Introduction to Fluorescence Time

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Fluorescence Time sentence examples within live cell imaging

live cell imaging

Here, we determine the siRNA-induced fold change in mRNA degradation kinetics from single-cell fluorescence time-courses obtained using live-cell imaging on single-cell arrays (LISCA).

Single-Cell Kinetics of siRNA-Mediated mRNA Degradation.

live cell imaging

Here, we describe a method to extract event times from fluorescence time traces of cell death-related markers in automated live-cell imaging on single-cell arrays (LISCA) using epithelial A549 lung and Huh7 liver cancer cells as a model system.

A high-throughput microscopy method for single-cell analysis of event-time correlations in nanoparticle-induced cell death

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Fluorescence Time sentence examples within Dimensional Fluorescence Time

Dimensional Fluorescence Time

Three-dimensional fluorescence time-lapse imaging of structural, cellular and sub-cellular processes in the beating heart is an increasingly achievable goal using the latest imaging and computational techniques.

Hybrid optical gating for long-term 3D time-lapse imaging of the beating embryonic zebrafish heart

Dimensional Fluorescence Time

Three-dimensional fluorescence time-lapse imaging of the beating heart is extremely challenging, due to the heart’s constant motion and a need to avoid pharmacological or phototoxic damage.

Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart

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Fluorescence Time sentence examples within Reporter Fluorescence Time

Reporter Fluorescence Time

By fitting a translation-maturation model to hundreds of individual eGFP reporter fluorescence time courses, the protein expression onset times and the expression rates after transfection are determined.

Correlation of mRNA delivery timing and protein expression in lipid-based transfection.

Reporter Fluorescence Time

By fitting a translation-maturation model to hundreds of individual eGFP reporter fluorescence time courses, the protein expression onset times and the expression rates after transfection are determined.

Correlation of mRNA delivery timing and protein expression in lipid-based transfection

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Fluorescence Time sentence examples within fluorescence time trace

fluorescence time trace

Here, we describe a method to extract event times from fluorescence time traces of cell death-related markers in automated live-cell imaging on single-cell arrays (LISCA) using epithelial A549 lung and Huh7 liver cancer cells as a model system.

A high-throughput microscopy method for single-cell analysis of event-time correlations in nanoparticle-induced cell death

fluorescence time trace

Here, we describe a method to extract event times from fluorescence time traces of cell death-related markers in automated live-cell imaging on single-cell arrays (LISCA) using epithelial A549 lung and Huh7 liver cancer cells as a model system.

A high-throughput microscopy method for single-cell analysis of event-time correlations in nanoparticle-induced cell death.

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Fluorescence Time sentence examples within fluorescence time course

fluorescence time course

By fitting a translation-maturation model to hundreds of individual eGFP reporter fluorescence time courses, the protein expression onset times and the expression rates after transfection are determined.

Correlation of mRNA delivery timing and protein expression in lipid-based transfection.

fluorescence time course

To meet this need, custom ImageJ plugins were written to array 4D data on a computer screen, identify structures of interest, edit the data to isolate individual structures, quantify the fluorescence time courses, and make movies of the projected Z-stacks.

4D Microscopy of Yeast.

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10.2152/jmi.66.65

The relationship between the fluorescence time (FT) of the oral stump and AL was investigated retrospectively.

Usefulness of blood flow evaluation by indocyanine green fluorescence system in laparoscopic anterior resection.

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10.1007/s11120-019-00663-4

The fluorescence time-course depends on the leaf growth conditions and actinic light quality.

Slow induction of chlorophyll a fluorescence excited by blue and red light in Tradescantia leaves acclimated to high and low light

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10.1039/c9pp00108e

The mechanism of Zn(ii) detection has been delineated using electrospray ionization-mass spectrometry (ESI-MS), Fourier-transform infrared spectroscopy (FTIR) and fluorescence time resolved studies coupled with theoretical calculations.

Evaluating the merit of a diethylamino coumarin-derived thiosemicarbazone as an intramolecular charge transfer probe: efficient Zn(ii) mediated emission swing from green to yellow.

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10.3390/cells8060582

Using microfluidics and fluorescence time-lapse microscopy, we studied how yeast responds to short, pulsed hyperosmotic stresses at the single-cell level by analyzing the dynamic behavior of the stress-responsive STL1 promoter (pSTL1) fused to a fluorescent reporter.

Hyperosmotic Stress Response Memory is Modulated by Gene Positioning in Yeast

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10.1016/J.JMS.2019.05.006

In the supersonic jet setup (collision-free), fluorescence time-traces at selected wavelength regions are analyzed.

One-color (212–220 nm) resonantly-enhanced (S1–S0) multi-photon dissociation of acetylene

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10.1002/smll.201804576

Here, the response of murine embryonic stem cells to different growth media, 2i and N2B27, is studied, showing that the exit from pluripotency can be monitored by fluorescence time-lapse microscopy, by immunostaining and by reverse-transcription and quantitative PCR (RT-qPCR).

