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Exact(23)
(102.4 mm) were determined for the two layer and three layer repairs.
Inhibition zones (mm) were determined using an agar diffusion assay when target bacteria were used as indicator organisms.
Engineering parameters such as weight per unit of volume, mechanical strength of produced control brick (with a dimension of 50 × 100 × 100 mm) were determined and optimized.
In addition, the specific activities of DHQases at 3-dehydroquniate concentration of 0.5 mM were determined and DHQase (Code 3016) from S. acdiscabies showed the highest activity (501.87 units/mg).
In a first step, the spectroscopic properties of GdBN (1 mM) were determined by performing the fluorescence excitation spectroscopy and the fluorescence emission spectroscopy of NPs diluted in ultra-pure water (Figure 1).
Methyl-beta cyclodextrin (MbCD) concentrations of up to 10 mM were determined to be sublethal using a standard viability assay (Figure 2A).
Similar(37)
Clearing zone (mm) was determined after appropriate incubation time.
An optimum electrode gap of 25 mm is determined.
Particle trajectories on the order of 700 mm are determined accurately to within 0.7 mm.
The level of precision, with a correction of 0.5 mm, was determined and its use was recommended for longitudinal studies.
Maximum theoretical specific gravity (G MM) was determined for each mixture in loose uncompacted form using asphalt density tester, as per ASTM D 2041.
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