ライフサイエンスコーパス: luminescence

1 for accommodating guests, and characteristic luminescence.

2 600 GM and two-photon-excited intense green luminescence.

3 termined through 2-deoxy glucose 6 phosphate luminescence.

4 of mechanically tunable circularly polarized luminescence.

5 ies and angle/electrical-potential-dependent luminescence.

6 at derivatives of DIPYR have modest, if any, luminescence.

7 prising gold nanoparticles provided enhanced luminescence.

8 triggered by tripropylamine (TPrA) to yield luminescence.

9 egation of the C-dots and quenching of their luminescence.

10 was defined by the color of the upconversion luminescence.

11 y transfer processes that give rise to metal luminescence.

12 the Gac/Csr cascade and induction of bright luminescence.

13 e products also display circularly polarized luminescence.

14 lecular identity of the cluster and its high luminescence.

15 mperature-dependent PL lifetimes and magneto-luminescence.

16 e was followed in vivo and ex vivo using NIR luminescence.

17 s diverse mechanisms to generate and control luminescence [1-5].

18 rspectral diffuse reflectance (400-2500 nm), luminescence (400-1000 nm), and X-ray fluorescence (XRF,

19 s, digital imaging measured higher SBRs than luminescence (6.1 +/- 0.2 vs. 4.3 +/- 0.4, p = 0.001).

20 Luminescence ability of elutriate fractions was tested w

21 tensity of both upconversion and downshifted luminescence across different excitation wavelengths (98

22 The optically stimulated luminescence ages suggest that Neandertals repeatedly vi

23 d a chronology based on optically stimulated luminescence ages.

24 ia typically rely on optical assays, such as luminescence and absorbance, to probe the viability of t

25 Here, we review the physics behind Cerenkov luminescence and associated applications in biomedicine.

26 We mapped the propagation of photogenerated luminescence and charges from a local photoexcitation sp

27 incremental differences in fluorescence than luminescence and digital imaging (Ln[SBR] = 6.8 +/- 0.6,

28 field, this plasmoid is shown to emit strong luminescence and discrete-frequency radio waves.

29 sy matrix were studied, using the methods of luminescence and FTIR.

30 correlated with the ratio between the defect luminescence and NBE.

31 eous solution, giving rise to changes in the luminescence and NMR spectra.

32 avelengths, with contributions from material luminescence and radiative decay of electromagnetic eige

33 and their potential applications, including luminescence and radioactive waste storage forms.

34 y reduced band gap (1.8-2.2 eV), solid state luminescence and reversible electrochemical doping creat

35 The luminescence and scintillation properties of ZnO single

36 these materials seem to be well explored for luminescence and second-harmonic generation (SHG) phenom

37 with respect to its ability to image Tb(III) luminescence and Tb(III)-mediated FRET in cultured mamma

38 ys with concomitant loss of both the Bk(III) luminescence and the broadband feature.

39 Luminescence and uranium-series techniques applied to bo

40 The nanoaggregates displayed increased luminescence and were successfully used to image bacteri

41 produce highly efficient below-gap broadband luminescence, and opens up a new route towards superior

42 on tomography, computed tomography, Cerenkov luminescence, and photoacoustic tomography.

43 anisms including radioluminescence, Cerenkov luminescence, and scintillation.

44 ities enabled the comparison of reflectance, luminescence, and XRF spectra at each pixel in the image

45 ally intense chiroptical activity and strong luminescence are prepared using gold nanorods and upconv

46 , aerotaxis, and social behaviors, including luminescence as well as biofilm establishment and disper

47 e infrared excitation spectra of the 1800 nm luminescence, as well as the visible excitation spectra

48 A luminescence assay adapted for high-throughput screening

49 Herein, we demonstrate a simple yet novel luminescence assay for visual chiral discrimination of c

50 chemical defects and emit long-NIR afterglow luminescence at 780 nm with a half-life of approximately

51 doped semiconductor NCs show similar mid-gap luminescence at slightly ( approximately 0.3 eV) higher

52 n of changes and behavior of a corresponding luminescence band.

