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AAT Bioquest

XFD532 PEG4 DBCO

Product key features

  • Ex/Em: 534/553 nm
  • Extinction coefficient: 81,000 cm-1M-1
  • Reactive Group: DBCO
  • Copper-Free Bioorthogonal Labeling: Enables rapid and efficient azide conjugation via copper-free SPAAC
  • Bright and Stable: Offers high fluorescence intensity, photostability, and consistent performance across pH 4—10
  • Hydrophilic PEG4 Spacer: Enhances solubility and minimizes steric hindrance for enhanced biocompatibility

Product description

XFD532, manufactured by AAT Bioquest, is structurally identical to Alexa Fluor™ 532 (ThermoFisher). It is a bright yellow-fluorescent dye with an excitation optimized for use with the 532 nm line of the frequency-doubled Nd:YAG laser. The incorporation of a PEG4 linker enhances the aqueous solubility of XFD532, while its pH-insensitivity across a broad pH range (pH 4–10) ensures reliable and stable signal generation under diverse experimental conditions. XFD532 is particularly suited for multicolor fluorescence microscopy and flow cytometry, as well as advanced applications in super-resolution imaging techniques such as dSTORM.

The DBCO derivative of XFD532 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, XFD532 DBCO serves as an effective alternative to copper-dependent fluorescent alkynes.

Spectrum

References

View all 3 references: Citation Explorer
Bivalent EGFR-Targeting DARPin-MMAE Conjugates.
Authors: Karsten, Lennard and Janson, Nils and Le Joncour, Vadim and Alam, Sarfaraz and Müller, Benjamin and Tanjore Ramanathan, Jayendrakishore and Laakkonen, Pirjo and Sewald, Norbert and Müller, Kristian M
Journal: International journal of molecular sciences (2022)
Metabolism-Based Click-Mediated Platform for Specific Imaging and Quantification of Cell Surface Sialic Acids.
Authors: Liang, Yong and Jiang, Xin and Yuan, Rong and Zhou, Yang and Ji, Caixia and Yang, Limin and Chen, Haifeng and Wang, Qiuquan
Journal: Analytical chemistry (2017): 538-543
Multifunctional porous silicon nanoparticles for cancer theranostics.
Authors: Wang, Chang-Fang and Sarparanta, Mirkka P and Mäkilä, Ermei M and Hyvönen, Maija L K and Laakkonen, Pirjo M and Salonen, Jarno J and Hirvonen, Jouni T and Airaksinen, Anu J and Santos, Hélder A
Journal: Biomaterials (2015): 108-18
Page updated on April 25, 2025

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Catalog Number1719
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Additional ordering information

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Physical properties

Molecular weight

1233.50

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.24

Correction Factor (280 nm)

0.09

Extinction coefficient (cm -1 M -1)

81000

Excitation (nm)

534

Emission (nm)

553

Quantum yield

0.611

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
Product Image
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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.