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The fracture surfaces were examined using a microscope to verify the fracture behaviors.
Suspensions stained with 0.02% Janus Green B were tested by oil lens of microscope to verify the quality of mitochondria.
The electrolytic lesion was examined under a light microscope to verify the recording electrode position.
The worms were checked under a microscope to verify complete homogenization.
After dissection the spinal cords were carefully examined in a dissection microscope to verify the completeness of the lesion.
Slides were examined under a light microscope to verify the location of the injections.
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Coronal 50-μm sections were cut in a cryostat, stained with cresyl violet, and examined with a computerized Olympus microscope camera to verify cannula placement.
A small sample of cell suspension was examined on a microscope slide to verify the presence of green fluorescent protein (GFP -positive sinGFP -positive the overall effectivenesinglethe cellsdissociandon.
The sections were analyzed with a light field microscope (Nikon) to verify the presence of Chicago Sky Blue dye in the RVLM. Figure 1 shows a typical example of KYN injection sites in the RVLM (top) and depicts the site of dye deposition (−12.48 mm from bregma according to the atlas of Paxinos and Watson [ 36]) (2009) (bottom).
An optical microscope was used to verify the particle size of the TPU adhesive powder and the evaluation of the results obtained is shown in Fig. 4b.
A light microscope was used to verify the histopathological findings.
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