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. 2015 May 19;6:427. doi: 10.3389/fmicb.2015.00427

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Copyright © 2015 Shen and Fulthorpe.

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) or licensor 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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DGGE gel of 341GC-MOD783R PCR amplifications on DNA samples from (1) original Acer negundo DNA, (2) MscI digested Acer negundo DNA, (3) PvuII digested Acer negundo DNA, (4) original Ulmus parvifolia DNA, (5) MscI digested Ulmus parvifolia DNA, (6) PvuII digested Ulmus parvifolia DNA, (7) original Ulmus pumila DNA, (8) MscI digested Ulmus pumila DNA, (9) PvuII digested Ulmus pumila genomic DNA and L–DGGE ladder. Note products are all bacterial due to use of 783 primer, but are not well amplified from undigested targets.