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. 2022 Jul 29;12:13089. doi: 10.1038/s41598-022-17382-x

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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2% agarose-TAE gel displaying the efficacy of the Multiplex PCR assay to identify wild, trap-collected specimens with examples of non-specific amplification. Species-specific amplicon sizes are indicated. Lanes 1 & 2: C. capitata, Lanes 3 & 4: C. cosyra, Lanes 5 & 6: C. quilicii, Lanes 7 & 8: C. rosa, Lanes 9 & 10: B. dorsalis, Lane 11: No template control, Lane L: GeneRuler 100 bp DNA ladder (Thermo Scientific). The original gel is presented in Supplementary Fig. S3.