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PC-PLC activity in thawed CSF was measured using a fluorometric enzyme assay.
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The activity of the peroxisomal enzyme catalase was evaluated in astrocyte cell culture using a fluorometric assay.
To determine whether complex 1 and 2's ability to reactivate virus was as a result of inhibiting HDAC, the activity of this enzyme in the presence of non-toxic concentrations of the complexes was evaluated using a fluorometric assay.
Lysine availability of extracted protein was measured using a fluorometric technique (Ferrer et al. 2003).
The non-covalent DNA-binding properties of 12, 13 have been examined using a fluorometric technique.
Serum paraoxonase-1 activity (PON1), which has been suggested as a marker of hepatotoxicity, was determined using a fluorometric assay.
Caspase-3 activity was measured using a fluorometric assay.
Following this result, PGF was tested for the presence of an DNase I inhibitor using a fluorometric assay [33].
We determined cell viability by using a fluorometric resazurin reduction method (CellTiter-Blue, Promega, Madison, WI) following the manufacturer's instructions.
The cytotoxic activity of the CGs was measured by using a fluorometric microculture cytotoxicity assay (FMCA) as previously described [23], [24].
A portion of each tissue homogenate was evaluated for IDUA activity using a fluorometric assay.
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