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. 2016 May 23;17(5):792. doi: 10.3390/ijms17050792

Figure 2.

Figure 2

Comparison of the PCR and DNA sequencing data with our visualization data using the ARPS method to detect the EGFR L858R mutation in NSCLC cells. (A) The PCR and DNA sequencing data; (B) The specificity and timely sensitivity of the ARPS method for detection of the EGFR L858R mutation. The “+” was the positive control in the RPA reaction kit (143 bp in size), which was detected between 10 and 20 min. The target mutated band size was 201 bp, and 300 ng of the DNA template was used. Results of ARPS were negative in red, positive in green.