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. 2015 May 18;16(5):11417–11438. doi: 10.3390/ijms160511417

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© 2015 by the authors; licensee MDPI, Basel, Switzerland.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).

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qPCR analysis of 12 differentially expressed genes in pepper. Two independent experiments were performed in the year 2014 (A) and 2015 (B), respectively. PI: “PI 201234” inoculated with P. capsici zoospore suspension; PI MOCK: “PI 201234” inoculated with sterile-distilled water; QM: “Qiemen” inoculated with P. capsici zoospore suspension; QM MOCK: “Qiemen” inoculated with sterile-distilled water. Gene expression was normalized to actin with the data displayed as a mean ± SD of three biological replicates and an asterisk indicating statistical significance between infected and corresponding mock treatments. T-test was performed at different levels of significance. One asterisk represents that the differences reach 0.05 level of significance and two asterisks represent the differences reach 0.01 level of significance.

qPCR analysis of 12 differentially expressed genes in pepper. Two independent experiments were performed in the year 2014 (A) and 2015 (B), respectively. PI: “PI 201234” inoculated with P. capsici zoospore suspension; PI MOCK: “PI 201234” inoculated with sterile-distilled water; QM: “Qiemen” inoculated with P. capsici zoospore suspension; QM MOCK: “Qiemen” inoculated with sterile-distilled water. Gene expression was normalized to actin with the data displayed as a mean ± SD of three biological replicates and an asterisk indicating statistical significance between infected and corresponding mock treatments. T-test was performed at different levels of significance. One asterisk represents that the differences reach 0.05 level of significance and two asterisks represent the differences reach 0.01 level of significance.