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. 2017 Jun 30;83(14):e00721-17. doi: 10.1128/AEM.00721-17

FIG 2.

FIG 2

qRT-PCR of RNA isolated from the Xanthomonas sp. strain 35Y wild type. Cells were grown on nutrient broth (yellow columns) or Tuschii and Takeda medium with polyisoprene latex (gray columns) for 4 days, respectively, and RNA was isolated and quantified as described in Materials and Methods. RNA levels were normalized to gyrA RNA levels. Three technical replicates were performed. Error bars show standard deviations.