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The effect size was small to medium at d = 0.29.
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Glucose and xylose consumptions rates and butyric acid production rates and yields obtained with wheat straw hydrolysate and synthetic medium at 1 d HRT with in situ acid removal by REED are shown in Fig. 4.
Fig. 4 Glucose and xylose consumption rates and butyric acid production rate and yield obtained in the continuous experiments with wheat straw hydrolysate and synthetic medium at 1 d HRT and in situ acid removal by REED with an influent sugar concentration of 54 55 and 34 35 g L−1 glucose and xylose, respectively.
To obtain cells in the exponential phase [ 55], yeast cells were subcultured three times in YPD medium at 5-d intervals.
Therefore, we estimate the effect size at d = 0.5 (medium effect).
First, a yeast culture in synthetic complete medium (FPM) was grown in chemostat mode at D = 0.3 h-1.
These amniotic fluid cells were a fraction of the cells obtained for cytogenetic analysis, and they were grown to confluency in T-12.5 cm flasks for approximate 10 to 14 days in 50% (v/v) AmnioMax C100 combined media (17% AmnioMax C100 Supplement, 83% AmnioMax C100 Basal media) and 50% Chang Medium D, at the Cytogenetics Laboratory of Mount Sinai Hospital.
For example, in E. coli cultures at D above 0.4 h-1 acetate accumulates in the medium [ 32].
Piglets were sacrificed at d 28.
After ATDC5 cells transfected with PxRe reporter gene grew to confluence in the maintenance medium, perfusion cultures were performed by perfusing the chondrogenic medium including D-luciferin at a flow rate of 1.0 mL/h by a peristaltic pump.
Conidia of M. fructicola were collected from 12 d-old cultures grown on modified V-8TM medium at 25°C.
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