
FAM DBCO, 6-isomer
| Catalog Number | R09-0008 |
| Category | Cycloalkyne Dyes (DBCO) |
| Molecular Formula | C42H32N2O7 |
| Molecular Weight | 676.71 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Fluorescein (FAM) is one of the oldest yet well known fluorescent dyes. This derivative of FAM contains cyclooctyne group (dibenzocyclooctyne, abbreviated as DBCO or ADIBO) for the conjugation with azides via copper-free, strain-promoted azide alkyne cycloaddition (spAAc).FAM DBCO can be used for the labeling of proteins, peptides, nucleic acids, and other molecules containing azide groups. Azides react with DBCO spontaneously upon simple mixing. The reaction does not require any catalysts, and it is very efficient.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | N-[6-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-6-oxohexyl]-3',6'-dihydroxy-1-oxospiro[2-benzofuran-3,9'-xanthene]-5-carboxamide |
| SMILES | C1C2=CC=CC=C2C#CC3=CC=CC=C3N1C(=O)CCCCCNC(=O)C4=CC5=C(C=C4)C(=O)OC56C7=C(C=C(C=C7)O)OC8=C6C=CC(=C8)O |
| InChI | InChI=1S/C42H32N2O7/c45-30-16-19-33-37(23-30)50-38-24-31(46)17-20-34(38)42(33)35-22-28(15-18-32(35)41(49)51-42)40(48)43-21-7-1-2-12-39(47)44-25-29-10-4-3-8-26(29)13-14-27-9-5-6-11-36(27)44/h3-6,8-11,15-20,22-24,45-46H,1-2,7,12,21,25H2,(H,43,48) |
| InChIKey | QAATVTNRYVCIIR-UHFFFAOYSA-N |
| Solubility | good in DMF, DMSO |
| Appearance | orange solid |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 75000 |
| Fluorescence Quantum Yield | 0.9 |
| Excitation | 494 |
| Emission | 520 |
| 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. Desiccate. |
Application
FAM DBCO, 6-isomer is a fluorescein-based labeling reagent combining a DBCO (dibenzocyclooctyne) click handle with a fluorescein (FAM) fluorophore for strain-promoted azide-alkyne cycloaddition (SPAAC). This design supports copper-free click conjugation workflows that are widely used to attach fluorescent tags to biomolecules, polymers, and surfaces while enabling fluorescence readout on standard fluorescence imaging and detection platforms.
1. Biomolecule Fluorescent Labeling
FAM DBCO, 6-isomer is used by chemical biology and glycobiology groups to fluorescently label azide-functional biomolecules such as peptides, proteins, and oligonucleotides via SPAAC. Researchers typically incorporate it into labeling workflows where copper-free conditions are preferred to preserve sensitive biomolecular activity or compatibility with downstream assays. The fluorescein fluorophore enables visualization and quantification of labeled conjugates in microscopy-based studies, gel-based fluorescence readouts, and fluorescence detection assays, supporting rapid tracking of conjugation efficiency and conjugate localization in complex experimental mixtures.
2. Click-Constructed Fluorescent Probes
FAM DBCO, 6-isomer is frequently employed in fluorescent probe development where a DBCO-bearing fluorophore is needed as a modular click component. In probe construction, it is conjugated to azide-bearing targeting ligands, affinity reagents, or scaffold molecules to generate fluorescent imaging reagents with defined attachment points. This approach is common in assay development laboratories that build custom fluorescent reagents for binding studies, reagent screening, and molecular imaging method development, leveraging the straightforward SPAAC coupling to rapidly generate probe libraries with consistent fluorescein labeling.
3. Surface And Material Functionalization
FAM DBCO, 6-isomer is applied in biomaterials and materials science workflows to create fluorescently traceable surfaces and coatings using azide-functional substrates. Researchers use it to introduce fluorescein signal onto polymer films, hydrogel matrices, and other azide-present materials where subsequent characterization by fluorescence microscopy or fluorescence quantification is required. The DBCO handle enables efficient conjugation without added copper, which is particularly useful when immobilizing fluorescent tags onto materials intended for sensitive biological compatibility studies, imaging-based material tracking, or fluorescence-guided process development.
4. Flow Cytometry Labeling Workflows
FAM DBCO, 6-isomer supports fluorescence labeling strategies for flow cytometry when azide-functional ligands or biomolecule conjugates are available for click attachment. In cell analysis workflows, it is used to generate fluorescein-labeled reagents that can be used to monitor binding, uptake, or surface association of click-constructed conjugates. The fluorescein output is compatible with standard blue-excitation flow cytometry configurations, enabling researchers to assess labeling performance and quantify fluorescent signal across experimental conditions in high-throughput studies.
Computed Properties
| XLogP3 | 6.4 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 7 |
| Exact Mass | 676.22095136 g/mol |
| Monoisotopic Mass | 676.22095136 g/mol |
| Topological Polar Surface Area | 125Ų |
| Heavy Atom Count | 51 |
| Formal Charge | 0 |
| Complexity | 1340 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry