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The TCID50 per milliliter for each sample at each time point was calculated by using the Spearman-Karber method (11 ).
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The limits of detection (LODs) were in the low nanogram per milliliter range for each phthalate metabolite.
Adjusted mean serum f-DNA concentrations were 41.2 genomic equivalents (GE) per milliliter for the Down syndrome cases and 24.2 GE/mL for the euploid controls (P =.002).
DX-88 or aprotinin was added to blood at 200 and 800 kallikrein inhibitory units (KIU) per milliliter for aprotinin, and at 1.1, 2.2, or 8.8 μg/ml for DX-88.
The results were expressed as picograms per milliliter for E2.
Densitometry results were analyzed and concentrations of antigen levels were calculated in micrograms per milliliter for NanA and milligrams per milliliter for Ply per CSF sample.
From the prepared microbial solutions, other dilutions with sterile physiological solution were prepared to give a final concentration of 10 colony- forming units (CFU) per milliliter for bacteria and 2 × 10 spores per milliliter for yeasts.
From the prepared microbial solutions, other dilutions with sterile physiological solution were prepared to give a final concentration of 10 colony- forming units (CFU) per milliliter for bacteria and 2 × 10 spores per milliliter for yeasts [ 10].
Then, the result was compared to the quantitative culture with a threshold at 104 colony-forming units per milliliter for bronchoalveolar lavage and 103 colony-forming units per milliliter for minibronchoalveolar lavage.
Results are given in gene copies (gc) per milliliter for water samples or per two hands for HRs.
Cells were counted at the time of collection to quantify the concentration in picograms per milliliter for 1 × 106 cells.
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