
BCN-PEG3-Biotin (exo)
| Catalog Number | R16-0052 |
| Category | BCN Reagents |
| Molecular Formula | C29H46N4O7S |
| Molecular Weight | 594.31 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
BCN-PEG3-Biotin (exo) is a bioconjugation reagent that features a bicyclo[6.1.0]nonyne (BCN) moiety, which is known for its participation in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions. The incorporation of a triethylene glycol (PEG3) spacer enhances solubility and flexibility, facilitating efficient biotinylation of biomolecules or surfaces without interfering with biological activity. Biotin, a well-established affinity tag, allows for subsequent interaction with streptavidin or avidin, enabling diverse applications in molecular labeling, affinity purification, and detection assays within the realms of click chemistry and bioorthogonal conjugation strategies.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >90% |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | White waxy |
Product Specification
| Storage | -20 °C |
Application
BCN-PEG3-Biotin (exo) is a biotinylated BCN (bicyclononyne) click chemistry reagent designed for strain-promoted cycloaddition with tetrazines, enabling fast, catalyst-free labeling in complex biological and materials settings. The structure combines a BCN cyclooctyne handle, a short PEG3 spacer for improved solubility and reduced steric effects, and an exo-oriented biotin motif for downstream avidin/streptavidin recognition. This reagent is commonly used to introduce biotin tags onto biomolecules, surfaces, and assemblies that require orthogonal click-compatible workflows for imaging, affinity capture, and modular probe construction.
1. Biotin Affinity Tagging
BCN-PEG3-Biotin (exo) is used to install biotin functionality on targets that are compatible with tetrazine-based click labeling, including proteins, peptides, and other biomolecular conjugates prepared for affinity workflows. The PEG3 spacer helps maintain accessible biotin for subsequent binding to streptavidin or avidin reagents, which is advantageous when biotinylated constructs must be captured, enriched, or immobilized without extensive optimization. Researchers often select this reagent when they need a robust handle for pull-down experiments, immobilization on streptavidin-coated surfaces, or modular assembly of multi-component complexes.
2. Molecular Imaging Probes
BCN-PEG3-Biotin (exo) supports the generation of imaging reagents by enabling tetrazine-mediated click attachment of biotin-bearing moieties that can then be linked to imaging platforms using avidin/streptavidin chemistry. This approach is frequently adopted in chemical biology and molecular imaging workflows where biotin serves as a universal connector between a click-labeled targeting component and an imaging scaffold, such as fluorescent or radiolabel-bearing streptavidin conjugates. The exo biotin orientation and short PEG linker are particularly useful for producing probes with consistent binding behavior in labeling and wash steps typical of imaging assay pipelines.
3. Surface Functionalization And Assays
BCN-PEG3-Biotin (exo) is applied to functionalize assay surfaces and biomaterial interfaces where biotin provides a standardized method for immobilizing capture reagents or organizing recognition elements. In practice, the reagent is used to create biotin-presenting layers on polymers, nanoparticles, or membrane-associated constructs that can later recruit streptavidin/avidin partners for assay development. This strategy is widely used in research settings to build reproducible binding architectures for biosensing, binding studies, and platform prototyping that benefit from modular assembly and straightforward surface regeneration concepts.
4. Proteomics And Enrichment Workflows
BCN-PEG3-Biotin (exo) is commonly incorporated into proteomics-oriented enrichment and sample preparation workflows that rely on biotin affinity to isolate labeled biomolecules from complex mixtures. By using BCN-mediated click labeling to introduce biotin tags under conditions compatible with downstream streptavidin capture, laboratories can streamline workflows for studying labeled subsets of proteins, interaction partners, or post-labeling modifications. The PEG3 spacer and biotin handle make the reagent useful when efficient recovery and consistent capture are required across multiple samples and experimental batches.
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