolism and its implications for cellular physiology. The availability of a wide range of ASM substrates allows for tailored experimental approaches that can address specific aspects of sphingomyelin metabolism, advancing research in cell biology, biochemistry, and related fields. View detailed information on our available ASM Substrates by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

2-(N-Hexadecanoylamino)-4-nitrophenylphosphocholine Hydroxide

60438-73-5sc-396222
10 mg
$380.00
(0)

2-(N-Hexadecanoylamino)-4-nitrophenylphosphocholine Hydroxide exhibits distinctive properties as an acid halide, characterized by its amphiphilic nature, which facilitates interactions with lipid membranes. Its nitrophenyl group enhances electron-withdrawing capabilities, influencing reaction kinetics and promoting nucleophilic attack. The hydroxide moiety contributes to its reactivity, enabling unique pathways in phospholipid synthesis and modulation of membrane dynamics, thereby affecting molecular assembly and stability.