The survey period was divided into five non-equal study period for enough quantity isolates in statistic analysis.
It is necessary to note, a considerable quantity isolates (30/98, 30%) were resistant to all tested drugs, however we were not able to designate these isolates as XDR due to lack of fluorquinolones resistance data [ 27, 28].
By using this method, the quantity of isolated SWNTs deposited can be controlled by varying the deposition time.
The sample preparation determines quality and quantity of isolated colorants.
The quality and quantity of isolated pDNA were determined using spectrophotometer (Epoch Microplate Spectrophotometer, Take3 Micro-Volume Plate, BioTek, Bad Friedrichshall, Germany) and agarose gel electrophoresis.
Quality and quantity of isolated total RNA was measured spectrophotometrically (NanoDrop; PeqLab Biotechnology, Erlangen, Germany), whereas RNA integrity was assessed by the 2100 Agilent Bioanalyser (Life Science Group, Penzberg, Germany).
Integrity and quantity of isolated RNA were assessed using a RNA Pico chip on an Agilent Bioanalyzer 2100 (Agilent Technologies) (Additional file 7: Table S5).
The quantity of isolated total RNA was checked for integrity by 2 % agarose gel electrophoresis as well as on an Agilent 2100 Bioanalyzer.
Quality and quantity of isolated total RNA is measured spectrophotometrically (NanoDrop, PeqLab Biotechnology, Erlangen, Germany) while RNA integrity is assessed by the 2100 Agilent Bioanalyser (Life Science Group, Penzberg, Germany).
Quality and quantity of isolated total RNA and miRNA were determined using an Agilent 2100 Bioanalyzer for RNA (Agilent Technologies, Santa Clara, CA).
