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The passive film on nuclear-grade stainless steels was evaluated by quantifying its color changes.
The antibacterial activities of EG12 and GWPU were evaluated by quantifying the minimal inhibitory concentration.
The photocatalytic activity was evaluated by quantifying the hydrogen production under UV light irradiation using gas chromatography.
The composition of hECM was evaluated by quantifying the content of sulphated glycosaminoglycans (sGAG), fibronectin and laminin.
The resistance was evaluated by quantifying the decrease of acidification activity during freezing and throughout 8 weeks of storage.
The protective nature of the coating was evaluated by quantifying its effectiveness in protecting the metal particles during oxidative annealing treatments.
Additionally, the pozzolanic activity of nanosilica was evaluated by quantifying the fixation of calcium hydroxide and its impact on the development of the compressive strength.
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Vertical bars indicate standard deviations Fig. 4 Brain expression levels of Bax, Bcl-2, and Bax/Bcl-2 ratios evaluated by immunoblotting, quantified by measuring band intensity with ImageJ, normalized by β-actin expression, and expressed as arbitrary units.
Fig. 2 Brain expression levels of complement factors and complement inhibitors evaluated by immunoblotting, quantified by measuring band intensity with ImageJ, normalized by β-actin expression, and expressed as arbitrary units.*p < 0.05; ***p < 0.001.
The effect of BPA-G on the differentiation of human and 3T3L1 murine preadipocytes was evaluated in vitro by quantifying lipid accumulation and the expression of adipogenic markers.
Subsequently, we evaluated cell migration by quantifying the number of cells in the scratched region at 0, 248 48, and 72 hours after scratching (Fig. 5A).
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