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The SnO2 nanotube arrays on FTO glass prepared above were put in an aqueous solution of 0.2 M TiCl4 at room temperature.
Glycome profiling of the sequential extracts prepared above was carried out as described previously [ 55].
Low passage clinical isolates prepared above will be inoculated onto the HEp-2 cells at 2500 and 5000 IFU per well.
A total of 10 μl of serially diluted extracts from the watery plates prepared above were transferred into the test plates containing parasitized RBCs and incubated in a candle jar at 37°C for 72 hours.
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CPLA microparticles were prepared by adding collagen acetic acid solution into PMAA-PLA microsphere suspension prepared above.
Hydrogels prepared below 25 °C were transparent and homogeneous whereas those prepared above 25 °C were slightly hazy to opaque.
The soft packed NCM/LTO batteries were assembled with Li(Ni1/3Co1/3Mn1/3 O2 (NCM) as the cathode, the LTO prepared above as the anode, and 1 M LiPF6/EC+DMC+EMC as the electrolyte solution.
Molecular orientation and mechanical properties of miscible poly styrene)/poly vinyl methyl ether) (PS/PVME) blends were compared with those of heterogeneous PS/PVME blends prepared above their temperature of phase separation.
As prepared, above 90% of the added catalyst existed in the third-liquid phase, and after 4-h on stream for a large excess of n-butyl bromide to sodium salicylate, the fraction of catalyst retaining in the reactor was reduced to around 80%.
The feedstock prepared above was injected into a stainless steel autoclave with a Teflon lining.
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