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The position of the central venous catheter was verified using a standard chest radiogram.
The probe concept was studied using a Finite Element Method (FEM) tool and experimental verified using a standard defect.
Secretion of the CCR2-inhibiting fusokine by the engineered mesenchymal stromal cells was verified using a standard ELISA for detection of CCL2 (eBioscience).
The change in scattering upon Hoechst staining was verified using a standard flow cytometer -FACSCalibur flow cytometer (Becton-Dickinson, Franklin Lakes, NJ).
The capacity for each assay to discriminate between SNP alleles was verified using a standard curve of artificially created allelic ratios using DNA from samples homozygous for the major and the minor alleles.
The single gene deletion of random strains was verified using a standard genomic DNA PCR protocol with primers flanking 100 bp upstream of the transcriptional start site and 100 bp downstream of the stop site of the specific gene knocked out.
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The wavelength accuracy of the instrument was verified using a holmium oxide standard (NIST SRM 2034), and the linearity of the spectrophotometer was verified with NIST SRM 930D glass filters.
The accuracy of calculation is verified using an industry standard finite element solver.
The accuracy of method was verified using a real sample (spiked tap water) by standard addition calibration technique.
The results were verified using a breath test.
This was verified using a simulated exercise.
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