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Luciferase reporter assay, antibody label assay and fluorescence protein assay are frequently used by researchers in screening small compounds.
At present, there are many methods utilized in differentiation assays to screen small molecules, including luciferase reporter assay, antibody label assay and fluorescence protein assay [8], [9], [10], [11], [12], [13].
Next we detected the proliferation of cells in both groups by BrdU label assay.
We next explored the effect of activin treatment on induction of apoptosis in LE6 cells using an AnnexinV/PI double label assay.
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The One-Cycle Eukaryotic Target Labeling Assay protocol was used.
Endothelial apoptosis was assessed by TdT-mediated dUTP nick end labeling assay.
In this study, we used an in vivo ubiquitin labeling assay to investigate the circadian ubiquitylated proteome of Drosophila melanogaster.
Extent of apoptosis was defined morphologically and by the TUNEL (Tdt-mediated dUTP biotin nick end labelling) assay.
They utilized an ELISA-based colorimetric assay to detect PI3K activity and a fluorescent metabolic labeling assay to detect protein synthesis in FXS lymphocytes.
In the glr3.1 mutant, excessive programmed cell death, as detected by the terminal transferase uridyl nick end labeling assay, was observed throughout the RAM.
Immuno-gold labeling assay showed that ORF38 is only present on virions that have entered the cytoplasmic vesicles, indicating that ORF38 is packaged into virions during secondary envelopment.
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