Skip to main content
. 2014 Jan 22;47(1):20–27. doi: 10.1111/cpr.12086

Figure 1.

Figure 1

Scattergram ( FSC ‐height versus SSC ‐height; formatted without smoothing and with threshold 0.5%) of a sample containing all three cell lines treated following the reviewed procedure, upper left panel. Dot plot (FL2‐A: Eth‐Br versus FL2‐H: Eth‐Br) of R1‐gated cells used to select single events (R2 gate). Contour graph (FL2‐A: Eth‐Br versus FL4‐H: TelC Cy5; formatted without smoothing and with threshold 0.5%) of logical gated (R1 and R2) cells illustrates double fluorescence (total versus telomeric DNA) of 1301, Ramos and Daudi hybridized cells and their negative controls (N.C.). Biparametric regions (R7, R6 and R5 for hybridized cells; R4 and R3 control cells) drawn around G1–G0 events to calculate geometric mean of Cy5 fluorescence.