
DBCO-PEG12-Mal
| Catalog Number | R01-0284 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C52H74N4O17 |
| Molecular Weight | 1027.16 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
DBCO-PEG12-Mal is a heterobifunctional crosslinker that features a dibenzocyclooctyne (DBCO) group and a maleimide moiety, connected via a polyethylene glycol (PEG) spacer with twelve ethylene glycol units. The DBCO group participates in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, enabling copper-free click chemistry applications, while the maleimide group is reactive towards thiol groups, facilitating bioconjugation. This reagent is used in the construction of multifunctional biomolecular assemblies, where it supports the conjugation of azide-functionalized biomolecules to thiol-containing substrates or surfaces.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >95% |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Light yellow oil |
Product Specification
| Storage | -20 °C |
Application
DBCO-PEG12-Mal is a difluorobenzocyclooctyne (DBCO) functionalized, PEG12-based linker bearing a terminal maleimide (Mal), enabling strain-promoted azide–alkyne cycloaddition (SPAAC) chemistry while providing a second, orthogonal thiol-reactive handle for conjugation. The PEG spacer supports solubility and reduces steric constraints, which is particularly useful when building multi-component bioconjugates, surface coatings, and imaging probes. This reagent is commonly selected for workflows that require sequential or modular attachment of DBCO-bearing constructs to azide-functional targets followed by maleimide-mediated capture of thiol-containing biomolecules, linkers, or nanoparticles.
1. Protein And Peptide Conjugation
DBCO-PEG12-Mal is widely used to generate site-defined protein and peptide conjugates for chemical biology and biomaterials research, where a DBCO handle enables efficient SPAAC coupling to azide-functional biomolecules or surfaces. The maleimide terminus then serves as a convenient thiol-reactive group for installing the conjugate onto cysteine-bearing proteins, engineered peptides, or thiol-terminated affinity tags. The PEG12 chain helps maintain colloidal stability and accessibility of both reactive termini, supporting downstream applications such as probe assembly, affinity reagent construction, and multivalent labeling strategies.
2. Surface Functionalization For Biomaterials
DBCO-PEG12-Mal supports modular modification of biomaterial surfaces and polymeric scaffolds by combining azide-reactive SPAAC targeting with maleimide-based attachment of thiol-bearing components. Researchers use this reagent to create functional coatings where DBCO-bearing layers are first positioned onto azide-present substrates, followed by maleimide capture of thiolated biomolecules such as peptides, enzymes, or linker constructs. The PEG spacer improves wetting and reduces nonspecific adsorption in many surface workflows, making DBCO-PEG12-Mal a practical choice for building biofunctional interfaces used in materials screening and mechanistic studies.
3. Multicomponent Probe Assembly
DBCO-PEG12-Mal is frequently employed in the assembly of multicomponent molecular imaging and diagnostic research probes, where modular coupling reduces the need for complex one-pot synthesis. The DBCO group allows rapid attachment to azide-functional reporters, carriers, or targeting vectors, while the maleimide group provides a handle for coupling to thiol-functional dyes, nanoparticles, or engineered binding domains. This dual-reactivity format is particularly valuable when teams need to standardize probe architecture across a series of targets, enabling consistent conjugation chemistry and streamlined reagent-to-assay integration.
4. Nanoparticle And Colloidal Labeling
DBCO-PEG12-Mal is used to functionalize nanoparticles and other colloidal platforms by enabling orthogonal conjugation steps that fit common industrial and research labeling pipelines. Azide-bearing nanoparticle formulations can be coupled via SPAAC to introduce the PEG-linked maleimide functionality, after which thiol-containing ligands, capture molecules, or surface modifiers are installed through maleimide–thiol coupling. The PEG12 spacer helps preserve colloidal stability and improves accessibility of the reactive maleimide group, supporting reproducible surface coverage and consistent performance in downstream labeling and assay development workflows.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry