
DBCO-PEG4-APN
| Catalog Number | R01-0316 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C39H40N4O7 |
| Molecular Weight | 676.76 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
DBCO-PEG4-APN is a reagent that features a dibenzocyclooctyne (DBCO) moiety, known for its ability to participate in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions. It bears a polyethylene glycol (PEG) spacer with four ethylene glycol units, which enhances solubility and flexibility, facilitating its use in bioconjugation and surface modification applications. This compound is incorporated into experimental protocols for labeling and crosslinking biomolecules, supporting the development of bioorthogonal chemistry strategies without the need for copper catalysis.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >90% |
| Solubility | DCM, acetonitrile, DMF and DMSO |
| Appearance | Oil |
Product Specification
| Storage | -20 °C |
Application
DBCO-PEG4-APN is a strain-promoted azide–alkyne cycloaddition (SPAAC) click chemistry reagent built on a DBCO (dibenzocyclooctyne) cyclooctyne scaffold linked to a PEG4 spacer and an APN functional handle. This design supports efficient, catalyst-free conjugation to azide-bearing biomolecules, targeting ligands, and material surfaces, while the PEG spacer helps tune solubility and reduce nonspecific interactions. DBCO-PEG4-APN is commonly used in chemical biology and biomaterials workflows where modular attachment of the DBCO-bearing component to azide-functional partners is required for probe, surface, and delivery-platform construction.
1. Receptor-Targeted Probe Building
DBCO-PEG4-APN is used to assemble azide-functional imaging or binding probes by providing a SPAAC-compatible DBCO handle that reacts cleanly with azide-bearing components under mild conditions. The PEG4 spacer supports conjugate solubility and helps maintain accessibility of the APN-associated functionality in probe constructs. Researchers in molecular imaging and chemical biology frequently incorporate this reagent into multicomponent probe designs where the DBCO-bearing module is introduced as a late-stage coupling step, enabling rapid swapping of azide-tagged reporters, affinity elements, or scaffold formats.
2. Surface Functionalization For Platforms
DBCO-PEG4-APN is well suited for functionalizing azide-present surfaces and coatings used in biomaterials and lab-on-chip research. By coupling to azide groups on polymer films, hydrogel networks, or nanoparticle surfaces, the reagent enables installation of an APN-bearing interface with improved hydrophilicity from the PEG4 linker. This approach is commonly adopted when building reusable assay platforms, immobilized binding surfaces, or spatially patterned materials where modular click attachment provides consistent grafting and straightforward reconfiguration of surface chemistry.
3. Multivalent Ligand Conjugation
DBCO-PEG4-APN is frequently employed to generate multivalent conjugates by clicking the DBCO moiety onto azide-functional ligands, peptide constructs, or scaffold backbones. The PEG4 linker helps manage steric presentation, which is important when constructing higher-order architectures such as ligand clusters, affinity arrays, or polymer–ligand hybrids. Chemical biology groups use this reagent as a modular building block to control conjugation geometry and to streamline workflows that require sequential assembly of complex macromolecular constructs from azide-functional intermediates.
4. Diagnostic Reagent And Assay Development
DBCO-PEG4-APN supports the construction of assay reagents where azide-tagged components (such as capture elements, reporter conjugates, or assay-specific reagents) must be coupled to a DBCO-bearing module without harsh conditions. The PEG4 spacer improves dispersion and conjugate handling in aqueous assay buffers, while the APN functional handle provides a chemically defined point of integration into the final assay format. Diagnostic reagent development teams and research laboratories often rely on SPAAC-based conjugation strategies to produce consistent reagent batches for screening assay chemistries, signal readouts, and modular assay component libraries.
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