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. 2019 Mar 13;9:4389. doi: 10.1038/s41598-019-39732-y

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© The Author(s) 2019

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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ELISA performed with 15 individual phage clones randomly picked up from the eluted phage pool after the 3rd round of bio-panning. The B1 peptide (a) or HeLa cell lines (b), were coated and 10¹⁰ pfu of each phage were added. Blocking buffer without B1 peptide was used as negative control for (a), and HeLa/Gpt cells were used as negative control for (b). Data represent the binding of the phage clones to the B1 target (a) and HeLa cells (b) as the mean ± SD of three separate experiments.