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Detectors may be nondestructive, whereby sensing does not alter the nature of the solutes, as in the case of light absorption, so they may be collected for further use.
The final pellet was collected for further use.
The obtained complex (MWCNTs-PEG-Mal) was then purified by Millipore ultrafiltration tube (MWCO = 100 kDa) and dried in vacuum at 60 °C and collected for further use.
Cells were seeded at a concentration of 4×10 cells/mL and incubated for 48 h at 37°C, in a humidified atmosphere containing 5% CO2, before being collected for further use.
Each run was performed for 1.5 h, after which the reaction mixtures were centrifuged, the upper lipid layer was collected for analysis and lower glycerol layer including the enzyme was collected for further use.
After separation of the liquid hydrolyzate from the solid residue, the liquid portion was collected for further use and stored at 50°C in an incubation shaker (Infors HT, Bottmingen, Switzerland) to prevent precipitation of high degree of polymerization (DP) xylo-oligomers [ 21].
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The products obtained were collected for further used.
After thermal treatment, the light yellow g-C3N4 powders were collected for further using.
Four fractions, marked as 1, 2, 3, and 4 in Figure 2, were collected for further characterization using the semi-preparative column with a maximal load of 0.3 mg of the isolate per injection.
GC cells and PBMCs were collected separately for further use.
After the solution was cooled to room temperature, NaOH was added to adjust the pH to 4 5, and the precipitated crude [D4] 3 or [C6] 3 was collected for further purification by HPLC using a linear gradient from 100%155 mM NH4OAc to 20%155 mM NH4OAc and 80% CH3CN over 50 min, at 0.7 mL/min.
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