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ATTO 647 acid

With EDAC or other equivalent activating coupling agents, fluorescent ATTO dyes 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.
With EDAC or other equivalent activating coupling agents, fluorescent ATTO dyes 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.
With EDAC or other equivalent activating coupling agents, fluorescent ATTO dyes 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.
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Physical properties
Molecular weight706.81
SolventDMSO
Spectral properties
Correction Factor (260 nm)0.08
Correction Factor (280 nm)0.04
Extinction coefficient (cm -1 M -1)120000
Excitation (nm)646
Emission (nm)666
Quantum yield0.20
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC12352200
Alternative formats
ATTO 647 maleimide

OverviewpdfSDSpdfProtocol


Molecular weight
706.81
Correction Factor (260 nm)
0.08
Correction Factor (280 nm)
0.04
Extinction coefficient (cm -1 M -1)
120000
Excitation (nm)
646
Emission (nm)
666
Quantum yield
0.20
ATTO 647 is rhodamine-based fluorescent label for the red spectral region that has similar spectral properties to Cy5. It has strong absorption, high fluorescence quantum yield, high thermal and photostability, and its absorption and fluorescence are independent of pH from 2 to 11. ATTO 647 is suitable for single-molecule detection applications, high-resolution microscopy (such as SIM, STED), flow cytometry (FACS) and fluorescence in-situ hybridization (FISH).

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of ATTO 647 acid to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM141.481 µL707.404 µL1.415 mL7.074 mL14.148 mL
5 mM28.296 µL141.481 µL282.961 µL1.415 mL2.83 mL
10 mM14.148 µL70.74 µL141.481 µL707.404 µL1.415 mL

Molarity calculator

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Spectrum


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spectrum

Spectral properties

Correction Factor (260 nm)0.08
Correction Factor (280 nm)0.04
Extinction coefficient (cm -1 M -1)120000
Excitation (nm)646
Emission (nm)666
Quantum yield0.20

Product Family


NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
ATTO 488 acid499520900000.800.250.10
ATTO 532 acid5315521150000.900.220.11
ATTO 647N acid6456631500000.6510.060.05
ATTO 594 acid6026211200000.850.260.51
ATTO 514 acid510531115,0000.850.210.08

Images


Citations


View all 21 citations: Citation Explorer
Single-molecule enzymatic reaction dynamics and mechanisms of GPX3 and TRXh9 from Arabidopsis thaliana
Authors: Kuang, Yanmin and Guo, Xing and Guo, Aiyu and Ran, Xia and He, Yulu and Zhang, Yu and Guo, Lijun
Journal: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy (2020): 118778
A novel nanocomposite based on fluorescent turn-on gold nanostars for near-infrared photothermal therapy and self-theranostic caspase-3 imaging of glioblastoma tumor cell
Authors: Wang, J., Zhou, Z., Zhang, F., Xu, H., Chen, W., Jiang, T.
Journal: Colloids Surf B Biointerfaces (2018): 303-311
Cell-permeable organic fluorescent probes for live-cell long-term super-resolution imaging reveal lysosome-mitochondrion interactions
Authors: Han, Y., Li, M., Qiu, F., Zhang, M., Zhang, Y. H.
Journal: Nat Commun (2017): 1307
Field-Controlled Charge Separation in a Conductive Matrix at the Single-Molecule Level: Toward Controlling Single-Molecule Fluorescence Intermittency
Authors: Kennes, K., Dedecker, P., Hutchison, J. A., Fron, E., Uji, I. H., Hofkens, J., Van der Auweraer, M.
Journal: ACS Omega (2016): 1383-1392
Determination of equilibrium and rate constants for complex formation by fluorescence correlation spectroscopy supplemented by dynamic light scattering and Taylor dispersion analysis
Authors: Zhang, X., Poniewierski, A., Jelinska, A., Zagozdzon, A., Wisniewska, A., Hou, S., Holyst, R.
Journal: Soft Matter (2016): 8186-8194
A Cystine Knot Peptide Targeting Integrin alphavbeta6 for Photoacoustic and Fluorescence Imaging of Tumors in Living Subjects
Authors: Zhang, C., Kimura, R., Abou-Elkacem, L., Levi, J., Xu, L., Gambhir, S. S.
Journal: J Nucl Med (2016): 1629-1634
Tracking structural transitions of bovine serum albumin in surfactant solutions by fluorescence correlation spectroscopy and fluorescence lifetime analysis
Authors: Zhang, X., Poniewierski, A., Hou, S., Sozanski, K., Wisniewska, A., Wieczorek, S. A., Kalwarczyk, T., Sun, L., Holyst, R.
Journal: Soft Matter (2015): 2512-8
The effect of local dynamics of Atto 390-labeled lysozyme on fluorescence anisotropy modeling
Authors: Babcock, J. J., Brancaleon, L.
Journal: Biopolymers (2015): 285-95
Application of single molecule fluorescence microscopy to characterize the penetration of a large amphiphilic molecule in the stratum corneum of human skin
Authors: Volz, P., Boreham, A., Wolf, A., Kim, T. Y., Balke, J., Frombach, J., Hadam, S., Afraz, Z., Rancan, F., Blume-Peytavi, U., Vogt, A., Alexiev, U.
Journal: Int J Mol Sci (2015): 6960-77
The key role of geminate electron-hole pair recombination in the delayed fluorescence in rhodamine 6G and ATTO-532
Authors: Aydemir, M., Jankus, V., Dias, F. B., Monkman, A.
Journal: Phys Chem Chem Phys (2014): 21543-9

References


View all 1 references: Citation Explorer
Quantitative comparison of long-wavelength Alexa Fluor dyes to Cy dyes: fluorescence of the dyes and their bioconjugates
Authors: Berlier JE, Rothe A, Buller G, Bradford J, Gray DR, Filanoski BJ, Telford WG, Yue S, Liu J, Cheung CY, Chang W, Hirsch JD, Beechem JM, Haugl and RP., undefined
Journal: J Histochem Cytochem (2003): 1699