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Each ML contained 20 [SRSO/SiO2] periods.
The dichloromethane solution (50 mL) contained TBAB.
The standard residual activity assay mixture (1.0 ml) contained 0.67 mM urea in 0.02 M KH2PO4-K2HPO4 buffer (pH 7.4).
The reaction mixture (0.9 mL) contained 1 mM substrate (either 2-cyclohexenone or 3-hydroxycyclohexanone) and 60 μM dichlorophenol indophenol (DCPIP) as the electron acceptor.
The reaction mixture (3 ml) contained 100 mM potassium phosphate buffer (pH 7.8), 0.1 mM EDTA, 13 mM methionine, 2.25 mM NBT, 60 μM riboflavin and enzyme extract.
The reaction mixture (3 ml) contained 100 mM potassium phosphate buffer (pH 6.1), 96 mM guaiacol, 12 mM H2O2 and enzyme extract.
The preformed Fe3O4@SiO2 nanoparticles were dispersed in ethanol (80 mL) contained in a three-necked round-bottom flask and sonicated for 5 min.
The assay mixture (1.0 ml) contained 40 mg L-1 urea, 6 μg ml-1 urease and different concentrations Hg2+ in 0.02 M KH2PO4-K2HPO4 buffer (pH=7.4).
The reaction system (1 mL) contained 200 mM PBS (pH 7.4), 5 mM (E/Z -citral, 40 g/L wE/Z -citrald 0.2 mM NAD+.
The standard reaction mixture (total volume: 1.00 ml) contained 200 mM carbonate-KOH (pH 10.5), 10 mM meso-DAP, 1.25 mM NADP and enzyme.
The assay mixture (1 mL) contained: 0.1 mM linoleic acid, the sample (or the same quantity of solvent as reference) and 50 mM sodium phosphate, pH 6.8.
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