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177Lu-DOTATATE/-TOC was prepared with minor modifications as previously reported [14],[14].
Sample preparation was carried out with modifications as previously reported (Atherton et al. 2006; Moazzami et al. 2011).
Cells were prepared following the protocol by Sana et al., with minor modifications as previously reported.
RNA isolation from Arabidopsis plants was performed with the RNA Aqueous-Midi kit (Ambion, Inc; catalog: #1911) following the manufacturer's recommendations with modifications as previously reported [ 27].
DNA was extracted from leaves and AFLP analysis was performed based on the protocol by Voss et al. [ 2] with minor modifications as previously reported [ 25, 26], using eight primer combinations (Table 1).
The flushed material was centrifuged and the pellet was processed to extract bacterial DNA, using the QIAamp DNA Stool Mini Kit (Qiagen, Valencia, CA, USA) with minor modifications as previously reported [ 4].
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Genomic DNA (1 μg) from each sample was modified by sodium bisulfite as described by Herman et al (1996) with slight modification as previously reported (Sriraksa et al, 2010).
With a well-established tip-modification method as previously reported [20], glycine molecules were introduced to the AFM tips.
Dose and schedule modifications were carried out as previously reported (Kunitoh et al, 2009).
Determination of the amino acid sequence of BacCH91 using Edman degradation required chemical modification of multiple residues, as previously reported for other lantibiotics (Meyer et al. 1994).
The amount of DNA/well, an indication of cell numbers, was assayed using a microplate modification of the diphenylamine assay as previously reported [ 16, 17, 23].
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