The proposed method was simple, highly sensitive, precise and accurate and retention time less than 4 min indicating that the method is useful for routine quality control.
The cracking path became dominantly intergranular if the hold time increased to 2 min, indicating that the time-dependent creep damage mechanisms were in control.
Rapid hydrolysis was observed within the first 60 min, indicating that a large number of peptide bonds were hydrolyzed (Shahidi et al. [1995]).
The firstly eluted peak showed retention time similar to that of LND (4.5 min) indicating that this peak corresponded to the unreacted LND.
However, the width of Doppler signal was rapidly reduced after 50 W pHIFU treatment for 15 min, indicating that the blood flow was reduced in femoral tissue.
Cinnamaldehyde was detected in the sediments of CC1 and CC2 at 0 and 180 min, indicating that the sediments without bacteria cells contain cinnamon oil.
Using a Platinum EPS column (150 mm × 4.6 mm ID, 3 μm) kept at 45 °C, 22 components could be separated within 45 min indicating that this method is much more selective than other already published ones.
When standing on rubber, muscle-activity movements among legs remained stable (0.6 0.7 movements per min) over 1 h but increased on concrete (0.6 0.9 movements per min), indicating that, like humans, cattle may sway to counteract effects of standing.
While the half-life of Nrf2 protein was 16.9 min in the absence of obacunone, the half-life of Nrf2 protein in the presence of obacunone was increased to 35.9 min, indicating that obacunone stabilizes Nrf2 protein (Fig. 1G).
Moreover, the resistance-activating ability of the extract was not reduced by exposure to 100°C for 20 min or autoclaving for 20 min, indicating that only chemical substances were involved in resistance activation.
