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(F) Merged image of (D) and (E).
BF, bright field; GFP, green fluorescent protein channel; Mer, merged image of each channel.
Figure 3 Epifluorescence microscopy of human astrocytoma cells exposed to CNT/DNA-Cy5 conjugates:a phase contrast image;b merged image of the phase contrast and Cy5 images c CNT/DNA-Cy5 (red) fluorescence image; andd merged image of the CNT/DNA-Cy5 and DAPI-stained cells (blue).
(a) the distribution of nuclei (blue), (b) the distribution of TiO2 nanoparticles (red), (c) DIC micrograph, and (d) the merged image of (a), (b), and (c), in which the violet color denotes the co-localization of TiO2 nanoparticles with nuclei.
(a) The distribution of Golgi complexes (green), (b) the distribution of TiO2 nanoparticles (red), (c) differential interference contrast (DIC) micrograph, and (d) the merged image of (a), (b), and (c), in which the yellow color denotes the co-localization of TiO2 nanoparticles with Golgi bodies.
Figure 1b is Differential Interference Contrast (DIC) image and Fig. 1c is merged image of Fig. 1a and b.
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b, OsRUS1 1-160aa)::GFP. Individual and merged images of GFP and chlorophyll autofluorescence (Chl), and brightfield (Bright) images of protoplasts are shown.
DAPI stained, GFP, bright field and merged images of onion epidermal cells expressing 35S::GFP as a control (a-d) and 35S::dep-GFP (e-h).
Figure 9 shows DAPI, RB, and merged images of HeLa cells incubated with RBFe3O4@SiO2 (20 μg mL-1, control) and RBFe3O4@SiO2-OCMCS-FA (20 μg mL-1) for 2 h.
Single channel and merged images of SPB.
Single channel and merged images of the SPB region(s).
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com