Fig. 4
From: Resource-efficient internally controlled in-house real-time PCR detection of SARS-CoV-2
RKI/ZBS1 SARS-CoV-2 protocol performance on different PCR cyclers. To show that the presented protocol can be run on several cyclers, we used 10 clinical samples of different RNA load, negative as well as positive controls and set up one master mix that was distributed to the different cyclers as shown above. Different colors represent 10 different samples used for comparison. Mean values of duplicates are shown, also for SARS-CoV-2-positive controls (crosses); negative controls are not shown