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Convergence of the parameters sampled was checked in TRACER v.1.5 and combined with Log-Combiner v.1.5.4 [ 56].
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This particular sample was checked and sent to lower-level labs after 24 hours".
The purity of each step protein sample was checked by SDS-PAGE.
The sample was checked for fluoride detection using spectrophotometer at wavelength 570 nm.
The structure of the phase-change samples was checked by X-ray diffraction [8].
Additionally, the surface roughness of each sample was checked after electropolishing with the aid of Atomic Force Microscopy (AFM).
The homogeneity of purified sample was checked using 10% SDS-PAGE prepared according to Laemmli (Laemmli [1970]).
The sample was checked for species absent from the sub-sample.
Successful amplification of the samples was checked by agarose gel electrophoresis.
The quality of each sample was checked by a Bioanalyzer 2100 (Agilent, Waldbronn, Germany).
The integrity of each RNA sample was checked with an Agilent Bioanalyzer® (Agilent Technologies).
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