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1 ulting in a large red-shift (~110 nm) in the fluorescence spectrum.
2  differentiating fluorophores based on their fluorescence spectrum.
3 scribed here bind thioflavin T and shift its fluorescence spectrum.
4 oduce red-shifted intensities in the Dronpa2 fluorescence spectrum.
5 pposite polarities in different parts of the fluorescence spectrum.
6  opens a pathway to in situ control over the fluorescence spectrum.
7                                       A 77 K fluorescence spectrum analysis of treated PSII membranes
8  of CoPhMoRe by considerably simplifying the fluorescence spectrum and background emission of the sen
9                                     From the fluorescence spectrum and from an inversion of the Debye
10 dye environment and dramatically altered the fluorescence spectrum and intensity, resulting in a stro
11                   However, inspection of the fluorescence spectrum and LC-MS analysis of the reaction
12 transect in the Deltalambda = 25 synchronous fluorescence spectrum and with the preexponential terms
13  leptosperin not only displayed an identical fluorescence spectrum, but supplementation of leptosperi
14       Using an intracellular substrate whose fluorescence spectrum changes after hydrolysis by Bla, w
15 mophore exhibits a nonshifted absorption and fluorescence spectrum characteristic of its native, exte
16 s at megapixels per hour with the full X-ray fluorescence spectrum collected per pixel.
17 n olive oil gave a different but interesting fluorescence spectrum, composed of three bands: one low
18 e donor and acceptor even though the donor's fluorescence spectrum does not overlap with absorption s
19 ctroscopy (XPS), particle size analysis, and fluorescence spectrum (FL) are applied to study the CL m
20            The ability to measure the entire fluorescence spectrum from each sensor simultaneously du
21                            We observe the UV fluorescence spectrum from naturally occurring tryptopha
22 r describes a method to measure the complete fluorescence spectrum from numerous fluorescent microsph
23 p, NFK and ArgP emission dominates the total fluorescence spectrum in both emulsified post-surgical h
24 orption spectrum and a red-shifted, quenched fluorescence spectrum, indicating aggregation of the con
25                                              Fluorescence spectrum investigations showed that Al(3+)
26 ing cluster size (the onset of the PH(+)(aq) fluorescence spectrum is 600 nm and the maximum is 518 n
27               An unusual and highly quenched fluorescence spectrum is also observed for Trp 38.
28 ly impossible for both UV-vis absorption and fluorescence spectrum measurements.
29                                          The fluorescence spectrum observed after entrapping MgADP-fl
30                             For example, the fluorescence spectrum of 7AW is sufficiently separated f
31             Here we simulate a time-resolved fluorescence spectrum of a dye in aqueous solution, the
32                                          The fluorescence spectrum of a solution of selected dyes all
33 e) bond is correlated with alteration of the fluorescence spectrum of the active PLP ketoenamine taut
34 cent quantum yields where the absorbance and fluorescence spectrum of the fluorophore was not affecte
35      It is clear from these results that the fluorescence spectrum of the introduced tryptophans in t
36 meric state, circular dichroism spectrum, or fluorescence spectrum of the sensor domain but do stabil
37 r the on-chip recording of protein intrinsic fluorescence spectrum originating from aromatic amino ac
38                The blue-shift of the Citrine fluorescence spectrum resulting from the bending of the
39                                          Its fluorescence spectrum shows two major peaks at 718 and 7
40  from a denaturing polyacrylamide gel, has a fluorescence spectrum similar to that of activated NCS-c
41 erent from established UV-vis absorption and fluorescence spectrum techniques where large amounts of
42  a chemical system often creates a congested fluorescence spectrum that is difficult to interpret.
43  the active site gorge, shows changes in its fluorescence spectrum that reflect the fluorescent side
44 e process by comparison of the laser-induced fluorescence spectrum to the ultraviolet depletion spect
45  the component parts, while in each case the fluorescence spectrum upon illumination of the Zn porphy
46 involving the lipophilic dye Nile Red, whose fluorescence spectrum varies according to the chemical p
47                                          The fluorescence spectrum was less intense and more red-shif
48                During refolding, the initial fluorescence spectrum was not that of native or unfolded