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These mouse samples were processed with the same reagents and procedures as used for human samples.
These experiments were done using the same technique as used for the sample shown in the old Figure 2 (now Figure 3) and are therefore directly comparable.
The samples on fused silica plates were fabricated with the same preparation and post-fabrication processing conditions as used for preparing the samples on Si.
Mock-infected cells were exposed to the same dilution of mock HEp-2 supernatant as used for rgRSV-infected samples.
Bioanalysis of PK was performed using the same method as used for the preclinical samples.
These cells were mounted in the same 90% glycerol solution as used for the calibration sample in section 3.3.
β-actin served as reference gene and was used for samples normalization.
The samples were depleted using the same procedure as used for preparation of the peptidomic samples.
RNA for quantitative PCR analysis was the same samples as used for DGE.
The second mean was calculated from the same duplicate samples as used for intra-assay CV.
Analytical blanks were made at each location using the identical water and aluminium foil as was used for the sampling.
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