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AAT Bioquest

ATTO 680 PEG4 DBCO

Product key features

  • Ex/Em: 679/696 nm
  • Extinction coefficient: 125,000 cm-1M-1
  • Reactive group: DBCO
  • Copper-Free Bioorthogonal Labeling: Enables efficient azide conjugation via SPAAC without copper, ideal for sensitive systems
  • High Quantum Yield & Stability: Provides bright fluorescence with high photostability and thermal resilience
  • Zwitterionic: Minimizes non-specific binding to biological surfaces, reducing background noise in live-cell imaging and super-resolution microscopy
  • Hydrophilic PEG4 Spacer: Enhances solubility and minimizes steric hindrance for enhanced biocompatibility

Product description

ATTO 680 PEG4 DBCO is manufactured by AAT Bioquest for research and development use. ATTO 680 is a far-red fluorescent dye characterized by its strong absorption, high photo and thermal stability, and good aqueous solubility. It is optimally excited within the 645-695 nm wavelength range, which aligns with the 670 nm line of diode laser and the 676 nm line of Krypton-Ion laser. As a zwitterionic compound, ATTO 680 remains electrically neutral when conjugated to biomolecules or other substrates. Its strong electron-accepting properties result in efficient fluorescence quenching by electron donors such as guanine and tryptophan. These properties make ATTO 680 ideal for precise applications including single-molecule detection and super-resolution microscopy techniques like PALM, dSTORM, and STED. Furthermore, ATTO 680 is compatible with flow cytometry (FACS), fluorescence in situ hybridization (FISH), and a variety of other biological assays, making it a versatile tool in advanced fluorescence-based research.<?p>

The DBCO derivative of ATTO 680 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, ATTO 680 PEG4 DBCO serves as an effective alternative to copper-dependent fluorescent alkynes.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
ATTO 514 PEG4 DBCO510531115,0000.850.210.08
ATTO 532 PEG4 DBCO5315521150000.900.220.11
ATTO 594 PEG4 DBCO6026211200000.850.260.51
ATTO 647 PEG4 DBCO6466661200000.200.080.04
ATTO 647N PEG4 DBCO6456631500000.6510.060.05
ATTO 655 PEG4 DBCO6616791250000.310.240.08
ATTO 700 PEG4 DBCO6997151200000.250.260.41

References

View all 3 references: Citation Explorer
Avidin/Biotin Bioinspired Platform for Dual In Vivo 18F-PET/NIRF Molecular Imaging.
Authors: Damont, Annelaure and Boisgard, Raphael and Dollé, Frédéric and Hollocou, Morgane and Kuhnast, Bertrand
Journal: Bioconjugate chemistry (2017): 2524-2529
Oxazine dye-conjugated dna oligonucleotides: Förster resonance energy transfer in view of molecular dye-DNA interactions.
Authors: Kupstat, Annette and Ritschel, Thomas and Kumke, Michael U
Journal: Bioconjugate chemistry (2011): 2546-57
Inter- and intramolecular fluorescence quenching of organic dyes by tryptophan.
Authors: Marmé, Nicole and Knemeyer, Jens-Peter and Sauer, Markus and Wolfrum, Jürgen
Journal: Bioconjugate chemistry (2003): 1133-9
Page updated on May 19, 2025

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Catalog Number70295
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Physical properties

Molecular weight

1031.24

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.30

Correction Factor (280 nm)

0.17

Extinction coefficient (cm -1 M -1)

125000

Excitation (nm)

679

Emission (nm)

696

Quantum yield

0.30

Storage, safety and handling

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

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12352200
Product Image
Product Image
Gallery Image 1
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.