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A positive correlation was observed between cell detection with optical microscopy and with electrical scanning.
To identify the phenotype of cells seeded on the rhBMP-2-conjugated scaffold, cellular activity was evaluated with scanning electron microscopy and with viability, histological, and immunohistochemical testing.
E.L.F., with Q.P.H.N. and V.M., performed the SIM-3D on human sperm; with C.S. and G.S., performed the bovine zygote staining; and with A.L.M., performed the Xenopus egg extract experiments; D.K. and J.L. performed correlative light and electron microscopy and with E.L.F., Bovine STORM.
The crystallization behavior of a linear polyethylene has been studied using conventional isothermal hot stage microscopy and with the Ding Spruiell method of rapid cooling.
The appearance of these under microscopy and with visual comparison under discrete hyperspectral wave bands, appears to be consistent with yellow ochre, yellow lake and gamboge.
It was also proved that the degradation products may only be detected in microsamples, both by Raman microscopy and with SEM EDS analysis.
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After washing with PBS, the cells were detected with fluorescence microscopy, and cells with condensed and/or fragmented chromatin indicative of apoptosis were not counted as living cells.
We appreciate the assistance of Dr. Rebecca Lee and Genevieve Phillips with confocal microscopy and Dr. Stephen Jett with electron microscopy.
VCCs were evaluated with 3D confocal microscopy and correlated with electron microscopy.
Images were taken with a Zeiss LSM510 confocal microscopy and processed with Adobe Photoshop.
Autophagic cell death was characterized with different methods (monodansylcadaverine [MDC] staining, electron microscopy) and compared with the findings obtained through QD imaging.
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