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IGF1R cell-based assays were based on established procedures (Liu et al., 2012).
The DPPH-scavenging and ABTS+-scavenging assays were based on previous reports [13].
The CA activity assays were based on methods from Sundaram et al. [27] and Fasseas et al. [4] with some modifications.
The treatment assays were based on different types of biostimulants, such as a slow or fast-release fertilizer, combined with commercial surfactants.
These specific and sensitive Real-Time PCR assays were based on the quantification of the copy number of the gene that encodes the alpha subunit of the PAH-ring hydroxylating dioxygenases (PAH-RHDα), involved in the initial step of the aerobic metabolism of PAH.
Assays were based on the reaction of transglutaminase with a cadaverine coated 96-well plate.
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Most protein assays are based on recognition of protein by one aptamer.
The statistics for the cell viability assays was based on mixed design ANOVA model.
The design of these assays is based on immunoluminometric assays described previously [20], [21].
These assays are based on completely different principles.
FFA and TG assays are based on enzymatic reactions.
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