ライフサイエンスコーパス: fluorescence

1 ich caused disaggregation and enhancement in fluorescence.

2 green fluorescent protein, and activate its fluorescence.

3 ation of the light and negligible background fluorescence.

4 visualization of previously undetectable GFP fluorescence.

5 ar sensitivity with visual detection of bead fluorescence.

6 Fluorescence activated cell sorting and Western blot wer

7 ll subsets (RRMS; n = 7) were isolated using fluorescence activated cell sorting for bulk RNA sequenc

8 In this study, fluorescence-activated cell sorted photosynthetic picoeu

9 y the earliest responding cell type, we used fluorescence-activated cell sorting (FACS) to sort the g

10 ofluorescence, Luminex assay, ELISA, UniCAP, fluorescence-activated cell sorting, and PCR.

11 ption templates regulates the synthesis of a fluorescence-activating RNA aptamer.

12 S3 cleavage site linker reported the highest fluorescence activation in stably transduced mammalian c

13 the reactivity of free sulfhydryl groups and fluorescence analysis, showed that the increase of ethan

14 pproach, complemented by intrinsic extrinsic fluorescence analysis.

15 of the host-guest complex WP5 G quenches the fluorescence and inhibits ROS generation of G.

16 Most HTS platforms use fluorescence and luminescence technologies, representing

17 simultaneously label mitochondria with blue fluorescence and lysosomes with red fluorescence, and th

18 Here we show by in vivo fluorescence and MR imaging, that LN paracortical zones

19 vior of the dynamic junction, quantified via fluorescence and NMR spectroscopy and DFT calculations.

20 ibutions of both thermally activated delayed fluorescence and phosphorescence.

21 Fluorescence and photoacoustic imaging are cost-effectiv

22 In vivo fluorescence and photoacoustic imaging studies highlight

23 hesis, characterisation and determination of fluorescence and photophysical properties of various nov

24 ural amino acid incorporation, time-resolved fluorescence, and (19)F nuclear magnetic resonance spect

25 s unambiguously supported by confocal Raman, fluorescence, and analytical transmission electron micro

26 ues, including synchrotron X-ray absorption, fluorescence, and diffraction methods, support successfu

27 s including isothermal calorimetry analysis, fluorescence, and FRET quenching, and a range of K(d) va

28 itration calorimetry (ITC), tryptophan (Trp) fluorescence, and microscale thermophoresis measurements

29 ith blue fluorescence and lysosomes with red fluorescence, and the correlation between the red-blue f

30 cy calculated from the fit of the eGFP15eGFP fluorescence anisotropy decays with a stretched exponent

31 We used fluorescence anisotropy imaging of histone H2B-EGFP to i

32 e fluidity of the lipid bilayer expressed as fluorescence anisotropy of the probe N,N,N-Trimethyl-4-(

33 Quantitative DNA binding studies with fluorescence anisotropy-based titrations revealed that M

34 asts and stromal cores using a dextran-based fluorescence assay and changes in HA receptor expression

35 In this study, a high-throughput fluorescence assay method for determination of xanthine

36 hlorin byproduct (1.4% relative to BC-1 upon fluorescence assay).

37 plication of mesoscopic imaging, a widefield fluorescence-based approach that balances high spatiotem

38 Our fluorescence-based assay offers distinct advantages over

39 roblem by introducing new, to our knowledge, fluorescence-based assays that overcome the restrictions

40 stop codons of MTCH2 using luminescence- and fluorescence-based assays, and by analyzing ribosome-pro

41 e neoplastic lesion detection by employing a fluorescence-based endoscopic approach.

42 are previously difficult or undesirable with fluorescence-based technologies.

43 Using kinetic analyses, fluorescence binding, X-ray crystallography, and gel fil

44 (ER-GCaMP6-150) in the ER, and measured its fluorescence both in dissociated ommatidia and in vivo f

45 Adsorption of ssDNA quenches intrinsic GQD fluorescence by 31.5% for low-oxidation GQDs and enables

46 performed in vivo FME and quantification of fluorescence by multidiameter single-fiber reflectance/s

47 Widefield fluorescence can originate from indicator molecules at a

48 mission, attributed to their single-emission fluorescence centre.

