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After sonodynamic treatment, colony forming unit assay and bacterial viability assay were conducted.
Bacteria was then enumerated by colony-forming unit assay to determine concentration, which was plotted as a percentage of untreated sample.
The antimicrobial activity of ABF-2 against S. aureus ATCC6538P and E. coli K12 was tested by a colony-forming unit assay.
Strain tolerance was examined using both a growth assay as well as viable cell counts employing a CFU (colony-forming unit) assay.
To confirm that refolded ABF-2 was correctly folded and active, purified ABF-2 was evaluated by a colony-forming unit assay as well as by CD and NMR spectroscopy (Table 3, Figures 4, 5).
Several analyses were performed including histological examination, nucleated marrow cell counts, colony forming unit assay (CFUs), and stem cell quantification.
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Phase 2 was a randomized, placebo-controlled trial to determine the effects of 6-month pioglitazone treatment in vivo on hBMSC differentiation using AD/OB colony forming unit assays in patients with type 2 diabetes.
Colony-forming unit assays with either Stro-1 positive or negative cells showed no formation of colonies (Fig. 5h).
Flow cytometry, colony-forming unit assays (CFU-Fs) and differentiation assays were utilized to study cell behavior.
Upon killing, marrow was taken from the mouse femurs to perform colony-forming unit assays for granulocytes and macrophages (CFUgm).
Similarly, no significant decrease in marrow toxicity, as assessed by colony-forming unit assays for granulocytes and macrophages (CFUgm), was seen.
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