Introduction to Fluorescence Depolarization
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Fluorescence Depolarization sentence examples within Resolved Fluorescence Depolarization
In this article we have investigated the solvation, rotational dynamics and photo physics of diketone derivatives DK-2 and DK-3 in alcohols and alkanes at room temperature through both a time-resolved fluorescence depolarization technique and steady state.
In this article we have investigated the solvation, rotational dynamics and photo physics of diketone derivatives DK-2 and DK-3 in alcohols and alkanes at room temperature through both a time-resolved fluorescence depolarization technique and steady state.
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Using time-resolved fluorescence depolarization studies, here we report complete reversal of trends in anisotropy decay traces up on increasing fluorophore concentration while traversing a series of solvent mixtures (water and glycerol) with increasing viscosity.
Using time-resolved fluorescence depolarization studies, here we report complete reversal of trends in anisotropy decay traces up on increasing fluorophore concentration while traversing a series of solvent mixtures (water and glycerol) with increasing viscosity.
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Fluorescence Depolarization sentence examples within fluorescence depolarization measurement
Using highly sensitive picosecond time-resolved fluorescence depolarization measurements, we directly capture rapid large-amplitude torsional fluctuations in the extended chains that can control the relay of making-and-breaking of noncovalent intermolecular contacts maintaining the internal fluidity.
Using highly sensitive picosecond time-resolved fluorescence depolarization measurements, we directly capture rapid large-amplitude torsional fluctuations in the extended chains that can control the relay of making-and-breaking of noncovalent intermolecular contacts maintaining the internal fluidity.
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Using highly-sensitive picosecond time-resolved fluorescence depolarization measurements, we directly capture rapid large-amplitude torsional fluctuations in the extended chains that can control the relay of making-and-breaking of noncovalent intermolecular contacts maintaining the internal fluidity.
Using highly-sensitive picosecond time-resolved fluorescence depolarization measurements, we directly capture rapid large-amplitude torsional fluctuations in the extended chains that can control the relay of making-and-breaking of noncovalent intermolecular contacts maintaining the internal fluidity.
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10.1021/acs.jpclett.1c01354
We relate these dynamical processes to the predicted fluorescence depolarization, extract the time scales corresponding to them, and thus interpret the observed sub-ps fluorescence depolarization.
We relate these dynamical processes to the predicted fluorescence depolarization, extract the time scales corresponding to them, and thus interpret the observed sub-ps fluorescence depolarization.
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10.1016/j.bpj.2021.01.035
Herein, we investigated the fluorescence depolarization dynamics of recently developed ionic-strength biosensors (mCerulean3-linker-mCitrine) in Hofmeister salt (KCl, NaCl, NaI, and Na2SO4) solutions.
Herein, we investigated the fluorescence depolarization dynamics of recently developed ionic-strength biosensors (mCerulean3-linker-mCitrine) in Hofmeister salt (KCl, NaCl, NaI, and Na2SO4) solutions.
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10.1088/1361-6501/abeccb
This technique exploits fluorescence depolarization due to rotational Brownian motion of fluorophores and determines fluid viscosity in microchannel flow by measuring steady-state fluorescence polarization.
This technique exploits fluorescence depolarization due to rotational Brownian motion of fluorophores and determines fluid viscosity in microchannel flow by measuring steady-state fluorescence polarization.
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10.1021/acs.jpcb.1c04426
In this study, we employed sensitive fluorescence depolarization kinetics by following picosecond time-resolved fluorescence anisotropy decays to directly capture the essential dynamical features of intrinsically disordered α-synuclein (α-syn) site-specifically labeled with thiol-active fluorophores.
In this study, we employed sensitive fluorescence depolarization kinetics by following picosecond time-resolved fluorescence anisotropy decays to directly capture the essential dynamical features of intrinsically disordered α-synuclein (α-syn) site-specifically labeled with thiol-active fluorophores.
