Not exact matches
Immunoreactions were developed using a fluorescently labeled secondary antibody, and samples visualized in a Leica Biosystems epifluorescent microscope or using a secondary antibody linked to horseradish peroxidase and developed
with a 3,3 ′ -
diaminobenzidine kit.
Stainings were developed
with 0.06 % 3,3 ′ -
diaminobenzidine (Sigma - Aldrich, USA) and 0.01 % hydrogen peroxide (Sigma - Aldrich, USA) in PBS and then mounted on subbed slides.
Antibodies are labeled
with DAB (3,3» -
diaminobenzidine) and the resulting brown staining indicates where an antibody has bound to its corresponding antigen.
Slides were then incubated
with Envision secondary followed by 3,3 ′ -
diaminobenzidine.