ATTO 495 amine
Product key features
- Ex/Em: 497/525 nm
- Extinction coefficient: 80,000 cm-1M-1
- Reactive group: amine
- Versatile Conjugation: Efficiently labels carbonyl groups and also serves as an amine donor for enzymatic transamination labeling
- Superior Brightness & Stability: Delivers intense fluorescence with high photostability and thermal stability
- Long-Lived Phosphorescence: Enables sustained emission in solid matrices or at low temperatures, ideal for time-resolved spectroscopy
Product description
ATTO 495 is a green fluorescent dye derived from acridine orange, known for its strong absorption, high fluorescence quantum yield, excellent photostability, and superior thermal stability. It exhibits moderate hydrophilicity and is highly soluble in polar solvents such as DMF and DMSO, with an optimal excitation range of 465-510 nm. Notably, ATTO 495 exhibits intense and long-lived phosphorescence in solid matrices or at low temperatures. This dye is well-suited for advanced applications in single-molecule detection and high-resolution microscopy techniques, such as PALM, dSTORM, and STED microscopy. It is also compatible with flow cytometry (FACS), fluorescence in situ hybridization (FISH), and a wide range of other biological assays.
ATTO 495 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 amine | 438 | 484 | 45000 | 0.90 | 0.19 | 0.17 |
ATTO 495 DBCO | 497 | 525 | 80000 | 0.2 | 0.45 | 0.37 |
ATTO 495 TCO | 497 | 525 | 80000 | 0.2 | 0.45 | 0.37 |
ATTO 495 Tetrazine | 497 | 525 | 80000 | 0.2 | 0.45 | 0.37 |
References
Authors: Rode, Sascha and Hayn, Manuel and Röcker, Annika and Sieste, Stefanie and Lamla, Markus and Markx, Daniel and Meier, Christoph and Kirchhoff, Frank and Walther, Paul and Fändrich, Marcus and Weil, Tanja and Münch, Jan
Journal: Bioconjugate chemistry (2017): 1260-1270
Authors: Wang, Yi-Rou and Yang, Yuan-Han and Lu, Chi-Yu and Chen, Su-Hwei
Journal: Analytica chimica acta (2015): 76-82