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AAT Bioquest

ATTO 700 PEG4 DBCO

Product key features

  • Ex/Em: 699/715 nm
  • Extinction coefficient: 120,000 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 700 PEG4 DBCO is manufactured by AAT Bioquest for research and development use. ATTO 700 is a near-infrared fluorescent dye characterized by its strong absorption, high photo and thermal stability, and good aqueous solubility. It is optimally excited within the 670-715 nm wavelength range. As a zwitterionic compound, ATTO 700 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 700 ideal for precise applications including single-molecule detection and super-resolution microscopy techniques like PALM, dSTORM, and STED. Furthermore, ATTO 700 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.

The DBCO derivative of ATTO 700 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 700 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 680 PEG4 DBCO6796961250000.300.300.17

References

View all 6 references: Citation Explorer
Whole blood multiplex measurements using electrochemical aptamer-based biosensors.
Authors: d'Astous, Élodie V and Dauphin-Ducharme, Philippe
Journal: Chemical communications (Cambridge, England) (2024): 6419-6422
Multiphoton absorption enhancement by graphene-gold nanostructure.
Authors: Izadshenas Jahromi, Saeid and Słowik, Karolina
Journal: Optics letters (2024): 3914-3917
Near infrared-emitting multimodal nanosystem for in vitro magnetic hyperthermia of hepatocellular carcinoma and dual imaging of in vivo liver fibrosis.
Authors: Nazeer, Shaiju S and Saraswathy, Ariya and Nimi, Nirmala and Santhakumar, Hema and Radhakrishnapillai Suma, Parvathy and Shenoy, Sachin J and Jayasree, Ramapurath S
Journal: Scientific reports (2023): 12947
Spatial distribution of single guest molecules along thickness of thin films of poly(2-hydroxyethyl acrylate).
Authors: Ito, Syoji and Hiratsuka, Kengo and Takei, Satoshi and Nishi, Hiroyasu and Kitagawa, Daichi and Kobatake, Seiya and Miyasaka, Hiroshi
Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society (2022): 175-184
Application of single molecule fluorescence microscopy to characterize the penetration of a large amphiphilic molecule in the stratum corneum of human skin.
Authors: Volz, Pierre and Boreham, Alexander and Wolf, Alexander and Kim, Tai-Yang and Balke, Jens and Frombach, Janna and Hadam, Sabrina and Afraz, Zahra and Rancan, Fiorenza and Blume-Peytavi, Ulrike and Vogt, Annika and Alexiev, Ulrike
Journal: International journal of molecular sciences (2015): 6960-77
Page updated on May 19, 2025

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Catalog Number70305
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Physical properties

Molecular weight

1071.30

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.26

Correction Factor (280 nm)

0.41

Extinction coefficient (cm -1 M -1)

120000

Excitation (nm)

699

Emission (nm)

715

Quantum yield

0.25

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.