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For growth, mycelia plugs of 3 mm ×3 mm were transferred from 7-day-old CM plates and inoculated on fresh medium (CM, MM, V8, OMA, and RTC) followed by incubation at 28°C with a 12 hour interval photophase.
Two tissue cores with a diameter of 2 mm were transferred from each donor block to the recipient TMA block.
The transformed hygromycin-resistant regenerated shoots about 2 to 3 mm were transferred to β-estradiol induction medium without hygromycin to induce marker excision.
Compounds (8 concentrations, 3 fold dilutions starting at 10 mM) were transferred via pin tool at 300 nL, giving final compound concentrations from 100 μM to 15 nM.
The hygromycin-resistant shoots at about 2 3 mm were transferred onto β-estradiol induction medium without hygromycin to induce marker excision.
Per patient, three tumour tissue cores of size 0.6 mm were transferred to a recipient paraffin block using a custom-made precision instrument.
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Mechanical vibration having resonance frequency of 300 Hz and amplitude of 0.5 mm was transferred to the molten weld pool of 6 mm thick mild steel butt-welded joints during the welding operation.
A weight of 500 mg of air-dried sample (<2 mm) was transferred into the pre-weighted china crucible.
Afterwards a focal female (36.4 ± 1.1 mm) was transferred into the central compartment.
Two fragments of a previous crop in 2% WA of D. flagrans, A. musiformis, C. rosea, and T. esau, with approximately 4 mm being transferred alone or associated with other fungi to Petri dishes of 600 × 15 mm (08 replicates) containing 10 mL of 2% WA culture medium, were maintained at room temperature and protected from light for 7 days.
Two fragments of a previous crop in 2% WA of D. flagrans, A. musiformis, C. rosea, and T. esau, with approximately 4 mm being transferred alone or in association with other fungi to Petri dishes of 100 × 15 mm (06 replicates) containing 20 mL of 2% WhA culture medium, were maintained at room temperature and protected from light.
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