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. 2018 Apr 18;2018:7360147. doi: 10.1155/2018/7360147

Figure 3.

Figure 3

The results of amplification of nucleic acids extracted from the samples using universal primers specific for the 16S rRNA gene. Lane 1: tampon number 1, 2: washout from the cavity number 1, 3: membrane of tampon number 2, 4: washout from the tampon number 2, 5: membrane of washout number 2, 6: washout from the cavity number 2, 7: membrane of washout number 1, 8: tampon number 2, 9: tampon number 2, 10: membrane of tampon number 1, 11: negative control (PCR k−). Molecular weight markers (step 100 bp.) are applied on the last lane.