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Fig. 2 | BMC Infectious Diseases

Fig. 2

From: Evaluation of a direct phage DNA detection-based Taqman qPCR methodology for quantification of phage and its application in rapid ultrasensitive identification of Acinetobacter baumannii

Fig. 2

Efficiency of the amplification obtained after directly loading phages as the template without DNA extraction based on ten-fold serially diluting by the phage DNA detection-based Taqman qPCR (A) and quantification result comparison of three fresh phage solution between the phage DNA detection-based Taqman qPCR and double layer plaque assay (B). “No” indicates no statistical difference.

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