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Then, two solutions were mixed together and stirred for 30 min, at an ice-cold bath.
The first film grew to 250 nm in 39 min at an average growth rate of 6.4 nm/min.
The assay was performed in 40 min at an optimal temperature of 58 °C, with endpoint results visualized directly.
After mixing of the reagent, the contents were sonicated for 5 20 min at an interval of 5 min.
It was found that the optimum time of contact was 25 min at an optimum pH of 3 (fast process).
GdSL3 was irradiated by 20-kHz ultrasound for 5 min at an intensity of 63.5 W/cm2.
The specific LAMP primer set designed in this study could amplify the msrA gene within 25 min at an isothermal temperature of 62 °C.
The results showed that target DNA was amplified and visualised by monitoring turbidity and adding calcein detection methods within 70 min at an isothermal temperature of 63 °C.
The results showed that target DNA was amplified and visualized by the two detection methods within 40 min at an isothermal temperature of 61 °C.
For example, one particle was produced and observed for over 6 min at an average pressure of 15.022 MPa and an average temperature of 5.1 °C.
The temporal FE current stability was measured over 120 min at an anode-cathode separation of 100 μm at a fixed voltage of 500 V.
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