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(Plasma concentration is corrected for metabolites).
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Experimental conditions were changed directly in the cells by adding concentrated solutions of potassium chloride and the final sample concentration was corrected for the volume increase.
The ammonia concentration was corrected for the shifted ammonia-ammonium equilibrium (see experimental section, equation 3).
DMSO concentration was corrected to 1% in all wells.
The dialysate creatinine concentration was corrected for interference by glucose according to our laboratory standards.
Urinary THP concentration was corrected according to the urinary creatinine level.
The biomass concentration was corrected for evaporation using C x, corrected = C x, oberved V observed V without evaporation.
After centrifugation, supernatant was transferred to a fresh tube and protein concentration was corrected to 1 μg/μL.
The extinction coefficient (ε592 = 9,000 M−1 cm−1), referred to total powder concentration, was corrected taking into account the purity.
Each PAH concentration was corrected using the recovery rate of the surrogate standard and expressed on a dry-weight basis.
Hindered settling due to high solids concentration was corrected for using the methodology described by (Tustian et al., 2007).
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