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Subsequent haematoxylin staining was carried out in DAB-stained samples.
48 h later, immunofluorescence staining was carried out using BCCIP antibody.
To confirm purity and cell shape, Gram staining was carried out on the respective isolates.
Protein staining was carried out on embedded cross sections following a method detailed by Schäfer [8].
Toluidine blue staining was carried out to investigate the synthesis of proteoglycan extracellular matrix.
Fluorescent double-immunocytochemical staining was carried out to evaluate the protein expression levels of HPV-E6 oncogene and caspase-3.
Staining was carried out as described [62].
Antibody staining was carried out as described [30].
Hoechst staining was carried out as described [22].
Surface staining was carried out by standard procedures.
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Counter-staining was carried out with Harris hematoxylin.
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