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2 protocols using anti gfap rabbit pab

1

Immunohistochemical Analysis of Hippocampal Neuroinflammation

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Brains were rapidly removed, frozen at −80 °C, and cut into 2-mm coronal slices in a rat brain matrix. After 10% formalin fixation, hippocampal tissue samples were processed into paraffin-embedded blocks and 5-μm-thick sections were cut for immunostaining. Hippocampal CA1 region sections were deparaffinized and treated with EDTA antigen repair buffer (pH 8.0). Antibodies used were anti-ionized calcium binding adaptor molecule 1 (IBA-1; anti-Iba1 rabbit pAb, Servicebio, HRP anti-rabbit IgG (HRP-conjugated goat anti-rabbit IgG, Servicebio), anti-glial fibrillary acidic protein (anti-GFAP; anti-GFAP rabbit pAb, Servicebio), and Cy3 anti-rabbit (Cy3-conjugated goat anti-rabbit IgG, Servicebio). Finally, the sections were sealed with the antifluorescence solution (G1401-5ML, Servicebio), and the immunofluorescence images were observed and recorded with fluorescence microscope (NIKON ECLIPSE C1, NIKON DS-U3).
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2

Multi-Modal Analysis of Neural Tissue

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The PZT was obtained from SCH Technology Co. Ltd. The 443 nm μ-LEDs were obtained from Shenzhen Rico Photoelectric Technology Co., Ltd. The red μ-LEDs were obtained from Shenzhen Super high-brightness Electronics Co., Ltd. The following reagents and antibodies were used in the study: Anti- IBA 1 Mouse mAb (Servicebio, GB12105; diluted: 1:100), Cy3 conjugated Goat Anti-mouse IgG (H + L) (Servicebio, GB21301; diluted: 1:100), Anti- GFAP Rabbit pAb (Servicebio, GB11096; diluted: 1:100), fluorescein isothiocyanate (FITC)–conjugated goat anti-rabbit IgG secondary antibody (Servicebio, GB22303; diluted: 1:100), TMR (Red) Tunel Cell Apoptosis Detection Kit (Servicebio, G1502-50T; Recombinant TdT enzyme: TMR-5-dUTP Labeling Mix: Equilibration Buffer (1: 5: 50)), Hematoxylin (Servicebio, G1004), Eosin Y (Biobomei, YE2080), 4′,6-diamidino-2-phenylindole (Servicebio, G1012), Toluidine blue (Servicebio, G1032).
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