Sentence examples for conversion samples from inspiring English sources
Low conversion samples were collected and copolymer compositions were determined with 13C n.m.r. by integration of the carbonyl resonances.
Copolymer compositions of low conversion samples were determined from 13C n.m.r. by integration of the carbonyl resonances.
Prior to cDNA conversion, samples were treated with RNase-free DNAse (QIAGEN) to eliminate any contamination with genomic DNA.
After conversion, samples were desulfonated and purified using column preparation.
Note there were distinct differences between clusterings of BS and oxBS conversion samples in brain tissue, implying a considerable amount of 5hmC in the brain.
The two additional bioactive compounds were the main conversion products, being identified as the quinoneimine (m/ z 413.1985, C25H25N4O2+, Δ 115.0990 u) and the hydroquinone (m/ z 415.2134, C25H27N4O2+, Δ 113.0841 u), both being present in all conversion samples.
The P OH, HPO42 −, PO43 −, CeO2 and a little Ce(OH 2 exist in the surface of the composite coating and the composite sample has best corrosion resistance than the untreated sample, chromate conversion sample and phytic acid conversion sample.
A novel environmentally-friendly composite coating with a cerium conversion coating deposited on the phytic acid conversion sample was formed on an AZ31B magnesium alloy.
Similar to previous results in human cell lines (Komor et al., 2016), besides C→T conversion, we observed rare C→G substitution (sample #21) and C→A conversion (sample #22).
The analysis process used by RNA-eXpress involves six phases: data import and conversion, sample merging, algorithm execution, and optionally external GTF comparison, sequence extraction and read counting.
To measure and remove timing-induced phase error [ 19] due to the random delay between the trigger signal and the subsequent A-to-D conversion (sample clock), a calibration signal was generated using a stationary mirror in the calibration arm (Fig. 3) as described in [ 19].
