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Endodermal cells are also positive for Nkx2 5 (left lower panel, open arrowhead).
Co-localization between segment 3 RNA and PA protein of the virus encoding PA-GFP was also detected (Fig. 2c, left lower panel).
In the parental TrxR1-YFP clone only a 414 bp product was amplified (Figure 2A, left lower panel).
In contrast, CX3CR1+, CD27+ GC B cells contained IgG+, IgM+, CD95+, Bcl-2+, CD44− cells, with lower proportions of cells expressing Ki-67 or IgD (Fig. 5A, left lower panel).
Western blot data (Fig. 8, left lower panel) indicated that Eda-peptide protected furin from self-degradation as the 55 kDa soluble furin band gradually became more intense as the concentration of Eda-peptide was increased.
Fig. 6 (left lower panel) showed the western blot results using FLAG antibody on the effect of furin-Eda-peptide (50 µM) on furin processing of FLAG-labeled proPDGF-A in CHO cells.
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Data are presented as percentage of increase in diameter (left panels) and changes in mean arterial blood pressure (mm Hg, right panels) induced by CGS21680 (left lower panels).
Representative morphology of distal airspaces shows that increased NE activity on BAL neutrophils is associated with airspace enlargement and destruction in βENaC-Tg mice that is substantially reduced by genetic deletion of NE (left lower panels).
The left lower panels show the residual fringes after fitting the raw data with modeled curves.
Upon TI treatment in the absence of silibinin greater apoptosis 3.98% to 14.99% (Fig. 4B, left lower panels) was observed in HCT116 but not HepG2 (4.35% to 5.48%, Fig. 4B, right lower panels) cells.
Yellow fluorescence detected in the root tip (upper panel) and the first true leaves (lower panel).
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