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Take a fixed mouse brain section containing the nucleus basalis of Meynert, rich in nerve fibers expressing the enzyme choline acetyltransferase.
The section is pretreated to deactivate endogenous peroxidase.
Add a detergent to permeabilize cellular membranes, followed by a blocking solution to prevent non-specific antibody binding.
Replace the solution with primary antibodies that bind to choline acetyltransferase.
Wash with buffer to remove unbound antibodies. Incubate with biotin-tagged secondary antibodies, which bind to the primary antibodies.
Remove unbound antibodies and add avidin-biotin-peroxidase complexes, which bind to the secondary antibodies.
Wash to remove excess complexes.
Add a chromogenic substrate that reacts with peroxidase, forming a colored precipitate.
Rinse with distilled water to remove excess precipitate.
Transfer the section onto a gelatinized slide.
Next, dehydrate the section using increasing ethanol concentrations, followed by xylene.
Mount the section and observe under a microscope to visualize the stained nerve fibers.
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