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Sections were then mounted on slide glasses and hydrated by ethanol and xylene.
The sections were then mounted on slide, dehydrated with xylene and then cover-slipped with permount (Fisher Scientific).
Sputum from patients was mounted on slide.
Slides were counter-stained with haematoxylin, and mounted on slide using Aquatex (Merck, Darmstadt, Germany).
They were microdissected and mounted on slide glasses for whole mount staining.
After rinsing with PBS, slices were mounted on slide glass and scanned by confocal microscopy (TCS SP2 AOBS).
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After incubation, sections were rinsed in PBS and immediately mounted on slides.
Coverslips were mounted on slides with gelutol.
Coverslips were mounted on slides with aqua polymount.
Sections of transgenic mouse brains are mounted on slides for viewing under a microscope.
Coverslips were washed with PBS, mounted on slides with DAPI, and analyzed by fluorescence microscopy.
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