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Subsequent amplification step and labeling with fluorophore gives a fluorescent dot at the exact site of protein interaction, which can be visualized by microscopy.
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During cross-flow membrane emulsification, droplet formation at a micro-engineered membrane with uniform pores was visualized by microscopy.
FipA-KO complemented with fipAMTB, was visualized by microscopy before and after subjecting to oxidative stress.
S-phase cells were visualized by microscopy and quantitated by counting 3 fields of 100 in quadruplicate.
When calpain activity was visualized by microscopy, the three inhibitors blocked formation of fluorescent CMAC and caused an elongated morphology (Fig. 3A).
Ten fields from each slice were visualized by microscopy (×200).
The lipid content of stained cells was visualized by microscopy (Olympus IX71, Tokyo, Japan).
After 18 h of culture, the cell rearrangement and tube formation were visualized by microscopy.
Microtubules were visualized by microscopy and photographed using a digital camera.
Cells that passed through the membrane were visualized by microscopy and pixel counts were determined using ImageJ software.
Migrated cells were visualized by microscopy and the number of cells in the center of each well was counted.
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