
BCN-PEG4-NHS (exo)
| Catalog Number | R16-0040 |
| Category | BCN Reagents |
| Molecular Formula | C26H38N2O10 |
| Molecular Weight | 538.59 |
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Product Introduction
BCN-PEG4-NHS (exo) is a bioconjugation reagent featuring a bicyclononyne (BCN) moiety, a polyethylene glycol (PEG) spacer, and an N-hydroxysuccinimide (NHS) ester. The BCN moiety participates in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions, facilitating copper-free click chemistry applications. The NHS ester functionality enables covalent attachment to primary amines, making this reagent suitable for biomolecule conjugation and surface modification in a variety of experimental contexts.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | >90% |
| Solubility | DCM, THF, Acetonitrile, DMF and DMSO |
| Appearance | Colorless oil |
Product Specification
| Storage | -20 °C |
Application
BCN-PEG4-NHS (exo) is a BCN-functionalized, PEGylated NHS ester designed for strain-promoted click chemistry conjugation. As an NHS-activated ester, it readily reacts with primary amines on proteins, peptides, and biomolecular surfaces to introduce a BCN handle, enabling subsequent bioorthogonal cycloaddition with tetrazine reagents. The PEG4 spacer supports improved solubility and spacing between the targeting/bioconjugation moiety and the click-active BCN group, which is commonly leveraged in molecular imaging, diagnostic reagent development, and biomaterials functionalization workflows.
1. Protein Surface Labeling
BCN-PEG4-NHS (exo) is widely used to install BCN click handles onto proteins and antibody fragments through NHS ester coupling to lysine residues and N-terminal amines. This approach is favored in research and industrial bioconjugation pipelines because it provides a controllable means to create tetrazine-reactive bioconjugates without requiring additional synthetic steps on the target biomolecule. The PEG4 linker helps reduce steric congestion and can improve handle accessibility for downstream tetrazine ligation, supporting consistent labeling of conjugate libraries used in assay development and molecular probe generation.
2. Antibody-Tetrazine Conjugates
BCN-PEG4-NHS (exo) supports the preparation of antibody-derived imaging and detection reagents by enabling modular assembly of BCN-bearing binding reagents that can be coupled to tetrazine-functional partners. In common workflows, researchers first functionalize the antibody or affinity reagent with the BCN handle using the NHS ester chemistry, then perform strain-promoted click conjugation to attach fluorophores, affinity tags, or other reporter constructs. The exo-oriented BCN functionality and PEG spacer are particularly relevant when maintaining binding-site accessibility and minimizing nonspecific interactions during probe construction.
3. Diagnostic Reagent Building Blocks
BCN-PEG4-NHS (exo) is used as a standardized click handle for constructing diagnostic and analytical reagents that require robust, bioorthogonal conjugation strategies. Teams developing labeled affinity reagents, multiplexing components, or surface-tethered detection platforms often rely on BCN installation via NHS coupling to introduce a reactive handle onto carrier proteins, peptide scaffolds, or other amine-containing components. Subsequent tetrazine-based ligation enables rapid assembly of reporter conjugates under conditions compatible with sensitive biomolecular formats, facilitating reproducible reagent manufacturing for research assays and analytical workflows.
4. Biomaterials Functionalization
BCN-PEG4-NHS (exo) is applied to functionalize amine-bearing biomaterial surfaces and polymeric scaffolds with BCN groups for later tetrazine-mediated attachment of imaging, sensing, or binding elements. In materials science and chemical biology, PEGylated NHS esters are commonly used to tune surface chemistry by spacing reactive BCN groups away from the underlying matrix, which can improve accessibility and reduce steric hindrance during subsequent click conjugation. This makes BCN-PEG4-NHS (exo) a practical reagent for creating modular, surface-derivatized materials used in probe immobilization and platform development.
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