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Exact(38)
The successful binding was visualized by EM and AFM measurements, and the functioning of the RC was checked by flash photolysis experiments.
After rinsing with 0.1 % PBS-Tween® 20 for 3 × 5 min, antibody binding was visualized by 3,3′-diaminobenzidine using the DAB Peroxidase Substrate Kit Vector Laboratories Ltd.., Peterborough, UK) at room temperature for 5 min.
After washing, protein binding was visualized by incubation with HRP-conjugated His antibody or FLAG antibody.
Antibody binding was visualized by chemiluminescence (Supersignal West Pico Chemiluminescence Kit from Pierce, Bonn).
Antibody binding was visualized by the Dako Envision system (cat #K4011).
Protein binding was visualized by detecting HRP with the OPD reagent (Pierce, Rockford, IL, USA) that resulted in a colored product.
Similar(22)
The biotin-free polymeric horseradish peroxidase-linker antibody conjugate system was used in the Bond-maX automatic slide stainer (Vision BioSystems), and antibody-binding was visualized by staining with 3,3-diaminobenzidine (DAB) solution.
Briefly, unspecific binding sites were blocked with 1% blocking reagent for 30 min, successively the labeled probes were bound to anti-digoxigenin Fab-fragments conjugated to alkaline phosphatase for 30 min and, finally, antibody-binding was visualized by membrane incubation in NBT/BCIP solution until the color reaction was completed (30 60 min).
The membranes were then incubated with the respective primary antibodies in Tris-buffered saline milk overnight at 4°C, and specific binding was visualized using species-specific IgG followed by enhanced chemiluminescent detection (ECL kit; Amersham Bioscience, Pittsburg, PA, USA) and exposure to enhanced chemiluminescent X-ray film.
Antibody binding was visualized using ECL.
The impact of this enhanced binding to actin was visualized by changes in podocyte morphology.
More suggestions(16)
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