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Open image in new window Fig. 2 Confocal microscopy images for the dyed PS/PA6 blend webs: red represents PS fibers and green represents PA6 fibers.
The extent of newly formed bone around the implant was measured from 200× fluorescence microscopy images for each type of implant.
Fig. 5 Optical microscopy images for PLA/PBS blends: a PLA; b PLA/PBS (90/10); c PLA/PBS (70/30), d PLA/PBS (50/50); e PLA/PBS (30/70); f PBS. Figure 6 shows the stress strain curves of the PLA/PBS blends with various weight ratios.
Figure 4 shows laser scanning confocal microscopy images for each fluorescent dye and a corresponding brightfield image.
Representative microscopy images for quantifications shown in Figure 2B.
The normalized microscopy images for each perturbation are shown in Figure 3b and are in agreement with the MFI cytometry data.
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In Figure 1a, we present a polarizing optical microscopy image for the mesophase of the microemulsion with silver nanoparticles synthesized inside of the mesophase.
Ten electron microscopy images of tissues for peroxisomes and mitochondria were counted in tissues of adult zebrafish fed different concentrations of clofibrate.
Fig. 2 Scanning electron microscopy images of the nanostructures for Al- and Ga-doped ZnO seed layers for selected temperatures and concentrations.
Fig. 9 Typical fluorescent microscopy images of HUVECs cultured for 24 and 72 h on the respective substrates.
Representative optical fluorescence microscopy images) of hABMSCs cultured for 7 days in static conditions (A) or LIPUS induction at 20% duty cycle (B) or 50% duty cycle (C) after the addition of differentiation media: cell nuclei, actin filaments, osteocalcin and merged images of the fluorescence stains.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com