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Confirmation in at least the case of ATP6V0C-MO that the phenotype observed was also validated by the hi1207mutant of an insertional mutagenesis screen[12], further demonstrated the validity and sensitivity of the screen.
The simulation was also validated by the experiment.
This difference was also validated by both SPECT and in excised xenografts (Figure 3a, Figure 2).
This proposed ultrasensitive electrochemical aptasensor method was also validated by comparison with the classic instrumental methods.
A Computational fluid dynamics (CFD) model was also validated by the experimental results.
High specificity of the qPCR assay was also validated by both in silico and experimental analyses.
The expression of miR-638 target gene in clinical CRC tissues was also validated by immunohistochemical assay.
The BSA grafting protocol was also validated by comparing the analyte adsorptions with simply drop casted modifications.
The three-dimensional dynamic simulation model, based on the chemical reaction kinetics, was also validated by the experimental data.
The importance of ascB for cell growth on cellobiose was also validated by overexpression and knockout studies.
The model was also validated by an independent set of experimental results from two different concrete mixtures.
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CEO of Professional Science Editing for Scientists @ prosciediting.com