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AAT Bioquest

XFD660 PEG4 DBCO

Product key features

  • Ex/Em: 663/691 nm
  • Extinction coefficient: 132,000 cm-1M-1
  • Superior Fluorescence Performance: High quantum yield, exceptional photostability, and pH-independent fluorescence across pH 4–11.
  • Reactive Group: DBCO
  • Copper-Free Bioorthogonal Labeling: Enables rapid and efficient azide conjugation via copper-free SPAAC
  • High Water-Solubility: Prevents aggregation and enhances signal clarity for advanced imaging and live-cell applications

Product description

XFD660, manufactured by AAT Bioquest, is a far-red fluorescent dye structurally equivalent to Alexa Fluor™ 660 (ThermoFisher). The dye demonstrates high fluorescence quantum yield, photostability, and aqueous solubility, with pH-independent fluorescence across a broad range (pH 4–11), providing consistent performance across diverse experimental conditions.

XFD660 is optimized for red laser excitation and is compatible with flow cytometers equipped with spectral detection systems. It provides robust and uniform labeling with high signal intensity and reproducibility, making it ideal for fluorescence imaging, flow cytometry, and other analytical techniques. XFD660 demonstrates versatility in labeling a wide range of targets, including cell surface, intracellular, and intranuclear antigens. Its spectral properties position it between XFD647 and XFD700, making it a valuable intermediate fluorophore for constructing complex multicolor panels and enabling precise experimental designs in advanced research workflows.

The DBCO derivative of XFD660 is a highly reactive cycloalkyne optimized for copper-free click chemistry (SPAAC, strain-promoted azide-alkyne cycloaddition). This derivative exhibits a significantly higher reaction rate with azides compared to other cyclooctynes and copper-catalyzed click reactions (CuAAC). Uniquely, DBCO does not react with tetrazines, allowing for its use in bioorthogonal reactions alongside trans-cyclooctenes and tetrazines. For applications where the presence of copper is problematic, XFD660 DBCO serves as an effective alternative to copper-dependent fluorescent alkynes.

Spectrum

Page updated on April 15, 2025

Ordering information

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Catalog Number70096
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Additional ordering information

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Physical properties

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.00

Correction Factor (280 nm)

0.10

Extinction coefficient (cm -1 M -1)

132000

Excitation (nm)

663

Emission (nm)

691

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501
Schematic illustrating the strain‐promoted azide–alkyne cycloaddition (SPAAC) between a dibenzocyclooctyne (DBCO)–dye conjugate and an azide‐modified biomolecule. The DBCO’s ring strain drives the copper‐free reaction with the azide to form a stable 1,2,3-triazole linkage, avoiding potential toxicity of copper catalysts. This bioorthogonal labeling strategy proceeds efficiently under mild conditions, making it especially valuable for live‐cell imaging, in vivo studies, and other sensitive bioconjugation applications.
Schematic illustrating the strain‐promoted azide–alkyne cycloaddition (SPAAC) between a dibenzocyclooctyne (DBCO)–dye conjugate and an azide‐modified biomolecule. The DBCO’s ring strain drives the copper‐free reaction with the azide to form a stable 1,2,3-triazole linkage, avoiding potential toxicity of copper catalysts. This bioorthogonal labeling strategy proceeds efficiently under mild conditions, making it especially valuable for live‐cell imaging, in vivo studies, and other sensitive bioconjugation applications.
Schematic illustrating the strain‐promoted azide–alkyne cycloaddition (SPAAC) between a dibenzocyclooctyne (DBCO)–dye conjugate and an azide‐modified biomolecule. The DBCO’s ring strain drives the copper‐free reaction with the azide to form a stable 1,2,3-triazole linkage, avoiding potential toxicity of copper catalysts. This bioorthogonal labeling strategy proceeds efficiently under mild conditions, making it especially valuable for live‐cell imaging, in vivo studies, and other sensitive bioconjugation applications.