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Δ G values were obtained from fluorescence at maximum emission using methods described previously [ 25].
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The evaluation of the fluorescence spectrum indicated that the maximum emission wavelength for QDs used here was around 605 nm, indicative of red light.
The maximum emission current can be achieved using a hemispherical-geometry cathode with a radius of 1 mm.
The process consists of a photocatalytic treatment under UV radiation at a maximum emission wavelength of 365 nm using a solid by-product obtained from the titanium dioxide production industry, which contains TiO2 and Fe(III) as a catalyst.
Plates were then read at 480 nm excitation and 520 nm emission maxima using a fluorescent spectrophotometer.
This maximum is characteristic of unbound ANS and contrasts with the 470 nm emission maximum seen using the vertebrate 27 kDa 7B2 protein.
The maximum emission intensities of the markers were used to evaluate the correlation of retinol concentration with fluorescent markers and to establish the corresponding prediction models of retinol concentration.
One LED lamp with a maximum emission wavelength of 465 nm was used to excite the pH fluorescent indicator, 5 6 -carboxyfluorescein (CF), and the other LED lamp with red color emission (λmax 660 nm) was selected to supply a stable color background (the reference light).
The λab value was used to determine the maximum emission wavelength (λmax- em) by fluorimetry with a spectrofluorometer (Cary® 100, Agilent, Santa Clara, CA, USA).
Wang et al. (2004) used quantum dots with maximum emission wavelength 605 nm (QD605) to detect the ovarian carcinoma marker CA125 in fixed cells.
To determine the peak of maximum emission due to tryptophan, the excitation wavelength used was 280 nm and the emission wavelength detection ranged from 300 to 400 nm.
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