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The morphologies and composition of the samples are controlled by adjusting some parameters, including reaction pH, Pb/Bi molar ratio, and temperature.
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The temperature of the samples was controlled from 40 to −196 °C.
The elution behaviors of these samples were controlled by the temperature changes without organic solvents in the mobile phase.
The mass loading of all tested samples was controlled to be ~ 400 μg cm− 2.
The incorporation process of Ca(NO3 2 molecules on blend samples were controlled by chemical and physical mechanisms.
Efficiency of the SLO-treatment in the different samples was controlled by WB developed with anti-GFP mAb (Fig. 2D).
The quality of the samples is controlled by several factors.
The quality of all RNA samples was controlled using an Agilent 2100 Bioanalyzer (Agilent Technologies).
The temperature of the samples was controlled using a Julabo F25/HP thermostatic bath.
Quality of all samples was controlled in a 2100 bioanalyzer (Fig. 1).
Variance in the amount of RNA between samples was controlled for by normalizing to 18S.
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