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Printing was carried out using two cartridges, in which 8 mL of the TiO2 ink and 6 mL of the AlOOH ink were preliminarily placed.
For measuring stability against Li2O2, 1 mg Li2O2 were stirred in 2 mL of the electrolyte.
Typically, 0.5 ml of the ink was loaded in a fountain pen for writing tests.
Then 1.7 ml of the cell suspension (50000 cells) were mixed to the complex.
Then were added 0.2 ml chloroform per each ml of the used Trizol.
The solutions were mixed immediately before analysis in a proportion, which achieved a 1 1 molar ratio of 1 3 (10 ml of the cage 3 solution + 7.1 ml of the cage 1 solution).
At a para-H2 flow rate of approx. 1.5 l/h, roughly 3 4 ml of the substrate evaporated.
To ensure water-saturated conditions throughout the incubation period, 2 ml of the seawater obtained from the cores was added.
30 mL of the overnight starter culture is inoculated into 3 L of LB media and grown for 16 h.
After exposure, desiccated and irradiated cells on glass slides were immediately resuspended in 10 ml of the mineralization solutions.
Next day, 1 mL of this culture was used to inoculate 50 mL of the same medium.
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