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The present work proposes an analytical procedure to determine sulfathiazole in milk by using molecular fluorescence spectroscopy.
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We do this by using molecular markers.
Using molecular probes and fluorescence endoscopy, the molecular signature of cells can be detection in real-time visualization with advanced targeted molecular imaging techniques [ 3].
By using bi-molecular fluorescence complementation, Pu et al. (2011) identified several interactions of LD-resident proteins with peroxisomal and mitochondrial proteins, indicating their direct physical interaction.
By using fluorescence technique, molecular interaction between mesogenic moieties of liquid crystal polymer has been proved to show various patterns of changes during phase transition processes.
To explore the mechanism of TRIS-based separation of 1-propanol/2-propanol from their aqueous solutions, the interactions between different pairs of molecules were also investigated by using fluorescence analysis and Molecular Dynamic (MD) simulation.
Cao et al. [ 59] investigated the interactions between polyamidoamine-C (a dendrimers) and curcumin by using fluorescence spectroscopy and molecular modeling methods.
The fluorescence signal from the adherent cells was measured by using a fluorescence plate reader (FLEXstation™, Molecular Devices) at an excitation wavelength of 494 nm and an emission wavelength of 517 nm.
MitoSOX™ Red has excitation/emission maxima of approximately 510/580 nm and the fluorescence was measured by using the fluorescence plate reader Softmax Pro 5 (Molecular Devices).
Activity of proteases was verified by using a standard fluorescence casein based assay (Molecular Probes).
More recent work with an orthotopic mouse brain tumor McCann, et al. successfully applied fluorescent molecular tomographic imaging to monitor protease activity in tumor by using protease activatable fluorescence, ProSense680 (peak light emission at 680 nm).
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