ライフサイエンスコーパス: fluorescence lifetime

1 ng like time-of-flight, gated detection, and fluorescence lifetime.

2 e speed of raster-scanned imaging imposed by fluorescence lifetime.

3 ics of their direct surroundings, with their fluorescence lifetime.

4 ned intracellular localization of MB and its fluorescence lifetime.

5 and GAF show blue-shifted emission with long fluorescence lifetimes.

6 rinsic fluorophores, based on their distinct fluorescence lifetimes.

7 ts ((13)C-AKIE) and decrease of 4-Cl-aniline fluorescence lifetimes.

8 ed substantial intermolecular variability in fluorescence lifetimes.

9 orescence quantum yields, Stokes shifts, and fluorescence lifetimes.

10 The dyes feature long fluorescence lifetimes (17-20 ns), high quantum yields (

11 nt component (qE) and stable (1) chlorophyll fluorescence lifetime; (2) amplitude of the fluorescence

12 ts strong fluorescence ( F = 0.48) with long fluorescence lifetime (5.6 ns) and large Stokes' shift,

13 onds of folding by monitoring the tryptophan fluorescence lifetime (60 mus dead time).

14 he absorption and emission while maintaining fluorescence lifetimes above 10 ns.

15 The instrument is capable of near real-time fluorescence lifetime acquisition in multiple spectral b

16 concentration information is encoded in the fluorescence lifetime across multiple spectral bands.

17 nced fluorescence emission, and an increased fluorescence lifetime, all indicating strong excitonic c

18 The tryptophan fluorescence lifetimes also suggest a deviation from nat

19 Single-molecule tracking combined with fluorescence lifetime analysis can be a powerful tool fo

20 Calorimetry and fluorescence lifetime analysis of labeled RNAs shows tha

21 Fluorescence lifetime analysis showed that mutations wit

22 ication of the phasor approach to study NADH fluorescence lifetime and emission allowed us to identif

23 Independent classification analysis based on fluorescence lifetime and on Raman spectra discriminated

24 orophore libraries, simultaneously measuring fluorescence lifetime and photobleaching.

25 An anomalous increase in the fluorescence lifetime and relative intensity takes place

26 The long fluorescence lifetime and small mass of LUMP are exploit

27 urement that captures information about both fluorescence lifetime and spatial position of the probes

28 Additionally, the long fluorescence lifetime and the surface-bound fluorescent

29 e of plasma membrane tension by changing its fluorescence lifetime and thus allows tension imaging by

30 T spectroscopy that includes measurements of fluorescence lifetime and two- and three-color FRET effi

31 ree' approach, combining 2-photon excitation fluorescence lifetimes and emission spectral imaging wit

32 pic methods such as fluorescence anisotropy, fluorescence lifetimes and fluorescence quenching measur

33 Fluorescence lifetimes and intensities of NAD(P)H and FA

34 ch is supported by an overall increased mean fluorescence lifetimes and significantly reduced water a

35 rption in a wide range of UV/vis, acceptable fluorescence lifetime, and effective intramolecular char

36 he combination of a high quantum yield, long fluorescence lifetime, and emission above 600 nm is poss

37 f their brightness, fluorescence anisotropy, fluorescence lifetime, and emission spectra.

38 steady-state fluorescence, phosphorescence, fluorescence lifetime, and phosphorescence lifetime meas

39 tween phycobilisome components, (ii) shorter fluorescence lifetimes, and (iii) red shift in the emiss

40 emissive substitute for G with good QY, long fluorescence lifetimes, and exquisite sensitivity to loc

41 alize AuNPs with CdTe/CdS QDs to modulate QD fluorescence lifetimes, and nucleate the formation of fl

42 absorption and emission spectra, luminosity, fluorescence lifetimes, and two-photon absorptivity.