49 DNA base excision activity by a ratiometric fluorescence change.

50 al activity in the mouse visual cortex, with fluorescence changes of up to 25%.

51 uced chirality, stimuli-responsive dynamics, fluorescence changes, organocatalysis, anion transport,

52 Non-cognate sequences display little to no fluorescence changes, showing that strand separation is

53 g multi-year changes in weather, chlorophyll fluorescence, chloroplast ultrastructure, and changes in

54 Using bimolecular fluorescence complementation and immunocytochemistry, we

55 Through a functional fluorescence conversion, Coupa can simultaneously label

56 ombined with spectroscopy techniques such as fluorescence correlation spectroscopy (FCS) and spectral

57 s, with thermophoresis, gel electrophoresis, fluorescence correlation spectroscopy (FCS), and microfl

58 ce spectroscopy, Circular Dichroism (CD) and Fluorescence Correlation Spectroscopy (FCS).

59 ysis (FPA) and photo-induced energy-transfer fluorescence correlation spectroscopy (PET-FCS) to show

60 will find use in the application of FRET and fluorescence correlation spectroscopy for the analysis o

61 with diverse CRISPR tools including our dual fluorescence CRISPRi/a cell lines, this system can facil

62 nt3 to its receptor, Frizzled1 (Fzd1), using fluorescence cross-correlation spectroscopy and show tha

63 Here, using FRET and fluorescence cross-correlation spectroscopy, we introduc

64 The fractal topology minimises fluorescence crosstalk and allows quantitative decoding

65 r average of both effects, possibly with the fluorescence data showing somewhat greater weighting of

66 ctor (PARAFAC) analysis where absorption and fluorescence data were combined.

67 9)Fe]Ent binding and uptake experiments, and fluorescence decoy sensor assays.

68 nce energy transfer efficiencies measured by fluorescence depolarization allowed us to construct a tw

69 is absorption and ORF, but it reduces the QD fluorescence depolarization.

70 Here, using a bulk fluorescence dequenching assay and single-molecule Forst

71 id quantification without need for expensive fluorescence detection equipment.

72 uminol and an ionic liquid in water exhibits fluorescence detection of SM within seconds.

73 We have explored a novel turn-on fluorescence detection of sulfur mustard (SM) at "room t

74 ased FITC molecules, leading to an amplified fluorescence detection signal.

75 Fluorescence detection, either involving propagating or

76 ing a common quantitative PCR instrument for fluorescence detection.

77 rated ME instrument coupled to laser-induced fluorescence detection.

78 romatography method coupling diode-array and fluorescence detectors (DAD and FLD, respectively) has b

79 We observed that background fluorescence due to leaky H2B-FP expression, occurring i

80 ion device to collect visible absorption and fluorescence EEM spectra of reacting solutions.

81 omplex is designed that achieves synchronous fluorescence-electron microscopy correlation.

82 Time-resolved fluorescence emission and resonance-enhanced second harm

83 pressure-induced bathochromic shifts in both fluorescence emission and UV/Vis absorption spectra of a

84 From the analysis of trans-parinaric acid fluorescence emission lifetimes, we could determine that

85 Herein, we report that red-shifting of the fluorescence emission of Au nanoclusters (AuNCs) into NI

86 S(1) -> Q(x) route because the S(1) -> S(0) fluorescence emission of zeta-carotene overlaps almost p

87 onic and neutral species that have different fluorescence emissions and different abilities to diffus

88 fast protein assay based on protein-induced fluorescence enhancement (PIFE), that can dynamically me

89 probe into a microtubule triggers remarkable fluorescence enhancement and promising electron contrast

90 NBD-Bu shows a significant fluorescence enhancement upon selective binding to the t

91 In systems with > 2.4% water addition fluorescence (excitation 325 nm / emission 410 nm) as in

92 e SA-DTP system to produce strong, amplified fluorescence for detection.

93 d not to undifferentiated MSCs, and emit NIR fluorescence for functional detection.

94 ic agents have the potential to combine both fluorescence for image-guided surgery (IGS) and photodyn

95 up to 130-fold enhancement of near-infrared fluorescence for ultra-sensitive and quantitative detect

96 of metastatic lung cancer, as well as during fluorescence-guided robotic surgery.

97 ep, and a liquid chromatography-ultra violet-fluorescence (HPLC-UV/FL) analysis.

