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Relative magnetometers must be calibrated by reference to a known, accurately measured magnetic field.
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The energy scale was internally calibrated by referencing to the binding energy of the C 1s peak of a carbon contaminant at 284.6 eV.
Peak positions were calibrated by referencing a value of 284.6 eV for the peaks corresponding to C C and C H in the C 1s spectrum.
One would need only to calibrate the clock by reference to an outside source, such as the fossil record, that would provide the actual geologic time elapsed in at least one specific lineage.
ICD-QD2 is not directly calibrated, but the calibration factor can be inferred by reference to another detector (ICD2).
Subsequently, sensors were calibrated by comparison to corresponding reference blood glucose measurements using a two-point retrospective calibration.
Absolute magnetometers are calibrated with reference to their own known internal constants.
Chemical shifts are calibrated with reference to the residual proton and carbon resonances of the solvent (CDCl3: δC=77.0ppmC=77.0ppm).
Serum creatinine was measured using a Roche enzymatic assay, calibrated by the manufacturer to be traceable to reference method procedures (standard creatinine).
The reference is calibrated by averaging three to five FLIM measurements of a freshly prepared 1 mg/ml solution of erythrosine B (cat # 198269, Sigma-Aldrich, Zwijndrecht, The Netherlands) in H2O, which has a known short fluorescence lifetime of 0.086 ns [49], [50].
The reference was calibrated by averaging three to five FLIM measurements of a 1 mg/ml solution of erythrosine B (cat # 198269, Sigma-Aldrich, Zwijndrecht, The Netherlands) in H2O, which has a known short fluorescence lifetime of 0.08 ns [ 19, 20].
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