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ATTO 565 maleimide

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Fax1-800-609-2943
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Physical properties
Molecular weight733.17
SolventDMSO
Spectral properties
Correction Factor (260 nm)0.34
Correction Factor (280 nm)0.16
Extinction coefficient (cm -1 M -1)120000
Excitation (nm)563
Emission (nm)589
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
Alternative formats
ATTO 565 acid

OverviewpdfSDSpdfProtocol


Molecular weight
733.17
Correction Factor (260 nm)
0.34
Correction Factor (280 nm)
0.16
Extinction coefficient (cm -1 M -1)
120000
Excitation (nm)
563
Emission (nm)
589
Quantum yield
0.90
ATTO 565 Maleimide is a commonly used thiol-reactive rhodamine dye. It might be used for labeling peptides, proteins and other thiol-containing compounds such as thiol-modified oligos. It readily reacts with compounds containing thiol groups, forming a chemically stable thiol ether bond between the dye and thiol compounds. The optimum pH range for maleimide coupling is pH 5.5 – 7.0. ATTO 565 Maleimide has strong absorption, high fluorescence quantum yield and high thermal/photostability. However, it has low water solubility. For the applications that require high water solubility, you may consider iFluor® 568 Maleimide that has almost identical fluorescence properties with greatly enhanced water solubility. In addition, the protein conjugates made from iFluor® 568 Maleimide are much brighter than those from ATTO 565 Maleimide.

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of ATTO 565 maleimide 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 mM136.394 µL681.97 µL1.364 mL6.82 mL13.639 mL
5 mM27.279 µL136.394 µL272.788 µL1.364 mL2.728 mL
10 mM13.639 µL68.197 µL136.394 µL681.97 µL1.364 mL

Molarity calculator

Enter any two values (mass, volume, concentration) to calculate the third.

Mass (Calculate)Molecular weightVolume (Calculate)Concentration (Calculate)Moles
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Spectrum


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spectrum

Spectral properties

Correction Factor (260 nm)0.34
Correction Factor (280 nm)0.16
Extinction coefficient (cm -1 M -1)120000
Excitation (nm)563
Emission (nm)589
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 maleimide499520900000.800.250.10
ATTO 532 maleimide5315521150000.900.220.11
ATTO 647 maleimide6466661200000.200.080.04
ATTO 647N maleimide6456631500000.6510.060.05
ATTO 594 maleimide6026211200000.850.260.51
ATTO 514 maleimide510531115,0000.850.210.08

Images


References


View all 32 references: Citation Explorer
Time-resolved fluorescence anisotropy with Atto 488-labeled phytochrome Agp1 from Agrobacterium fabrum.
Authors: Elkurdi, Afaf and Guigas, Gernot and Hourani-Alsharafat, Latifa and Scheerer, Patrick and Nienhaus, Gerd Ulrich and Krauß, Norbert and Lamparter, Tilman
Journal: Photochemistry and photobiology (2024): 561-572
Analysis of photon trajectories from diffusing single molecules.
Authors: Gopich, Irina V and Kim, Jae-Yeol and Chung, Hoi Sung
Journal: The Journal of chemical physics (2023)
Curvature preference of cubic CsPbBr3 quantum dots embedded onto phospholipid bilayer membranes.
Authors: Chairil, Ricki and Malmstadt, Noah
Journal: Soft matter (2023): 3966-3974
Interactions of the Kv1.1 Channel with Peptide Pore Blockers: A Fluorescent Analysis on Mammalian Cells.
Authors: Orlov, Nikita A and Kryukova, Elena V and Efremenko, Anastasia V and Yakimov, Sergey A and Toporova, Victoria A and Kirpichnikov, Mikhail P and Nekrasova, Oksana V and Feofanov, Alexey V
Journal: Membranes (2023)
Spatial distribution of single guest molecules along thickness of thin films of poly(2-hydroxyethyl acrylate).
Authors: Ito, Syoji and Hiratsuka, Kengo and Takei, Satoshi and Nishi, Hiroyasu and Kitagawa, Daichi and Kobatake, Seiya and Miyasaka, Hiroshi
Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society (2022): 175-184
Atto488-Agitoxin 2-A Fluorescent Ligand with Increased Selectivity for Kv1.3 Channel Binding Site.
Authors: Denisova, Kristina R and Orlov, Nikita A and Yakimov, Sergey A and Kirpichnikov, Mikhail P and Feofanov, Alexey V and Nekrasova, Oksana V
Journal: Bioengineering (Basel, Switzerland) (2022)
Lipophilic probe behavior in microemulsions evaluated by fluorescence correlation spectroscopy.
Authors: Yamamoto, Johtaro and Suzuki, Yoshio and Ogawa, Yoshikatsu and Kamata, Tomoyuki and Hashimoto, Hinako and Kunitake, Masashi and Kato, Dai
Journal: Analytical sciences : the international journal of the Japan Society for Analytical Chemistry (2022): 401-408
A Model of F-actin Organization in Granuloreticulopodia in Foraminifera: Morphogenetic and Evolutionary Implications from Novel Fluorescent and Polarised Light Observations.
Authors: Goleń, Jan and Tyszka, Jarosław and Godos, Karolina and Janse, Max
Journal: Protist (2022): 125886
Evaluation of [Cys(ATTO 488)8]Dermorphin-NH2 as a novel tool for the study of μ-opioid peptide receptors.
Authors: Giakomidi, Despina and Bird, Mark F and McDonald, John and Marzola, Erika and Guerrini, Remo and Chanoch, Serena and Sabu, Nidhuna and Horley, Barbara and Calo, Girolamo and Lambert, David G
Journal: PloS one (2021): e0250011
Multimodal fluorescently labeled polymer-coated GdF3 nanoparticles inhibit degranulation in mast cells.
Authors: Shapoval, Oleksandr and Sulimenko, Vadym and Klebanovych, Anastasiya and Rabyk, Mariia and Shapoval, Pavlo and Kaman, Ondřej and Rydvalová, Eliška and Filipová, Marcela and Dráberová, Eduarda and Dráber, Pavel and Horák, Daniel
Journal: Nanoscale (2021): 19023-19037