Fig. 2
From: Heterologous avian system for quantitative analysis of Syncytin-1 interaction with ASCT2 receptor
Cellular localisation of protein products of FuTraP variants. Confocal microscopy analysis showing the channels separately in grayscale and together in colourised composite. From top to bottom: the IRES-driven iRFP713 (red channel); AcGFP fused with ASCT2 (green channel); the stained cellular membrane (blue channel); merge of previous channels. Scale bars represent 10 μm. NC, negative control (ggTvbS1 or hEAAT1)