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All the synthesized compounds were assayed to evaluate their ability to block acrolein-mediated activation of native human and rat TRPA1 channels employing a fluorometric calcium imaging assay.
After evaluating the mineralization activity of scaffolds in osteogenic differentiation of MC3T3- E1 cells, the actin cytoskeleton organization of scaffold seeded with cells is also assayed to evaluate the effect of scaffolds on osteogenesis.
After investigating the influence factors of the CEC monolithic columns, four flavonoids (i.e., Rutin, Quercetin, Kaempferol, and Quercitrin) were separated and assayed to evaluate this monolithic column with CEC method.
Corticosterone levels were assayed to evaluate the impact of social partners' change on the females' physiology.
Plasma aminotransferases were assayed to evaluate hepatotoxicity in Coilia nasusu.
DCF fluorescence was, therefore, assayed to evaluate the extent of amyloid-β-induced oxidative stress in the low-glucose cultures.
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The colorimetric assays to evaluate the aforementioned enzymes were conducted following the manufacturer's protocol (Quibasa, Bioclin, Brazil).
In light of these limitations and uncertainties, we used all three serological assays to evaluate the humoral response induced by the plant-made H5 VLP vaccine in humans.
We established assays to evaluate BMTP-11 in vitro, in vivo, and ex vivo.
Therefore, we performed xenograft formation assays to evaluate the effect of miR-144 overexpression on tumorigenicity.
We performed radio-receptor binding, real-time RT-PCR, multiplexed IHC, and ISH assays to evaluate receptor expression.
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