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Dissolution medium (water and hydrochloric acid pH 1.2), apparatus (paddles and baskets) and time (30 and 60 min) were analyzed.
It was then further used for long-term planning, where all areas of the country not reachable within 20 min were analyzed and four new units were established.
The compositions of the three particle types, that is, large particles, small particles, and black particles of films oxidized for 50 min, were analyzed using EDS.
Experimental data obtained from images captured at different drying temperatures (100 130 °C) and several time intervals (15 180 min) were analyzed with a complete randomized block design (CRBD), and the means were compared with Duncan's multi-range test.
(C and D) H292 cells (C) or A549 cells (D) pretreated with N-6 (10 μmol/L) for 2 h in serum free medium before being exposed to TNFα (10 ng/mL) for an additional 30 min were analyzed for p85α/tRXRα interaction by co-immunoprecipitation assay using anti-RXRα antibodies of D20 or ΔN197.
Nonartifactual stationary global data segments of 1.5 2 min were analyzed using single time windows of 25 s which were successively shifted by 5 beats for temporal determination of frequency and amplitude.
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The mice were left in the chamber for 11 min, and the freezing time during the initial 5 min was analyzed.
Trisilylated-glycerol (tR: 7.33 min) was analyzed using the SCAN mode program (calibration curve (duplicates, R2 = 0.99): 10 10, 50, 100, 1000 mg/l).
The accumulated distance that cells travelled over a period of 10 min was analyzed.
[C] 8 (tR, ca. 6.8 min) was analyzed as described for [C] 7, except that the HPLC mobile phase was MeCN: 1 mM aq.
The fluorescence response of ArsR-GFP to the As (III) within 40 min was analyzed in milk and yoghurt with a microplate fluororeader and a portable fluorometer.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com