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. 2015 Aug 4;31(1):69–81. doi: 10.1093/mutage/gev055

Figure 2.

Figure 2.

Confirmation of genotype of DT40 clones that were used in this study. (A) Southern blot analysis of indicated gene disrupted DT40 clones using the gene specific probes. (B) Liquid survival assay after exposure to ionising radiation. Cells were cultured for 48h after IR. Cellular ATP level was used to measure cell survival. The survival of untreated cells was set as 100%. (C) Colony survival assay after exposure to IR. Percent survival was determined relative to numbers of colonies from untreated cells. For both B and C, error bars represent SD from at least three independent experiments.