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By employing enrichment technique in BSMY1 medium containing varying concentrations of CuSO4.
E. coli cells carrying pUC118 (filled triangles), pMKY12 (filled circles), or pMRA114 (filled diamonds) were grown in liquid medium containing varying concentrations of HgCl2 (A) or C6H5HgOCOCH3 (B).
The medium was removed and replaced with fresh medium containing varying MOIs of recombinant adenovirus or different concentrations of synthetic Tat-MIP.
After 18 hr, medium was changed and cells were incubated for either 6 or 24 hr in 100 μL medium containing varying doses of F−.
Cell culture medium containing varying concentrations of Paclitaxel (10−9 mol/l to 10−6 mol/l) or vehicle alone was added to the wells.
After this time, the medium was removed and replaced with fresh culture medium containing varying concentrations of docetaxel and incubated for a further 24 hours.
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Decolorization potential of the strain GGUPV1 was studied in minimal medium BSMY1 containing varying concentration of MG (50 400 mg/L).
Uptake experiments were initiated by addition of 500 μL BME medium prewarmed to 37°C and containing varying concentrations of either [H]TC (3.7 kBq/mL) or [H]ES (3.7 kBq/mL) and unlabeled TC (7, 40, 60, 80, and 100 μM) and ES (7, 10, 20, 30, 40, and 50 μM), respectively.
Then, to test the possible cytotoxicity of V. tricolor, the culture medium was changed by fresh one containing varying concentrations (0 800 μg/mL) of the HAE and its fractions.
The degradation characteristics of αTCP-PLGA 50 50 αTCP-PLGA 50 50 conanocompositesng containingight loadings in an aqueous medium havarying assessed using X-ray miceramicgraphy (XμT).
An overnight culture of F. tularensis subsp. novicida was harvested by centrifugation, diluted to an OD595 = 1.0, then used to inoculate modified Chamberlain's Defined Medium (using a 96-well plate; 17 µL of inoculum was added to 158 µL media containing varying concentrations of fosmidomycin).
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