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As the use of the A1C test gained traction, dozens of different analytical methods based on different assay principles (e.g., ion-exchange chromatography, affinity chromatography, immunoassay, and electrophoresis) were used to measure glycated hemoglobin.
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High correlations between oxidative potential and transition metals such as Cu and Fe have been reported previously based on different assays (Briedé et al. 2005; Mudway et al. 2004; Shi et al. 2006).
The APC ratio was cross-checked using three different assays based on different FV activation pathways, which yielded consistent, normal results (Table I).
Quantification accuracies of real-time PCR assays based on different standards were compared.
Therefore, using multiple assays based on different antioxidant mechanisms would be crucial in providing a more reliable assessment of the samples antioxidant capacity [ 4, 24].
Several commercial multiplex assays, based on different techniques such as conventional polymerase chain reaction (PCR) (VYOO®, Analytik Gena, Germany), real-time PCR (Magicplex™ Sepsis Real-time Test, Seegene, Korea; LightCycler® SeptiFast, Roche, Switzerland; Sepsitest™, Molzym, Germany) and microarray (Prove-it™ Sepsis, Mobidiag, Finland) are now on the market.
These two assays are based on different principles and were used to eliminate a possible interference of tested nanozeolites with the assay [26, 27].
The comet assay is based on different migration velocities of DNA fragments of different sizes in agarose gels.
The treatment assays were based on different types of biostimulants, such as a slow or fast-release fertilizer, combined with commercial surfactants.
These assays are based on different technologies but they all rely on the principle to measure reduction of virus infectivity in susceptible cells in the presence of inhibitory reagents.
To compare the effect of different labels on the assay sensitivity, LFIAs based on different gold nanoparticles and silver enhancement procedure were performed.
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