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The residual enzyme activity was assayed under standard assay conditions.
Protease activity was determined by following the standard assay procedure.
The residual activity was measured under standard assay condition.
The initial velocity of the reductive reaction was analyzed using the standard assay conditions.
The residual activity was subsequently measured under standard assay conditions (see above).
The residual activity of modified enzyme was determined under standard assay conditions.
The aliquots were removed for the determination of residual enzyme activity under standard assay conditions.
At different intervals, samples were withdrawn and the residual activity was measured under standard assay condition.
Protein concentrations were determined by the standard assay procedure using Pierce Coomassie® Plus Protein Assay Reagent.
Twelve standard assay points were used to generate a standard curve.
Residual activities were measured periodically at an interval of 4 h under standard assay conditions.
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