
DBCO-PEG11-DBCO
| Catalog Number | R01-0308 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C62H78N4O15 |
| Molecular Weight | 1119.30 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
DBCO-PEG11-DBCO is a bifunctional compound featuring two dibenzocyclooctyne (DBCO) groups connected by an 11-unit polyethylene glycol (PEG) linker. The presence of DBCO groups allows the compound to participate in strain-promoted azide-alkyne cycloaddition reactions, facilitating bioorthogonal conjugation with azide-functionalized molecules. This reagent is often used in applications requiring the linking of biomolecules, surface modification, and the creation of complex macromolecular assemblies through its flexible PEG spacer and reactive DBCO moieties.
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-PEG11-DBCO is a bifunctional, PEG-based dibenzocyclooctyne (DBCO) click chemistry reagent designed for strain-promoted azide–alkyne cycloaddition (SPAAC). The linear PEG spacer and two terminal DBCO groups enable multivalent conjugation and controlled spacing between biomolecules, surfaces, or nanoparticles without requiring copper catalysis. This structure is widely used in chemical biology and biomaterials workflows where efficient, bioorthogonal labeling and modular assembly are needed for probes, coatings, and functionalized materials.
1. Multivalent Biomolecule Labeling
DBCO-PEG11-DBCO is commonly used to build multivalent conjugates for protein labeling, antibody or ligand functionalization, and nucleic-acid or peptide tagging workflows that rely on azide-bearing partners. The two DBCO termini provide a convenient way to link two azide-functional targets or to create higher local density of reactive handles, improving the practical robustness of downstream conjugation steps in research settings. Its PEG11 spacer helps reduce steric congestion compared with shorter linkers, supporting more reliable coupling in complex mixtures such as lysates, purified protein panels, or assay reagent formulations.
2. Surface and Bead Functionalization
DBCO-PEG11-DBCO is well suited for functionalizing solid supports such as agarose beads, magnetic beads, polymer surfaces, and microarray platforms that present azide groups or are designed to incorporate azide handles. By using this reagent as a bifunctional linker, researchers can immobilize biomolecules with defined spacing, enhancing accessibility of binding moieties and improving reproducibility across parallel experiments. The PEG spacer also supports more uniform surface coverage and can reduce nonspecific interactions relative to more hydrophobic or rigid linkers, which is valuable when developing screening libraries, capture reagents, and modular affinity platforms.
3. Nanoparticle and Hydrogel Crosslinking
DBCO-PEG11-DBCO is frequently applied in the preparation of functional nanoparticles and PEG-based hydrogels where azide-functional components are available for SPAAC-driven assembly. The dual DBCO groups allow network formation or particle-to-particle tethering while maintaining a copper-free click environment compatible with sensitive materials and labeling strategies. In biomaterials development, the PEG11 length provides a tunable balance between crosslink density and chain mobility, supporting formation of stable, processable constructs used as carriers, imaging scaffolds, or customizable matrices for chemical biology studies.
4. Imaging Probe and Reporter Assembly
DBCO-PEG11-DBCO is used to assemble azide-tagged imaging reporters and fluorescent or luminescent probe constructs through copper-free SPAAC conjugation. The bifunctional design enables linking of two components, such as a targeting module and a reporter payload, or installing multiple reporter units to increase signal density in research assays. PEG spacing can help preserve probe performance by reducing steric hindrance around bulky fluorophores or detection handles, which is particularly relevant for developing consistent labeling reagents for microscopy, flow-based readouts, and molecular imaging toolkits.
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