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AAT Bioquest

XFD594 Tetrazine

Product key features

  • Ex/Em: 590/618 nm
  • Extinction coefficient: 90,000 cm-1M-1
  • Reactive Group: Tetrazine
  • Click Chemistry Conjugation: Provides rapid, copper-free labeling of TCO-modified biomolecules
  • Bright & Stable: Provides high quantum yield with resilience to photobleaching and pH variations from 4 to 10
  • Hydrophilic: Minimizes aggregation, enhancing signal clarity for advanced imaging and live-cell studies

Product description

XFD594, manufactured by AAT Bioquest, is structurally identical to Alexa Fluor™ 594 (ThermoFisher). This bright red-fluorescent dye is efficiently excited by the 561 nm or 594 nm laser lines and is compatible with RFP filters like Texas Red. It demonstrates excellent solubility in aqueous solutions and is pH-insensitive across a broad range (pH 4–10), ensuring reliable and stable signal generation under diverse experimental conditions. XFD594 is particularly well-suited for multicolor fluorescence microscopy, flow cytometry, and advanced SRM imaging techniques like dSTORM, SIM, STED and TPE. It can be conjugated to proteins at high molar ratios with minimal self-quenching, resulting in brighter conjugates. Moreover, the superior fluorescence quantum yield and photostability of XFD594 make it ideal for detecting low-abundance biological targets, enabling greater precision and sensitivity in quantitative fluorescence assays.

XFD594 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

References

View all 4 references: Citation Explorer
In vitro and in vivo evaluation of a tetrazine-conjugated poly-L-lysine effector molecule labeled with astatine-211.
Authors: Timperanza, Chiara and Jensen, Holger and Hansson, Ellinor and Bäck, Tom and Lindegren, Sture and Aneheim, Emma
Journal: EJNMMI radiopharmacy and chemistry (2024): 43
Metal-ion coordinated self-assembly of human insulin directs kinetics of insulin release as determined by preclinical SPECT/CT imaging.
Authors: Engudar, Gokce and Rodríguez-Rodríguez, Cristina and Mishra, Narendra Kumar and Bergamo, Marta and Amouroux, Guillaume and Jensen, Knud J and Saatchi, Katayoun and Häfeli, Urs O
Journal: Journal of controlled release : official journal of the Controlled Release Society (2022): 347-360
Covalent Immobilization of Antibodies through Tetrazine-TCO Reaction to Improve Sensitivity of ELISA Technique.
Authors: García-Maceira, Tania and García-Maceira, Fé I and González-Reyes, José A and Torres-Sánchez, Luis A and Aragón-Gómez, Ana Belén and García-Rubiño, María Eugenia and Paz-Rojas, Elier
Journal: Biosensors (2021)
Tetrazine-TCO Ligation: A Potential Simple Approach to Improve Tumor Uptake through Enhanced Blood Circulation.
Authors: Wang, Mengzhe and Wang, Hui and Niu, Crystal Q and Zhang, Tao and Wu, Zhanhong and Li, Zibo
Journal: Bioconjugate chemistry (2020): 1795-1803
Page updated on April 25, 2025

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Catalog Number1733
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Physical properties

Molecular weight

906.00

Solvent

DMSO

Spectral properties

Absorbance (nm)

592

Correction Factor (260 nm)

0.43

Correction Factor (280 nm)

0.56

Extinction coefficient (cm -1 M -1)

90000

Excitation (nm)

590

Emission (nm)

618

Quantum yield

0.661

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
Product Image
Gallery Image 1
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.