53 sed to develop a heterogeneous time-resolved luminescence based assay for the monitoring of GTP conce

54 Herein, we present the validation of a new luminescence-based assay (UMP-Glo) for measuring activit

55 main PGT from Campylobacter concisus Using a luminescence-based assay, together with substrate labeli

56 on level, which makes it the best performing luminescence-based chemical sensor to date.

57 stic tracers), this review attempts to place luminescence-based interventional molecular imaging tech

58 t three-hybrid assays, pulldown experiments (luminescence-based mammalian interactome), and fluoresce

59 Observatory for Roots (GLO-Roots) that uses luminescence-based reporters to enable studies of root a

60 and SRFA concentrations, it appears that two luminescence behaviors of Eu(III) are occurring.

61 n-off" luminescent switching probe, with its luminescence being quenched upon urea being enzymaticall

62 Using chitosan foam and a luminescence bioassay we obtained maximum inhibition at

63 ng a broader interest in developing chemical luminescence biosensors and improving their commercial e

64 bed in the literature, the field of chemical luminescence biosensors has yet to demonstrate commercia

65 creens permit a readout (e.g., fluorescence, luminescence, cell morphology) from each cell in the pop

66 200-800 nm and created circularly polarized luminescence centered at 510 nm and Raman OA at 50-1400

67 rosamples revealed the presence of different luminescence centers emitting in the visible spectrum, w

68 ion, confirming the trap state nature of the luminescence centers.

69 on emission tomography/fluorescence/Cerenkov luminescence/Cerenkov radiation energy transfer) imaging

70 Luminescence characteristics (band position, lifetime) o

71 stituted naphthalenes that display promising luminescence characteristics.

72 The characteristic blue glow of Cerenkov luminescence (CL) arises from the interaction between a

73 ig challenge in the clinical use of Cerenkov luminescence (CL) imaging is its low signal intensity, w

74 ped a highly specific and robust bimolecular luminescence complementation (BiLC) reporter system to f

75 resent study shows that circularly polarized luminescence (CPL) induced in europium complexes provide

76 wever, the limited precision and accuracy of luminescence dating methods commonly used in loess depos

77 We use optically stimulated luminescence dating of dunes, shorelines, and fluviolacu

78 Using optically stimulated luminescence dating of sand grains, we demonstrate that

79 We combined optically stimulated luminescence dating of sediments with U-Th and palaeomag

80 The luminescence decay keeps on evolving but link to hydrati

81 Additionally, the luminescence decay kinetics transform from multiexponent

82 minescence yield and comparable reduction of luminescence decay time are observed.

83 optical biosensors, those based on chemical luminescence detection (including chemiluminescence, bio

84 in the Z-axis in real time, we increase the luminescence detection efficiency by 35% with an improve

85 f ATP, thereby allowing sensitive isothermal luminescence detection of nucleic acids as diverse as ph

86 arly polarized luminescence with an absolute luminescence dissymmetry factor, |glum|, of 1.3 x 10(-3)

87 m H(+)-induced quenching of Tb(III)-centered luminescence due to protonation of Tb(III) complexes loc

88 These compounds combine strong luminescence due to the CuI inorganic modules and signif

89 in the design of LEDs is to maximise electro-luminescence efficiency at high current densities.

90 sion efficiency from the overall upconverted luminescence efficiency, allowing more targeted engineer

91 They exhibit high luminescence efficiency, significantly improved chemical

92 ductors with high absorption coefficient and luminescence efficiency.

93 assessed by in vivo calliper and luciferase luminescence emission measurements along with postmortem

94 The bioconjugate maintained an intense luminescence emission, slightly red-shifted as compared

95 The preferential luminescence enhancement observed with mismatches result

96 sing porous silicon (pSi) microcavities as a luminescence-enhancing optical biosensing platform.

97 lowest CSRFA values, is showing the typical luminescence evolution of Eu(III) complexed by humic sub

98 produce efficient green and red upconversion luminescence for optical imaging; 2) Efficient nonradiat

99 ely high viral replication, as visualized by luminescence, for 2 wpi.

