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All liquid samples were stabilized with 1 M anoxic HCl.
The soil samples were stabilized with 3% lime and cured for 28 days at 20 °C.
The soil samples were stabilized with 3% lime and subjected to different curing times of up to 28 days, then exposed to 6 wetting drying cycles of 96 h each.
Water samples were stabilized with 1 mL nitric acid.
The blood samples were stabilized with heparin for biochemical examination (final heparin concentration in blood samples < 1%).
Upon processing, thawed samples were stabilized with a sodium azide and a protease inhibitor cocktail containing 100 ug/mL aprotinin and 5% (w/v) sodium azide, which were added to the plasma at a volume ratio of 1 100.
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The sample is stabilized with an epoxy resin.
The pressurized sample was stabilized with hydrogen bonds, while disulfide bond was the dominant bonding in samples that were pressurized at 800 MPa and heated.
Blood samples were stabilized immediately at the time of collection by diluting them 1 10 with 0.1 M NaPO4 buffer (pH 8.0) containing 1% Triton X-100.
Maternal oral mucosa samples were stabilized in 50 mM NaOH.
All samples were stabilized for 20 min before the measurement.
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