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The polymerase was expressed and purified from the baculovirus system as we described previously [17].
Wound-healing assay and transwell assay were performed following protocols as we described previously.
Western blotting as well as total protein extraction and quantification were performed following procedures as we described previously.
We described previously a novel DNA amplification technique, termed ramification amplification (RAM) (Zhang et al., Gene 211 (1998) 277).
γFe2O3 NPs were prepared according to the method we described previously [12].
For these simulations, we used the same sampling process as we described previously.
The experimental system for DC treatment is the same as we described previously (Niepa et al. 2012, 2016b).
Western blotting was carried out as we described previously [14].
The immersion AMG was performed as we described previously [40].
RNA preparation was done as we described previously [26].
Recombinant hBD-3 was produced and tested for endotoxin contamination as we described previously [25].
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