43 Specifically, longer fluorescence lifetimes are observed in vitro for G-quadr

44 g a large emission cross-section and a short fluorescence lifetime as the gain medium, a stable LGS Q

45 Using fluorescence lifetime as the readout modality offers mor

46 We used a fluorescence-lifetime based leakage assay to examine the

47 To address this need, we developed a fluorescence lifetime-based approach (VF-FLIM) to visual

48 brane leakage was separately measured by the fluorescence lifetime-based calcein leakage assay and th

49 Specifically, we used a fluorescence lifetime-based high-throughput screen and b

50 e have designed a cell-permeable T-sensitive fluorescence lifetime-based nanoprobe based on lipophili

51 and mechanism of leakage is measured by the fluorescence lifetime-based vesicle leakage assay using

52 leads to consistent results when compared to fluorescence-lifetime-based FRET.

53 We found that fluorescence lifetime better distinguishes subtle differ

54 analysis of the correlation function of the fluorescence lifetime by improving the estimation of the

55 nerate spatially controlled gradients in the fluorescence lifetime by stimulated emission.

56 The fluorescence lifetime can be sensitive to the local pola

57 chlorophyll fluorescence quantum yields and fluorescence lifetimes clearly indicate that the presenc

58 Fluorescence lifetime correlation spectroscopy (FLCS) an

59 e, we take advantage of previously published fluorescence lifetime correlation spectroscopy which rel

60 properties and to use them for single-color fluorescence lifetime cross-correlation spectroscopy (sc

61 Fluorescence lifetime data are compatible with a model i

62 s a large Stokes shift and a monoexponential fluorescence lifetime decay.

63 a machine learning algorithm to process the fluorescence lifetime distribution patterns.

64 Measurements of NBD fluorescence lifetime distributions reveal that alpha-sy

65 Fluorescence lifetime estimation is performed via a pre-

66 n, multi-modal - two-photon fluorescence and fluorescence lifetime (FLIM) - microscopy and imaging fl

67 ingle-cell imaging methods for metabolism by fluorescence lifetime (FLIM) of NADH and signaling by ki

68 We propose that the long fluorescence lifetime follows from (i) a sterically more

69 of ex vivo viable epidermis showed a stable fluorescence lifetime for unpatched areas of ~1000 ps up

70 myosins tested, we found two populations of fluorescence lifetimes for individual myosin molecules,

71 concentrations with linear reduction of the fluorescence lifetime from 4.3 to 2.6 ns.

72 pmental, or "D-trajectory", that consists of fluorescence lifetime from different stages of mouse pre

73 uantum yields ranging from 0.01 to 0.29, and fluorescence lifetimes from 3 to 42 ns.

74 As minocycline and tazarotene have distinct fluorescence lifetimes from the lifetime of the skin's a

75 ave a large fluorescence quantum yield, long fluorescence lifetime, good photostability, and an emiss

76 y limited class of fluorophores, with a long fluorescence lifetime (>10 ns) and fluorescence beyond 5

77 spectrometry, immunoelectron microscopy and fluorescence lifetime image microscopy based on Forster

78 Fluorescence lifetime images of a 30 degrees retinal fie

79 nent analysis to analyze pairs of two-photon fluorescence lifetime images of stratum basale and strat

80 ual colour FLIM method we are able to detect fluorescence lifetime images of two donors to simultaneo

81 M and a viable route towards multi-megapixel fluorescence lifetime images, with a proof-of-principle

82 Here we present a technique using two-photon fluorescence lifetime imaging (2pFLIM) with new FRET bio

83 Fluorescence lifetime imaging (FLI) provides unique quan

84 veloped an analytical strategy based on FRET-fluorescence lifetime imaging (FLIM) and fluorescence cr

85 Combining TPE with fluorescence lifetime imaging (FLIM) and spectral analys

86 to perturb NAD(P)H metabolism, we find that fluorescence lifetime imaging (FLIM) differentiates quan

87 Luminescence using fluorescence lifetime imaging (FLIM) enables real-time i

88 Fluorescence lifetime imaging (FLIM) is a quantitative,

89 mer to its micelle displays that time-domain fluorescence lifetime imaging (FLIM) is able to rapidly

