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The HPV 16 samples were verified by a standard PCR test.
The crystallinity and purity of the samples were verified by XRD (Cu-Kαradiation) and thermo gravimetric measurements (20 °C/min).
The SH and DH structures of the samples were verified by high-resolution transmission electron microscopy (HRTEM).
The pigment samples were verified analytically as described in [53] and the paint samples were prepared in animal glue and painted on paper [52].
Our previous study on Streptococcus mutans showed the mechanical evolution on bacterial surface for 2 h, monitored by continuous AFM mechanical mapping, and the microbial samples were verified to remain alive within such duration [8 10].
The morphology, structure, and interplanar distance of the samples were verified using a focused-ion beam-scanning electron microscope dual-beam system (FIB-SEM, FEI Helios Nanolab 600i), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM JEOL JEM-2100F).
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An extended stability of the DNPH-glucose derivative in spiked plasma samples was verified via the employed HPLC-UV method.
The quality of the extracted samples was verified by polymerase chain reaction (PCR) and gel-electrophoresis after the extractions.
The presence of tumor tissue on the arrayed samples was verified on hematoxylin eosin stained section.
The quality of the samples was verified by hybridization with specific probes to detect viral RNA and viral/endogenous sRNAs.
The absence of DNA from RNA samples was verified by PCR prior to reverse transcription, using rpoB-specific primers.
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CEO of Professional Science Editing for Scientists @ prosciediting.com