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The results demonstrated that the fluorescence of HSA would be quenched with the addition of paeoniflorin.
With increase in temperature above 100 K, the PL peak intensity is observed to be quenched with large activation energy of 84.8 meV.
Since the chemical reduction of Cu2+ to Cu+ lies between the conduction band and valence band of g-C3N4, the PL of g-C3N4 can be quenched with a low detection limit of 0.5 nM [103].
Since reaction of 1 with N,N-diisopropylbenzamide could be quenched with iodine and the iodinated product isolated in 88%% yield, other electrophiles were considered (Scheme 1).
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Quench-Phrase The reaction was quenched with methanol.
The reaction was quenched with 100 μL of methanol.
Tissue sections (4 μm) were rehydrated, and endogenous peroxidases were quenched with 3% hydrogen peroxide.
Labeling was quenched with FBS.
Endogenous peroxidases were quenched with 0.3% H202.
Endogenous peroxidases were quenched with 3% H2O2 in methanol.
The reaction was quenched with 130 mM glycine.
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