90 ascular ultrasound (IVUS) with multispectral fluorescence lifetime imaging (FLIm) that enables label-

91 ion was characterized nondestructively using fluorescence lifetime imaging (FLIm) to identify regions

92 Fluorescence lifetime imaging (FLIM), a technique which

93 Using multiangle light scattering (MALS), fluorescence lifetime imaging (FLIM), and FRET analyses,

94 tilization, measured with two-photon NAD(P)H fluorescence lifetime imaging (FLIM), was matched in the

95 Using fluorescence lifetime imaging (FLIM), we observed that P

96 ctions in situ Here, we used high-resolution fluorescence lifetime imaging (FLIM)-FRET of HeLa cells

97 directly image islet metabolism with NAD(P)H fluorescence lifetime imaging (FLIM).

98 ransfer (FRET) pair optimized for dual-color fluorescence lifetime imaging (FLIM).

99 energy transfer (FRET) read out by automated fluorescence lifetime imaging (FLIM).

100 resonance energy transfer (FRET) measured by fluorescence lifetime imaging (FLIM-FRET) and identified

101 eveloped to perform quantitative macroscopic fluorescence lifetime imaging (MFLI) over a large field

102 advanced quantitative-time-resolved imaging (Fluorescence Lifetime Imaging and Fluorescence Correlati

103 fields of biomedical sensors, spectroscopy, fluorescence lifetime imaging and in the design of many

104 In this study, we describe a fluorescence lifetime imaging approach for real-time mon

105 These results establish 2P fluorescence lifetime imaging as a viable means of measu

106 Fluorescence lifetime imaging demonstrates that molecule

107 monitoring kinase activity under two-photon fluorescence lifetime imaging microscopy (2pFLIM).

108 Multiphoton fluorescence lifetime imaging microscopy (FLIM) allows l

109 s been delineated through spatially resolved fluorescence lifetime imaging microscopy (FLIM) and fluo

110 Using fluorescence lifetime imaging microscopy (FLIM) and phas

111 -factors NADH and FAD with quantitation from Fluorescence Lifetime Imaging Microscopy (FLIM) as a mea

112 Fluorescence lifetime imaging microscopy (FLIM) can meas

113 By recording fluorescence lifetime imaging microscopy (FLIM) data of

114 sment of processes such as fibrosis, whereas fluorescence lifetime imaging microscopy (FLIM) enables

115 We used fluorescence lifetime imaging microscopy (FLIM) in live

116 Fluorescence lifetime imaging microscopy (FLIM) is a key

117 phases could be imaged with high contrast by fluorescence lifetime imaging microscopy (FLIM) on giant

118 This approach uses fluorescence lifetime imaging microscopy (FLIM) paired w

119 Subsequently, we evaluated the probe and fluorescence lifetime imaging microscopy (FLIM) techniqu

120 In this work, we employ two-photon fluorescence lifetime imaging microscopy (FLIM) to creat

121 We used phasor fluorescence lifetime imaging microscopy (FLIM) to disti

122 rescent molecular rotors in combination with Fluorescence Lifetime Imaging Microscopy (FLIM) to image

123 l two-photon microscopy and frequency-domain fluorescence lifetime imaging microscopy (FLIM) to map c

124 Here, we used the phasor approach and Fluorescence Lifetime Imaging Microscopy (FLIM) to measu

125 e use of pulsed interleaved excitation (PIE)-fluorescence lifetime imaging microscopy (FLIM) to measu

126 Using biochemical assays and fluorescence lifetime imaging microscopy (FLIM) to probe

127 We have used Fluorescence Lifetime Imaging Microscopy (FLIM) to quant

128 ssected into its components, and chlorophyll fluorescence lifetime imaging microscopy (FLIM) was used

129 t of microscopic viscosity in live cells via fluorescence lifetime imaging microscopy (FLIM) while al

