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Samples from the same individuals and from individuals with the same measuring point or treatment were allocated on different plates, in order to minimize a between-plate effect.
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A practical solution is to apply normalization techniques prior to the statistical analysis to minimize between-plate variation.
We used video animated males to minimize an effect of behavioural differences between ecotypes.
To minimize possible biological differences between plate-attached and suspension specimens, isolated mouse liver mitochondria respiring uncoupled on succinate (10 mM) in the presence of rotenone (1 μM), cytochrome c (10 μM) and FCCP (0.5 μM/no BSA) were used.
Furthermore, to minimize plate-to-plate variability between real-time PCR assays, the signal from LPS-treated RNA was normalized to the signal from PBS-treated RNA from the same subject (at the same time points), assayed together on the same plate.
The backflow was minimized with narrow plates between the cells.
The majority of the test specimens were initially fabricated as larger loaf specimens, to achieve proper fiber directionality in the out-of-plane direction, and then cut and trimmed, with steel brush platens used for loading to minimize friction between the testing machine and the plate specimens.
To minimize butanol evaporation, plates were sealed with a gas-impermeable film, thereby reducing evaporation to a maximum of 10% after 48 h.
From each ECG recording, a 1-min period was analysed, to minimize variations between beats.
All four dilutions against a single bacterial lysate were run on the same plate to minimize plate-to-plate variations.
Each subject's samples were prepared on the same plate to minimize inter-plate variability.
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CEO of Professional Science Editing for Scientists @ prosciediting.com