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Test samples, control and loperamide were given orally by means of a feeding needle.
Non-irradiated samples (control cells) underwent all procedures except the irradiation step and were kept on ice.
The three samples: control, case and internal standard (combination of equal amounts of tested samples) are pooled after labeling and separated simultaneously.
All frozen samples (control and test serum samples) were thawed for approximately half an hour at room temperature, vortexed before processing and transferred to appropriately labelled tubes.
All statistical analysis was considered significant when p value <0.05. Figure 3 presents the SEM micrographs of zirconium samples (control and anodised).
Three samples (control sample, kitchen waste, and kitchen waste plus poultry faeces) were heated in an oven at 50 °C to remove any moisture.
Thus, 41 commercially available potting media and media components and two soil samples (Control) were assessed for hydrophobicity at different moisture levels via Water Droplet Penetration Test (WDPT).
Cells were incubated with the four samples: control (cells in RPMI media), ATO 5 μM (ATO5), liposomes only (Lip) and lipo-ATO 5 μM (ATO5 + Lip) for 48 h.
On comparing paired samples (control and irradiated for implants and femurs) there were no significant differences in mean colony counts after inoculation between the control and experimental femurs at 24 and 48 h.
These bins were then used to analyze the other two samples (control siRNA and UNG siRNA).
The control samples (control; n = 5) were found to form a separate cluster from that of LA and CEmb.
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