130 time property could be visually mapped using fluorescence lifetime imaging microscopy (FLIM), allowin

131 We used cryo-SEM, fluorescence lifetime imaging microscopy (FLIM), autoflu

132 ed the fluorescence decay of anthocyanins by fluorescence lifetime imaging microscopy (FLIM), in both

133 We show multi-label fluorescence lifetime imaging microscopy (FLIM), single-

134 ET imaging advantages normally attributed to fluorescence lifetime imaging microscopy (FLIM), such as

135 or image-correlation spectroscopy of histone fluorescence lifetime imaging microscopy (FLIM)-Forster

136 luidic mixer and two-color two-photon (2c2p) fluorescence lifetime imaging microscopy (FLIM).

137 ed a novel Forster resonance energy transfer-fluorescence lifetime imaging microscopy (FRET-FLIM)-bas

138 e, we used Forster resonance energy transfer/fluorescence lifetime imaging microscopy (FRET/FLIM) com

139 Specifically, Molecular Tension-Fluorescence Lifetime Imaging Microscopy (MT-FLIM) produ

140 ng the first single-shot spectrally resolved fluorescence lifetime imaging microscopy (SR-FLIM).

141 Using automated Fluorescence Lifetime Imaging Microscopy - Fluorescence

142 Fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy analyses show t

143 Fluorescence lifetime imaging microscopy analysis demons

144 rmore, our Forster resonance energy transfer-fluorescence lifetime imaging microscopy analysis indica

145 Here, we introduce fluorescence lifetime imaging microscopy and fluorescenc

146 We used in planta fluorescence lifetime imaging microscopy and fluorescenc

147 scopy techniques, including FRET detected by fluorescence lifetime imaging microscopy and single-cell

148 Fluorescence lifetime imaging microscopy and single-part

149 Forster resonance energy transfer by fluorescence lifetime imaging microscopy assays revealed

150 tracing, histone mass spectrometry, and NADH fluorescence lifetime imaging microscopy in these cells,

151 des an additional channel for multiparameter fluorescence lifetime imaging microscopy of green fluore

152 Here we report the use of fluorescence lifetime imaging microscopy of the molecula

153 Finally, fluorescence lifetime imaging microscopy studies in rat

154 ing two- and three-color dSTORM supported by fluorescence lifetime imaging microscopy we identified h

155 We adapted this setup for fluorescence lifetime imaging microscopy with phasor ana

156 , using fluorescence confocal microscopy and fluorescence lifetime imaging microscopy with the phasor

157 ologic evaluation, we apply the phasor-FLIM (Fluorescence Lifetime Imaging Microscopy) method to capt

158 channels (Forster resonance energy transfer-fluorescence lifetime imaging microscopy).

159 rmed "molecular rotors", in combination with Fluorescence Lifetime Imaging Microscopy, for monitoring

160 raction with beta2 integrins, as revealed by fluorescence lifetime imaging microscopy, leading to int

161 Furthermore, using fluorescence lifetime imaging microscopy, live-cell imag

162 vo by fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy, mediated throu

163 We now show, as determined by fluorescence lifetime imaging microscopy, that motile ce

164 According to fluorescence lifetime imaging microscopy, the new flippe

165 By fluorescence lifetime imaging microscopy, we also demons

166 ransfer-based sensor for TrkB and two-photon fluorescence lifetime imaging microscopy, we monitor Trk

167 Along with cell cycle progression, utilizing fluorescence lifetime imaging microscopy-based Forster r

168 ing a fluorescence resonance energy transfer/fluorescence lifetime imaging microscopy-based Ras imagi

169 minescence-based mammalian interactome), and fluorescence lifetime imaging microscopy-fluorescence re

170 ted primary bronchial epithelial cells using fluorescence lifetime imaging microscopy.

171 Rab1 and K-Ras activity in live cells using fluorescence lifetime imaging microscopy.

172 UVs) and cells by confocal laser scanning or fluorescence lifetime imaging microscopy.

173 sing donor recovery after photobleaching and fluorescence lifetime imaging microscopy.

