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. Author manuscript; available in PMC: 2013 Nov 26.
Published in final edited form as: Insect Mol Biol. 2005 Oct;14(5):10.1111/j.1365-2583.2005.00578.x. doi: 10.1111/j.1365-2583.2005.00578.x

Figure 2.

Figure 2

qRT-PCR analysis of differentially expressed genes of An. gambiae in ONNV infection. For cDNA construction total RNA was isolated from ONNV-infected and non-infected control mosquitoes. Biological replicates were used to generate fold changes and error bars for qRT-PCR experiments (n = 3). Each bar represents standard deviation. The fold changes were calculated to the average transcript level of ONNV infected mosquitoes divided by that of non-infected control mosquitoes. However, there was a fold change decrease in the value of MRpL7 (white bar), therefore, the value was negatively inversed. RpS4 gene (black bar) shows no significant loading variation of the samples.