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Images of calcein and alizarin-labelled bone sections were visualized using the argon 488-nm laser and the HeNe 543-nm laser, respectively, of a confocal laser scanning microscope (LSM 510; Carl Zeiss MicroImaging GmbH, Jena, Germany) at similar regions as the μCT analysis.
Images of calcein and alizarin labeled bone sections were visualized using the argon 488 nm laser and HeNe 543 nm laser, respectively, of a confocal laser scanning microscope (LSM 510; Carl Zeiss MicroImaging GmbH, Jena, Germany) at similar regions as the μCT analysis.
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Immunoperoxidase labelled sections were visualized by brightfield microscopy.
Sections were visualized on a NanoZoomer 2.0-HT slide scanner (Hamamatsu).
Sections were visualized under the FV1000 confocal microscope (Olympus, USA).
Sections were visualized using Nikon fluorescent microscopy and images were acquired using a Zeiss Axiocam camera.
Sections were visualized by using BM purple substrate together with 2 mM levamisole.
After dehydration and embedding, ultra-thin sections were visualized using a Phillips 410 transmission electron microscope.
Sections were visualized by diaminobenzidine (DAB) (2 min) and methyl-green counterstain.
Sixty minutes after FM-4-64 injection, leaf sections were visualized under a laser-scanning confocal microscope.
Sections were visualized by fluorescent microscopy on a Ziess Axioplan 2 microscope.
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