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Prepare above materials.
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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.
The feedstock prepared above was injected into a stainless steel autoclave with a Teflon lining.
CPLA microparticles were prepared by adding collagen acetic acid solution into PMAA-PLA microsphere suspension prepared above.
The mordanted silk sample was dyed using the mixed dye solution prepared above for 1 hour at 60°C.
Based on the aligned fibrous array prepared above, we fabricated twisted ropes using the setup shown in Fig. 1(c).
Hydrogels prepared below 25 °C were transparent and homogeneous whereas those prepared above 25 °C were slightly hazy to opaque.
The TiO2 nanobranches were grown by immersing the TiO2 nanorod arrays prepared above in a bottle filled with an aqueous solution of 0.2 M TiCl4.
Then, the magnetite suspension prepared above (20 mL) was placed in a 250 mL round-bottom flask and allowed to settle.
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