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Since a single dipstick test has a sensitivity of 96% and a specificity of 85%, the total test result was considered positive (i.e. elevated albumin levels in the urine) when in at least two out of three dipstick tests a concentration of 30 mg/l or higher was found.
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C. albicans reached log-phase growth at 30 hours of incubation at 30°C, and we tested a concentration of 10 CFU/ml (Fig. 1C).
Testing a concentration of 40% (v/v) in all three laboratories residual infectivity could be detected after one or two minutes.
When testing PAA a concentration of 0.1% (1000 ppm) and when testing GDA a concentration of 0.25% (2500 ppm) was needed to inactivate 99.99% of the viruses.
The tested oxcarbazepine solution was saturated at 26°C; a solubility test showed a concentration of 8.7 ± 0.3 mg L-1.
None of the tested spiroindolones had any effect on parasite ATP levels when tested at a concentration of 50 nM and measured over a period of 60 min.
Povidone iodide was tested as a 10% weight by volume solution; lidocaine was tested at a concentration of 12 μg/mL, as recommended by the CLSI EP7-A2 Guideline [ 15].
Sulfhydryl-specific reagents effect was tested using a concentration of 0.5, 1.5 and 2.5 mM.
AY1 and its nano-conjugate, AY1-AgNP was non-toxic, with only 5% of cell lysis tested upto a concentration of 100 μM.
As shown in Fig. 4a, LPS in citrate/BSA and in citrate/Triton X-100 was only barely detectable in the LAL-test at a concentration of 10 EU/ml, which exceeds the range of the assay.
However, no modifications were detected on the adhesion levels of the pathogenic strains tested at a concentration of 1 mg/mL of EPS.
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