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AAT Bioquest

ATTO 514 azide

Product key features

  • Ex/Em: 510/531 nm
  • Extinction coefficient: 115,000 cm-1M-1
  • Reactive group: azide
  • Click Chemistry Conjugation: Efficiently and rapidly labels terminal alkynes via CuAAC and copper-free SPAAC
  • Superior Brightness & Stability: Provides robust quantum yield with high photostability and thermal stability
  • Excellent Hydrophilicity: Prevents aggregation and enhances signal clarity for advanced imaging and live-cell applications

Product description

ATTO 514 azide is manufactured by AAT Bioquest for research and development use. ATTO 514 azide is used to label terminal alkynes on peptides, antibodies, and other biomolecules via click chemistry with the bright, green fluorescent ATTO 514 dye. It participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) with alkyne-containing molecules and strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO- or BCN-containing molecules.

ATTO 514 is a hydrophilic fluorescent dye characterized by excellent aqueous solubility, strong molar absorptivity, high fluorescence quantum yield, and notable thermal and photostability. These properties make it well-suited for advanced imaging techniques, including single-molecule detection and super-resolution microscopy methods such as PALM, dSTORM, and STED. ATTO 514 is also compatible with flow cytometry (FACS), fluorescence in situ hybridization (FISH), and other fluorescence-based assays. The dye is optimally excited within the 510–535 nm range, with the 514 nm line of an Argon-Ion laser providing efficient excitation.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
ATTO 390 azide39047524000.900.460.09
ATTO 425 azide438484450000.900.190.17
ATTO 488 azide499520900000.800.220.09
ATTO 495 azide497525800000.20.450.37
ATTO 514 TCO510531115,0000.850.210.08
ATTO 514 Tetrazine510531115,0000.850.210.08
ATTO 550 azide5535741200000.800.230.10
ATTO 565 azide5625891200000.900.270.12
ATTO 590 azide5926211200000.800.390.43
ATTO 610 azide6156321500000.700.030.06
ATTO 620 azide61964112000010.510.040.06
ATTO 633 azide6296511300000.6410.040.05
ATTO 647N azide6456631500000.6510.060.05
Show More (4)

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 May 19, 2025

Ordering information

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Catalog Number2845
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Additional ordering information

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Fax1-800-609-2943
Emailsales@aatbio.com
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Physical properties

Molecular weight

1055.07

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.21

Correction Factor (280 nm)

0.08

Extinction coefficient (cm -1 M -1)

115,000

Excitation (nm)

510

Emission (nm)

531

Quantum yield

0.85

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 azide–alkyne cycloaddition (“click chemistry”) between an azide‐functionalized dye and an alkyne‐presenting biomolecule. In the presence of a copper catalyst (CuAAC) or under strain‐promoted conditions (SPAAC), the azide and alkyne react to form a stable 1,2,3‐triazole linkage. This highly selective and robust reaction proceeds under mild conditions and tolerates a wide range of functional groups.