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The direct labeling protocol was performed for sample RNAs, which included steps of first strand synthesis, slide preparation, hydrolysis, cDNA purification, hybridization and array washing.
A comparison of the two pretreatment methods applied in this study was performed for sample J12sc24 (VERA-4982), and the resulting 14C ages are in excellent agreement.
At first, a PCA was performed for sample distribution overview.
Beta-actin western blotting was performed for sample loading controls.
Furthermore 190.5 million reads belonged to whole genome sequencing performed for sample 1.
Runs were performed for sample duplicates and readings were carried out at default settings in an ABI7500 real time PCR system equipped with the SDS v1.4 software.
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High Resolution Transmission Electron Microscopy imaging combined with Electron Diffraction analysis were performed for samples synthesized at 2.6, 5.0 and 8.5 GPa and 1100 K.
Comparison of the PL intensity from NPs of different sizes was performed for samples matched in OD at 250 nm.
As is shown in Figure 4, since XPS analysis was performed for samples A, B, and C, Ga2p and N1s core level spectra were measured.
Serial dilutions were performed for samples exceeding 5.3 log10 copies/mL.
These were performed for samples from the same genotype but for different treatments or time-points.
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