
BDP TR DBCO
| Catalog Number | F01-0253 |
| Category | BODIPY |
| Molecular Formula | C42H35N4BF2O3S |
| Molecular Weight | 724.63 |
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Product Introduction
BDP TR is a bright and photostable red-fluorescent dye. Because of its hydrophobic properties, BDP TR can readily permeate cell membranes and is an excellent fluorophore for staining various lipophilic compounds. This dye is an analog of BODIPY™ TR and similar to ROX by its spectral characteristics.,BDP TR has a long excitation lifetime; besides conventional fluorescence microscopy, it can be used in various fluorescence anisotropy assays.,Being an alternative to alkynes, dibenzocyclooctyne (DBCO) readily reacts with azides in copper-free Click Chemistry reactions, which result in BDP TR-biomolecule conjugates.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | NMR 1H, HPLC-MS (95%) |
| Solubility | Good in DMF, DMSO, DCM |
| Appearance | Copper-violet foam |
Product Specification
| CF260 | 0.15 |
| CF280 | 0.19 |
| Fluorescence Quantum Yield | 0.9 |
| Excitation | 589 |
| Emission | 616 |
| Storage | Storage: 24 months after receival at -20 °C in the Dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. |
Application
BDP TR DBCO is a DBCO-functionalized BODIPY-based fluorescent building block designed for copper-free click chemistry labeling. Its cyclooctyne (DBCO) group enables fast strain-promoted azide-alkyne cycloaddition with azide-bearing biomolecules, while the BDP TR fluorophore supports fluorescence readouts in labeling workflows used for microscopy and fluorescence-based assays. Researchers rely on this reagent to attach bright BODIPY dyes to proteins, peptides, and other azide-tagged targets without introducing copper, which is often beneficial for sensitive biomaterials and live-cell-adjacent labeling protocols.
1. Biomolecule Labeling
BDP TR DBCO supports fluorescent labeling of azide-modified proteins, peptides, and affinity reagents for downstream imaging and quantification. In chemical biology and molecular imaging workflows, investigators use the DBCO handle to generate defined fluorescent conjugates for tracking binding interactions, monitoring biomolecule localization, and comparing labeling efficiency across experimental conditions. The BODIPY fluorophore is commonly selected when robust fluorescence labeling is needed for visualization and assay development, including studies where minimal perturbation of the biomolecule is important.
2. Fluorescence Microscopy
BDP TR DBCO is used to construct fluorescent staining reagents for cellular and subcellular imaging experiments where azide-functional probes or targeting ligands are available. By clicking the DBCO dye onto azide-bearing targeting constructs, researchers can visualize labeled structures with fluorescence microscopy while maintaining modular control over the final conjugate composition. This approach is frequently applied in microscopy-based studies that require flexible probe assembly, such as generating matched dye conjugates for co-localization experiments or validating labeling patterns using standardized fluorophores.
3. Flow Cytometry Labeling
BDP TR DBCO enables fluorescent tagging of azide-containing biomolecules for flow cytometry workflows that require consistent dye chemistry and reproducible conjugate construction. In cell-surface labeling and biomolecule binding assays, the DBCO click handle allows researchers to prepare fluorescent conjugates that can be used to quantify binding or uptake signals by flow cytometry readouts. The BODIPY-based fluorescence provides a practical route to generate cytometry-compatible staining reagents when click-assembled labeling is preferred over pre-conjugated dyes.
4. Fluorescent Probe Construction
BDP TR DBCO is frequently incorporated into fluorescent probe development pipelines where modular assembly of dye-ligand conjugates is required. By reacting with azide-functional recognition elements, the reagent helps researchers generate custom fluorescent probes for fluorescence imaging and assay development, including probe formats used to validate binding behavior and optimize labeling strategies. This click-based construction is particularly valuable in research settings that iterate rapidly on probe design, since the DBCO dye can be swapped into new azide-bearing scaffolds while keeping the fluorophore component consistent.
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