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In the Masson lesion photo, the margins of each sample were labeled as M. It was demonstrated that tumor invasion ability in PVP group was most powerful, followed by pure CUR and CUR@PVP groups.
We used two chips in which RNAs from each sample were labeled either with cy3 or with cy5.
50 micrograms of protein from each paired sample and from an aliquot of the pooled CSF sample were labeled with one of three N-hydroxysuccinimide cyanine dyes.
Peptides from the rapamycin treated sample were labeled with 13C6-PIC, while those from the non-rapamycin treated sample (methanol alone) with 12C6-PIC (Figure 1A).
Amino groups of surface (non-lysed sample) or total proteins (detergent-treated sample) were labeled for 20 min at 4°C with 1 mM sulfo-NHS-Biotin.
Two µg of total RNA from each sample were labeled using the miRCURY™ Hy3™/Hy5™ labelling kit and hybridized on the miRCURY™ LNA Array (v.8.0) (Exiqon, Vedbaek, Denmark).
Similar(29)
The sample was labeled as ZnAl LDH.
This powdered sample was labeled as sample A (MnFe2O4).
This coal sample was labeled as 'raw coal (RC)'.
This sample was labeled as the raw Macadamia nutshells (RMN).
The unetched sample was labeled as A. The etching rate was about 0.2 μm min-1.
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