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. Author manuscript; available in PMC: 2014 Apr 1.
Published in final edited form as: Exp Eye Res. 2013 Jan 18;109:8–16. doi: 10.1016/j.exer.2013.01.005

Figure 4. GFP expression in mouse aqueous humor outflow pathway following fast intracameral infusion of adenovirus encoding GFP.

Figure 4

Ad.cmv.gfp (5×105 particles in 10 µl volume) was infused into mouse anterior chamber over 3 minutes (flow rate 3.33 µl/min). Three to five days after transduction, mouse eyes were fixed and dissected. The anterior segments were then processed by cryosectioning (10 µm), semi-thin sectioning (0.5 µm) or thin sectioning (65 nm). A) Immunofluorescence image of sagittal plane section through mouse angle structures; B) Sagittal plane semi-thin section (60 × amplification) through angle structures of mouse eye. The section was immunostained with anti-GFP primary antibody and Alexa Fluor®488 goat anti-rabbit IgG (H+L) secondary antibody. Nuclei were stained with DAPI. The image was captured with a confocal microscope; C) Sagittal plane thin section through trabecular meshwork and Schlemm's canal. The section was immunostained with specific anti-GFP primary antibodies and 6 µm immunogold anti-rabbit secondary antibodies. Images were captured with a JEM-1400 electron microscope. Data are representative of 3 experiments using C57BL/6 mice (8–22 weeks old).