Exact(1)
Sections were counterstained with hematoxylin and the ratio of TUNEL-positive cells to TUNEL-negative cells was calculated from 3 random areas within each specified brain region (internal capsule, hippocampus and thalamus) under bright microscopy at a magnitude of 40x.
Similar(59)
The autoradiographs were analyzed by conventional bright field microscopy as well as by dark field microscopy.
c, d Bright field microscopy images showing the production of hydrogel using microfluidic device and e, f bright field microscopy images of microbeads formed after crosslinking the hydrogel at 10× and 20× magnifications.
Stained sections were observed using bright field microscopy [36].
Finally, parasites were mounted in neutral glycerin jelly and examined by bright field microscopy.
Bright field microscopy was used to image trichrome stained tissue sections as previously described [9].
Cell periphery is shown by white line (from the corresponding bright field microscopy images).
Morphological resembling of aerial and branched mycelia (Fig. 1) of the isolate was examined under bright field microscopy.
Bright field microscopy was used for counting c-Fos-positive cells.
The first experiment uses optical trapping, bright field microscopy and laser position detection.
The cells were observed by bright field microscopy in order to distinguish attached from internalized parasites.
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