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From the results observed, we conclude that the percentage formation of triangularly shaped AuNPs increased with decreasing the reaction temperature, while the percentage formation of spherically shaped particles increased with increasing the reaction temperature (Table 1), which can be explained by the higher reactivity of the detergent at a higher temperature.
The maximum percent conversion of 7-DHC (> 20%) and percentage formation of previtamin D3 (> 18%) occurred from December to July with exception of the month of January (7-DHC-18% and previtamin D3 -12.9%) and March 7-DHC-17.3 7-DHC-17.3 7-DHC-17.33.5%) (Figs. 3 and 4).
The percentage formation was calculated as the number of 4',6-diamidino-2-phenylindole (DAPI -positive nuclei in myotubes (positive cells) DAPI -positive total nuclei of nucleinin the area, and the obtained fusion index ranged fromyotubes 90% (Additional file 1a).
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The results demonstrated that by increasing the n-butanol percentage, soot formation was suppressed.
Percentage complex formation was plotted against [protein]/[DNA].
Percentage appressorium formation was determined by counting the number of germinated conidia which had produced an appressorium.
CD24+ cells formed relatively high numbers of tumorspheres, which were counted under a light microscope, and the percentage tumorsphere formation efficiency (TFE) was calculated (Fig. 2b).
Proliferation rates and percentage tumorsphere formation efficiency (TFE) of CD24− cell extracted from CD24− developed tumors and CD24− and CD24+ cells extracted from CD24+ developed tumors were compared.
All parameters were calculated and expressed according to standard formulas and nomenclatures (27): mineral apposition rate (micrometers per day), mineralizing surface per bone surface (percentage), bone formation rate (cubic micrometers per square micrometer per day).
Dauers and normal larvae were scored 72 hr after the midpoint of the egg lay and the percentage dauer formation was calculated by dividing the number of dauer larvae by the total number of offspring.
Percentage complex formation was plotted as a function of protein concentrations and fitted to the Hill equation: f = f max ([ Ku ] n / K d n ) / (1 + ([ Ku ] ) n / K d n ) where [Ku] is the protein concentration, f is the fractional saturation, Kd reflects the apparent equilibrium dissociation constant and n is the Hill coefficient.
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