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Temporal resolution was high (5 min), allowing the study of the short-term dynamics of the interception process.
The hydrogel bound promptly to phosphorus, reducing the phosphorus content 78% within 5 min. The viscous hydrogel settled to the bottom of the container within 10 min allowing the supernatant to be easily decanted.
As a result, the fluorescence quenching by Hg2+ was completed almost within 1 min, allowing the rapid detection of Hg2+.
Briefly, in the first step, 50 μL of patient's serum is incubated with the solid phase (polystyrene bead) for 30 min, allowing the TRAbs in the sample to bind through one arm of the capture receptor.
After 20 min of uptake, PET scans were started for a total duration of 110 min allowing the reconstructions of PET frames of 30 ± 10 min, 60 ± 10 min and 120 ± 10 min of uptake.
Using this HPLC method, the simultaneous separation of sorafenib and nucleolipids was achieved in 12 min, allowing the individual quantization of compounds in SLNs (Additional file 1: Figure SI1 4).
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Baking in convection oven at 250 °C for 45 min allowed the full consolidation of the composite coatings.
The high temporal resolution of GROMOS (30 min) allows the analysis of short-term fluctuations.
Continuous heating at 310°C for 10 min allowed the QDs to emit green color of fluorescence.
Preference test durations of 15 min allowed the animals time to interact with the feeding tubes, but typically not enough time to empty them.
As shown in Fig. 3E and F, treatment with EtOH NaOH for 3.5 or 5 min allowed the microspheres to fuse.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com