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The introduction of a resting period for thawed cells is known to be advantageous since apoptotic cells die during the resting period, and final dilutions for the assay are based on a more homogenous population of viable cells [ 16, 18].
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The assay was based on the published protocol (Thakur et al., 2015).
This assay is based on the cleavage activity of the light chain.
SOD activity assay was based on the method described by Giannopotitis and Ries ([1977]).
The assay was based on the published protocol (Li et al., 2016).
This assay is based on the TdT-mediated dUTP nick end labeling method (TUNEL method).
This assay is based on the ability of the antioxidant to scavenge the radical cation DPPH.
ABTS radical scavenging assay is based on biamperometric measurements using ABTS+/ABTS redox couple.
The assay was based on the methodology of Benzie and Strain [25].
The assay is based on the reduction of Fe3+ to Fe2+ by AsA.
The SmartRNAplex miRNA detection assay is based on proprietary Firefly hydrogel technology.
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