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P. falciparum cultures stained with JC-1 dye and by TUNEL assay were visualized by fluorescence microscopy.
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Cell viability assay was visualized by the Evans blue staining.
Lysates were then analyzed through western blot assay, and the immunoreactive bands were visualized by using ECL kit (Bio-Rad, Hercules, CA).
Probe-target hybrids were visualized by chemiluminescent assay, using the chemiluminescent alkaline phosphatase substrate CSPD according to manufacturer's directions.
The immune complexes were visualized by an ECL assay.
The free radical scavenging activity, determined by the DPPH assay, is visualized in Fig. 2.
To check enzyme activity, elution fractions were subjected to native PAGE and esterase activities were visualized by α/β-naphthyl acetate assay, as described in [16].
The apoptotic tumor cells were visualized by an in situ TUNEL assay.
Foci of infected cells were visualized by using peroxidase-based foci staining assay as described previously [ 62, 65].
Liquid droplets were visualized by DIC microscopy.
Nuclei were visualized by DAPI (blue).
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