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The cells on the top membrane and the bottom surface were observed and recorded under the microscope (Carl Zeiss, Canton, China).
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The fluorescence changes were recorded under the fluorescence microscope.
The increasing fluorescence signal, generated by the calcium bound to Fluo-8 inside the cells through the binding of PGE2 to its receptor, was recorded under the fluorescence microscope and analyzed.
The images were recorded under a fluorescence microscope (Nikon H600L microscope; Nikon, Japan [16]. Dead cells were quantified by flow cytometry (BD FACS Diva™ software).
Generally speaking, the etching rate anisotropy can be recorded under a microscope upon anodization through a mask with the simplest configuration.
The inhibitory effects of the E1R-j fermentation liquid on the conidial germination and the appressorial formation of Bgt were recorded under light microscope.
The number of cells in each detection point was recorded under optical microscope using cell count plates, so as to draw the cellular proliferation curve.
At the indicated time points, morphological changes were examined and recorded under light microscope (Carl Zeiss, Germany).
Shrinkage activity was recorded under a microscope (Olympus C × 41 × 40 magnification).
Raman spectra were recorded under a microscope with a × 40 objective in range of 0 1,600 cm-1 and 3 mW of power at the sample.
Details of this process were recorded under a microscope in real-time using a high-sensitivity video camera.
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