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Exact(12)
Small drops of this mixture were placed on Parafilm and the grids were floated on it for 5 minutes.
The components of the mixture were placed inside a beaker glass, with a capacity of 1,000 mL.
Tubes containing a final volume of 13.5 µL of this mixture were placed in a thermal cycler at 95 °C for 5 min to separate the RNA strands present in the solution.
H2S gas is passed in to the warmed acidified with dilute HCl solution for about 5 8 min. The sealed 25 mL Teflon lined autoclaves containing above solution mixture were placed for hydrothermal treatment at 180 °C for several hours.
PCR tubes containing reaction mixture were placed in the block of PCR (GenePro-Bioer) and programmed for initial denaturation at 94 °C for 4 min followed by denaturation (94 °C; 1 min), annealing (37 °C; 1 min) and extension (72 °C; 2 min) for 45 cycles.
Aliquots of 50 µl of the cells-Glycerol mixture were placed in 1.5 ml microfuge tubes containing 1 ml of PBS.
Similar(48)
The reaction mixture was placed on a shaker at 300 rpm and incubated at 37 °C for 10 min.
Approximately 3.0 g of the powder mixture was placed into a tungsten carbide ball mill jar, which was ball milled (SpexSamplePrep 8000 M) for 30 min.
The mixture was placed in cylindrical sample holder.
The mixture was placed in the dark for 72 h.
The mixture was placed in a water bath at 50°С.
More suggestions(15)
mixture were given
mixture were carried
mixture were tested
mixture were investigated
mixture were studied
mixture were observed
mixture were measured
mixture were recorded
mixture were engineered
mixture were captured
mixture were found
mixture were calculated
mixture was placed
mixture were transferred
mixture were formed
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CEO of Professional Science Editing for Scientists @ prosciediting.com