ライフサイエンスコーパス: fluorescence lifetime

1 cence emission, high quantum yield, and long fluorescence lifetime.

2 of serine/threonine protein kinases based on fluorescence lifetime.

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

4 ed substantial intermolecular variability in fluorescence lifetimes.

5 nd detected with on-the-fly determination of fluorescence lifetimes.

6 in larger emission quantum yields and longer fluorescence lifetimes.

7 mbrane-associated species by their differing fluorescence lifetimes.

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

9 rinsic fluorophores, based on their distinct fluorescence lifetimes.

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

11 e, excitation intensity, and geometry, makes fluorescence lifetime a practical alternative to the est

12 ssay based on detection of changes in global fluorescence lifetime above a gold substrate, with super

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

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

15 The tryptophan fluorescence lifetimes also suggest a deviation from nat

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

17 Calorimetry and fluorescence lifetime analysis of labeled RNAs shows tha

18 Fluorescence lifetime analysis showed that mutations wit

19 ross-correlation spectroscopy (PIE-FCCS) and fluorescence lifetime analysis.

20 insertion into live cell membranes, the GPs' fluorescence lifetime and diffusion time were measured i

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

22 Fluorescence lifetime and one-photon ratiometric imaging

23 orophore libraries, simultaneously measuring fluorescence lifetime and photobleaching.

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

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

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

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

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

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

30 Measurements of fluorescence lifetimes and rotational correlation times

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

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

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

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

35 Subnanosecond-resolved detection of fluorescence lifetime, anisotropy, and quenching was use

36 arboxyl terminal of [Ru(bpy)(2)PICH(2)](2+) (fluorescence lifetime approximately 682+/-5 ns) dye was

37 es including fluorescence quantum yields and fluorescence lifetimes are briefly introduced.

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

39 The decrease in average fluorescence lifetime as measured in a recently develope

40 hnique to measure the changes in chlorophyll fluorescence lifetime as photosynthetic organisms adapt

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

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

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

44 his article describes novel data analysis of fluorescence lifetime-based protein kinase assays to ide

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

46 We found that fluorescence lifetime better distinguishes subtle differ

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

48 The fluorescence lifetime can be sensitive to the local pola

49 only the colors of the photons but also the fluorescence lifetimes can be monitored.

50 e amplitudes of 65 ps and 305 ps chlorophyll fluorescence lifetime components that was reversed after

51 Fluorescence lifetime correlation spectroscopy (FLCS) an

52 rate for the first time the applicability of fluorescence lifetime correlation spectroscopy (FLCS) to

53 nd that DSBNI aggregation leads to increased fluorescence lifetimes, coupled with hypsochromic shifts

54 EGFR neutralizing antibody was confirmed by fluorescence lifetime cross-correlation measurements and

55 Fluorescence lifetime data are compatible with a model i

56 ate-limiting step, fitting kinetic models to fluorescence lifetime data cannot be used to derive mech

57 Steady-state fluorescence quenching and fluorescence lifetime data indicate that there are exten

58 Fluorescence lifetime data reveal no significant Forster

59 Fluorescence lifetime data revealed that TMSs occupied a

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

61 After addition of KI, the fluorescence lifetime decreased to 3.1 ns.

62 The differential change of fluorescence lifetime demonstrates the shift in position

63 joint distribution of FRET efficiencies and fluorescence lifetimes determined from bins (or bursts)

64 ility has been hampered by the complexity of fluorescence lifetime distributions in solution.

65 Modulation of the fluorescence lifetime (FLT) of CdTeSe/ZnS quantum dots (

66 In this study, fluorescence lifetime (FLT) was evaluated before and aft

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

68 rrelated single-photon counting, we measured fluorescence lifetimes for all CaRubies and demonstrate

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

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

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

72 We use the phasor-fluorescence lifetime image microscopy approach to spati

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

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

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

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

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

78 Fluorescence lifetime imaging (FLIM) is widely applied t

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

80 Using fluorescence lifetime imaging (FLIM) we show that MCAK b

81 Fluorescence lifetime imaging (FLIM), a technique which

82 Fluorescence lifetime imaging (FLIM)-FRET microscopy dem

83 lifetime cross-correlation measurements and fluorescence lifetime imaging (FLIM).

