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The dynamic shock-loading-induced damage evolution and failure response of all three 316L SS materials was quantified using flyer-plate impact driven spallation experiments at peak stresses of 4.7 and 6.5 GPa.
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The flavonoid content of the plant materials were quantified using the aluminium chloride colorimetric method [ 29].
The fraction of released material was quantified using fluorescence spectroscopy.
The radioactive material was quantified using the Imagequant software (GE Healthcare, Munich, Germany).
Total iridoid content of the plant material was quantified using the method described by Levieille and Wilson [ 26].
A total of 5 μl of the eluted DNA was run on a 1.5% agarose gel, and the remaining material was quantified using a NanoDrop.
The derived material was quantified using an isocratic HPLC method and fluorimetric detection (λ excitation 386 nm, λ emission 451 nm).
"Unbound" (remaining in the tube), "bound" (remaining on the microspheres), and "eluted" P-containing material was quantified using a scintillation counter (Supplementary Figure 1a, Supporting Information).
The optimized procedure was validated with powdered milk certified reference material, which was quantified using external calibration and standard addition protocols.
Cellulose pellets were washed using acetic acid-nitric acid reagent and water to remove the non-cellulosic material; cellulose then was quantified using anthron in a colorimetric method.
The cell lysate was ultracentrifuged to remove the undissolved materials, and the protein was quantified using bicinchoninic acid assay (BCA1; Sigma-Aldrich).
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