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(A) Direct fluorescence image of mouse lung transplanted with 1 × 106 GFP-labeled SOX9+ BCs under dissection microscope.
Twenty five amphistomes were incubated and the motility of control and test group was observed under dissection microscope at a regular time interval of (0, 10, 15, 30 and 60) min respectively.
The vertebrae were counted under dissection microscope after the whole vertebral column from one side was exposed with the aid of a scalpel.
Same stage leaves were brushed in imbibition buffer to remove trichomes and checked under dissection microscope.
We examined the collected feathers of these ten birds under dissection microscope (×20) to score potential ectoparasites (presumably feather lice).
After 25 d of incubation, colonies were stained with 0.005% crystal violet overnight and were counted under dissection microscope.
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The whole aortas (from the sinotubular junction to aortic bifurcation) were dissected out under the dissection microscope and rinsed with saline to remove the blood.
They were dissected manually under a dissection microscope using a fine glass needle to separate eight mesomeres.
The mouse forebrains around the implantation site were harvested under a dissection microscope and the dissected samples were homogenised.
Brains were dissected on ice under a dissection microscope to remove all traces of the optic lobe and then stored at −80°C.
Cortices were dissected from embryonic brains under a dissection microscope, and placed in Hanks Balanced Salt Solution (HBSS) media (Invitrogen) on ice.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com