Long-Term Perfusion Culture of Monoclonal Embryonic Stem Cells in 3D Hydrogel Beads for Continuous Optical Analysis of Differentiation.

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10.3791/58618

To meet this need, custom ImageJ plugins were written to array 4D data on a computer screen, identify structures of interest, edit the data to isolate individual structures, quantify the fluorescence time courses, and make movies of the projected Z-stacks.

4D Microscopy of Yeast.

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10.1101/749739

Fluorescence time traces are used to report on dynamical properties of molecules.

Pitching single-focus confocal data analysis one photon at a time with Bayesian nonparametrics

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10.1101/625756

Using microfluidics and fluorescence time-lapse microscopy, we studied how yeasts respond to short-pulsed hyperosmotic stresses at the single-cell level by analyzing the dynamical behavior of the stress responsive STL1 promoter fused to a fluorescent reporter.

The memory of hyperosmotic stress response in yeast is modulated by gene-positioning

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Keywords related to Fluorescence

Fluorescence Time
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What is/are Fluorescence Time?

Fluorescence Time - The relationship between the fluorescence time (FT) of the oral stump and AL was investigated retrospectively. [1] The fluorescence time-course depends on the leaf growth conditions and actinic light quality. [2] The mechanism of Zn(ii) detection has been delineated using electrospray ionization-mass spectrometry (ESI-MS), Fourier-transform infrared spectroscopy (FTIR) and fluorescence time resolved studies coupled with theoretical calculations. [3] Using microfluidics and fluorescence time-lapse microscopy, we studied how yeast responds to short, pulsed hyperosmotic stresses at the single-cell level by analyzing the dynamic behavior of the stress-responsive STL1 promoter (pSTL1) fused to a fluorescent reporter. [4] In the supersonic jet setup (collision-free), fluorescence time-traces at selected wavelength regions are analyzed. [5] Here, the response of murine embryonic stem cells to different growth media, 2i and N2B27, is studied, showing that the exit from pluripotency can be monitored by fluorescence time-lapse microscopy, by immunostaining and by reverse-transcription and quantitative PCR (RT-qPCR). [6] To meet this need, custom ImageJ plugins were written to array 4D data on a computer screen, identify structures of interest, edit the data to isolate individual structures, quantify the fluorescence time courses, and make movies of the projected Z-stacks. [7] Fluorescence time traces are used to report on dynamical properties of molecules. [8] Using microfluidics and fluorescence time-lapse microscopy, we studied how yeasts respond to short-pulsed hyperosmotic stresses at the single-cell level by analyzing the dynamical behavior of the stress responsive STL1 promoter fused to a fluorescent reporter. [9]

live cell imaging

Here, we determine the siRNA-induced fold change in mRNA degradation kinetics from single-cell fluorescence time-courses obtained using live-cell imaging on single-cell arrays (LISCA). [1] Here, we describe a method to extract event times from fluorescence time traces of cell death-related markers in automated live-cell imaging on single-cell arrays (LISCA) using epithelial A549 lung and Huh7 liver cancer cells as a model system. [2] Here, we describe a method to extract event times from fluorescence time traces of cell death-related markers in automated live-cell imaging on single-cell arrays (LISCA) using epithelial A549 lung and Huh7 liver cancer cells as a model system. [3]

Dimensional Fluorescence Time

Three-dimensional fluorescence time-lapse imaging of structural, cellular and sub-cellular processes in the beating heart is an increasingly achievable goal using the latest imaging and computational techniques. [1] Three-dimensional fluorescence time-lapse imaging of the beating heart is extremely challenging, due to the heart’s constant motion and a need to avoid pharmacological or phototoxic damage. [2]

Reporter Fluorescence Time

By fitting a translation-maturation model to hundreds of individual eGFP reporter fluorescence time courses, the protein expression onset times and the expression rates after transfection are determined. [1] By fitting a translation-maturation model to hundreds of individual eGFP reporter fluorescence time courses, the protein expression onset times and the expression rates after transfection are determined. [2]

fluorescence time trace

Here, we describe a method to extract event times from fluorescence time traces of cell death-related markers in automated live-cell imaging on single-cell arrays (LISCA) using epithelial A549 lung and Huh7 liver cancer cells as a model system. [1] Here, we describe a method to extract event times from fluorescence time traces of cell death-related markers in automated live-cell imaging on single-cell arrays (LISCA) using epithelial A549 lung and Huh7 liver cancer cells as a model system. [2] Fluorescence time traces are used to report on dynamical properties of molecules. [3]

fluorescence time course

By fitting a translation-maturation model to hundreds of individual eGFP reporter fluorescence time courses, the protein expression onset times and the expression rates after transfection are determined. [1] To meet this need, custom ImageJ plugins were written to array 4D data on a computer screen, identify structures of interest, edit the data to isolate individual structures, quantify the fluorescence time courses, and make movies of the projected Z-stacks. [2] By fitting a translation-maturation model to hundreds of individual eGFP reporter fluorescence time courses, the protein expression onset times and the expression rates after transfection are determined. [3]