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

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

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

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

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

89 uscle segment length) were synchronized with fluorescence lifetime imaging and force measurements to

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

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

92 eport, we apply the phasor representation of fluorescence lifetime imaging data to the quantitative s

93 Fluorescence lifetime imaging demonstrates that molecule

94 , and fluorescence resonance energy transfer-fluorescence lifetime imaging experiments revealed direc

95 Taken together, quantitative in vivo fluorescence lifetime imaging illustrated that RhoA is n

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

97 Concomitantly, fluorescence lifetime imaging microscopy (FLIM) analyses

98 y simultaneous use of the phasor approach to fluorescence lifetime imaging microscopy (FLIM) and cros

99 Using fluorescence lifetime imaging microscopy (FLIM) and phas

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

101 Fluorescence lifetime imaging microscopy (FLIM) can meas

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

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

104 Fluorescence lifetime imaging microscopy (FLIM) is now r

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

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

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

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

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

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

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

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

113 enerate efficient FRET, and steady-state and fluorescence lifetime imaging microscopy (FLIM) were use

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

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

116 with fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy (FRET-FLIM) and

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

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

119 o, by fluorescence resonance energy transfer/fluorescence lifetime imaging microscopy (FRET/FLIM), th

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

121 Fluorescence lifetime imaging microscopy analysis demons

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

123 Here, we introduce fluorescence lifetime imaging microscopy and fluorescenc

124 We used in planta fluorescence lifetime imaging microscopy and fluorescenc

125 ergy transfer-based system using multiphoton fluorescence lifetime imaging microscopy and its applica

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

127 Fluorescence lifetime imaging microscopy and single-part

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

129 escence resonance energy transfer (FRET) and fluorescence lifetime imaging microscopy between fluores

130 scence biomarkers and the phasor approach to fluorescence lifetime imaging microscopy in conjunction

131 Fluorescence lifetime imaging microscopy is used to demo

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

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

134 Finally, fluorescence lifetime imaging microscopy studies in rat

135 Fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy studies showed

136 Fluorescence lifetime imaging microscopy supports P450 c

137 g the fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy technique.

138 excitation-Forster resonance energy transfer-fluorescence lifetime imaging microscopy to determine th

139 We applied fluorescence lifetime imaging microscopy to map the micr

140 Here we used two-photon fluorescence lifetime imaging microscopy to monitor the

141 Herein we combine confocal fluorescence lifetime imaging microscopy with a statisti

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

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

144 We used a combination of fluorescence lifetime imaging microscopy, cell biology,

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

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

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

148 r aggregates of LHCII-HL have been shown, by fluorescence lifetime imaging microscopy, to be particul

149 By fluorescence lifetime imaging microscopy, we also demons

150 Using two-photon-induced fluorescence lifetime imaging microscopy, we corroborate

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

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

153 We also discuss anisotropy and fluorescence lifetime imaging microscopy-based FRET tech

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

155 A fluorescence lifetime imaging microscopy-fluorescence re

156 vity at a subcellular level using FLIM-FRET (fluorescence lifetime imaging microscopy-fluorescence re

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

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

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

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

161 sing comparative colocalization analysis and fluorescence lifetime imaging microscopy.

162 ll beta2 integrins and CD47 were detected by fluorescence lifetime imaging microscopy.

163 tween hBVR and PKCdelta was detected by FRET-fluorescence lifetime imaging microscopy.

164 ssociation by both coimmunoprecipitation and fluorescence lifetime imaging microscopy.

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

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

167 expressed in N. benthamiana leaf tissues and fluorescence lifetime imaging microscopy/Forster resonan

168 myces cerevisiae) two-hybrid analysis and by fluorescence lifetime imaging microscopy/Forster resonan

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

170 Fluorescence lifetime imaging of cells expressing lipid-

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

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

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

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

175 Fluorescence lifetime imaging results indicate that Pil1

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

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

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

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

180 We apply fluorescence lifetime imaging to show that shell viscosi

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

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

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

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

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

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

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

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

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

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

191 The maximum chlorophyll fluorescence lifetime in isolated photosystem II (PSII)

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

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

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

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

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

197 by Zn(2+) and Cd(2+) ions inside MOFs shows fluorescence lifetimes in line with those of close-packe

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

199 model that sets constraints on the values of fluorescence lifetimes in the time responses of the assa

200 ers were moved from relaxation to rigor, the fluorescence lifetime increased for all label positions.

201 Measurements of pigments and chlorophyll fluorescence lifetimes indicated that the additional NPQ

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

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

204 We use the fluorescence lifetime information to perform a robust du

205 A change of the fluorescence lifetime is achieved by the phosphorylated

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

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

208 developed method, information about analyte fluorescence lifetimes is collected by time-correlated s

209 of 700-1000 fs and low anisotropy (~0.1) in fluorescence lifetime kinetic studies.

