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In the present study, this chip was divided into two samples (sample x and sample y), the former of which containing the large anorthosite clast was used for PTS x-1 (Figure 1b).
Cultured human MDDCs (1×106cells) were divided into two samples (5×105cells each).
Beads were washed as previously described and divided into two samples for subsequent protein or RNA analysis.
The sRNA-pool was then divided into two samples (each 5 μg).
After dissection, gray matter was divided into two samples (Fig. 1).
The supernatant was divided into two samples, which were directly used for the filter retardation assay.
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For analysis, the microarray data were divided into two sample subsets.
The samples were randomly divided into two sample plates and screening using the panel of 352 antibodies was performed for both plates.
In brief, a sub-experiment essentially consists of a collection of microarrays that is divided into two sample categories, or phenotypes.
One sample for each as-deposited pair was divided into three samples using a diamond scriber.
The above-prepared compounds are divided into five samples and the mechanical hardness is tested by Monsanto and Vickers hardness tests.
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