Sentence examples for min of sampling from inspiring English sources

Enhanced glucose clearance was achieved when plasma NEFA was reduced by NA, despite lower insulin concentration (70.0 vs. 97.9 ± 13.4 μIU/mL) and a tendency for smaller insulin response area under the curve during 180 min of sampling [7,646 vs. 12,104 ± 2,587 (μIU/mL) × 180 min], reflecting an increased response to endogenous insulin.

The reduction of plasma NEFA concentration led to significantly greater glucose clearance rate (1.9 vs. 1.2%/min) and to decreased glucose half-life (37 vs. 58 min), time to reach basal concentration (81 vs. 114 min) and glucose response area under the curve during 180 min of sampling [6,942 vs. 10,085 (μIU/mL) × 180 min].

The samples were analyzed in a standardized manner within 2 min of sampling.

Following centrifugation, the supernatant was transferred to a 15-mL polypropylene falcon tube and divided in 0.5-mL aliquots, placed on dry ice within 30 min of sampling and transferred to −80 °C for storage within 60 min of sampling.

Blood samples were collected in EDTA tubes and centrifuged at 2000  g for 10 min within 30 min of sampling.

No B. anthracis was identified on any of the SSSB plates during the 20 min of sampling.

The upper and lower bounds depend on max and min values of sampled path loss data.

A preconcentration factor of 20 and a detection limit (3sb) of 2.1 ng L−1, along with a sampling frequency of 28 h−1 were achieved with 1.4 min of sample loading time and with 2.8 mL sample consumption.

The resulting DNA duplexes could be visualized trapped at the LFD strip test line within 5 min of sample exposure.

Fig. 3 Plot of particle sizes (μm) versus ground time (min) of samples S4, S5, S6, S7, and S8.

Disintegration was performed at 4000 rpm in three cycles consisting of 2 min of disruption and 2 min of sample cooling on ice.