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The main parameters used for the determination were a wavelength of 283.3 nm, current of 8 mA, a slit width of 1.00 nm, drying at 150°C, ashing at 325°C, and atomization at 1,400°C.
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Peak areas were integrated at a wavelength of 215 nm.
The viable cells were measured at a wavelength of 570 nm using a VersaMax microplate reader.
The latest images were recorded at a wavelength of 1.3 millimeters in the microwave band.
Absorbance profiles were acquired at a wavelength of 335 nm, chosen according to the protein concentration.
Samples and standards were read at a wavelength of 412 nm.
The emission spectra were recorded over a wavelength of 300 400 nm with an excitation wavelength of 280 nm.
Both compounds were detected at a wavelength of 282 nm.
Chromatograms were monitored at a wavelength of 280 nm [ 7].
Xanthophylls were detected at a wavelength of 452 nm.
The polyphenols were detected at a wavelength of 280 nm.
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