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Brain slices were fixed in 4% PFA at 4 °C o/n with shaking and washed in PBS for 30 mins at room temperature (RT).
After recording, brain slices were fixed with 2% paraformaldehyde and 1% glutaraldehyde and histochemically stained.
Brain slices were fixed in 4% paraformaldehye and permeabilized with ice cold methanol at −20°C for 5 minutes and then processed as above for cofilin.
The brain slices were fixed in 4% paraformaldehyde/PBS (10 mM Na-phosphate and 140 mM NaCl, pH 7.4) overnight at 4°C.
Brain slices were fixed with 10%% formaldehyde for 10 min and washed twice with PBS.
After 10 days in culture, tumor-implanted brain slices were fixed and stained for laminin.
Similar(51)
The brains were cut in 12-μm coronal sections using a cryostat (CM3050S, Leica, Heidelberg, Germany), and the slices were fixed with 4% paraformaldehyde and stained with a monoclonal antibody against phosphorylated NF-H, MAP2, synaptophysin or MBP.
Subsequently, slices were fixed overnight in 2% paraformaldehyde at 4°C.
Immediately after incubation, slices were fixed in 4% buffered formaldehyde.
Slices were fixed, permeabilized, washed, and blocked as outlined above.
Tissue slices were fixed in 10% phosphate-buffered formalin.
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