Figure 3.
Figure 3. Analysis of GloFli fish thrombocytes by flow cytometry. Representative dot plots show the presence of GFP+ and RFP+ thrombocytes in whole blood of Glo fish (A), Fli fish (B), GloFli fish (C), and GloCD41 fish (D). FL1 and FL2 channels are shown as FL1-A and FL2-A on the x-axis and y-axis, respectively. Forward scattering in FL1 and FL2 channels measures green and red fluorescence from GFP+ and RFP+ thrombocytes and is shown in Q4-LR and Q4-UL gates, respectively. DP thrombocytes (GFP+/RFP+) are shown in the Q4-UR gate. The percentages of thrombocytes are shown in the respective gates. The large percentage of cells shown in Q4-LL (lower left quadrangle) gates represents other blood cells. Gating was according to the fluorescence intensities of thrombocytes in the side scattering.

Analysis of GloFli fish thrombocytes by flow cytometry. Representative dot plots show the presence of GFP+ and RFP+ thrombocytes in whole blood of Glo fish (A), Fli fish (B), GloFli fish (C), and GloCD41 fish (D). FL1 and FL2 channels are shown as FL1-A and FL2-A on the x-axis and y-axis, respectively. Forward scattering in FL1 and FL2 channels measures green and red fluorescence from GFP+ and RFP+ thrombocytes and is shown in Q4-LR and Q4-UL gates, respectively. DP thrombocytes (GFP+/RFP+) are shown in the Q4-UR gate. The percentages of thrombocytes are shown in the respective gates. The large percentage of cells shown in Q4-LL (lower left quadrangle) gates represents other blood cells. Gating was according to the fluorescence intensities of thrombocytes in the side scattering.

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