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Its viability was assessed using the Cell Titer 96 aqueous one solution assay (Promega, Madison, WI).
Good agreement is demonstrated between rates measured from the solution assay data and those calculated from mineralogy using kinetic databases.
Similarly, Kim et al. [87] demonstrated the use of time-resolved fluorescence measurements to study the enhanced FRET efficiency and increased fluorescent lifetime of immobilized quantum dots on a paper platform in comparison to a solution assay.
To enumerate the cell growth on the PU films and PU-MWNT composite films, cell proliferations were carried out using cellTiter 96 aqueous one solution assay after being cultured for 24, 48 and 72 h (Fig. 4p).
Cell proliferations were quantified using a CellTiter 96 aqueous one solution assay (Promega, USA) which contained tetrazolium compound [3- 4,5-dimethylthiazol-2-yl -5- 3-carboxymethoxyphenyl -2- 4-sulphonyl -2H tetrazolium, inner salts; MTS(a)] with electron coupling reagent (phenazine ethosulfate).
To determine the hemolymph Mg2+ concentration using a solution assay, we adapted a procedure described previously [28].
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Methods to estimate ANRnc, based on silicate mineralogy and solution assays from long-term column leach tests, are compared.
We examined these MBs by solution assays and established their specificity using NPPA-overexpressing CHO cells as well as hPSC-CMs.
To further confirm the oligomerization of Uch37 in solution, assays based on fluorescence resonance energy transfer (FRET) were used to monitor both the oligomers of Uch37 in solution and their de-oligomerization by Rpn13C.
Midgut samples were tested for trypsin-like activity in solution assays using a specific substrate.
For TRAP solution assays, cells were fixed with 10% formalin, permeabilized with methanol/acetone (1∶1), dried, and then incubated with TRAP substrate solution for 30 minutes at room temperature.
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