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. 2020 Oct 20;11:5300. doi: 10.1038/s41467-020-19150-9

Table 1.

Quantitative analysis of Cx40+-derived clones.

4’OH E9.5 4’OH E10.5 4’OH E14.5 4’OH E18.5
Ctrl Nkx2-5+/− Ctrl Nkx2-5+/− Ctrl Nkx2-5+/− Ctrl Nkx2-5+/−
Total hearts 10 15 16 10 8 9 6 4
Total clones 36 48 64 50 118 128 105 58
Frequency/heart 3.6 3.2 4 5 14.75 14.2 17.5 14.5
% GFP+  39.1 30.4 37.5 44 39.3 37.5 34.3 37.9
% CFP+  4.3 4.3 1.6 2 0.85 0 0.95 0
% RFP+  43.5 52.2 42.2 40 38.5 41.4 45.7 43.1
% YFP+  13.0 13.0 18.75 14 21.4 21.1 19.0 19.0
% Cond. clones 36.1 47.9 53.1 18 57.6 32.8 95.2 44.8
% Mixed clones 27.8 25 12.5 16 11.0 9.4 0 17.2
% Non-cond. clones 36.1 27.1 34.4 66 37 57.8 5 36.2
Size cond. clones 5.4 5.1 4.5 3.9 2.6 2.5 3.18 1.9
Size mixed clones 27.7 13.3 31.1 9.25 6.5 7.25 0 6
Size non-cond. clones 16.9 27.7 31.6 16.1 6.5 6.7 4.8 3.0

Table represents the n values of hearts and clones analyzed in this study, using Cx40-CreERT2::R26R-Confetti mouse line. Only clones observed in the subendocardial surface of the inter-ventricular septum within the left ventricle are analyzed. Percentages of colors and type of clones are represented. The size of clones are measured by quantifying the number of cells per clone.