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After completing the block construction, four micrometer sections of the resulting tumor tissue microarray block were cut for further analysis.
After completing the block construction, four micrometer sections of the resulting tumour tissue microarray block were cut for further analysis.
After completing the block construction, 4 μm sections of the resulting tumour TMA block were cut for further analysis.
After completing block construction, 4 µm sections of the resulting tumor TMA block were cut for further analysis.
After the block construction was completed, 4.0-μm sections of the resulting tumour tissue microarray block were cut for further analysis.
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Using a water-cooled-wheel diamond saw, the bone/implant specimen blocks were cut into 2 transverse blocks: a 3-mm thick block of the outermost part of the specimen block was cut and returned to the freezer for mechanical testing and a 6-mm thick block of the innermost part of the specimen block was cut for histomorphometrical analysis.
Two-micrometre sections of the TMA blocks were cut for further analysis.
Consecutive 3 μm sections from each TMA block and the six whole tissue blocks were cut for processing of FISH.
5 μm serial sections from routinely formalin-fixed paraffin-embedded blocks were cut for each case, and one section stained with haematoxylin-eosin (H.E).
Serial sections (4 μm) from formalin-fixed, paraffin-embedded blocks were cut for each case, and one section stained with H&E was used to confirm the histopathological diagnosis.
Paraffin sections of 5 μm were cut from each piece and stained with hematoxylin and eosin (H&E) for histological examination and from same paraffin blocks, sections were cut for immunohistostainings.
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