
TCO-PEG2-DBCO
| Catalog Number | R01-0341 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C35H43N3O6 |
| Molecular Weight | 601.7 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
TCO-PEG2-DBCO is a heterobifunctional crosslinker that integrates a trans-cyclooctene (TCO) moiety and a dibenzylcyclooctyne (DBCO) group, interconnected by a polyethylene glycol (PEG) spacer. This reagent is utilized in bioorthogonal chemistry, where its TCO component can undergo inverse electron-demand Diels–Alder reactions, while the DBCO moiety is compatible with strain-promoted azide-alkyne cycloaddition (SPAAC). The PEG linker enhances solubility and flexibility, making TCO-PEG2-DBCO suitable for applications in biomolecule conjugation and surface modification.
Product Specification
Application
Product Specification
| Storage | -20 °C |
Application
TCO-PEG2-DBCO is a bifunctional click chemistry reagent designed for strain-promoted inverse electron-demand Diels–Alder cycloaddition (SPAAC) using a trans-cyclooctene (TCO) handle paired with a DBCO (dibenzocyclooctyne) cyclooctyne. The PEG2 linker provides aqueous compatibility and spatial separation between the two reactive termini, enabling efficient dual-labeling workflows and modular assembly of complex conjugates. Because TCO and DBCO react rapidly and selectively under bioorthogonal conditions, this reagent is widely used in chemical biology, molecular imaging, and biomaterials research to build multivalent constructs, surface-functional materials, and probe libraries.
1. Dual-Functional Probe Assembly
TCO-PEG2-DBCO is commonly used to generate dual-reactive probe platforms where two different capture chemistries are required in a single construct. Researchers employ this reagent to pre-organize labeling handles for subsequent attachment to two distinct biomolecular targets, such as pairing a TCO-reactive site with a DBCO-reactive site on different carriers or surfaces. The PEG2 spacer supports consistent conjugate formation in aqueous buffers, which is particularly valuable for building multivalent imaging probes, affinity reagents, and screening libraries that benefit from controlled valency and reduced steric interference.
2. Multivalent Biomolecule Conjugation
TCO-PEG2-DBCO is frequently selected for multivalent bioconjugation strategies that aim to increase labeling density or enable stepwise assembly of larger molecular architectures. In chemical biology workflows, the reagent can be incorporated into labeling schemes for antibodies, proteins, peptides, and nucleic-acid-binding components where orthogonal or sequential attachment is needed to produce well-defined conjugates. The presence of both TCO and DBCO functionalities supports flexible downstream design, including constructing conjugates with two different attachment points, improving robustness of conjugate generation across diverse labeling formats used in assay development and molecular tool production.
3. Surface and Hydrogel Functionalization
TCO-PEG2-DBCO is used to functionalize material surfaces and soft biomaterials, including polymer coatings, nanoparticles, and hydrogel networks, where SPAAC handles provide rapid, catalyst-free coupling. Materials scientists and biomaterials teams often incorporate the reagent into surface modification protocols to introduce two reactive termini that can be captured by complementary partners, enabling patterned functionalization and multicomponent assembly. The PEG2 linker helps maintain reactivity in hydrated environments, supporting uniform surface chemistry and facilitating the creation of materials used for imaging reagent immobilization, affinity capture surfaces, and modular scaffold construction.
4. Molecular Imaging Reagent Building
TCO-PEG2-DBCO is well suited for building imaging and detection reagents that require controlled conjugate architecture and reliable bioorthogonal attachment to targeting or reporter components. In molecular imaging and diagnostic reagent development, the reagent is used as a versatile linker to connect reporter moieties, targeting ligands, and scaffold elements through SPAAC-compatible chemistry while maintaining aqueous solubility. The dual-reactive design supports assembly of multicomponent imaging constructs, including probe formats that benefit from adjustable spacing and multivalent presentation of binding or signal-generating elements.
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