98 near-infrared window (NIR-II, 1000-1700 nm) fluorescence imaging (FI) and photoacoustic imaging (PAI

99 Ex vivo fluorescence imaging after overnight cold exposure and f

100 Using live and fixed fluorescence imaging and electrophysiological techniques

101 vity and subcellular localization, live-cell fluorescence imaging and stimulated emission depletion s

102 Indocyanine green fluorescence imaging demonstrated complete coverage of t

103 For this type of problem, fluorescence imaging is usually the primary tool of choi

104 Live-cell single-molecule fluorescence imaging of G4s was carried out under condit

105 ovel method for targeted near-infrared (NIR) fluorescence imaging of glucagonlike peptide 1 receptor

106 ha(IIb)beta(3) (GPIIb/IIIa) through confocal fluorescence imaging of primary rat megakaryocytes.

107 Earlier single-molecule fluorescence imaging of the archaeal model glutamate tra

108 microscopy of proteins and synchrotron X-ray fluorescence imaging of trace metals, both performed wit

109 in vivo SPECT imaging, biodistribution, and fluorescence imaging on BALB/c nude mice with orthotopic

110 Subsequently, high-resolution fluorescence imaging results consolidated the potential

111 In vivo fluorescence imaging revealed that PEG30 kDa-conjugated

112 co predictions, complemented with time-lapse fluorescence imaging to study live interactions of bacte

113 ements in planar lipid bilayers, and in vivo fluorescence imaging, we demonstrate here that ColN uses

114 llenge could be overcome with intraoperative fluorescence imaging, which provides real-time lesion de

115 roteins (RSFPs) serve as markers in advanced fluorescence imaging.

116 rgery, the ILM flap may be visualized by ICG fluorescence imaging.

117 In this work a new fluorescence immunosensor with use of graphene oxide and

118 luorescence in vitro, but they exhibit lower fluorescence in mammalian cells.

119 ecific protein (PLIN2) that exhibits altered fluorescence in response to LD interactions with the lys

120 d staining and catalysed reporter deposition fluorescence in situ hybridization (CARD-FISH) on >14 50

121 Fluorescence in situ hybridization (FISH) is a powerful

122 sion, and we observed > 70% concordance with fluorescence in situ hybridization (FISH) results.

123 elomeres, ChIP, telomere immunofluorescence, fluorescence in situ hybridization (FISH), micronuclei i

124 s of eight breast cancer genes by multicolor fluorescence in situ hybridization, and targeted sequenc

125 cells and test their expression with double fluorescence in situ hybridization.

126 nsparent, have expanded the applicability of fluorescence in the biomedical field.

127 maging intervals showed significantly higher fluorescence in the colorectal lesions than in surroundi

128 Neurons labeled with NeuroPAL do not exhibit fluorescence in the green, cyan, or yellow emission chan

129 pinach/Broccoli-DFHBI complexes exhibit high fluorescence in vitro, but they exhibit lower fluorescen

130 Using Cy3 fluorescence in vivo imaging, we showed that unlike non-

131 proteins due to the ambiguity in microarray fluorescence intensity and complexity in branched glycan

132 uorescence protein (RFP) exhibited increased fluorescence intensity in media containing 2'-FL.

133 ce, and the correlation between the red-blue fluorescence intensity indicates the progress of mitocho

134 It was observed that fluorescence intensity of SGQDs could be substantially q

135 mula: see text] caused an average normalized fluorescence intensity recordings >1.40 for the calcium

136 (microdroplets) in oil were excited, and the fluorescence intensity was recorded as function of time.

137 Fluorescence intensity was recorded as the number of cel

138 midine analog, exhibiting a 28-fold brighter fluorescence intensity when base paired with A as compar

139 The individual change in log median fluorescence intensity(MFI-BG) values was -0.15 overall

140 between neural activity and calcium-related fluorescence involves nonlinearities and low-pass filter

141 Moreover, because its fluorescence is sensitive to viscosity, Coupa allowed us

142 hoton adsorption, accompanied by anti-Stokes fluorescence, is achieved under near-infrared femtosecon

143 a Cys-lite variant needed for site-specific fluorescence labeling.

