Sentence examples for min to identify from inspiring English sources

The ultrasound examination took approximately 3 min to identify these findings.

Vascular networks were photographed and traced every 30 min to identify changes over time.

Normal human fibroblasts were incubated with 30 μM EdU or IdU for 20 min to identify sites of DNA replication.

Each US examination took 15±4.3 min, whereas it took only 5 min to identify the thyroid BFI-TS.

The samples were assessed for elemental composition for 5 min to identify and map silicon at two positions (Gong et al. 2006).

Cultures were stained with propidium iodide (7.5 μg/ml) for 30 min to identify cell membrane damage, washed with PBS and fixed with 4% paraformaldehyde.

After initial denaturation, amplification was done using a PCR thermal cycler (BioRad) for 35 cycles of 94°C/40 sec, 64°C/1 min, 72°C/1 min followed by a final extension of 72°C/7 min. To identify the flanking sequences of the 386 bp region, another set of primers were used (moaFP: 5'-CCCATCGTGGTCGTTCACC-3' and moaRP: 5'-CGATGGCAGCGGTTTACAG-3') which was expected to amplify a 1254 bp product.

PCR amplification of gDNA of C. olitorious and C. trilocularis with XTH5′F and XTHGR primers (35 cycles, 95°C for 1 min, 59°C for 40 sec, and 72°C for 1 min) helped to identify the introns of CtXTH1 and CoXTH1.

The remaining cells of eight clones each were pooled, suspended in 50 µl of water, heat-lysed at 95°C for 10 min, and digested with 10 µg of proteinase K at 55°C for 30 min. To identify homologous recombinants, we used aliquots of the pooled lysates to PCR amplify a 1.2 kb genomic fragment.

Subsequent blood samples were drawn every 10 min over a 180-min period to identify time to peak HCO3 −.

Immunostained sections were then incubated with Hoechst 33342 dye (1 μg/ml, 8 min; Life Technologies) to identify nuclei, rinsed thoroughly, mounted in ProLong Gold anti-fade reagent (Life Technologies), and then air-dried for ≥8 h in the dark.