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. 2022 Aug 18;13:953654. doi: 10.3389/fpls.2022.953654

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Copyright © 2022 Singh, Pillay, Naicker, Alexandre, Malatji, Mach, Steinkellner, Vorster, Chikwamba and Tsekoa.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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SDS-PAGE and Western Blot analysis of the purification of CAP256-VRC26 mAbs produced in N. benthamiana (ΔXTFT) with and without genome editing vectors. (A,B) SDS-PAGE and Western blot analysis of the purification of CAP256-VRC26.25 without genome editing vectors. (C,D) SDS-PAGE and Western blot analysis of the purification of CAP256-VRC26.25 produced with genome editing vectors. M represents the molecular weight marker (PageRuler™ Plus Prestained Protein Ladder).