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Specific binding was visualised by standard techniques.
Specific binding was visualised by chemiluminescence (ECL Western Blotting Analysis System, Amersham Biosciences).
Subsequently, the level of P-GTP binding was visualised by autoradiography.
Peroxidase binding was visualised by enhanced chemiluminescence and detected as described previously (Thomas et al, 2010).
Antibody binding was visualised by tetramethylbenzidine and hydrogen peroxide and the colour reaction was measured at 450 nm.
After applying a biotinylated secondary antibody and tertiary reagent (Vector-Laboratories, Bulingam, CA, USA) the antibody binding was visualised by diaminobenzidine (Serva, Heidelberg, Germany) and H2O2.
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OPG binding was visualised using TMB Pierce Chemical Coo).
Antibody binding was visualised using AEC-solution (for LSAB2-Kit).
Antibody binding was visualised using 3-diaminobenzidine (Sigma-Aldrich).
Antibody binding was visualised Proteins were detected using an enhanced chemiluminescence kit (Amersham/GE Healthcare, UK).
Antibody binding was visualised using Cy3-labelled anti-mouse IgG (Amersham).
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