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SOD activity assay was based on the method described by Giannopotitis and Ries ([1977]).
The assay was based on the published protocol (Thakur et al., 2015).
The assay was based on the methodology of Benzie and Strain [25].
The assay was based on the published protocol (Li et al., 2016).
The assay was based on a set of four primers matching the specific region of the CChMVd genome.
The assay was based on the competition between a quantum dots labeled CEA and analyte CEA using concanavalin A (Con A) as the recognition element.
The biotoxicity assay was based on the respiratory activity of E. coli cells estimated by the oxidation current of microbially reduced benzoquinone.
The assay was based on the hydrolysis of N-hippuryl-His-Leu hydrate (HHL) by the angiotensin-converting enzyme as described by Cushman and Cheung [18].
EG activity assay was based on the ability of catalyzing the hydrolysis of standard CMC-Na to reducing sugar (Dashtban et al. 2010).
SOD activity assay was based on the method of Beauchamp and Fridovich ([1971]) which measures the inhibition of the photochemical reduction of NBT.
This assay was based on a Biuret reaction where the presence of protein in an alkaline medium reduces Cu2+ to Cu1+.
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