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The first was monitoring at 305 nm with excitation at 280 nm, showing the increase in tyrosine fluorescence after dephosphorylation.
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The most preferred strategy was monitoring at-risk populations (coefficient=13.75).
was monitored at 265 nm.
The eluent was monitored at 245 nm.
The absorbance was monitored at 215 nm.
Absorbance was monitored at 210 nm.
The detection was monitored at 210 nm.
The activity was monitored at 590 nm in a spectrophotometer.
For chymotrypsin, the reaction was monitored at 253 nm.
The absorbance of the eluate was monitored at 280 nm.
Variation in lead concentration was monitored at room temperature.
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