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PNA melting point differences between perfect match and single insertion were measured by melting point analysis.
The high reproducibility of LightCycler determinations is especially important when small melting point differences are to be determined.
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The formation of the solid-phase and liquid-phase sintered regions in the partially melted region is attributed to the melting point difference of A12O3 and TiO2.
Crystallization by slow cooling creates non-statistical concentration fluctuations which result in excess forward SANS, so a melting point difference of 1°C is still sufficient to trigger 'clustering' or 'segregation' of PE and DPE.
Therefore, at similar distances from the melting point, the differences in translational motion are attenuated by the relative quantities of thermal energy.
Furthermore, measured densities and melting points, indicated differences in molecular packing for odd and even chain length compounds, attributed to geometries necessary for higher packing efficiencies and greater lattice stability.
Here, we have shown that full base dual-labeled PNA is apt material for fluorescence probe-based melting point analysis with large difference in the melting temperature between full specific hybridization and that of partial hybridization, including insertion and deletion.
It can be easily fused and spliced with SiO2 fibers due to a small difference of melting point between them.
There was a large temperature difference between melting point and decomposition point of about 50°C for these complex salts.
Despite the big difference in melting point, both oxide and metal fuels have a relatively similar margin to melting during postulated accidents.
The large difference in melting point between the HEA and the substrate material (AZ91D), and the limited reaction and the lack of fusion between the HEA and Mg have made it possible that a metal particles reinforced AZ91D composite material was produced.
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