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Flow cytometry, western blot, and fluorescence microscopy analysis were employed to investigate the apoptosis-related proteins and the BRAF signaling.
Scanning electron and confocal microscopy analysis were used to study cell adhesion and proliferation at the scaffold surface and within their structure.
Atomic force microscopy (AFM) and optical microscopy analysis were used to corroborate the topological changes of the modified dendronized side of the ChPW film.
X-ray diffraction, scanning electron microscopy, field emission scanning electron microscopy and transmission electron microscopy analysis were performed in order to give information on the crystal phase and structure of both TiO2 coatings and size of particles.
The samples for transmission electron microscopy analysis were prepared by ultra cryo-microtomy using aLeica Ultracut UCT (Wien, Austria).
Total viable count (TVC) and epifluorescence microscopy analysis were studied to evaluate antimicrobial efficiency of ZrO2 and Ag ZrO2 composite coatings using gram negative (gram −ve) Escherichia coli (E.coli) and gram positive (gram +ve) Staphylococcus aureus (S.aureus).
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Confocal microscopy analysis was applied to detect and localize insulin protein in the human primary visceral preadipocytes.
Confocal microscopy analysis was used to localize Insulin and Glucagon in insulin dependent diabetes mellitus (IDDM) and control rats.
From A to F, confocal microscopy analysis was applied to detect and localize insulin protein in the human primary visceral adipocytes.
Scanning electron microscopy analysis was used to characterise the as-grown films for morphology and crystallinity.
Microscopy analysis is developed for determing whether flexural or inter-laminar shear failure modes are obtained experimentally.
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