144 The use of fluorescence labels has enabled new cell-sorting strateg

145 ore and after fungal interaction using X-ray fluorescence, laser ablation inductively coupled plasma

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

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

148 Fluorescence lifetime estimation is performed via a pre-

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

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

151 Fluorescence lifetime imaging microscopy (FLIM) is a key

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

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

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

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

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

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

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

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

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

161 However, cryogenic fluorescence localization methods are, in their majority

162 me that correlates cryogenic single-molecule fluorescence localizations with CET reconstructions.

163 pplication to imaging platforms ranging from fluorescence, luminescence, photoacoustic, magnetic reso

164 multispectral imaging (MSI), and macro X-ray fluorescence (MA-XRF) with minimally invasive surface-en

165 hput workflows such as liquid chromatography-fluorescence-mass spectrometry (LC-FLR-MS) workflows hav

166 ntration elements and optical components for fluorescence measurement of specific cyanobacterial pigm

167 s, such as those afforded by single-molecule fluorescence measurements.

168 anate and DPPP (diphenyl-1-pyrenylphosphine) fluorescence methods were comparatively examined to dete

169 When used appropriately, a confocal fluorescence microscope is an excellent tool for making

170 itation, having deep penetration depth, by a fluorescence microscope on a coverslip, or uptaken in a

171 es an open-top, single-objective light sheet fluorescence microscope with an atomic force microscope

172 Miniaturized fluorescence microscopes (miniscopes) have been instrume

173 ows super-resolution imaging on conventional fluorescence microscopes, but has been limited to protei

174 h-affinity lanthanide ion binding, and X-ray fluorescence microscopy (XFM).

175 Further combination with fluorescence microscopy allows users to determine cells

176 Here, fluorescence microscopy and genetics were used to confir

177 tic combination of total internal reflection fluorescence microscopy and image correlation spectrosco

178 lysed on-chip at different time points using fluorescence microscopy and Lactate dehydrogenase (LDH)

179 Mating experiments, fluorescence microscopy and TEM revealed indigenous bact

180 Fluorescence microscopy can provide extensive informatio

181 In vivo fluorescence microscopy can reveal cellular and subcellu

182 Super-resolution fluorescence microscopy has enabled important breakthrou

183 UV absorbance, circular dichroism and fluorescence microscopy indicated that the microfluidic

184 To this end, one of the primary tools in fluorescence microscopy is that of computational deconvo

185 Widefield fluorescence microscopy is used to monitor the spiking o

186 cal microscopy and total internal reflection fluorescence microscopy on fixed specimens.

187 Spectrally resolved fluorescence microscopy on single block copolymerized or

188 olecular biology, mammalian cell culture and fluorescence microscopy skills.

189 with confocal and total internal reflection fluorescence microscopy suggested that Amot's role in ac

190 reening, oil and water phases were imaged by fluorescence microscopy to reveal the micro to macro sca

191 Biomolecules were fluorescently labeled, and fluorescence microscopy was employed to assess their ele

192 In this work, X-ray fluorescence microscopy was used to measure diffusion co

193 ng single molecule total internal reflection fluorescence microscopy we show that Wsp1 synergizes wit

194 X-ray micro-computed tomography (micro-CT), fluorescence microscopy, and fine root hydraulic conduct

195 Here, using human cell lines, fluorescence microscopy, and pulldown and immunoblotting

196 Using fluorescence microscopy, fluorescence spectroscopy, and

197 elle dynamics are challenging to detect with fluorescence microscopy, making it difficult to determin

198 ess of HIV membrane fusion can be tracked by fluorescence microscopy, the 3D configuration of protein

199 lity assays, LC3B immunoblots, and live-cell fluorescence microscopy, we report here that in the pres

200 mmunostaining, H&E staining, and light-sheet fluorescence microscopy.

201 and pathologists experienced in conventional fluorescence microscopy.

202 oral organs of Arabidopsis using light sheet fluorescence microscopy.

203 as assessed in a salivary rinse sample using fluorescence microscopy.

204 ia with a light-emitting diode (LED)-induced fluorescence module integrated into the device.