174 ecreased ER Ca(2+), which was measured using fluorescence lifetime imaging microscopy.

175 sing comparative colocalization analysis and fluorescence lifetime imaging microscopy.

176 fold and employed multiphoton microscopy and fluorescence lifetime imaging microscopy.

177 identification of submicroscopic domains by fluorescence lifetime imaging microscopy; 3), elucidatio

178 eep neural network (DNN) architecture, named fluorescence lifetime imaging network (FLI-Net) that is

179 y for minimizing the background influence in fluorescence lifetime imaging of live cells and sub-cell

180 sfunction and oxidative stress determined by fluorescence lifetime imaging of NADH and kidney fibrosi

181 determine oxygen-dependent lifetimes and for fluorescence lifetime imaging of oxygen.

182 The comparative fluorescence lifetime imaging of several full-length cis

183 this study was to investigate the benefit of fluorescence lifetime imaging ophthalmoscopy (FLIO) for

184 Fluorescence lifetime imaging ophthalmoscopy seems to de

185 ore specialized microscopy techniques, e.g., fluorescence lifetime imaging or two-photon excited fluo

186 Our analysis shows that two-photon fluorescence lifetime imaging permits the identification

187 Fluorescence lifetime imaging results indicate that Pil1

188 Furthermore, NAD(P)H fluorescence lifetime imaging revealed an increase in bo

189 NAD(P)H fluorescence lifetime imaging showed that EPA acts downs

190 le and can be applied to many multicomponent fluorescence lifetime imaging targets that require cellu

191 its activity directly in single cells using fluorescence lifetime imaging to detect Forster resonanc

192 by fluorescence resonance energy transfer by fluorescence lifetime imaging to interact directly with

193 We apply fluorescence lifetime imaging to show that shell viscosi

194 Spectrally resolved fluorescence lifetime imaging(1-3) and spatial multiplex

195 obtained by the phasor approach to confocal fluorescence lifetime imaging, a graphical method that d

196 XRD, He-ion imaging, HR-TEM, EELS, PL, fluorescence lifetime imaging, Raman, FTIR, TGA, KPFM, X

197 , brightfield microscopy, histochemistry and fluorescence lifetime imaging, these autofluorescent par

198 les a diverse range of applications, such as fluorescence lifetime imaging, time-of-flight depth imag

199 pines using a new FRET sensor and two-photon fluorescence lifetime imaging.

200 vity in spines using fast-framing two-photon fluorescence lifetime imaging.

201 ed via fluorescent ratiometric detection and fluorescence lifetime imaging; it was found that lysosom

202 Fluorescence-lifetime imaging (FLIM) and 3D structural i

203 ty in visualizing intracellular processes by fluorescence-lifetime imaging microscopy (FLIM) measurem

204 or can be used to image PI4KB in cells using fluorescence-lifetime imaging microscopy (FLIM) microsco

205 ally, fluorescence-resonance energy transfer-fluorescence-lifetime imaging microscopy experiments ind

206 arbons on the external surface, evidenced by fluorescence-lifetime imaging microscopy, are principall

207 findings are complemented experimentally by fluorescence-lifetime imaging microscopy/fluorescence re

208 study addressed this requirement by joining fluorescence-lifetime imaging microscopy/phasor multipho

209 n reaction,(13)C-nuclear magnetic resonance, fluorescence-lifetime imaging, mass spectrometry-based m

210 tudying 2D pH distributions with the help of fluorescence-lifetime-imaging techniques.

211 chondria of cancer cells, as well as shorter fluorescence lifetime in cancer relative to normal cells

212 Moreover, (th)G's dominant fluorescence lifetime in DNA is unusually long (9-29 ns)

213 The average fluorescence lifetime in RNA duplexes is 4.3 ns and gene

214 However, the use of fluorescence lifetime in this area has been limited by t

215 GFP and EGFP can be clearly distinguished by fluorescence lifetime in various models, including mamma

216 nts such as acetonitrile, MV(2+) has a short fluorescence lifetime in water.

