Thiol-ene Resin

Thiol-ene resin is a polymer-forming material that combines thiol groups with carbon-carbon double bonds to create crosslinked networks, making it useful for precisely engineered biomaterials. When activated by light and a photoinitiator, radicals drive thiol molecules to add across ene groups in a step-growth click reaction, rapidly producing a uniform polymer network with tunable stiffness and swelling. In bioengineering, these resins support photopatterned hydrogels, three-dimensional cell encapsulation, tissue-engineering scaffolds, and microfabricated devices. Their efficient curing and adjustable composition enable control over structure, mechanical properties, and biological presentation, supporting research in regenerative medicine and in vitro model development.

Thiol-ene Resin - Related Videos

Research

JoVE Journal - Biology

Clear Resin Casting of Arthropods for Use in Education, Outreach, and Research

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2026

Here we show key steps in the process of creating high-quality, resin-embedded arthropods for educational instruction and outreach.

Biliary System Resin Casting: A Technique for Analyzing 3D Architecture of Biliary System in Murine Model Using Radiopaque Resin Injection

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2025

This video describes the procedure for biliary system resin casting, for understanding 3D biliary architecture. This technique provides insights into the internal diameter and network connectivity of the biliary system, which could be used for liver regeneration analysis.

Research

JoVE Journal - Biochemistry

Resin-Assisted Capture Coupled with Isobaric Tandem Mass Tag Labeling for Multiplexed Quantification of Protein Thiol Oxidation

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Cited by 9 •

2021

Protein thiol oxidation has significant implications under normal physiological and pathophysiological conditions. We describe the details of a quantitative redox proteomics method, which utilizes resin-assisted capture, isobaric labeling, and mass spectrometry, enabling site-specific identification and quantification of reversibly oxidized cysteine residues of proteins.

Education

JoVE Core - Organic Chemistry

Preparation and Reactions of Thiols

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2023

Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol. This reaction fails because the thiol product can undergo a second nucleophilic substitution reaction in the presence of an excess alkyl halide to generate a sulfide as a by-product. This limitation can be overcome by using thiourea as the nucleophile. The reaction first produces an alkyl...

Research

JoVE Journal - Biology
Free Sample

Profiling Thiol Redox Proteome Using Isotope Tagging Mass Spectrometry

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Cited by 40 •

2012

Reactive oxygen species level is elevated when cells encounter stress conditions. Here we show the example of 3'-3' diaminobenzidine staining as well as cysTMT labeling and mass spectrometry to profile the redox proteome in Pseudomonas syringae treated tomato leaves.

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