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For the first time, nano- and submicron particles of street dust have been separated, weighted, characterized by electronic microscopy, and quantitatively analyzed by ICP-MS (after digestion).
The polyplexes cytotoxicity was determined using [3- 4,5-dimethylthiazol-2-yl -2,5-diphenyltetrazolium bromide] assay and its transfection efficiency was examined qualitatively by fluorescent microscopy and quantitatively by flow cytometery methods.
LMP was monitored qualitatively by fluorescence microscopy and quantitatively by flow cytometry, by measuring the percentage of cells with loss of lysosomal AO red fluorescence.
We investigated the in vitro transfection efficiency of the C20-18, C20-20, and C30-20 linoplexes in retinal cells using a plasmid coding for GFP and assessing its expression qualitatively by fluorescence microscopy and quantitatively by flow cytometry.
Examination of FAP-BKα expressing cells qualitatively by microscopy and quantitatively by flow cytometry showed a substantial and significant decrease in cell surface labeling accompanied by a meager reduction in internal labeling after fsk treatment.
Peroxidase activity (POX) in both inoculated and not inoculated leaves was evaluated qualitatively by transmission light microscopy, and quantitatively by spectrophotometry, exploiting the chromogenic property of TMB that undergoes a change in colour upon oxidation by peroxidase in presence of hydroperoxide [ 29, 30].
Similar(54)
Biofilm formation was confirmed qualitatively by scanning electron microscopy (SEM) and quantitatively by photometrical measurements according to Safranin O staining.
The fiber dispersion state was evaluated qualitatively by scanning electron microscopy (SEM) and quantitatively by the fiber distribution index (FDI).
The cellular uptakes of the DOX-loaded micelles and free DOX · HCl were qualitatively detected by confocal laser scanning microscopy (CLSM) and quantitatively estimated by flow cytometry (FCM) toward RenCa cells.
The nanodispersion of MMT is evaluated qualitatively by X-ray diffraction (XRD) and transmission electronic microscopy (TEM), and quantitatively by solid state nuclear magnetic resonance (NMR).
To compare with our model, we systematically analyze confocal microscopy images, and quantitatively estimate cup variability for the three different conditions using small (1.5 μm radius) and large (3 μm radius) particles.
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