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One sample for each as-deposited pair was divided into three samples using a diamond scriber.
After catapulting the cells of interest, each group of cells (normal ovarian cyst epithelium, normal ovarian surface epithelium, and ovarian carcinoma) was divided into three samples each, for a total of nine cell samples.
PBMC were divided into three samples, two were in vitro irradiated and the third sample was used as a control.
Once the GNSs were coated with mPEG-SH and PEG7, they were divided into three samples before conjugation to fluorescein.
At time of harvest, shoot and roots were weighted; aerial parts of each treatment were further divided into three samples for cadmium quantification, morphological parameter and pigment content measurements, and protein extraction.
Nuclei were resuspended in 1 ml of 20 mM Hepes pH 7.6, 150 mM NaCl, 2 mM EDTA, 1× protease inhibitor cocktail (Roche, Basel, Switzerland), 0.5 mM PMSF, 1 mM DTT, 0.5 U/ml of RNAseOUT/SUPERase-In (Invitrogen/Ambion), homogenized using a 1 ml dounce homogenizer (three times with loose pestle, two times with tight pestle), and divided into three samples of equal volume.
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The above-prepared compounds are divided into five samples and the mechanical hardness is tested by Monsanto and Vickers hardness tests.
Labelled MSCs were fixed in 4% paraformaldehyde and divided into four samples containing increasing numbers of cells (0.125 × 106, 0.25 × 106, 0.5 × 106, 1 × 106).
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.
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