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The best visualisation is achieved with individually adjusted narrow window settings (c).
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In addition, visualisation is achieved by conjugation of imaging agents such as radionuclides or paramagnetic/superparamagnetic metals.
However, visualisation is achieved using a peroxidase-based chromogenic reaction, similar to IHC.
Visualisation was achieved with a Vectastain ABC kit (Vector Laboratories, US) and peroxidase substrate kit (Vector VIP).
Protein visualisation was achieved using the ECL Western Blotting Reagent Kit (Amersham) and Hyperfilm-ECL photographic film (Amersham).
Visualisation was achieved using enhanced chemiluminesence (ECL) reagents (Amersham Biosciences; Little Chalfont, Buckinghamshire UK).
Band visualisation was achieved with Enhanced Chemiluminescence (Amersham Biosciences) using X-ray film.
Visualisation was achieved with 5-bromo-4-chloro-3-indolyl phosphate-nitroblue tetrazolium.
Visualisation was achieved using 3-amino-9-ethylcarbazol (AEC) containing H2O2 (DakoCytomation Denmark A/S, Glostrup, Denmark).
Visualisation was achieved by incubation at RT for 3 5 min in 3,3′-diaminobenzidine chromogen-buffered substrate solution (DakoCytomation).
Visualisation was achieved using DAB Sigma-Aldrichh Co Ltd, Poole, Dorset, UK) as an enzyme substrate, counterstained with haematoxylin, dehydrated and mounted.
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