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. 2019 Feb 26;63(3):e02190-18. doi: 10.1128/AAC.02190-18

FIG 1.

FIG 1

(A) Primers used to confirm each of the indicated A. baumannii mutants. The lengths of the resulting PCR products are shown in base pairs (bp). (B) PCR verification of each A. baumannii mutant generated by gene disruption. V Ladder NzyTech (lane M1) and ʎ BsteII-digested DNA (lane M2) were used as molecular size markers.