100 Plus One (android), which was able to detect luminescence from 10(6) CFU/mL of the bio-reporter, whi

101 In addition to luminescence from Bk(III) in the Bk(IO3)4 crystals, a br

102 s, together with the characteristically fast luminescence from Ce(3+), make this material also a stro

103 Upconversion luminescence from nanomaterials exhibits additional size

104 We show that luminescence from Sn-based perovskite nanocrystals occur

105 the top two candidates were used to evaluate luminescence from the bioluminescent reporter Pseudomona

106 The electrochemical stimulus used for luminescence generation does not suffer from background

107 ts for all the defects, except for the green luminescence (GL1) band, are independent of temperature.

108 n models), the use of Tb(3+) or Eu(3+) doped luminescence glass or CdS-QD coated glass lenses provide

109 e developed new optic devices - singly-doped luminescence glasses and nanoparticle-coated lenses that

110 donor, can be measured even after the donor luminescence has decayed.

111 Several biosensors based on chemical luminescence have been described for quantitative, and i

112 visible (Tb(3+)) and near-infrared (Yb(3+)) luminescence, (ii) PARACEST- (Tb(3+), Yb(3+)), or (iii)

113 Each luminescence image was fit to a three-dipole emission mo

114 Cerenkov luminescence images from incised BCS specimens were anal

115 s study, we investigated the use of Cerenkov luminescence imaging (CLI) as compared with PET as a mod

116 Cerenkov luminescence imaging (CLI) combines optical and molecula

117 increasing interest in noninvasive Cerenkov luminescence imaging (CLI) of in vivo radionuclide distr

118 Luminescence imaging has gained attention as a promising

119 hysiologic and even molecular interventional luminescence imaging is illustrated.

120 A major obstacle in luminescence imaging is the limited penetration of visib

121 Integrating luminescence imaging with three-dimensional radiologic-

122 rmance liquid chromatography-ultraviolet and luminescence imaging, revealed that carnosic acid and it

123 ph node resection, such as by using Cerenkov luminescence imaging.

124 ce, popliteal lymph nodes underwent Cerenkov luminescence imaging.

125 ion of high charge carrier mobility and high luminescence in an organic semiconductor is challenging.

126 Mid-gap luminescence in copper (Cu(+))-doped semiconductor nanoc

127 e multiphoton near-infrared, quantum cutting luminescence in Er(3+)/Tm(3+) co-doped telluride glass w

128 Luminescence in Motyxia stem-group taxa may have initial

129 G129 mice that survived infection maintained luminescence in the brain for up to 8 wpi.

130 in hexagonal lattice and exhibit narrowband luminescence in the red spectral range.

131 Luminescence in the respiratory tract and in less well-c

132 rities of 6 and 7 are their yellow color and luminescence in the visible region distinguishing them f

133 Luminescence in the visible region, especially by cluste

134 well matched DNA but exhibits a significant luminescence increase in the presence of a 27-mer DNA du

135 ed quorum sensing, raising the threshold for luminescence induction.

136 f advanced OSAM for robust quantification of luminescence intensities and lifetimes for a variety of

137 Antennae providing similar luminescence intensities with 2-4 Ln-emitters were ident

138 tase with approximately 170-fold increase in luminescence intensity and high selectivity for enzymati

139 ition, a similar linear relationship between luminescence intensity and the concentration of thrombin

140 thiophene rings) does not correlate with the luminescence intensity and, correspondingly, does not de

141 We find that their energy and luminescence intensity are highly tunable by an applied

142 a high quantum efficiency of 73.2%, and its luminescence intensity at 150 degrees C decreased simply

143 The remarkable quenching of the luminescence intensity at 457nm of nano Pd(atz,ur) doped

144 The remarkable quenching of the luminescence intensity at 528nm of nano binuclear Pt(pca

145 The remarkable enhancement of the luminescence intensity at 645nm of nano [Sm-(TC)2](+) co

146 We found that the near-infrared 1800-nm luminescence intensity of (A) Er(3+)(8%)Tm(3+)(0.5%):tel

147 Additionally, the luminescence intensity of the complex with DNA containin

148 Histidine enhances the luminescence intensity of the nano optical [Sm-(TC)2](+)

149 3-nitrotyrosine (3-Nty) quenches the luminescence intensity of the nano optical sensor binucl

150 ivity is carried out by the quenching of the luminescence intensity of the nano optical sensor binucl

151 The luminescence intensity showed a three-fold difference be

152 We further found that the luminescence intensity was strongly dependent on the par

153 stable chelate leading to a sample-dependent luminescence-intensity array.

