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. 2019 Nov 27;125(1):10–18. doi: 10.1080/03009734.2019.1690603

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© 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 5. — Protein composition of seminal prostasomes from oligozoospermic men separated by lectin-affinity chromatography. Seminal prostasomes separated by lectin-affinity chromatography were resolved on 10% SDS-PAGE under reducing and denaturing conditions and stained with silver. Representative total protein patterns of non-bound (nb) and bound (b) fractions separated on a Con A column and on a WGA column were shown. Samples were loaded as isolated (equal volume/line to reflect yield), and total protein amounts were: line 1 (19 μg), line 2 (10 μg), line 3 (14 μg), line 4 (11 μg), line 5 (50 μg), line 6 (6 μg), line 7 (24 μg), line 8 (13 μg). Characteristic prostasome-associated bands in the region of 90–150 kDa are marked (asterisk). Numbers indicate the position of molecular mass standards (kDa). sPro-O1 and sPro-O2: different isolates of seminal prostasomes from oligozoospermic men.