210 hoton absorption, fluorescence emission, and fluorescence lifetime kinetics.

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

212 n of Acd into proteins, using changes in Acd fluorescence lifetimes, Mcm/Acd FRET, or energy transfer

213 Despite these changes, the average fluorescence lifetimes measured in Fm and Fm' (with NPQ)

214 Fluorescence lifetime measurement reveals that the CT-ty

215 We used a time-domain fluorescence lifetime measurement to quantify the effect

216 Fluorescence lifetime measurements and confocal fluoresc

217 In agreement, fluorescence lifetime measurements confirm the exception

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

219 Fluorescence anisotropy and fluorescence lifetime measurements indicate that contact

220 Fluorescence lifetime measurements indicate the nature o

221 An understanding of the basic physics of fluorescence lifetime measurements is required to use th

222 Fluorescence lifetime measurements of sulfoindocarbocyan

223 Fluorescence lifetime measurements of the intrinsic flav

224 Fluorescence lifetime measurements revealed multiple tra

225 Fluorescence lifetime measurements suggest that the enha

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

227 Fluorescence lifetime measurements were employed to comp

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

229 Using steady-state and fluorescence lifetime measurements, we further demonstra

230 nsient absorption spectroscopy as well as by fluorescence lifetime measurements.

231 optical biomarker and the phasor approach to Fluorescence Lifetime microscopy (FLIM) we identify cell

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

233 nfirmed by Forster-resonance energy transfer fluorescence lifetime microscopy in Arabidopsis thaliana

234 Fluorescence lifetime microscopy of whole cells and ultr

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

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

237 e to be the first near-infrared pH-sensitive fluorescence lifetime molecular probe suitable for biolo

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

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

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

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

242 However, the excited-state fluorescence lifetime of an EGFP fusion of Orf1629 remai

243 The excited-state fluorescence lifetime of EGFP fused to VP39 or EXON0 was

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

245 FWPV; an avipoxvirus), and the excited-state fluorescence lifetime of EGFP was reduced from 2.5 +/- 0

246 Exploiting the different fluorescence lifetime of free and bound NADH has the pot

247 Here, we investigate the fluorescence lifetime of Laurdan at two different emissi

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

249 By also measuring the fluorescence lifetime of Oregon Green in SVs, we determi

250 reaking for the symmetric chromophore within fluorescence lifetime of several tens of ns.

251 H changes as measured using the pH-dependent fluorescence lifetime of SNARF-1 conjugated to urease we

252 The fluorescence lifetime of Spinach-DFHBI is 4.0 +/- 0.1 ns

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

254 The long fluorescence lifetime of the Pdots was used to distingui

255 and an iron(III) chelate that modulates the fluorescence lifetime of the peptide only when it is pho

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

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

258 EN1 (hFEN1) in the low-energy CD spectra and fluorescence lifetimes of 2-aminopurine in substrates an

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

260 al is found to be 6.7% and, coupled with the fluorescence lifetime on the millisecond time scale, beg

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

262 or complexes, based on analysis of the donor fluorescence lifetime or the spectrally resolved fluores

263 mpound, LS482, demonstrated steady-state and fluorescence-lifetime pH-sensitivity.

264 lifetime as measured in a recently developed fluorescence lifetime plate reader (Edinburgh Instrument

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

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

267 The chlorophyll fluorescence lifetime probes the excited-state chlorophy

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 We applied this technique to measure the fluorescence lifetimes responsible for the predominant,

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

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

273 itting differential scanning calorimetry and fluorescence lifetime spectroscopy denaturation data, an

274 hermore, we compare calcium titrations using fluorescence lifetime spectroscopy with the ratiometric

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 e oxidized materials, and an increase in the fluorescence lifetime (tau(F)), due to a decrease in the

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

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

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

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

283 bility, together with inherent advantages of fluorescence lifetime technology (FLT) as a homogeneous,

284 Furthermore, pHRed has a pH-responsive fluorescence lifetime that changes by ~0.4 ns over physi

285 they are used to measure the quenched donor fluorescence lifetime that results from Forster resonanc

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

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

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

289 logical applications was demonstrated with a fluorescence-lifetime tomography system.

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

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

292 A corresponding decrease in fluorescence lifetime was observed for each distance.

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

297 Fluorescence lifetimes were similar for the O- and S-con

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