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Absorbance given in absorbance units.
Absorbance given in absorbance units Open image in new window Fig. 6 Infrared spectra of (from bottom to top): sepiolite, nMFI and nMFIsep4 after calcination at 600 °C for 5 h.
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Given in seconds, t1/2 has the advantage of being independent from the absolute absorbance value and thus the initial protein concentration in the wells.
The absorbance of the effluent samples before and after treatment with the four adsorbents is given in Table 1.
The first exciton peak positions (E1s 1s) are given in Figure 8; they were calculated from the first minimum value of the second derivatives of the absorbance graphs.
Chlorophyll concentrations were calculated by the absorbance spectra of the extract at 647 and 663 nm, using the formula and extinction coefficients given in Porra et al. [48].
The absorbance ratios (post mortem blood/ ante mortem blood, post mortem body fluid/ ante mortem blood) of the samples from individual animals are given in Table 1.
The data were analyzed to give a continuous distribution of absorbance as a function of sedimentation coefficient, and one example of raw data, fit to give a continuous sedimentation coefficient profile, is given in Figure 1 of the Supporting Information.
The percentage of inhibition of ferrozine-Fe2+ ferrozine-Fe2+ion was given in the below formula: (2) % inhibition = [ 1 − (A P A complex 100, where A C is absorbance oformationtrol and A P is absorbance in the presence of the sample.
The percentage of inhibition of inhibition rate of 2-deoxyribose oxidation by hydroxyl radical was given in the following formula: (2) Hydroxyl radical scavenging activity = [ (A 0 − A 1 ) A 0 ] × 100, where A0 was the absorbance of the control and A1 was the absorbance in the presence of extracts.
One unit of MPO is defined as that giving an increase in absorbance of 0.001 per min and specific activity is given as U/L.
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