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Exact(17)
After infusion in 2.3 M sucrose overnight at 4°C, cell blocks were mounted on aluminum pins and frozen in liquid nitrogen.
Five microns width sections from the paraffin blocks were mounted on silane coated slides, deparaffinized for 18 h at 60°C and sequentially immersed in xylene (30 min at 37°C), absolute ethanol, 75 %, 50 %, 25ethanol and water.
Tissue blocks were mounted on glass slides by sequencing.
For sectioning, communities embedded in OCT blocks were mounted on a cryotome.
Tissue sections from TMA blocks were mounted on to slides, deparaffinized with xylene, and dehydrated in a graded ethanol series.
Sections (5μm) from archival formalin-embedded tissue blocks were mounted on the salinized slides, and baked overnight at 60°C.
Similar(43)
Sections 2.5 μm thick from each TMA block were mounted on silanised glass slides.
For immunohistochemical staining freshly cut 3 μm thick sections of the TMA block were mounted on superfrost slides (Menzel Gläser, Braunschweig, Germany).
Ultrathin sections from the donor block were mounted on charged slides permitting the simultaneous screening of tissue from a number of animals with antibodies.
The display unit and heating block were mounted on the withers of the horse with the help of a surcingle and Velcro strips.
Sections (4 μm) from this block were mounted on slides before they were deparaffinised, rehydrated and microwave-treated in target retrieval solution at pH 9.9 (Dako, Glostrup, Denmark), before being processed with an automated immunostainer (Techmate 500; Dako, Copenhagen, Denmark), using the Envision software (Dako, Glostrup, Denmark).
More suggestions(16)
blocks were cooled on
blocks were selected on
blocks were collected on
blocks were detected on
blocks were carved on
blocks were surveyed on
blocks were loaded on
blocks were raised on
blocks were deposited on
blocks were maintained on
blocks were performed on
blocks were sectioned on
blocks were solidified on
blocks were stacked on
blocks were frozen on
blocks were reassembled on
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