154 The new signal termed as Infra-Red Photo-Luminescence (IRPL) is a Stokes emission ( 1.30 eV) deri

155 Luminescence is an alternate optical technology that avo

156 The enhancement factor of upconversion luminescence is as high as 21.3 in aqueous phase.

157 Ag(+) is nonmagnetic, and the dopant-related luminescence is ascribed to decay of the conduction-band

158 g diode (LED) lamps with bright upconversion luminescence is designed.

159 The most efficient luminescence is forty times higher than in silicon-on-in

160 iple TFEL lamps, effective and area-scalable luminescence is realized.

161 on of ROS is provided using luminol-enhanced luminescence (LEL) in both model mixtures of ascorbic ac

162 Thus, the long luminescence lifetime can be further modulated and utili

163 e sensitized acceptor emission has prolonged luminescence lifetime compared to the donor and the long

164 d approach, relying on the millisecond-scale luminescence lifetime of the lanthanide ions, was applie

165 The dependence of the luminescence lifetime on the probe environment is the ba

166 A 4-fold increase in both quantum yield and luminescence lifetime was observed in viscous media for

167 uishable spectroscopic fingerprint, and long luminescence lifetime.

168 esent a simple method for the measurement of luminescence lifetimes on the microsecond scale based on

169 ively charged uncoated, "bare" CNP with high luminescence loses its PL when positively charged macrom

170 present study magnetic circularly polarized luminescence (MCPL) is explored as a more sensitive tool

171 cence (PL) and magnetic circularly polarized luminescence (MCPL) spectroscopies.

172 spectroscopy, magnetic circularly polarized luminescence (MCPL) spectroscopy, and time-dependent den

173 Real-time luminescence measurements and single-cell analysis demon

174 It also provided bulk luminescence measurements that were not affected by surf

175 0.3 eV) higher energy, suggesting a similar luminescence mechanism, but this suggestion appears inco

176 iewed in the context of the well-established luminescence mechanisms of bulk copper-doped semiconduct

177 e comparative advantages of using time-gated luminescence microscopy in combination with an emissive

178 Our results indicate that time-gated luminescence microscopy using Tb(III) labels can provide

179 At higher CSRFA, a second luminescence mode is detected as the asymmetry ratio is

180 m the insect bacterial pathogen Photorhabdus luminescence modifies actin to force its aggregation.

181 The luminescence nanoaggregates were elegantly exploited for

182 Near-infrared (NIR) persistent luminescence nanoparticles (PLNPs), possessing unique NI

183 This new persistent luminescence nanoparticles have been demonstrated for op

184 ncapsulation either changing or switching-on luminescence not present in the bulk phase.

185 integrated-imaging system called Growth and Luminescence Observatory for Roots (GLO-Roots) that uses

186 The luminescence observed is dependent on the solvent access

187 n more information about the redox-dependent luminescence of [Ru(bpy)3](2+) finding a continuous quen

188 ificant amount of experimental work into the luminescence of Au25(SR)18(-) clusters, the origin of ph

189 Fundamental investigations into the luminescence of copper-containing colloidal nanocrystals

190 The luminescence of CuInS2 nanocrystals is explained well by

191 lap and energy transfer between the infrared luminescence of Er(3+) donor ions and the infrared absor

192 Luminescence of lanthanide(III) ions sensitively reflect

193 erent timescales by combining the long-lived luminescence of Mn(2+) with the relatively short-lived e

194 robes mainly accumulate in the liver and the luminescence of nanoparticles remains suppressed owing t

195 mical demonstrations include electrochemical luminescence of ruthenium compounds and ligand exchange

196 strategy to take advantage of time-resolved luminescence of Tb(3+)-chelated phosphotyrosine-containi

197 Time-resolved studies of the upconversion luminescence of the UCNP donor revealed a considerable s

198 nd the label is typically detrimental to the luminescence of the unstable chelate leading to a sample

199 ct as a synergistic antenna to sensitize the luminescence of trivalent lanthanide and actinide ions i

200 excitation spectra of the 522 nm and 652 nm luminescence, of (A) Er(3+)(8%)Tm(3+)(0.5%):telluride gl

201 Most important of these properties is luminescence, often in the visible-near-infrared window,

202 We report a BODIPY-based luminescence ON reagent for detection of HNO in aqueous

203 on and monitoring of crucial biomarkers with luminescence ON response have significance in clinical d

204 FRET based luminescence ON responses are observed on formation of t

205 n the color and position of the upconversion luminescence on the array.