205 cohorts, respectively, and a mean intrinsic fluorescence of 0.035 vs. 0.023 mm(-1) (P < 0.0003), 0.0

206 sing ROS-responsive probes and found reduced fluorescence of a superoxide-selective probe within the

207 hat the near-infrared and shortwave-infrared fluorescence of lipofuscin can be used to monitor the pr

208 sessments of thermal gradients by changes in fluorescence of temperature-sensitive fluorescent dyes n

209 sis techniques focusing solely on either CNT fluorescence or metal fingerprints may misrepresent expo

210 We employed fluorescence polarization microscopy to show that cadher

211 rgy transfer between identical fluorophores) fluorescence polarization to monitor dynamic changes in

212 Synthesized probes also facilitated a fluorescence polarization-based screen for dGMII inhibit

213 increased the accumulation of the conjugated fluorescence probe in the placenta with a total accumula

214 heory (TDDFT) calculations indicate that the fluorescence properties of amyloid-bound MHB can be corr

215 Here, we showed that a green fluorescence protein (GFP) reporter becomes unstable whe

216 y co-expressing alpha-L-fucosidase and a red fluorescence protein (RFP) exhibited increased fluoresce

217 tion of a fluorescent label (enhanced yellow fluorescence protein, EYFP) with the target enzymes to c

218 t behavioural improvements compared to green fluorescence protein-treated controls (1012 vg per anima

219 through visual (stay-green) and chlorophyll fluorescence ( PSII) approaches.

220 was larger for flanking G/C residues but its fluorescence quantum yield (QY) and lifetime values were

221 outputted as a white light continuum with a fluorescence quantum yield of 29.9%.

222 C:POPG bilayers through the use of real-time fluorescence quenching assays and Forster resonance ener

223 Fluorescence quenching confirmed the delivery of exogeno

224 GI) tract imaging remains challenging due to fluorescence quenching in the digestive microenvironment

225 P-glycan-lectin binding affinities via a new fluorescence quenching method, but also reveal drastical

226 Here, we employ a fluorescence-quenching assay to study the binding of ssr

227 the interior of living cells with integrated fluorescence readout of metabolic activity.

228 was 100% specific and 100% sensitive with a fluorescence readout, and 100% specific and 97% sensitiv

229 Fourier transform fluorescence recovery after photobleaching (FT-FRAP) wit

230 Using fluorescence recovery after photobleaching microscopy, w

231 Fluorescence recovery after photobleaching of tagged Nex

232 For normal diffusion, the fluorescence recovery produced a simple single-exponenti

233 s: intrinsic blinking even in air, excellent fluorescence recovery, and stability over several months

234 ear fit to multiple spatial harmonics of the fluorescence recovery.

235 y, whereas microscale thermophoresis and Trp fluorescence represent a summary or average of both effe

236 se transposon sequencing in conjunction with fluorescence resonance energy transfer (FRET) microscopy

237 l periods (100-130 bp) using single-molecule fluorescence resonance energy transfer (FRET).

238 omic force microscopy (AFM), single-molecule fluorescence resonance energy transfer (smFRET), nanopor

239 Here, by quantifying single-molecule fluorescence resonance energy transfer between a first f

240 Subcellularly targeted fluorescence resonance energy transfer sensors can preci

241 ) model) incorporating parameters from rapid fluorescence response curves.

242 interference from the other tested BAs, the fluorescence response of the probes ZnO@PLP and ZnO@Py s

243 While delayed fluorescence results mainly from triplet-triplet annihil

244 Its emission equivalent, supercritical angle fluorescence (SAF), is comparably less established, alth

245 increased oxidative stress (dihydroethidium fluorescence: sham, 1.6x10(8)+/-6.1x10(7), banding, 2.6x

246 Transient absorption and time-resolved fluorescence show that, relative to the lifetime of the

247 Effective use of solar-induced chlorophyll fluorescence (SIF) to estimate and monitor gross primary

248 membrane; and (2) analyzing the differential fluorescence signal between the red and green color chan

249 With Bessel TPLSM, the fluorescence signal of a vessel becomes proportional to

250 ion and photobleaching to the time course of fluorescence signal per yeast cell expressing mEos3.2.

251 results in emission of a readily detectable fluorescence signal.

252 ength shift and an enhancement of the ligand fluorescence signal.

