
AF 488 DBCO
| Catalog Number | R01-0448 |
| Category | Alexa Fluor |
| Molecular Formula | C48H49N5O11S2 |
| Molecular Weight | 936.08 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
AF 488 is sulfonated rhodamine, a bright, photostable, and hydrophilic fluorophore that emits in the green channel. The absorption maximum is 495 nm. The emission maximum is 519 nm. AF 488 DBCO allows fluorescent labeling of azide-containing biomolecules inside living cells, whole organisms, and inanimate samples.
Chemical Information
Product Specification
Application
Chemical Information
| Appearance | Orange Solid |
Product Specification
| Excitation | 495 |
| Emission | 519 |
Application
AF 488 DBCO is a DBCO-functionalized fluorescent labeling reagent built for copper-free click chemistry workflows. It pairs the bright AF 488 fluorophore with a strained cyclooctyne handle, enabling efficient conjugation to azide-bearing biomolecules, polymers, and surfaces under mild conditions. This combination is widely used to generate fluorescent bioconjugates for imaging, tracking, and analytical assays where robust covalent attachment is required.
1. Biomolecule Labeling
AF 488 DBCO is used to fluorescently label azide-functionalized proteins, peptides, and affinity reagents for downstream fluorescence imaging and quantitative analysis. Researchers commonly incorporate the DBCO handle into biomolecules (or introduce azide groups into target systems) and then use AF 488 DBCO to install the AF 488 fluorophore via strain-promoted azide-alkyne cycloaddition. The resulting covalent conjugates are favored in workflows that require stable labeling for microscopy, recombinant protein tracking, and fluorescence-based characterization of bioconjugates.
2. Fluorescence Microscopy
AF 488 DBCO supports covalent fluorescent staining of azide-modified cell-surface components and biomaterial-associated targets for microscopy studies. In practice, labs use azide-functionalized targeting ligands, extracellular matrix components, or surface coatings and then apply AF 488 DBCO to visualize localization patterns with AF 488 emission in standard fluorescence imaging setups. This approach is particularly useful when researchers want a defined fluorescent tag installed after azide presentation, improving labeling consistency for fixed-sample imaging and multi-step staining workflows.
3. Surface Functionalization
AF 488 DBCO is applied to fluorescently functionalize azide-bearing surfaces, including polymer films, hydrogels, and nanoparticle coatings, for materials imaging and surface chemistry verification. By reacting the DBCO group with surface-presented azides, researchers obtain stable, covalently attached AF 488 fluorescence that can be monitored by fluorescence microscopy or plate-based fluorescence readouts. Such labeling is commonly used to confirm surface modification density, track biomaterial interactions, and generate fluorescent materials for cell-material interface studies.
4. Flow Cytometry Labeling
AF 488 DBCO is used to prepare fluorescently labeled azide-containing bioreagents for flow cytometry workflows where covalent attachment improves signal stability during washing and analysis. Laboratories often generate azide-tagged antibodies, ligands, or capture reagents and then label them with AF 488 DBCO to produce robust fluorescent conjugates for cell-surface binding experiments and fluorescence-based characterization of binding reagents. The DBCO click handle enables straightforward post-functionalization of azide-bearing targets, supporting reproducible labeling across experimental batches.
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