206 alculations are performed to investigate the luminescence origin and emission mechanism of these mate

207 outcrops and that their optically stimulated luminescence (OSL) age of about 20,000 years for the hum

208 use 16 new single-grain optically stimulated luminescence (OSL) dates to define three stages of rapid

209 loped, high sensitivity Optically Stimulated Luminescence (OSL) material of low effective atomic numb

210 ive and quantitative manner by measuring the luminescence output in a discontinuous coupled assay sys

211 ing 12 h of caerulein compared with baseline luminescence (p < 0.05).

212 ramework of PN4 tetrahedra and exhibits blue luminescence peaking at 455 nm.

213 llowed direct comparison of amperometric and luminescence performance.

214 the conjugated polymer MEH-PPV can generate luminescence persisting for an hour upon single excitati

215 multiphoton, near-infrared, quantum cutting luminescence phenomenon that occurs in novel Er(3+)-Tm(3

216 Here we report the use of a persistent luminescence phenomenon, which enables an external excit

217 alkane dehydrogenation (M = Cr) or efficient luminescence properties (M = Yb and Eu) essential for bi

218 and exhibit impressive circularly polarized luminescence properties (|g lum|: up to 0.16).

219 We also investigate the luminescence properties of a representative member of th

220 The interesting luminescence properties of lanthanide doped rare-earth c

221 ductivity, carrier mobility, dielectric, and luminescence properties of optically patterned layers ar

222 Overall, the luminescence properties of semi-polar AlGaN epilayers ar

223 Luminescence properties of the BODIPY-based chemodosimet

224 tallinity, surface area, pore structure, and luminescence properties of the polymers.

225 The extended analysis of the luminescence properties of these complexes, excited by t

226 explored further by leveraging its intrinsic luminescence properties to determine its intracellular l

227 aled LaPO4:Pr(3+) to have the most favorable luminescence properties, achieving over 2-log inactivati

228 ed by different light sources show different luminescence properties.

229 rotations, leading to desirable solid-state luminescence properties.

230 In the most widely used procedure for luminescence quantum yield determination, absorption and

231 ich allow large spectral tunability and high luminescence quantum yields at low excitation densities.

232 The cages are highly emissive (luminescence quantum yields of 16(1) to 18(1)%) and exhi

233 The highest lanthanide-centered luminescence quantum yields were 35% (Tb), 7.9% (Eu), 0.

234 Luminescence quenching at high dopant concentrations gen

235 hilic surface functionalization minimize the luminescence quenching effect by water.

236 n of the binding constant to the diamine via luminescence quenching.

237 activity concentration and in vivo Cerenkov luminescence (r(2) = 0.98).

238 The luminescence reaction occurred with luminol, hydrogen pe

239 o that of a full-size PerkinElmer laboratory luminescence reader.

240 Eu(II)-containing materials have unique luminescence, redox, and magnetic properties that have p

241 This differential luminescence reflects the sensitive detection of the mis

242 We developed a luminescence reporter system to facilitate a large-scale

243 Herein we present the application of luminescence resonance energy transfer (LRET) for invest

244 energy donor), which allows for upconversion luminescence resonance energy transfer (LRET) that can b

245 Here, we used luminescence resonance energy transfer (LRET) to measure

246 particle-based assay utilizing time-resolved luminescence resonance energy transfer (TR-LRET) was dev

247 Two mix-and-measure systems, time-resolved luminescence resonance energy transfer (TR-LRET) with do

248 Site-directed incorporation of a luminescence resonance energy transfer donor-acceptor pa

249 eactive bifunctional reagents as well as the luminescence resonance energy transfer measurements of i

250 Here, we used luminescence resonance energy transfer spectroscopy to s

251 ation densities to account for the nonlinear luminescence response of UCNPs.

