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2 protocols using clone m1 70

1

Immunohistochemical Analysis of Retinal Cells

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Anesthetized mice were perfused with 20 mL of PBS. Eyes were enucleated and fixed in 4% paraformaldehyde in 2× PBS for 15 min and then transferred to 2× PBS on ice for 10 min. After dissecting eyes, retinal whole mounts were prepared. Retinas were then transferred to ice-cold methanol and kept at −80 °C until use.
For immunohistochemistry, retinas were first blocked in a blocking buffer (0.3% Triton, 0.2% BSA, and 5% goat serum in PBS) for 1 h at room temperature and incubated with primary antibodies and Alexa Fluor 647-conjugated isolectin GS-B4 (1:100; Thermo Fisher Scientific) overnight at 4 °C. After washing, retinas were incubated with secondary antibodies for 4 h at 4 °C. Retinas were mounted after washing. Rabbit anti-P2ry12 antibody (1:500; a gift from H. Weiner, Brigham and Women’s Hospital), rat anti-CD11b antibody (1:100, clone M1/70; Abcam), rat anti-MHC class II (1:1,000, I-A/I-E; BD Pharmingen), rat anti-CD4 (1:200, RM4-5; BD Pharmingen), and rat anti-CD8a (1:200, 53-6.7; BD Pharmingen) were used for primary antibodies. Alexa Fluor 594-conjugated goat anti-rabbit antibody, and Alexa Fluor 488-conjugated goat anti-rat antibody (1:500; Thermo Fisher Scientific) were used for secondary antibodies.
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2

Multicolor Immunofluorescence Analyses

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The following antibodies were purchased and used: primary CD11b (Biolegend, Clone M1/70 cat#101202, 1:100), Fibronectin (Abcam, cat#ab23750, 1:100), IFNAR1 (Sino Biological Inc., cat#50469-RP02, 1:100), FAP (R&D, cat#AF3715, 1:100) and secondary antibodies: Alexa Fluor 488 Goat anti-Rat (Thermo Fisher Scientific, cat#A11006, 1:500) for CD11b, Alexa Fluor 488 Goat anti-Rabbit (Thermo Fisher Scientific, cat#A11070, 1:500) for Fibronectin, Alexa Fluor 594 Goat anti-Rabbit (Thermo Fisher Scientific, cat#A11072, 1:500) for IFNAR1, Alexa Fluor 488 Donkey anti-sheep (Thermo Fisher Scientific, cat#A11015, 1:500) for FAP. Immunofluorescence analyses were carried out as previously described18 (link). The images were taken using the Olympus BX51 microscope. The quantification of immunofluorescence intensity was performed by Image J. Three sections were analyzed for each mouse and six to ten fields in each section were quantified.
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