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Product Introduction
3'-DBCO CPG is a solid-phase support material that features dibenzocyclooctyne (DBCO) functionality, enabling bioorthogonal conjugation reactions. The DBCO moiety participates in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, facilitating the attachment of azide-containing biomolecules without the need for copper catalysis. This reagent is commonly incorporated into oligonucleotide synthesis workflows, where it supports the installation of clickable handles for subsequent conjugation and labeling applications.
Chemical Information
Application
Chemical Information
| Appearance | Off-white Solid |
Application
3'-DBCO CPG is a DBCO-functionalized controlled-pore glass (CPG) solid support designed for strain-promoted azide–alkyne cycloaddition (SPAAC)-based click conjugation workflows. The reagent combines a high-surface-area porous matrix with a stable cyclooctyne (DBCO) handle, enabling efficient immobilization and subsequent coupling of azide-bearing biomolecules, linkers, or imaging tags. 3'-DBCO CPG is commonly used in chemical biology and materials-oriented reagent development where solid-phase, modular assembly of clickable constructs is advantageous.
1. Solid-Phase Probe Immobilization
3'-DBCO CPG is widely used to immobilize azide-functional probes onto a robust solid support for downstream assay development and imaging workflows. Researchers in chemical biology and molecular diagnostics often prefer a solid-phase format to simplify separation steps, concentrate reagents at the surface, and enable rapid exchange of azide-bearing components across experiments. The porous CPG architecture supports high loading of clickable sites, which is particularly useful when building libraries of immobilized affinity reagents, affinity handles, or surface-tethered chemical probes for screening and characterization.
2. Surface Functionalization For Imaging
3'-DBCO CPG supports modular construction of imaging-ready materials by enabling SPAAC coupling of azide-containing fluorophores, biotin-like tags, or other imaging moieties to a solid matrix. In molecular imaging and diagnostic reagent development, the ability to attach diverse azide partners under catalyst-free conditions helps maintain compatibility with sensitive labeling chemistries and streamlined production of probe batches. The DBCO-bearing CPG format is also used to prepare clickable surfaces and bead-based or particle-based platforms where consistent tethering chemistry and straightforward post-coupling handling are important.
3. Clickable Linker And Reagent Libraries
3'-DBCO CPG is used as a platform for generating reagent libraries in which different azide-bearing building blocks are coupled to a common solid support to create matched sets of conjugates. This approach is common in biomaterials science and chemical biology laboratories that need rapid iteration of linker length, spacer chemistry, or functional group presentation while keeping the immobilization scaffold constant. By using SPAAC-compatible azide partners, teams can build structured collections of immobilized conjugates for binding studies, material characterization, and method development that require reproducible click chemistry attachment to a solid phase.
4. Biomolecule Conjugation On Solid Supports
3'-DBCO CPG is applicable to the preparation of immobilized biomolecule conjugates where azide-functional proteins, peptides, nucleic-acid components, or biomolecule-derived tags are attached to a solid matrix for workflow integration. Solid-phase conjugation is frequently selected for workflows that benefit from easy wash steps, reduced sample loss, and controlled presentation of biomolecular ligands at a surface. The DBCO handle on 3'-DBCO CPG enables SPAAC coupling to azide-bearing biomolecules, supporting the creation of stable, heterogeneous conjugate formats used in research-grade assay development and platform prototyping.
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