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In vitro treatment with MβCD, which allowed examination of labeling in individual axons, showed there to be a visually obvious but relatively small decrease in labeling intensity across the population of ORN axons.
An examination of labeling after a 2-h BrdU pulse administered at E11.5 reveals a similar labeling index in control (39%) and mutant brains (42%; Fig. 5 J), indicating that cell division rates are unaffected in the absence of Lhx2.
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Examination of labeled cells by flow cytometry and laser scanning confocal microscopy showed that LQ had higher fluorescence intensity due to the cluster formation and their distribution in cytoplasma while TQ were preferentially accumulated at peri-nuclear regions.
Electron microscopic examination of labeled tectoincertal terminals demonstrated that they contain mainly spherical vesicles and have slightly asymmetric to symmetric synaptic densities.
We analyzed the fine anatomical structure through confocal examination of labeled single neurons to determine the arborization patterns of each of the three FruM-positive OA SOG neurons.
Examination of labels on various chocolate powders sold in the United States show that the serving sizes are typically in the range of 15 25 g.
Examination of labeled cells after a 2-h pulse of BrdU administered at E11.5 reveals that the labeling index in control and mutant septum (45% and 47%, respectively) and hem (46%and45%5%, respectively) is similar.
Examination of EYFP labeling at the 14-day time point, however, revealed a dramatic decrease in the labeling index of ABKO acinar cells following regeneration (Fig. 7E I).
The examination of magnetic labeling of tumors by SSB, as shown in Figure 3, indicated that the accumulation of anti-CEA SPIONPs reached the highest level and gradually dissipated to the initial level at approximately the 72nd hour.
Dedifferentiation was assessed by morphologic examination of fluorescently labeled myotubes for signs of cleavage, and by the appearance of myotube-derived (i.e. fluorescently-labeled) mononucleated cells.
(B) SDS-PAGE examination of fractions labelled in (A).
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