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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).
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In permanent magnet based side wall flowmeter (SWFM), a permanent magnet block is mounted on one side of the large pipe and the magnetic field produced by the magnet penetrates through the pipe and interacts with the flowing sodium and induces an electro motive force (emf) proportional to the flow.
The die block is mounted on a table while a vertical-spindle milling machine with end cutters is used to shape the die.
Briefly, the resin-embedded tissue block was mounted on a high-precision three-axis stage, which, together with a confocal laser scanning microscope, was used to acquire extended images at a series of focal planes from the surface of the block to a depth of 35 μm.
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.
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