217 The method simultaneously images fluorescence lifetimes in 3D with multiple excitation la

218 s well suited to accurately quantify complex fluorescence lifetimes in cells and, in real time, in in

219 f 7-aminocoumarin dyes that have distinctive fluorescence lifetimes in different solvation environmen

220 Although it has long fluorescence lifetimes in polar solvents such as acetoni

221 Fluorescence lifetimes increased significantly with incr

222 o show that the origin of PIFE is the longer fluorescence lifetime induced by the local protein envir

223 The method makes use of fluorescence lifetime information from both donor and ac

224 ore the possibilities of using the available fluorescence lifetime information in PIE-FI experiments.

225 " embedded in the microbubble surface, whose fluorescence lifetime is directly related to the viscosi

226 With PSFC the fluorescence lifetime is taken as a cytometric parameter

227 tly labeled drugs, using fluorophores with a fluorescence lifetime larger than the rotational correla

228 ee Ag-In-S ternary quantum dots (t-QDs) with fluorescence lifetimes (LTs) of several hundred nanoseco

229 h high-performance liquid chromatography and fluorescence lifetime measured at 380-400 nm (R = -0.76,

230 Fluorescence lifetime measurement reveals that the CT-ty

231 Fluorescence lifetime measurements and confocal fluoresc

232 In agreement, fluorescence lifetime measurements confirm the exception

233 is the demonstration of how high-throughput fluorescence lifetime measurements correlate well to cha

234 fluorescence anisotropy decay and picosecond fluorescence lifetime measurements for the flavin reveal

235 Fluorescence lifetime measurements of the intrinsic flav

236 ic methods listed above and by time-resolved fluorescence lifetime measurements using a complementary

237 ques (UV, both steady state fluorescence and fluorescence lifetime measurements, circular dichroism (

238 Here we highlight the application of fluorescence lifetime microscopy (FLIM)-based biosensing

239 onance energy transfer measurements based on fluorescence lifetime microscopy (FRET-FLIM).

240 Fluorescence lifetime microscopy of whole cells and ultr

241 sessed using clinically available two-photon fluorescence lifetime microscopy systems.

242 phoresis, quantitative mass spectrometry and fluorescence lifetime microscopy to characterise a serie

243 vel microscopic technique, comparable to the fluorescence lifetime microscopy, enables its applicatio

244 -pull probes with the mechanosensitivity and fluorescence lifetime needed for practical use in biolog

245 ted single photon counting revealed that the fluorescence lifetime of (ts)T (tau = 4-11 ns) was short

246 en fluorescent protein (EGFP) and exhibits a fluorescence lifetime of 5.1 ns.

247 er by biophysical studies: the excited-state fluorescence lifetime of a complex between ReAsH and a p

248 onitored by atomic force microscopy, and the fluorescence lifetime of Alexa-labeled Tau (time-correla

249 phagosomes become acidified and the average fluorescence lifetime of EGFP is known to be affected by

250 the simultaneously recorded images based on fluorescence lifetime of LHCII and fluorescence anisotro

251 uantifying FRET is to measure changes in the fluorescence lifetime of the donor fluorophore using FLI

252 s, the polymer chain extends, increasing the fluorescence lifetime of the donor.

253 a(2+), but did correlate with differences in fluorescence lifetime of the dye.

