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We gathered our sample by placing the link to our survey on capital-market and SRI related websites or message boards and in newsletters for SRI.
Originally, we proposed to recruit the sample by placing mobile units in selected "hotspots" for both study arms to serve as recruitment venues.
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Some newer microscopes allow imaging of wet, nonconductive samples by placing them in a gaseous environment.
Hematocrit values were immediately determined after sampling by placing fresh blood in glass capillary tubes and centrifuging for 5 min in a microhematocrit centrifuge.
Root exudates from Eriophorum vaginatum and Rhododendron groenlandicum, grown in ombrotrophic bog cores removed from the field, were sampled by placing individual root segments of excavated roots into custom-designed root traps.
For the semiquantitative assessment, 9 vascular areas were identified and sampled by placing different regions of interest.
After rubbing, the fingers were sampled by placing the fingertips directly on the 5% sheep-blood agar plate.
Urine samples were obtained as spot samples by placing the rats in a metabolic cage for 30 to 60 min and waiting for them to urinate.
For children who were not toilet trained, we collected urine samples by placing a surgical insert into a clean diaper at the beginning of the study visit.
Threshold values for Ct calculation were manually selected for all samples by placing the threshold line at the intersection where the signal intensities of the fluorescence traces surpassed background levels and began to increase (i.e., the linear portion of the curve).
The formvar film on a Cu grid was used for samples preparation by placing 50 μL of silica suspensions in ethanol on abovementioned support, followed by drying at ambient conditions.
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