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Nematode DNA was quantified and used with a standard curve that was established with known amounts of DNA per nematodes.
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Nonlinear regression analysis of log-transformed concentration values was used to construct a standard curve with standard absorbance readings.
Kit standards were used to obtain a standard curve.
Concentrations were determined using a standard curve with high- and low-level control subjects.
Each experiment was set up using a standard curve, with each quantitative point represented in triplicate.
The total flavonoid content was determined using a standard curve with catechin (0 100 mg/L) as the standard.
TPC values were determined using a standard curve prepared with Gallic acid (GA).
Concentrations were calculated by using a standard curve generated with specific standards provided by the manufacturer.
Concentrations were calculated using a standard curve generated with specific standards provided by the manufacturer.
NS3 levels were estimated using a standard curve obtained with dilutions of recombinant NS3 (fig 1D).
The amount of H2O2 was calculated using a standard curve prepared with known concentrations of H2O2.
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