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The buffer was oxygenated with a 95%oxygas/5%CO2 gas mixture at 37°C.
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The bath solution was oxygenated with 95% O2/5% CO2 gas, and perfused continuously through the recording chamber at ∼1 ml/min.
The tissue was oxygenated with 95% O2 and 5% CO2.
The blood was oxygenated with 20% O2, 75% N2, and 5% CO2 carbogen gas.
Blood was oxygenated with a humidified gas mixture containing 6% CO2, 36% O2 and 58% N2 (v v−1).
Water was oxygenated with an air stone and circulated through an external charcoal filter (AquaClear 20 Power Filter; Hagen, Montreal, Canada).
The buffers were oxygenated by bubbling with 99.6% O2 for 15 min before mixing and the mixtures were also bubbled with O2 for 15 min. The resultant lysates were frozen in MB cups using liquid N2.
The initial oxygenators consisted of venous blood pools that were oxygenated with oxygen bubbles.
All the patients were oxygenated with an oxygen concentrator.
All solutions were oxygenated with 95%O2/5%% CO2.
Both the cutting solution and ACSF were oxygenated with a gas mixture of 95% O2 and 5% CO2.
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