Selected article for: "citrate buffer and light microscope"

Author: Yuan, Chen; Zhang, En; Huang, Lulu; Wang, Jialu; Yang, Qian
Title: Oral administration of inactivated porcine epidemic diarrhea virus activate DCs in porcine Peyer’s patches
  • Document date: 2018_8_16
  • ID: 184kmuiy_18
    Snippet: After deparaffinization and rehydration, paraffin sections were put in citrate buffer (pH 6) at 90-95°C for 15 min to retrieve antigen. Then, the sections were put in 0.3% H 2 O 2 to quench endogenous peroxidase and washed in PBS. 5% bovine serum albumin were incubated on sections for 30 min to close the non-specific antibody binding sites. After blocking with 5% bovine serum albumin, sections were incubated with goat anti-pig IgA overnight at 4.....
    Document: After deparaffinization and rehydration, paraffin sections were put in citrate buffer (pH 6) at 90-95°C for 15 min to retrieve antigen. Then, the sections were put in 0.3% H 2 O 2 to quench endogenous peroxidase and washed in PBS. 5% bovine serum albumin were incubated on sections for 30 min to close the non-specific antibody binding sites. After blocking with 5% bovine serum albumin, sections were incubated with goat anti-pig IgA overnight at 4°C. Biotinylated secondary antibodies were added to the sections for 1 h at room temperature, and treated with SABC for 60 min. Sections were counterstained with hematoxylin and images were obtained using a light microscope (BH-2; Olympus). Different fields of each tissue in each piglet were counted for the statistical analysis.

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