Figure EV2
- ID
- ZDB-FIG-220516-3
- Publication
- Karabid et al., 2022 - Angpt2/Tie2 autostimulatory loop controls tumorigenesis
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Expression of Angpt2 and Tie2 was assessed in Att20, GH3, LβT2 and αT3 cells by western blotting (WB) using specific antibodies. α‐Tubulin was included as loading control. Immunofluorescence (IF) of GH3 cells for Angpt2 (red) and Tie2 (green). Nuclei were counterstained with DAPI (blue). Original magnification: 400x; scale bar: 20 µm. Panels shown are representative of 3 independent experiments. Cell proliferation of GH3 cells transfected with si In samples parallel to (C), activated caspase‐3/7 was measured to assess for apoptosis. *** Cell proliferation of GH3 cells transfected with the individual siAngpt2 or scrRNA and incubated with rhANGPT2 (+rhANGPT2) or left untreated (−rhANGPT2) normalized against scrRNA‐transfected, untreated (scr‐rhANGPT2) cells. n.s., not significant; *** In samples parallel to (E), activated caspase‐3/7 was measured to assess for apoptosis. n.s., not significant; *** Cell proliferation of GH3‐sh In samples parallel to (G), activated caspase‐3/7 was measured to assess for apoptosis. *** GH3 cells transfected with si Cell viability of isolated rat primary EC cells incubated with CM from isolated rat primary PitNET cells. The experiments was performed independently 2 times, each with 3 technical replicates. Results are expressed as mean ± SEM. * |