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1 . Pt.1. Identifying sources of nonevanescent excitation light).
2 ferases have emerged, as they do not require excitation light.
3 inescence imaging of tumor in the absence of excitation light.
4 alyte-mediated inner filtering of sub-330 nm excitation light.
5 has been handicapped by poor penetration of excitation light.
6 ing, is their ability to efficiently scatter excitation light.
7 t on the presence of an IFP that absorbs the excitation light.
8 ticle orientation and on polarization of the excitation light.
9 und to depend on wavelength and intensity of excitation light.
10 ET dynamic range, phototoxicity from the CFP excitation light and complex photokinetic events such as
11 n functions of absorption of energy from the excitation light and emission of that energy in the form
12 ther factors were the improved absorption of excitation light and the increase of light extraction ra
13 he reaction proceeds only in the presence of excitation light and the rate and extent of reaction can
14 ide of the beads and is fully exposed to the excitation light, and a strong increase in fluorescence
15 nce angle alters the interference pattern of excitation light, and hence the intensity of detected fl
22 surface in response to point illumination of excitation light by using a gain-modulated intensified c
27 roscope that extends the wavelength range of excitation light, expands the number of simultaneously u
28 mtosecond pulse shaping was used to generate excitation light fields that were directed toward distin
29 w-coherence interferometric detection of the excitation light for depth-resolved aberration correctio
30 thin-film interference filter that prevents excitation light from inhibiting the fluorescence detect
31 ated scanning schemes are used to manage the excitation light going to and emission light coming from
32 ring is not the dominant source of far-field excitation light in objective-type TIRF, at least for mo
33 ging of fluorescent proteins (FPs) using red excitation light in the 'optical window' above 600 nm is
35 ce generated by the substitution reduced the excitation light-induced photoactivation from the dark t
36 s show a non-linear relationship between the excitation light intensity and mitotic arrest, and the f
40 rate shows a non-linear relationship to the excitation light intensity, and a good correlation exist
43 oisson kinetics in the presence of scattered excitation light is resolved by filtering the prior mode
45 ective Si surface and the incidence angle of excitation light is varied by placing annular photomasks
47 reflection fluorescence microscopy in which excitation light only penetrates several hundred nanomet
48 ion fluorescence (TIRF) microscopy, in which excitation light only penetrates several hundred nanomet
51 re overcome in two ways: (1) by limiting the excitation light power and gradually increasing the powe
52 otoluminescence instruments by replacing the excitation light source (short duty cycle rectangular si
53 ht filters were integrated for filtering the excitation light source and, thereby, increasing the con
55 of organic light emitting diodes (OLEDs) as excitation light sources for quantum dot-based fluoresce
57 amentally address the problem of propagating excitation light that is contaminating objective-type TI
61 By varying the angle of incidence of the excitation light, we are able to obtain fluorescent cont
62 of the capillary leads to refraction of the excitation light, which affects the point spread functio
63 yet this traditionally relies on delivery of excitation light, which can trigger autofluorescence, ph
64 gs, material autofluorescence and leakage of excitation light, which deteriorates its detection limit
65 fluidic waveguide and efficiently guides our excitation light, which is butt-coupled from the side fa
66 sisted of a source that delivered 610-650-nm excitation light within a lighttight chamber, a 700-nm l
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