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The representative samples (5.0 g each) were extracted using the acetate buffered extraction under the optimized conditions and were analyzed using HPLC system of the reported methods.
The air-dried and powdered plant materials (10 g of each) were extracted with 400 ml methanol (CH3OH) by Soxhlet extraction for 8 hours.
The procedure to calculate the H/V spectra can be summarized as follows: First, a high-pass filter of 0.1 Hz was adopted, and seven time sections of 163.84 s each were extracted from the original data considering recorded noise.
Plasma samples (12 μL each) were extracted with 2 mL of ethyl ether, as described previously [ 79].
14 Two spots of 0.5 cm diameter, corresponding to 10 µL of blood each, were extracted and eluted in 100 µL miliQ water (Millipore, Billerica, MA).
The cells (10 cells each) were extracted using PCA (see above), and the high-performance liquid chromatography/mass spectrometry (HPLC/MS) method was validated (Klawitter et al, 2007).
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Unique DNA sequence of each was extracted as a text file and examined using blast analysis.
The air-dried fruit sample (100 g each) was extracted using 70% ethanol at room temperature.
If more than one miR-200 family member or cancer type was reported in one study, each was extracted separately.
After removing duplicates, methylation levels of each C were extracted by programs of each mapper.
SNPs within each group were extracted for the analysis.
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