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Dissolution of 3 (20 mg, 0.10 mmol) in this buffered solution resulted in a solution of pH* ~8.
The hydrolytic degradation study was carried out at 37°C in buffered solution at pH 7.4.
The analogous trends were observed in either alkaline or acid buffered solution.
These carbons were examined for adsorption of Lysozyme (Lz) from buffered solution at pH 10.8.
L6 cultures were fixed in 4% formaldehyde buffered solution and permeabilized with methanol.
Following the 30-min incubation period cells were washed four times with ice-cold physiological phosphate buffered solution.
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For citrate CVVH, RF used were citrate anticoagulation solution and bicarbonate-buffered solution and for heparin or no anticoagulation, only bicarbonate-buffered solution.
Cells were then rinsed slowly with sequential methanol dilution in phosphate-buffered solution (PBS).
Degradation of PLGA sponges in phosphate-buffered solution (PBS) was evaluated with the protocol.
The probe could discriminate GSH from cysteine and homocysteine within 1 min in PBS-buffered solution.
Frozen tissue sections were fixed in 4% paraformaldehyde (Wako) and then antigen retrieval was performed by heating at 100 °C in a citrate-buffered solution at pH 6.4.
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