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ATTO 633 acid

Product key features

  • Ex/Em: 629/651 nm
  • Extinction coefficient: 130,000 cm-1M-1
  • High Quantum Yield: Offers bright fluorescence, ideal for sensitive detection in various imaging techniques
  • Exceptional Stability: Maintains fluorescence under prolonged light exposure, temperature variations, and across a wide pH range (2–11)
  • Broad Applications: Suited for high-precision techniques such as single-molecule detection and super-resolution microscopy (PALM, dSTORM, STED)

Product description

ATTO 633 is a bright-red fluorescent dye, characterized by its strong absorption, high fluorescence quantum yield, and exceptional photo and thermal stability. It exhibits moderate hydrophilicity and is optimally excited within the 610-645 nm wavelength range, compatible with both the 633 nm line of the He-Ne laser and the 635 nm line of the diode laser. The dye maintains stable fluorescence over a wide pH range (2-11), allowing for its use in diverse experimental conditions. Upon conjugation to a substrate, ATTO 633 becomes cationic, carrying a net positive charge of +1. These properties make ATTO 633 particularly suitable for high-precision applications, including single-molecule detection and super-resolution microscopy techniques such as PALM, dSTORM, and STED. Additionally, it is compatible with flow cytometry (FACS), fluorescence in situ hybridization (FISH), and various other biological assays.

ATTO 633 acid is a non-reactive compound that can be employed as a reference standard in studies utilizing ATTO 633 conjugates. It is also suitable for use as a control in confocal microscopy, immunocytochemistry (ICC), high-content screening (HCS), flow cytometry, and live cell imaging applications. Furthermore, it can be utilized in the synthesis of activated esters and STP and can be coupled to hydrazines, hydroxylamines, or amines in aqueous solutions using water-soluble carbodiimides (e.g., EDAC). This allows for the conjugation of the dye to amino-containing molecules, such as proteins, antibodies, amine-modified oligonucleotides, and peptides.

Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
ATTO 488 acid499520900000.800.220.09
ATTO 532 acid5315521150000.900.220.11
ATTO 647 acid6466661200000.200.080.04
ATTO 647N acid6456631500000.6510.060.05
ATTO 594 acid6026211200000.850.260.51
ATTO 514 acid510531115,0000.850.210.08
ATTO 565 acid5625891200000.900.270.12
ATTO 390 acid39047524000.900.460.09
ATTO 425 acid438484450000.900.190.17
ATTO 495 acid497525800000.20.450.37
ATTO 550 acid5535741200000.800.230.10
ATTO 590 acid5926211200000.800.390.43
ATTO 610 acid6156321500000.700.030.06
ATTO 620 acid61964112000010.510.040.06
ATTO 633 DBCO6296511300000.6410.040.05
ATTO 633 TCO6296511300000.6410.040.05
ATTO 633 Tetrazine6296511300000.6410.040.05
ATTO 655 acid6616791250000.310.240.08
ATTO 680 acid6796961250000.300.300.17
ATTO 700 acid6997151200000.250.260.41
Show More (11)

References

View all 21 references: Citation Explorer
Defect-Engineered Metal-Organic Frameworks as Nanocarriers for Pharmacotherapy: Insights into Intracellular Dynamics at The Single Particle Level.
Authors: Huang, Ge and Dreisler, Marcus Winther and Kæstel-Hansen, Jacob and Nielsen, Annette Juma and Zhang, Min and Hatzakis, Nikos S
Journal: Advanced materials (Deerfield Beach, Fla.) (2024): e2405898
Confocal Microscopy to Measure Three Modes of Fusion Pore Dynamics in Adrenal Chromaffin Cells.
Authors: Han, Sue and Wang, Xin and Cordero, Nicholas and Wu, Ling-Gang
Journal: Journal of visualized experiments : JoVE (2022)
Measuring Photophysical Transition Rates with Fluorescence Correlation Spectroscopy and Antibunching.
Authors: Sakhapov, Damir and Gregor, Ingo and Karedla, Narain and Enderlein, Jörg
Journal: The journal of physical chemistry letters (2022): 4823-4830
Comparing lifeact and phalloidin for super-resolution imaging of actin in fixed cells.
Authors: Mazloom-Farsibaf, Hanieh and Farzam, Farzin and Fazel, Mohamadreza and Wester, Michael J and Meddens, Marjolein B M and Lidke, Keith A
Journal: PloS one (2021): e0246138
Structural Mechanism of the Arrestin-3/JNK3 Interaction.
Authors: Park, Ji Young and Qu, Chang-Xiu and Li, Rui-Rui and Yang, Fan and Yu, Xiao and Tian, Zhao-Mei and Shen, Yue-Mao and Cai, Bo-Yang and Yun, Youngjoo and Sun, Jin-Peng and Chung, Ka Young
Journal: Structure (London, England : 1993) (2019): 1162-1170.e3
Page updated on December 17, 2024

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Catalog Number70270
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Physical properties

Molecular weight

652.19

Solvent

DMSO

Spectral properties

Correction Factor (260 nm)

0.04

Correction Factor (280 nm)

0.05

Extinction coefficient (cm -1 M -1)

130000

Excitation (nm)

629

Emission (nm)

651

Quantum yield

0.641

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
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Gallery Image 1
With EDAC or other equivalent activating coupling agents, fluorescent dyes, such as ATTO 633 acid, can react readily with the primary amines (R-NH<sub>2</sub>) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The resulting dye conjugates are quite stable.