A 1∶1 mixture of the cultures was used to inoculate the animals intragastrically (200 µl for mice, 100 µl of concentrate for chicks (1 ml resuspended in 100 µl), 4 ml for pigs (1 ml diluted to 4 ml), 10 ml for calves, 1 ml for turtles, guinea pigs, and rabbits.
The tube capacity was 5 mL : 0.5 mL for sodium citrate and 4.5 mL for whole blood.
Average volume approximation obtained with the cuboid formula was 34.4 ml (+/−41.4 ml) for primary tumors and 18.5 ml (+/−33.4 ml) for the largest LNs (Table 2).
The resin was treated with 10 ml of a mixture of trifluoroacetic acid, water, and tri-isopropylsilane (9 ml:9 ml:1 ml) for 2.5 hours.
The simulation results for 75 mL, 100 mL, 150 mL, and 250 mL KCl tracer additions were compared.
40 g powder of XF was decocted with water (1000 mL, 800 mL, and 600 mL) for 3 times, respectively.
The concentrations of faecal indicator bacteria in untreated sewage are 8 log10 CFU/100 mL for TC, 7.48 log10 CFU/100 mL for FC and 6.6 log10 CFU/100 mL for enterococci (Wilén et al. 2012).
They reported mean volume of 3.04 ml (SD, ± 0.04 ml) for the medial menisci and 3.07 ml (SD, ± 0.07 ml) for the lateral menisci.
Therefore, 0.8 ± 0.2 mL for PSE, 1.0 ± 0.2 mL for PPA and 1.0 ± 0.5 mL for EPH were chosen as the optimum buffer volume for the analysis.
