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. 2017 Nov 6;45(21):12090–12099. doi: 10.1093/nar/gkx1045

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© The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 3. — Schematic illustration (left) and 2.5% agarose gel electrophoresis (right) for endonuclease digestion of the circular dimer, trimer and tetramer with MspI and BspHI. Lane L: DNA ladder with 100–1000 base pairs. Lane 1: tetrahedron monomer as a control; Lane 2: dimer without any enzyme; lane 3: dimer digested with MspI; lane 4: dimer digested with BspHI; lane 5: dimer digested by both of MspI and BspHI; lane 6: trimer without any enzyme; lane 7: trimer digested with MspI; lane 8: trimer digested with BspHI; lane 9: trimer digested by both of MspI and BspHI; lane 10: tetramer without any enzyme; lane 11: tetramer digested with MspI; lane 12: tetramer digested with BspHI; lane 13: tetramer digested by both of MspI and BspHI.