Exact(39)
The developed assay was used in analysing 469 soybean samples and five soybean products under different processing.
Two archaeal 16S rRNA gene libraries were constructed from free-living planktonic microbe samples and five from marine sponges, for the two environments, Guanabara Bay and Cagarras Archipelago.
All fields of the hemacytometer were examined thoroughly in low parasites densities samples and five fields were averaged for high parasite densities samples.
Both of these markers were positive in nine samples, kDNA alone was detected in six samples, and five were nDNA and kDNA-free.
Samples and five discs of graded hydroxyapatite phantoms were scanned with X-rays generated by a sealed micro-focus X-ray tube (tungsten anode) at 90 KeV and 110 µA with an integration time of 400 s.
Statistical analyses for differential protein expressions in cancerous versus non-cancerous tissue samples were performed on the basis of the following criteria: (1) Proteins had to have iTRAQ ratios determined in at least five of the EmCa samples and five of the normal proliferative samples.
Similar(21)
We distinguished three clusters of sediment samples and two clusters of pore water samples.
We detected nine soybean samples, six maize samples, seven potato samples and two rice samples by the MPCR MHA method; at the same time we also detected them with single PCR MHA method.
Three phases of fcc/L12-Ir3Nb/B2-IrAl fcc/L12-Ir3Nb/B2-IrAl fcc/L12-Ir3Nb/B2-IrAlof fcc/L12-Ir3Nb/L12-Ni3Al/B2-IrAl were characterized in one sample.
PCR detection demonstrated BKV genome in three of five PBMC samples, six of six urinary cell samples, and two of four renal biopsies.
SV40 genome was detected in two of five PBMC samples, one of six urinary cell samples, and two of four renal biopsies.
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