252 sorting phenomena with associated changes in luminescence responses that could be correlated for Bool

253 different inclusion complexes with distinct luminescence responses.

254 ted chemicals within the sample leading to a luminescence signal profile that is unique to the bacter

255 nonantenna ligands with sample leading to a luminescence signal profile, unique to the sample compon

256 ption properties, which are presented as the luminescence signal vs PEG mass concentration.

257 nked chimeric nucleotide (ARGO) that enables luminescence signaling of the enzymatic reaction, greatl

258 enabling sensitive detection via luciferase luminescence signaling.

259 edictive model was trained with the measured luminescence signals and its ability to differentiate al

260 w strategy is reported for the production of luminescence signals from DNA synthesis through the use

261 ns such as the limited tissue penetration of luminescence signals.

262 The luminescence spectra of the encapsulated guests are cons

263 experimental steady-state and time-resolved luminescence spectra of the oxyluciferin/luciferase comp

264 length, between 250 and 400 nm (4.9-3.1 eV), luminescence spectra were collected between 400 and 800

265 work, a compact instrument for time-resolved luminescence spectroelectrochemistry using low-cost disp

266 A direct luminescence spectroscopic experimental setup for the de

267 A correlation of luminescence spectroscopic features with Raman frequenci

268 In situ infrared and luminescence spectroscopic studies evidence the formatio

269 copic techniques (EPR, IR, XAS, UV-vis, NMR, luminescence spectroscopies).

270 speciation is investigated by time-resolved luminescence spectroscopy (TRLS) in the presence of Suwa

271 ared (ATR FT-IR) spectroscopy, time-resolved luminescence spectroscopy (TRLS), and surface complexati

272 urface sites according to reactivity for Cr, luminescence spectroscopy for Yb and Eu, and dynamic nuc

273 the mixed dppz/dppn complex also displays a luminescence "switch on" DNA light-switch effect.

274 Results indicated for the first time that luminescence switchable CNPs can be synthesized for effi

275 of TccC3 toxin and established Photorhabdus luminescence TccC3 as a toxin suitable for the developme

276 By providing an overview of the available luminescence technologies and the various clinically eva

277 ped with windows to measure the oxygen using luminescence technology.

278 Phosphorescence is a phenomenon of delayed luminescence that corresponds to the radiative decay of

279 lation dynamics in vivo, with mean bacterial luminescence that remained two orders of magnitude lower

280 bleach the chromophore and thus recover the luminescence, the presence of ONOO(-) in the liver leads

281 ccessfully generate persistent near-infrared luminescence through resonance energy transfer.

282 These NCs exhibit bright luminescence throughout the exchange, allowing their opt

283 and the endometrial surfaces were imaged for luminescence to localize adherent lux-labeled bacteria.

284 Raman and multiphoton luminescence together with transmission electron microsc

285 ile concurrently emitting strong upconverted luminescence (UCL) for visualized guidance under 980 nm

286 version by 9-fold to produce bright 1550 nm luminescence under 980 nm excitation.

287 t development of upconversion nanomaterials, luminescence upconversion has begun to receive renewed a

288 scriptions for all the processes involved in luminescence upconversion, which include absorption, emi

289 comprehensive framework for plasmon enhanced luminescence upconversion.

290 e substrates that can enhance lanthanide ion luminescence upon tyrosine phosphorylation enable rapid,

291 Luminescence using fluorescence lifetime imaging (FLIM)

292 on by grid test, myeloperoxidase activity by luminescence, vascular leakage by fluorescence in vivo i

293 The resulting Bk(IV) complex exhibits luminescence via sensitization through an intramolecular

294 ime-resolved spectroscopy, we establish that luminescence via triplets occurs within 350 nanoseconds

295 The conjugate shows weak luminescence when free in solution or with well matched

296 ving rise to an intense charge-transfer (CT) luminescence, while the closed structure without this em

297 m yield (up to 74%) and circularly polarized luminescence with an absolute luminescence dissymmetry f

298 electric field that is sufficient to excite luminescence without an electrical interface circuit.

299 udied by photoluminescence and X-ray-induced luminescence (XRIL) techniques.

300 Moreover, a threefold increase of the luminescence yield and comparable reduction of luminesce