Sentence examples for mounting of slides from inspiring English sources

Counterstaining with haematoxylin and mounting of slides with permanent mounting media.

Counterstaining of nuclei was performed using Harris haematoxylin (Surgipath) followed by mounting of slides with Aquamount (VWR).

The chromogenic substrate was 3,3-diaminobenzidine and sections were counterstained with Meyers' prior to dehydration and mounting of slides in Depex.

Following detection and mounting of slides with antifade Prolong GOLD without DAPI (Invitrogen), signals were identified in BrdU incorporated nuclei as replicated doublets (D), or un-replicated singlet's (S), using a DMRXA epifluorescence microscope, DFC340 FX camera and CW4000 Karyo software (Leica).

Tissue sections from whole tumors were obtained and (pre) treated in the same manner as the TMA slides (described above) except for the section thickness (6 μm) and the mounting of the slides in Pertex (Histolab) instead of malinol.

After rinsing, the slides were visualized by diaminobenzidine (DAB) chromogen solution (Dako) and counterstained with routine hematoxylin, followed by dehydration through graded ethanol and mounting of the slides.

Following microtome sectioning and mounting of tissue, slides were dried vertically at room temperature and incubated overnight at 37°C to ensure that the tissue was adhered to the slide.

Hybridization, washing, counterstaining and mounting of the slides were conducted following standard protocols [ 43].

The orientation of each histology image had random variations during the process of sectioning and mounting of histology slides.

They were then rinsed once with phosphate-buffered saline (PBS) and fixed with 4% paraformaldehyde, followed by mounting of coverslips on slides using Prolong Gold antifade reagent with 4', 6-diamidino-2-phenylindole (Invitrogen).

Two sets of serial sections (at intervals of 120  μm) were mounted on slides (Superfrost PLUS), using a solution of 0.1% BSA (albumin bovine, minimum 98%) in PBS.