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Figure 3 The viable cell counts of fungal cells.
The EMA assay was also more consistent at determining viable cell counts when compared to plating than fluorescent microscopy viable cell counts.
Figure 7 The logarithmic values of viable cell counts of P. aeruginosa cells.
Figure 3 The logarithmic values of viable cell counts of fungal cells.
The results of the viable cell counts in terms of colony-forming units (CFU) are represented in Table 1.
Figure 3 Viable cell counts recovered from S. aureus biofilms developed on the (nano-modified) catheter pieces.
A modified Microtiter count method was designed to assess viable cell counts in a rapid, easy, and accurate way.
Viable cell counts of LAB used for the production of both type chesses was high, over 106 cfu g−1.
The antimicrobial assay of the microbial biofilms formed on these films was assessed by the viable cell counts method.
Also, it makes viable cell counts more accurate, since it has been described that some pathogens that are present in a biofilm are not routinely culturable.
The viable cell counts of tester strains were 0.71 × 109 to 1.65 × 109 CFU/ml for TA strains, and 2.31 × 109 CFU/ml for WP2 uvrA.
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