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AAT Bioquest

XFD750 Tetrazine

Product key features

  • Ex/Em: 752/776 nm
  • Extinction coefficient: 240,000 cm-1M-1
  • Reactive Group: Tetrazine
  • Click Chemistry Conjugation: Provides rapid and copper-free labeling of TCO-modified biomolecules
  • Bright & Stable: Offers intense, photostable fluorescence for labeling low-abundance targets
  • Water Soluble: Minimizes aggregation, enhancing signal clarity for advanced imaging and live-cell studies

XFD750, manufactured by AAT Bioquest, is a bright near-infrared fluorescent dye structurally identical to Alexa Fluor™ 750 (ThermoFisher). It is efficiently excited by the 633 nm laser line and is compatible with the Cy7 filter set, making it well-suited for applications such as fluorescence microscopy and flow cytometry. The dye demonstrates excellent aqueous solubility and maintains pH stability across a broad range (pH 4–10), ensuring reliable and reproducible fluorescence signals under diverse experimental conditions. Its long-wavelength emission effectively reduces background autofluorescence, enhancing signal-to-noise ratios in complex biological samples, particularly in tissue imaging. Furthermore, XFD750 is widely utilized in stochastic optical reconstruction microscopy (STORM), providing exceptional performance in both dSTORM and nSTORM super-resolution imaging techniques.

XFD750 tetrazine is particularly useful for labeling TCO-modified biomolecules under copper-free conditions. It reacts with TCO-functionalized molecules, forming a stable conjugate via a dihydropyrazine moiety. This click reaction is favored over others due to its extremely fast kinetics and higher yields under mild reaction conditions, making it a popular choice for researchers.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
XFD488 tetrazine *Same Structure to Alexa Fluor™ 488 tetrazine*499520710000.9210.300.11
XFD555 Tetrazine5535681500000.110.080.08
XFD635 Tetrazine633647140,000---
XFD647 Tetrazine6506712390000.3310.000.03
XFD680 Tetrazine6817041840000.3610.000.05
XFD700 Tetrazine6967191920000.2510.000.07
XFD750 acid7527762900000.121-0.04
XFD750 alkyne7527762400000.1210.000.04
XFD750 amine7527762900000.121-0.04
XFD750 azide7527762400000.1210.000.04
XFD750 TCO7527762400000.1210.000.04
XFD790 Tetrazine782805260,000-0.090.08
Show More (3)

References

View all 17 references: Citation Explorer
Crosslinking intermodular condensation in non-ribosomal peptide biosynthesis.
Authors: Heberlig, Graham W and La Clair, James J and Burkart, Michael D
Journal: Nature (2025): 261-269
Conjugation of Multiple Proteins Onto the Surface of PLGA/Lipid Hybrid Nanoparticles.
Authors: Hu, He and Zhang, Chenming
Journal: Journal of biomedical materials research. Part A (2025): e37807
Fluorescence labeling strategies for cell surface expression of TRPV1.
Authors: Mott, Taylor M and Wulffraat, Grace C and Eddins, Alex J and Mehl, Ryan A and Senning, Eric N
Journal: The Journal of general physiology (2024)
Fluorescence labeling strategies for the study of ion channel and receptor cell surface expression: A comprehensive toolkit for extracellular labeling of TRPV1.
Authors: Mott, Taylor M and Wulffraat, Grace C and Eddins, Alex J and Mehl, Ryan A and Senning, Eric N
Journal: bioRxiv : the preprint server for biology (2024)
Broadening the Utility of Farnesyltransferase-Catalyzed Protein Labeling Using Norbornene-Tetrazine Click Chemistry.
Authors: Auger, Shelby A and Venkatachalapathy, Sneha and Suazo, Kiall Francis G and Wang, Yiao and Sarkis, Alexander W and Bernhagen, Kaitlyn and Justyna, Katarzyna and Schaefer, Jonas V and Wollack, James W and Plückthun, Andreas and Li, Ling and Distefano, Mark D
Journal: Bioconjugate chemistry (2024): 922-933
Page updated on April 15, 2025

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Catalog Number1742
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Physical properties

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.00

Correction Factor (280 nm)

0.04

Extinction coefficient (cm -1 M -1)

240000

Excitation (nm)

752

Emission (nm)

776

Quantum yield

0.121

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 inverse‐electron‐demand Diels–Alder (iEDDA) reaction between a tetrazine–dye conjugate and a trans‐cyclooctene (TCO)–modified biomolecule. The tetrazine–dye selectively and rapidly reacts with the TCO moiety on the biomolecule to form a stable linkage, labeling the nucleic acid with the dye. This bioorthogonal “click chemistry” process is fast, selective, and well‐suited for biocompatible labeling applications.
Schematic illustrating the strain‐promoted inverse‐electron‐demand Diels–Alder (iEDDA) reaction between a tetrazine–dye conjugate and a trans‐cyclooctene (TCO)–modified biomolecule. The tetrazine–dye selectively and rapidly reacts with the TCO moiety on the biomolecule to form a stable linkage, labeling the nucleic acid with the dye. This bioorthogonal “click chemistry” process is fast, selective, and well‐suited for biocompatible labeling applications.
Schematic illustrating the strain‐promoted inverse‐electron‐demand Diels–Alder (iEDDA) reaction between a tetrazine–dye conjugate and a trans‐cyclooctene (TCO)–modified biomolecule. The tetrazine–dye selectively and rapidly reacts with the TCO moiety on the biomolecule to form a stable linkage, labeling the nucleic acid with the dye. This bioorthogonal “click chemistry” process is fast, selective, and well‐suited for biocompatible labeling applications.