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The effect of gold concentration on Au@NP formation was tested within the range of 10 300 ppm Au3+.
In this work, a metabolically engineered Escherichia coli strain with strongly reduced acetate formation was tested for the production of a plasmid vaccine at high cell-densities.
Biofilm formation was tested 17 hours following each exposure.
Therefore, the influence of iron concentration on biofilm formation was tested.
The ability of IL-7 to induce OC formation was tested in cultures of purified monocytes alone and in co-cultures with purified T or B cells treated or untreated with IL-7 at 2,5 and 15 ng/ml.
Their ability for biofilm formation was tested and their cell invasiveness was confirmed by a flow cytometric invasion assay (FACS), fluorescent in situ hybridization (FISH) and immunohistochemistry. S. aureus was the predominant species (57.7%) in RT patients, whereas Streptococcus pyogenes was most prevalent (20.2%) in PTA patients.
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Endothelial cells were co-cultured with the degradation products and the angiogenic cell behaviors, including cell proliferation, migration and tube-like structure (TLS) formation, were tested by MTT assay, cell migration quantification method (CMQM), and tube-like structure quantification method (TLSQM) respectively.
Here, the effect of erythritol and castanospermine on α-glucosidase activity and Hz formation were tested.
The effects of AM peptide on osteoclast-like multinucleated cell formation were tested in vitro.
Human peripheral-blood mononuclear cells, separated by Isopaque-Ficoll flotation and E-rosette formation, were tested by the fluorescein fluorescence polarization method of Cercek & Cercek (the SCM test).
Several genes that are required or associated with fruiting body formation were tested for expression in Δsec22 and the complemented strains.
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