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Additionally, the flow patterns were visualised by using a rheoscopic fluid.
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After further incubation and washing steps, hybridisations were visualised by using a precipitating dye.
Nuclei were visualised by using Prolong Gold Antifade Reagent with DAPI (Invitrogen).
Immunoreactive bands were visualised by using Western Lightning Chemiluminescence Reagent Plus (Perkin Elmer, Cambridge, UK).
Fragments were visualised by using the 2100 Bioanalyzer Multi-Instrument system (Agilent Technologies, CA, USA).
Protein bands were visualised by using an ECL chemiluminescence detection system (GE, Healthcare Biosciences, Uppsala, Sweden).
Loss of heterozygosity were visualised by using an optical densitometry scanner.
Immunoreactivity was visualised by using DAB Chromogen followed by haematoxylin counterstain.
Immunolabelling was visualised by using the ECL procedure (Amersham Biosciences, USA).
Binding of streptavidin biotin-conjugated horstreptavidin biotin-conjugatedised by using 3,3'-diaminobenzidine tetrahorseradishde.
Immmunolabelling was visualised by using an appropriate combination of species-specific Alexafluor-conjugated secondary antibodies (Invitrogen).
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