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Bands were visualized onto autoradiography films, scanned and quantified with Image J. The signal intensity was normalized to β-actin expression.
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After washing, protein bands were visualized using chemiluminescence and developed onto film (KODAK).
Once separated in this way, the proteins were transferred onto nitrocellulose, and Aβ-immunoreactive bands were visualized using 6E10.
Bands were visualized by enhanced chemiluminescence (Pierce Biotechnology).
Protein bands were visualized by ECL.
The separated protein bands were visualized by staining with the Simply Blue Safe Stain solution (Life Technology, Frederick, MD, USA) or transferred onto nitrocellulose membranes for Western blot analysis.
Bands were visualized by chemiluminescence.
Bands were visualized with chemiluminescence.
Bands were visualized with an UV transilluminator.
Immunoreactive bands were visualized by chemiluminescence.
The bands were visualized using ECL Chemiluminescent Substrate Reagent (Amersham).
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