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The samples illustrated in this article were all from Ag NW isopropyl alcohol suspensions.
In general, the correlations appeared similar to those observed between replicate UHRR samples illustrated in Figure 4.
Sections (4 μm) were cut onto slides, and stained with the panel of antibodies at concentrations and with control samples illustrated in Table 2.
Figure 2 shows the results of immunoblotting obtained after incubation of the cereals samples, illustrated in Fig. 1, with polyclonal anti-gliadin antibodies.
Multiple dimeric bands are present for Prdx1 and Prdx2 in the samples illustrated in Fig. 1, although the extent of the dimeric bands is less for the equivalent samples shown in Fig. 5.
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The rating of color fastness to water of unmordanted and mordanted samples illustrates in Table 6.
The microRaman spectrum obtained from one of the green blue particles at the top right edge of the sample illustrated in Fig. 2B is shown in Fig. 6.
Finally, a 180-nm layer of ZEP 7000-22 electron beam resist was spin-coated on top, resulting in the sample illustrated in Figure 3a.
The SEM image of the 400 °C annealed sample illustrated in Fig. 1a shows the formation of nanoparticles having a pseudo-spherical morphology and exhibiting an agglomeration behavior.
Detailed investigation of the failure mechanism in these samples illustrated that trabecular bone often fails in delamination, providing a mechanism for energy dissipation while conserving trabecular bone architecture.
The synthesized TiO2-CNF catalyst supports were analyzed by FTIR to evaluate the chemical bonding in the samples, and the IR spectra of the samples are illustrated in Fig. 6.
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