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. 2017 Dec 19;18:974. doi: 10.1186/s12864-017-4355-5

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© The Author(s). 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 8 — qRT-PCR analysis of the expression levels of ten unigenes. X axis represents different unigenes. CL2742.Contig1_All, cytochrome P450 9G3; Unigene4872_All, HSP 19.7; Unigene7931_All, HSP 16.1; CL658.Contig2_All, aldehyde dehydrogenase family of seven members A1; CL2227.Contig1_All, acetyltransferase 1; Unigene5878_All, hemolymph juvenile hormone-binding protein; CL887.Contig1_All, aldose 1-epimerase-like; CL1060.Contig3_All, 17-beta-hydroxysteroid dehydrogenase; Unigene6918_All, Hematopoietically-expressed homeobox protein HHEX homolog; Unigene6953_All, cytochrome P450 B5. Y axis represents the relative expression levels of genes. Ribosomal protein L32 (Rpl32) was used as an internal control