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. 2020 Jun 15;37(4):485–498. doi: 10.1007/s10719-020-09931-1

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© The Author(s) 2020

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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Fig. 5 — Western blot analysis of protein extracts from animal heart valves, pericardia and HAECs using anti-Le^a (a), anti-Le^b (b), anti-sialyl Le^x (c), anti-Le^x (d), and anti-Le^y (e) antibodies. Positive control samples were Le^a-, Le^b- and sLe^x-BSA neoglycoconjugates. For Le^x and Le^y staining, recombinant mucin-type fusion proteins carrying Le^x (CP-Le^x) or Le^y determinants (CP-Le^y) were used as positive controls, while C-P55 was the negative control