iFluor® 594 azide
Product key features
- Bright, Red-Emitting Fluorophore: Excitation/emission maxima at ~588/604 nm, spectrally compatible with Texas Red® and Alexa Fluor® 594.
- pH-Independent Fluorescence: Maintains stable emission across a broad pH range, ensuring reproducibility in diverse experimental conditions.
- High-Specificity Bioconjugation: Azide functionality enables efficient and selective CuAAC-mediated labeling with alkyne-modified targets.
- Low Background Signal: CuAAC chemistry minimizes nonspecific interactions, enhancing signal-to-noise ratio.
- Broad Experimental Utility: Optimized for fluorescence microscopy, flow cytometry, and other fluorescence-based assays.
Product description
iFluor® 594 azide is a hydrophilic, red-emitting fluorescent dye engineered for efficient biomolecular labeling via click chemistry. It exhibits excitation and emission maxima at approximately 587 nm and 603 nm, respectively, aligning closely with dyes such as Texas Red® and Alexa Fluor® 594. A key advantage of iFluor® 594 is its pH-independent fluorescence, which remains stable across a broad pH range, ensuring consistent performance in different experimental conditions and improving reproducibility across diverse labeling applications.
The azide functionality of iFluor® 594 allows for precise and efficient bioconjugation with alkyne-functionalized molecules via copper-catalyzed azide-alkyne cycloaddition (CuAAC). Unlike conventional labeling strategies that modify amine or thiol groups, CuAAC provides exceptional chemoselectivity, minimizing nonspecific interactions and reducing background fluorescence. This improves labeling accuracy while maintaining the structural and functional integrity of biomolecules. iFluor® 594 azide is particularly suitable for applications including fluorescence microscopy, flow cytometry, and various fluorescence-based assays, providing researchers with a reliable tool for sensitive detection and imaging.
The azide functionality of iFluor® 594 allows for precise and efficient bioconjugation with alkyne-functionalized molecules via copper-catalyzed azide-alkyne cycloaddition (CuAAC). Unlike conventional labeling strategies that modify amine or thiol groups, CuAAC provides exceptional chemoselectivity, minimizing nonspecific interactions and reducing background fluorescence. This improves labeling accuracy while maintaining the structural and functional integrity of biomolecules. iFluor® 594 azide is particularly suitable for applications including fluorescence microscopy, flow cytometry, and various fluorescence-based assays, providing researchers with a reliable tool for sensitive detection and imaging.
Spectrum
Product family
Name | Excitation (nm) | Emission (nm) | Extinction coefficient (cm -1 M -1) | Quantum yield | Correction Factor (260 nm) | Correction Factor (280 nm) |
iFluor® 647 azide | 656 | 670 | 2500001 | 0.251 | 0.03 | 0.03 |
iFluor® 488 azide | 491 | 516 | 750001 | 0.91 | 0.21 | 0.11 |
iFluor® 555 azide | 557 | 570 | 1000001 | 0.641 | 0.23 | 0.14 |
iFluor® 594 Styramide *Superior Replacement for Alexa Fluor 594 tyramide* | 587 | 603 | 2000001 | 0.531 | 0.05 | 0.04 |
iFluor® 594 Tyramide | 587 | 603 | 2000001 | 0.531 | 0.05 | 0.04 |
iFluor® 594 TCO | 587 | 603 | 2000001 | 0.531 | 0.05 | 0.04 |
iFluor® 594 Tetrazine | 587 | 603 | 2000001 | 0.531 | 0.05 | 0.04 |
iFluor® 405 azide | 403 | 427 | 370001 | 0.911 | 0.48 | 0.77 |
iFluor® 790 Azide | 787 | 812 | 2500001 | 0.131 | 0.1 | 0.09 |
References
View all 50 references: Citation Explorer
Combination of atom transfer radical polymerization and alkyne-azide click-chemistry for the synthesis of phosphonic acid cation exchange materials.
Authors: Schipplick, Luca and Kahler, Philipp and Seubert, Andreas
Journal: Journal of chromatography. A (2025): 465675
Authors: Schipplick, Luca and Kahler, Philipp and Seubert, Andreas
Journal: Journal of chromatography. A (2025): 465675
Preparation of Protein A Membranes Using Propargyl Methacrylate-Based Copolymers and Copper-Catalyzed Alkyne-Azide Click Chemistry.
Authors: Osuofa, Joshua and Husson, Scott M
Journal: Polymers (2024)
Authors: Osuofa, Joshua and Husson, Scott M
Journal: Polymers (2024)
Universal Click-Chemistry Approach for the DNA Functionalization of Nanoparticles.
Authors: Siegel, Nicole and Hasebe, Hiroaki and Chiarelli, Germán and Garoli, Denis and Sugimoto, Hiroshi and Fujii, Minoru and Acuna, Guillermo P and Kołątaj, Karol
Journal: Journal of the American Chemical Society (2024): 17250-17260
Authors: Siegel, Nicole and Hasebe, Hiroaki and Chiarelli, Germán and Garoli, Denis and Sugimoto, Hiroshi and Fujii, Minoru and Acuna, Guillermo P and Kołątaj, Karol
Journal: Journal of the American Chemical Society (2024): 17250-17260
A facile strategy for tuning the density of surface-grafted biomolecules for melt extrusion-based additive manufacturing applications.
Authors: Beeren, I A O and Dos Santos, G and Dijkstra, P J and Mota, C and Bauer, J and Ferreira, H and Reis, Rui L and Neves, N and Camarero-Espinosa, S and Baker, M B and Moroni, L
Journal: Bio-design and manufacturing (2024): 277-291
Authors: Beeren, I A O and Dos Santos, G and Dijkstra, P J and Mota, C and Bauer, J and Ferreira, H and Reis, Rui L and Neves, N and Camarero-Espinosa, S and Baker, M B and Moroni, L
Journal: Bio-design and manufacturing (2024): 277-291
Halogenase-Assisted Alkyne/Aryl Bromide Sonogashira Coupling for Ribosomally Synthesized Peptides.
Authors: Saha, Nirmal and Vidya, F N U and Xie, Ramon and Agarwal, Vinayak
Journal: Journal of the American Chemical Society (2024): 30009-30013
Authors: Saha, Nirmal and Vidya, F N U and Xie, Ramon and Agarwal, Vinayak
Journal: Journal of the American Chemical Society (2024): 30009-30013
Page updated on March 11, 2025