254 Here, we find that the fluorescence lifetime of the red-shifted Ca(2+) indicato

255 room-temperature emission efficiency and the fluorescence lifetime of the restrained cyanine are not

256 We also find that the fluorescence lifetime of the restrained heptamethine cya

257 We observed lengthening of the fluorescence lifetime of these dyes at the water-oil per

258 We demonstrate that the fluorescence lifetime of this new probe changes consider

259 Significant differences between fluorescence lifetimes of "free" Trp derivatives hydroxy

260 in the absorption and emission spectra with fluorescence lifetimes of 1.3 ns, indicating the formati

261 Furthermore, the distinct fluorescence lifetimes of iRFPs enable lifetime multiple

262 We measured the fluorescence lifetimes on whole leaves of Arabidopsis th

263 demonstrate that mCherryTYG is an excellent fluorescence lifetime pH sensor that significantly expan

264 From kinetic modeling of our two fluorescence lifetime populations and earlier solution d

265 ty of responding to low pH by decreasing the fluorescence lifetime, present in the wild-type protein,

266 The chlorophyll fluorescence lifetime probes the excited-state chlorophy

267 This remotely manipulated fluorescence lifetime property could be visually mapped

268 are combined to correlate the dependence of fluorescence lifetime reduction on the spectral overlap

269 narrow defined tunable emission peak, longer fluorescence lifetime, resistance to photobleaching and

270 ser-induced fluorescence with wavelength and fluorescence lifetime selection.

271 1038 cm(-1)) bands in the Raman spectrum and fluorescence lifetime shortened by 0.4 ns compared to un

272 We observed that the tissue fluorescence lifetime shortened, and that Raman bands at

273 itation enhancement of circa 100 times and a fluorescence lifetime shortening to ~20 ps.

274 cP at 40 degrees C was completed within the fluorescence lifetime, so that the rotational time const

275 None of the mutations affect fluorescence lifetimes, Stokes shift relaxation rates, a

276 inding isotope effects (BIEs), time-resolved fluorescence lifetimes, Stokes shifts, and extended grap

277 n nuclear magnetic resonance ((1)H-NMR), and fluorescence lifetime studies.

278 account for fluorescence quenching based on fluorescence lifetime (tau) measurements is shown.

279 s high as 0.93 in nonpolar solvents, and the fluorescence lifetimes (tau(F)) vary from 1.50 to 3.01 n

280 g average homo-FRET rates (k(FRET)), average fluorescence lifetimes (tau), and average anisotropies o

281 hin plant cells, the amplitude-weighted mean fluorescence lifetime (taum ) correlated with distinct s

282 how in response to doxorubicin, NAD(P)H mean fluorescence lifetime (taum) and enzyme-bound (a2%) frac

283 The mean fluorescence lifetime, taum, was calculated from a 3-exp

284 frared region (730 nm) is observed with long fluorescence lifetimes that range from 30 to 860 ns, dep

285 which exploits high sensitivity of the OGB-1 fluorescence lifetime to nanomolar Ca(2+) concentration

286 , a technique which utilizes a fluorophore's fluorescence lifetime to probe changes in its environmen

287 jections) showed a reduction in the observed fluorescence lifetimes to between ~518-583 ps.

288 he CH3NH3SnI3 film effectively increases the fluorescence lifetime up to 10 times and gives diffusion

289 to-switchable nanogel that exhibits variable fluorescence lifetime upon photoisomerization-induced en

290 nditions are associated with altered NAD(P)H fluorescence lifetimes, use a simple cell model to confi

291 , followed by measurement and imaging of the fluorescence lifetime using multiphoton excitation.

292 ains in living cells on account of its large fluorescence lifetime variation in the two phases.

293 presentation to analyze changes in Laurdan's fluorescence lifetime we obtain two different phasor tra

294 th a time constant >10 ns, comparable to the fluorescence lifetime, we used electron spin resonance s

295 progressive internalization of EGFP-E. coli, fluorescence lifetimes were acquired and compared to con

296 Mean fluorescence lifetimes were calculated.

297 ncreases from 0.22 to 0.96) while long-lived fluorescence lifetimes were observed between 1.8-2.4 ns.

298 It is also able to recover fluorescence lifetime with sub-20ps accuracy as validate

299 Comparison of in situ fluorescence lifetimes with satellite retrievals of sola

300 It was hypothesized that fluorescence lifetimes would correlate well with phagocy