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10.1016/J.MOLLIQ.2021.116456
In this article we have investigated the solvation, rotational dynamics and photo physics of diketone derivatives DK-2 and DK-3 in alcohols and alkanes at room temperature through both a time-resolved fluorescence depolarization technique and steady state.
In this article we have investigated the solvation, rotational dynamics and photo physics of diketone derivatives DK-2 and DK-3 in alcohols and alkanes at room temperature through both a time-resolved fluorescence depolarization technique and steady state.
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10.1016/J.JPHOTOCHEM.2019.04.006
Using time-resolved fluorescence depolarization studies, here we report complete reversal of trends in anisotropy decay traces up on increasing fluorophore concentration while traversing a series of solvent mixtures (water and glycerol) with increasing viscosity.
Using time-resolved fluorescence depolarization studies, here we report complete reversal of trends in anisotropy decay traces up on increasing fluorophore concentration while traversing a series of solvent mixtures (water and glycerol) with increasing viscosity.
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10.1016/j.cbpb.2019.05.011
Fluidity of mitochondrial membranes was quantified by fluorescence depolarization for the white-blooded Chaenocephalus aceratus and the red-blooded Notothenia coriiceps.
Fluidity of mitochondrial membranes was quantified by fluorescence depolarization for the white-blooded Chaenocephalus aceratus and the red-blooded Notothenia coriiceps.
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10.1039/C9FD00054B
10 monomers) exciton-phonon correlation length causes ultrafast exciton-site decoherence, which is observable on conformationally disordered chains as fluorescence depolarization.
10 monomers) exciton-phonon correlation length causes ultrafast exciton-site decoherence, which is observable on conformationally disordered chains as fluorescence depolarization.
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10.1021/ACSOMEGA.8B03354
Presented herein is a combined computational and experimental study of the scattering and fluorescence depolarization enhancement induced by light scattering in turbid samples.
Presented herein is a combined computational and experimental study of the scattering and fluorescence depolarization enhancement induced by light scattering in turbid samples.
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10.1021/acs.jpclett.9b01731
Using highly sensitive picosecond time-resolved fluorescence depolarization measurements, we directly capture rapid large-amplitude torsional fluctuations in the extended chains that can control the relay of making-and-breaking of noncovalent intermolecular contacts maintaining the internal fluidity.
Using highly sensitive picosecond time-resolved fluorescence depolarization measurements, we directly capture rapid large-amplitude torsional fluctuations in the extended chains that can control the relay of making-and-breaking of noncovalent intermolecular contacts maintaining the internal fluidity.
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10.1101/621714
Using highly-sensitive picosecond time-resolved fluorescence depolarization measurements, we directly capture rapid large-amplitude torsional fluctuations in the extended chains that can control the relay of making-and-breaking of noncovalent intermolecular contacts maintaining the internal fluidity.
Using highly-sensitive picosecond time-resolved fluorescence depolarization measurements, we directly capture rapid large-amplitude torsional fluctuations in the extended chains that can control the relay of making-and-breaking of noncovalent intermolecular contacts maintaining the internal fluidity.
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10.1021/acs.analchem.9b01803
A polarized anti-Stokes'-shifted, on-resonance, and Stokes'-shifted spectroscopic method is developed for quantifying fluorophore absorption, scattering, one-resonance fluorescence (ORF) cross-section spectra, and scattering and ORF fluorescence depolarization spectra in this wavelength region.
A polarized anti-Stokes'-shifted, on-resonance, and Stokes'-shifted spectroscopic method is developed for quantifying fluorophore absorption, scattering, one-resonance fluorescence (ORF) cross-section spectra, and scattering and ORF fluorescence depolarization spectra in this wavelength region.
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10.1016/j.saa.2019.117326
A thorough mathematical analysis of the fluorescence depolarization results based on the two-step and wobbling in cone model yields critical insight into the complex rotational relaxation dynamics of the bound drug.
A thorough mathematical analysis of the fluorescence depolarization results based on the two-step and wobbling in cone model yields critical insight into the complex rotational relaxation dynamics of the bound drug.
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