Exact(9)
The diluted solution was plated on a nutrient agar and incubated for 24 h at 37°C ± 2°C.
0.5 ml of the solution was plated, and three serial 1 10 dilutions, (100, 10-1, 10-3, 10-3) onTSATSA plates.
This solution was plated on carbenicillin supplemented LB agar plates.
Cells were mixed with VEGF (25 ng/ml), and 250 μl solution was plated on top of Matrigel.
Following the digestions, the cell solution was plated in a cell-culture treated flask, followed by an incubation at 37C at 1% CO2 for three hours.
The remaining solution was plated on a single YPD plate and incubated at 30 °C for two nights to allow mass mating of the isolated spores.
Similar(51)
After a series of dilutions of the bacterial solutions using the DI water, 1 ml of the solution is plated in nutrient agar.
Serial tenfold dilutions of the samples in a 0.85% NaCl solution were plated in triplicate on PCA at 37 °C and Sabouraud containing chloramphenicol at 25 °C for total bacterial counts and for yeasts counting, respectively.
For each dilution, 3 µl of cell solution were plated on the appropriate agar plate and incubated over several days.
Finally, 50 ml of the solution were plated onto LB agar plates and the number of colonies was counted after overnight aerobic incubation at 37°C.
Two hundred μl of the AEC solution were plated per well.
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