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. 2016 Feb 9;16:17. doi: 10.1186/s12866-016-0631-9

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© Górska et al. 2016

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. 2 — Immunoblotting of proteins isolated from analyzed strains: M – low molecular mass marker: 94, 67, 43, 30, 20.1, 14.4 kDa, line 1 – L. johnsonii 142, line 2 – L. johnsonii 151, line 3 – L. rhamnosus LOCK 0900, line 4 – L. casei LOCK 0919, with sera: s1– rabbit polyclonal serum against L. paracasei LOCK 0912, s2 – rabbit polyclonal serum against L. animalis murinus 148, s3 – rabbit polyclonal serum against L. johnsonii 142, s4 – rabbit polyclonal serum against L. johnsonii 151, s5 – serum from germ free mouse, s6 – serum from mouse living under pathogen free conditions, s7 – serum from mouse living under conventional conditions, s8-s10 sera from human healthy adults, s11-s13 human umbilical cord blood sera. These images were cut from the same gel, merged and the appropriate scaling was used