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ATTO 390 amine

Product key features

  • Ex/Em: 390/475 nm
  • Extinction coefficient: 24,000 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
  • Large Stokes Shift: Enables effective signal separation, reducing background interference

Product description

ATTO 390 is a coumarin-based fluorescent dye characterized by its high fluorescence quantum yield, large Stokes shift, good photostability, and low molecular weight. It exhibits moderate hydrophilicity and is optimally excited within the 360-410 nm range, with a mercury arc lamp (emission lines at 365 nm and 405 nm) serving as an effective excitation source. This dye is well-suited for applications in single-molecule detection and advanced high-resolution microscopy techniques, including PALM, dSTORM, and STED. Additionally, ATTO 390 is compatible with flow cytometry (FACS), fluorescence in situ hybridization (FISH), and other diverse biological assays.

ATTO 390 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

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
ATTO 390 DBCO39047524000.900.460.09
ATTO 390 TCO39047524000.900.460.09
ATTO 390 Tetrazine39047524000.900.460.09
ATTO 425 amine438484450000.900.190.17
ATTO 495 amine497525800000.20.450.37

References

View all 7 references: Citation Explorer
The new live imagers MitoMM1/2 for mitochondrial visualization.
Authors: Maeda, Miwa and Suzuki, Mayu and Takashima, Shigeo and Sasaki, Tsutomu and Oh-Hashi, Kentaro and Takemori, Hiroshi
Journal: Biochemical and biophysical research communications (2021): 50-54
DNA-templated control of chirality and efficient energy transport in supramolecular DNA architectures with aggregation-induced emission.
Authors: Ucar, Hülya and Wagenknecht, Hans-Achim
Journal: Chemical science (2021): 10048-10053
Endoplasmic reticulum phospholipid scramblase activity revealed after protein reconstitution into giant unilamellar vesicles containing a photostable lipid reporter.
Authors: Mathiassen, Patricia P M and Menon, Anant K and Pomorski, Thomas Günther
Journal: Scientific reports (2021): 14364
Importance of probe design for bioanalysis of oligonucleotides using hybridization-based LC-fluorescence assays.
Authors: Ji, Yuhuan and Liu, Yijiang and Xia, Wanhong and Behling, Alexander and Meng, Min and Bennett, Patrick and Wang, Laixin
Journal: Bioanalysis (2019): 1917-1925
The effect of local dynamics of Atto 390-labeled lysozyme on fluorescence anisotropy modeling.
Authors: Babcock, Jeremiah J and Brancaleon, Lorenzo
Journal: Biopolymers (2015): 285-95
Page updated on December 17, 2024

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Catalog Number70208
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Physical properties

Molecular weight

499.53

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.46

Correction Factor (280 nm)

0.09

Extinction coefficient (cm -1 M -1)

24000

Excitation (nm)

390

Emission (nm)

475

Quantum yield

.90

Storage, safety and handling

Certificate of OriginDownload PDF
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12352200