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The materials show a maximum fluorescence emission at 480 and 530 nm.
Fluorescence spectroscopy showed that the fluorescence of HSA can be quenched remarkably by 3d under physiological condition with a slight shift of maximum fluorescence emission bands from 360 nm to 363 nm.
The maximum fluorescence emission spectrum intensity (Imax) of pure Hb arises around 340 nm.
The maximum fluorescence emission peak of InP/ZnS core/shell QDs was obtained at ~ 530 nm.
The wavelengths of maximum fluorescence emission were 567 nm (NC-RS100 and LNC-PCL) and 574 nm (NC-S100).
The figure showed the fluorescence spectrum of the protein when the excitation wavelength is 280 nm, the maximum fluorescence emission wavelength (λmax) of BSA is about 330 nm.
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As shown in Fig. 2, all the maximum fluorescence emissions of the BSA-GNPs were at about 640 nm, and the fluorescence intensity of the BSA-GNPs showed a gradual decrease with the concentration of Hg2+ increasing from 0.1 nM to 4 μM.
3. Stokes shift: difference between excitation maximum and fluorescence emission maximum.
After intercalation both the approximate fluorescence excitation maximum and fluorescence emission maximum are shifted to the right from 488 and 590 nm to 535 and 617 nm, respectively.
For each pigment, the observation wavelength used to acquire the excitation spectrum corresponds to the observed peak position of the maximum of fluorescence emission.
At the maximum of fluorescence emission between 500 and 512 nm of BRI1-GFP expressing hypocotyl cells (Fig. 1B), the lifetime was characterized by a mono-exponential decay (Fig. 1C) typical for GFP (Figure S1) [26]–[27].
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greater fluorescence emission
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