2022
DOI: 10.1016/j.xpro.2022.101672
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Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues

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“…compound and stored at − 80 °C before sectioning coronally at 40 µm using a Leica cryostat, with every third section saved for use in the present study. Tissue sections were immunofluorescently stained for OT and VP following previously established protocols 60 . Tissue was rinsed 5× for 10 min in 0.1 M PBS (pH 7.4), incubated for 1 h in a blocking solution (PBS + 10% normal donkey serum + 0.03% Triton-X-100) to prevent non-specific binding, and then incubated for approximately 48 h in primary antibodies diluted in PBS containing 5% normal donkey serum + 0.03% Triton-X-100.…”
Section: Partner Preference Testmentioning
confidence: 99%
“…compound and stored at − 80 °C before sectioning coronally at 40 µm using a Leica cryostat, with every third section saved for use in the present study. Tissue sections were immunofluorescently stained for OT and VP following previously established protocols 60 . Tissue was rinsed 5× for 10 min in 0.1 M PBS (pH 7.4), incubated for 1 h in a blocking solution (PBS + 10% normal donkey serum + 0.03% Triton-X-100) to prevent non-specific binding, and then incubated for approximately 48 h in primary antibodies diluted in PBS containing 5% normal donkey serum + 0.03% Triton-X-100.…”
Section: Partner Preference Testmentioning
confidence: 99%