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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).
Both electron and confocal microscopy of human gastric biopsies or cultured epithelial cells clearly separated PaCS from VacA-storing vacuoles and phagosomes, despite their common toxin content.
(MOV 18,900 kb) ESM Video 2 Combined bioluminescence fluorescence time-lapse microscopy of human islet cells.
(MOV 22,300 kb) ESM Video 3 Combined bioluminescence fluorescence time-lapse microscopy of human islet cells: close-up.
Confocal microscopy of human frozen LN sections overlaid with fluorescent gp120 and immunostained for the indicated markers.
In addition, immunofluorescence microscopy of human cell lines over-expressing NP_219484, NP_848545, AAK25825/NP_079514, NP_115683, AAP34400.1/JC5707 and NP_056520 has detected subcellular localization of the corresponding proteins.
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Here we determined the cryo-electron microscopy structure of human mTORC1 at 4.4 Å resolution.
Fluorescence microscopy images of human mesenchymal stem cells cultured on 1D and 2D structures demonstrate the short term biocompatibility of the ablated surfaces.
Microscopy image of human genomic DNA deposited from a droplet containing 200 pg of material.
The cell density results obtained using the proposed novel approach correlate well with previous work on computerized keratocyte cell counting from confocal microscopy images of human cornea.
Electron microscopy examination of human NK cells interacting with target cells expressing a ligand for the inhibitory receptor KIR2DL1 revealed the presence of wide and narrow regions between the apposing membranes, and accumulation of the ligand in the narrow regions, as predicted by the kinetic-segregation model 26.
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