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The comparison between the simulations and measurements confirms the validity of this system.
We fused the epitope tags at the 3′ region of global transcription factors of Streptomyces coelicolor to test the validity of this system.
Under conditions established through experiments with chemically synthesized model targets comprising both conserved and variable regions of 16S rDNA, we confirmed the validity of this system using real 16S rDNA targets.
The validity of this system has previously been demonstrated [ 37].
The microarray analysis provides firm support for the validity of this system as a model of human Ewing's sarcoma.
The reliability and validity of this system in measuring BF% has been previously verified in multiple ethnicities [ 20, 21].
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To test the biological validity of this systems level analysis implicating EMT in the origin of IPF myofibroblasts, we selected the epithelial intermediate filament component, Keratin 18, for further analysis.
However, our findings support the validity of this scoring system as a measure for severity of underlying illness.
The validity of this measurement system can be affected by atmospheric conditions, particularly temperature, humidity, and precipitation.
The validity of this isolation system was confirmed by the detection of CTCs in blood samples from 46 of the 60 (76.7%) HCC patients, including patients with tumors <3 cm in diameter and patients with Edmondson Steiner grade I or II.
The validity of this scoring system was confirmed in the body wall and mid-hindgut, where Likert-quantified scores were comparable to those obtained by counting or by semiautomated quantification respectively (data not shown).
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