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In this particular type of plot, the maximum wavelength is graphed against the square of the lattice constant of the salt under consideration [1].
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The adsorption spectrum of nZVMn as presented in Fig. 1 showed the maximum wavelength was observed at about 380 nm.
The excitation maximum wavelength was 310 nm, and the emission scan was carried out in the range from 350 to 550 nm.
The RTA treatments were realised by the illumination of structures under investigation by linear halogen lamps whose emission maximum wavelength was 1 μm.
With the introduction of the low-band-gap chromophore onto the porphyrins, the absorption spectra of the two porphyrin dyes in the range of 450 600 nm were broadened and the maximum wavelength was red-shifted compared with PZn as expected.
The red-shifted maximum wavelength was 356 nm in the presence of urea, indicating that the tryptophan residues were not fully exposed to the solvent despite urea concentration was raised up to 9 M.
In the case of SmTAL1 and SmTAL2, the spectra under these two conditions were noticeably different and the fluorescence intensity at the maximum wavelength was statistically significantly different (p < 0.02; unpaired t-test with Welch's correction).
No differences in the maxima wavelengths were observed for the three TRXs at the two excitation wavelengths (data not shown).
The maximum absorption wavelength of the FITC molecule is between 490 and 495 nm, and its maximum emission wavelength is around 525 530 nm, resulting in a bright yellow-green fluorescence.
The maximum excitation wavelength is at 358 (emission wavelength 436 nm) owing to the 340 nm of absorption peak.
The product of the NH3- o-phthalaldehyde (OPA) -Na2SO3 reaction is rose red at pH more than 10.4, and its maximum absorption wavelength is 550 nm.
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