253 multaneous collection of electrochemical and fluorescence signals gives valuable space- and time-reso

254 ithin 25 min and generated stronger specific fluorescence signals which were easily read and analysed

255 le neuronal media and show that BPI enhances fluorescence signals, reduces phototoxicity and optimall

256 ck probes, each rendering a unique two-color fluorescence signature to a nucleic acid target represen

257 -chemical, textural and color parameters and fluorescence spectra of aromatic amino acids and nucleic

258 positions were accompanied by a red shift of fluorescence spectra.

259 was determined by Hydride Generation-Atomic Fluorescence Spectrometry (HG-AFS).

260 nce spectrometry and Hg by cold vapor atomic fluorescence spectrometry after ultrasound-assisted emul

261 alm oil samples by hydride generation atomic fluorescence spectrometry and Hg by cold vapor atomic fl

262 The presented fluorescence spectroscopic toolkit will likely accelerat

263 radiation induced micro- and submicro-X-ray fluorescence spectroscopy (SR-XRF), gadolinium was detec

264 lculations support the results obtained from fluorescence spectroscopy and give insights into the int

265 were guided by findings from single-molecule fluorescence spectroscopy and molecular dynamics simulat

266 C in the presence of Gsp was demonstrated by fluorescence spectroscopy and PXRD analysis, respectivel

267 ameter single-fiber reflectance/single-fiber fluorescence spectroscopy in 15 patients with a dysplast

268 UV/vis and fluorescence spectroscopy reveals that the anthracene-su

269 Using fluorescence microscopy, fluorescence spectroscopy, and cell fractionation experi

270 c tools such as steady-state & time-resolved fluorescence spectroscopy, Circular Dichroism (CD) and F

271 nanomaterials, and compare it with ensemble fluorescence spectroscopy.

272 e to the presence of saponin was observed by fluorescence spectroscopy.

273 Fluorescence staining further revealed that OY phytoplas

274 a multiplexing approach using a three-color fluorescence staining method, which allowed for up to se

275 nd allows quantitative decoding of quantized fluorescence states.

276 au(av) = 366 ns) thermally activated delayed fluorescence (TADF) emitter with a radiative rate consta

277 eir potential as thermally activated delayed fluorescence (TADF) emitters for organic light-emitting

278 diodes based on thermally activated delayed fluorescence (TADF) from donor-acceptor exciplexes that

279 pounds exhibited thermally activated delayed fluorescence (TADF) in spite of a relatively large Delta

280 viours including thermally activated delayed fluorescence (TADF), room-temperature phosphorescence (R

281 we named "Rainbow-KSHV," that encodes three fluorescence-tagged KSHV proteins (mBFP2-ORF6, mCardinal

282 d the minimum of the different npai* states, fluorescence takes place in the visible (green) part of

283 in imaging with faster kinetics and brighter fluorescence than commonly used nuclear GCaMPs.

284 ical properties of the macrocycles came from fluorescence, time-correlated single-photon counting (TC

285 Using single molecule fluorescence, time-lapse TIRF microscopy and AFM imaging

286 assays, along with total internal reflection fluorescence (TIRF), confocal, and EM analyses, we show

287 is included and show the expected changes in fluorescence to accompany these reactions, the anthracen

288 zymatic system affords greater than 100-fold fluorescence turn on in buffer, is selective for glucose

289 s by hexylcreatinine produced supramolecular fluorescence turn-on sensors that work at micromolar ana

290 The discovery of fluorescence two centuries ago ushered in, what is today

291 ectroscopy (NIRS) and total reflection X-ray fluorescence (TXRF).

292 remarkable 75-fold enhancement of sulfo-Cy3 fluorescence upon target capturing.

293 r of cells responding and the area under the fluorescence versus time curve.

294 Using fluorescence vesicle leakage assays, we demonstrate that

295 in 3 to 4 h postinfection at 100 frames/s by fluorescence video microscopy.

296 of QDs, which gradually shows enhancement of fluorescence with the increment of distance and the smal

297 ing only terCBZ donor(s) exhibited deep blue fluorescence, with Commission Internationale de l'eclair

298 GRAB(DA) sensors exhibit a large increase in fluorescence, with subcellular resolution, subsecond kin

299 Synchrotron-based macro-X-ray fluorescence (XRF) mapping brings to light the presence

300 The relationship between the fluorescence yield and P(+) (fraction of closed RC) show