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The rat brain was preconditioned with 1 U thrombin by direct infusion into the left caudate nucleus.
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The nanofibers mat was preconditioned with 200 μL methanol and 200 μL water once each.
The tC18 Sep-Pak cartridge was preconditioned with EtOH (5 mL) and sterile water (10 mL).
The cartridge was preconditioned with 2 mL of ethanol and 1 mL of water, sequentially.
The SPE was preconditioned with 3 ml of methanol and 3 ml of water.
DGA columns were preconditioned with 3.0 M HCl.
Sample bottles were preconditioned with 5% nitric acid and rinsed with distilled deionized water.
Rat primary cortical neurons were preconditioned with 15 min OGD.
The columns were preconditioned with 1 ml methanol and 1 ml water.
SPE cartridges were preconditioned with 5 mL of MeOH and 5 mL of ultrapure water.
SEP-PAK light QMA cartridges were preconditioned with NaHCO3 aqueous (8.4%) and water before use.
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