ATTO 425 amine
Product key features
- Ex/Em: 438/484 nm
- Extinction coefficient: 45,000 cm-1M-1
- Reactive group: amine
- Versatile Conjugation: Efficiently labels carbonyl groups (e.g., aldehyde, ketone, and carboxy groups); also an amine donor for enzymatic transamination labeling
- High Quantum Yield & Photostability: Delivers strong, stable fluorescence for sensitive applications
- Enhanced Signal Separation: Minimal excitation and emission overlap reduces background interference
Product description
ATTO 425 is a coumarin-based fluorescent dye characterized by its high fluorescence quantum yield, large Stokes shift, excellent photostability, and low molecular weight. It exhibits moderate hydrophilicity and is optimally excited in the 405-455 nm wavelength range. These properties make ATTO 425 particularly suitable for applications in single-molecule detection and high-resolution microscopy techniques, including PALM, dSTORM, and STED microscopy. Additionally, ATTO 425 is well-suited for use in flow cytometry (FACS), fluorescence in situ hybridization (FISH), and various other biological assays.
ATTO 425 amine is a carbonyl-reactive building block for modifying carboxylic groups in the presence of activators such as EDC or DCC, or activated esters like NHS esters, through the formation of stable amide bonds. Additionally, it can be used as an amine donor for enzymatic transamination labeling.
Spectrum
Product family
Name | Excitation (nm) | Emission (nm) | Extinction coefficient (cm -1 M -1) | Quantum yield | Correction Factor (260 nm) | Correction Factor (280 nm) |
ATTO 390 amine | 390 | 475 | 24000 | .90 | 0.46 | 0.09 |
ATTO 425 DBCO | 438 | 484 | 45000 | 0.90 | 0.19 | 0.17 |
ATTO 425 TCO | 438 | 484 | 45000 | 0.90 | 0.19 | 0.17 |
ATTO 425 Tetrazine | 438 | 484 | 45000 | 0.90 | 0.19 | 0.17 |
ATTO 495 amine | 497 | 525 | 80000 | 0.2 | 0.45 | 0.37 |
References
Authors: Sun, Zhiwei and Li, Juan and Yang, Yufei and Tong, Yao and Li, Hui and Wang, Chuanxin and Du, Lutao and Jiang, Yanyan
Journal: Bioconjugate chemistry (2022): 1698-1706
Authors: Sun, Zhiwei and Li, Juan and Tong, Yao and Zhao, Li and Zhou, Xiaoyu and Li, Hui and Wang, Chuanxin and Du, Lutao and Jiang, Yanyan
Journal: Biosensors (2022)
Authors: Damont, Annelaure and Boisgard, Raphael and Dollé, Frédéric and Hollocou, Morgane and Kuhnast, Bertrand
Journal: Bioconjugate chemistry (2017): 2524-2529
Authors: Fonin, Alexander V and Sulatskaya, Anna I and Kuznetsova, Irina M and Turoverov, Konstantin K
Journal: PloS one (2014): e103878