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ATTO 532 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 weight848.08
SolventDMSO
Spectral properties
Correction Factor (260 nm)0.22
Correction Factor (280 nm)0.11
Extinction coefficient (cm -1 M -1)115000
Excitation (nm)531
Emission (nm)552
Quantum yield0.90
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 532 maleimide

OverviewpdfSDSpdfProtocol


Molecular weight
848.08
Correction Factor (260 nm)
0.22
Correction Factor (280 nm)
0.11
Extinction coefficient (cm -1 M -1)
115000
Excitation (nm)
531
Emission (nm)
552
Quantum yield
0.90
ATTO 532 is a rhodamine-based fluorescent labeling dye with high molecular high extinction coefficient and fluorescence quantum yield (0.90) as well as sufficient Stoke's shift (excitation maximum 532 nm, emission maximum 553 nm). The dye also has relatively good photostability. It is optimized for excitation with frequency doubled Nd:YAG-Laser.

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of ATTO 532 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 mM117.913 µL589.567 µL1.179 mL5.896 mL11.791 mL
5 mM23.583 µL117.913 µL235.827 µL1.179 mL2.358 mL
10 mM11.791 µL58.957 µL117.913 µL589.567 µL1.179 mL

Molarity calculator

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Spectrum


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Spectral properties

Correction Factor (260 nm)0.22
Correction Factor (280 nm)0.11
Extinction coefficient (cm -1 M -1)115000
Excitation (nm)531
Emission (nm)552
Quantum yield0.90

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 647 acid6466661200000.200.080.04
ATTO 647N acid6456631500000.6510.060.05
ATTO 594 acid6026211200000.850.260.51
ATTO 514 acid510531115,0000.850.210.08

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Citations


View all 20 citations: Citation Explorer
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
Fluorescence of dyes in solutions with high absorbance. Inner filter effect correction
Authors: Fonin, A. V., Sulatskaya, A. I., Kuznetsova, I. M., Turoverov, K. K.
Journal: PLoS One (2014): e103878
AMBER-DYES: Characterization of Charge Fluctuations and Force Field Parameterization of Fluorescent Dyes for Molecular Dynamics Simulations
Authors: Graen, T., Hoefling, M., Grubmuller, H.
Journal: J Chem Theory Comput (2014): 5505-12

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