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The scanning electron microscopy results also demonstrated that all bacteria treated with peptide L12D/L20D showed significant membrane damaging effect.
The electron microscopy results also corresponded to a diagnosis of TG.
Fluorescent microscopy results also suggested that zinc ferrite NPs treated cells show higher intensity of green fluoresce of DCF dye (ROS generation marker) than those of the control cells (Fig. 4b).
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The confocal microscopy result also showed externalization of phosphotydle serine on the surface of DTE treated U937 cells which support the earlier evident of apoptosis induction.
Immunoelectron microscopy results are also consistent with this localization [11], [20], [21].
Fluorescence microscopy results were also according to the quantitative data.
Microscopy results were also used if PCR result was negative (5 P. knowlesi infections and 1 P. knowlesi/P. falciparum infection) or if PCR result was positive for Plasmodium spp. (7 P. knowlesi infections).
Although only partially aligned, the pattern shown in Figure 2 D indicates that fundamentally identical results were obtained, confirming the electron microscopy results and also revealing a system of small angle (SAXS) rings around the beam‐stop which is consistent with previous investigations.
Transmission electron microscopy (TEM) results also showed the evidence of supplementary reaction between Co and WC/W2C to form Co3W3C during the SPS processing.
Scanning electron microscopy (SEM) and XRD results also suggest improvements in strengths of SCPs due to calcite (calcium carbonate).
Scanning electron microscopy and energy dispersive spectrometry results also reveal that SF and GO are homogeneous blended together.
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