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The sensing mechanism was based on the nanochannel blockage caused by MS2 binding to immobilized capture antibodies.
Previous molecular description of the mammalian timekeeping mechanism was based mainly on transcriptional/translational feedback loops (TTFLs).
The sensing mechanism was based on nucleophilic addition between CN− and indolium group, which was confirmed by 1H NMR and mass spectrum analysis.
The detection mechanism was based on nano-scale transduction of the detection of the localized binding event between the functional binding sites and the chemical species of interest.
This mechanism was based on our previous modeling of alkane combustion and, in particular, on our study of the oxidation of n-heptane.
The detection mechanism was based on the monitoring of the electrochemical current response change of TB by the square wave voltammetry (SWV) when immunoreaction occurred on the surface of electrode.
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The second mechanism is based on subcellular localization (Fig. 8b, bottom).
Our mechanism is based on stochastic datagram relocation.
The underlying mechanism is based on the interaction of para-H2 with a substrate of interest via an Ir-based catalyst system1.
The underlying mechanism is based on the shear stress transfer between hard fibers and soft matrix.
The sensing mechanism is based on the displacement of the metal ion from the NTA Ni2+ chelates.
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