ライフサイエンスコーパス: fluorescence signal

1 e of a target molecule into a dose-dependent fluorescence signal.

2 -catalyzed phosphorylation can switch on the fluorescence signal.

3 n contrast to the more dynamic chlorophyll a fluorescence signal.

4 lecules due to the overwhelming isoenergetic fluorescence signal.

5 d spectral information in the time dependent fluorescence signal.

6 rom miR-10c while generating an equally high fluorescence signal.

7 enic dye DFHBI, and thereby induces a strong fluorescence signal.

8 he scattered Raman signal from the competing fluorescence signal.

9 ccount for technical variation in background fluorescence signal.

10 ce of agonist binding but did not reduce the fluorescence signal.

11 iolet oxidation, obtaining a decrease in the fluorescence signal.

12 ound to the sensor surface and thus to lower fluorescence signal.

13 he dye cargo with detectable enhancements of fluorescence signal.

14 voltage-dependent binding, also reduced the fluorescence signal.

15 uld accelerate the elimination to generate a fluorescence signal.

16 e response kinetics and the intensity of the fluorescence signal.

17 re accurate quantitative measurements of the fluorescence signal.

18 ophages and neutrophils as the source of the fluorescence signal.

19 to a stable and long-lasting, highly intense fluorescence signal.

20 e by MazF results in a large increase in the fluorescence signal.

21 ingle-cells into an integrated, long-lasting fluorescence signal.

22 perty is used to generate a binding-specific fluorescence signal.

23 on sequence to simplify quantitative nuclear fluorescence signal.

24 the binding event directly into an enhanced fluorescence signal.

25 the ACC is released and produces a readable fluorescence signal.

26 quenchers and thus a significant increase in fluorescence signal.

27 bound to the sensor surface and thus reduced fluorescence signals.

28 the system of interest can be extracted from fluorescence signals.

29 DPA-713 abrogated both the SPECT and ex vivo fluorescence signals.

30 ce, and alters the time dependence of hEAAT3 fluorescence signals.

31 an express reporter genes and produce strong fluorescence signals.

32 inserted into the dsDNA, generating enhanced fluorescence signals.

33 n to allow high-quality imaging of even weak fluorescence signals.

34 ne encounter events into readable cumulative fluorescence signals.

35 agreement was observed between ripeness and fluorescence signals.

36 er ablation plume and saturation behavior of fluorescence signals.

37 can visualize H2 S and H2 Sn with different fluorescence signals.

38 ratiometric manner, in addition to enhanced fluorescence signaling.

39 ffers, and were used to predict the observed fluorescence signal after blurring by the microscope poi

40 ions by comparing the variations in the QD's fluorescence signals against variations of the backgroun

41 easurement of the needle bending and monomer fluorescence signal allows us to correlate the bending w

42 ing nicking endonuclease-assisted isothermal fluorescence signal amplification.

43 rom HSAF by other anesthetics attenuates the fluorescence signal and allows determination of K(d), as

44 utations in the orthosteric site abolish the fluorescence signal and concomitantly, the voltage-depen

45 We generated 3D maps of the fluorescence signal and fused them with anatomical compu

46 ontributes to the overall mitochondrial NADH fluorescence signal and provides an explanation for the

47 We compare fluorescence signal and signal-to-noise ratio at various

48 y images to show a close correlation between fluorescence signal and tumor burden.

49 The simultaneously recorded fluorescence signals and behavior events can be used to

50 p technique, we have simultaneously recorded fluorescence signals and gating currents from Xenopus la

51 both diffraction and non-diffraction-limited fluorescence signals and is scalable for high-throughput

52 On the basis of the fluorescence signals and labeling schemes, the count of

53 ltiple aptamers to a target protein based on fluorescence signals and sort individual particles harbo

54 photo-reactivity, leading to blinking of the fluorescence signal, and eventually to its loss by photo

55 at of vitamin K, provides a high-sensitivity fluorescence signal, and is compatible with biological c

56 al for increasing photostability, optimizing fluorescence signals, and adjusting kinetics of fluoresc

57 enerally causes a recovery or enhancement of fluorescence signals, and thus provides an interesting n

58 Encoding and detection fluorescence signals are distinguishable by nonoverlappi

59 llic nanoparticles to create a hotspot where fluorescence signals are enhanced by plasmonic effects.

60 d histological staining, confirming that the fluorescence signals are highly specific to tumor cells.

61 However, large fluorescence signals are obtained only at high DPA conce

62 by a factor of up to 5.39 +/- 1.44, whereby fluorescence signals are reversible.

63 s to incorporate nonlinear saturation of the fluorescence signal, as well external stimulus and spike

64 human tumor xenografts resulted in a near-IR fluorescence signal at ca. 700 nm, 24 h after administra

65 ho-FF-Van results in a significant increased fluorescence signal at the MRSA infected site.

66 minutes with the tube scanner set to collect fluorescence signals at 1-minute intervals.

67 Zn(2+) by bringing ratiometric change in the fluorescence signals at 390 and 490 nm, but in the case

68 N was used to record action potential-evoked fluorescence signals at consecutive locations separated

69 Fluorescence-signal-averaging is performed on each tempo

70 le 12-24 hours after injection as background fluorescence signals began to disappear.

71 of hydroxyl radical based on the ratiometric fluorescence signal between 7-hydroxy coumarin 3-carboxy

72 parian zone, there were clear differences in fluorescence signals between the leaching methods.

73 Fluorescence signals (blips) arising from single functio

74 tical axis and (2) removing the out-of-focus fluorescence signal by a deconvolution method to reconst

75 HS-ssDNA monolayers initially increases DNA fluorescence signal by densifying the chemisorbed monola

76 otic shock greatly decreased the periplasmic fluorescence signal by loss of the protein but had no ef

77 es selective electrochemical modulation of a fluorescence signal by sequentially oxidizing the analyt

78 o convert the weak CL signal into a stronger fluorescence signal by using CL-activated formation of n

79 With this strategy, the fluorescence signal can be amplified to as high as 70-fo

80 lecule dynamics in living cells in which the fluorescence signal can be controlled by the addition of

81 The nucleus is preserved, and its DNA fluorescence signal can be measured independently.

82 ter dye (e.g. ROX, HEX, ATTO647N, FAM) whose fluorescence signal can be monitored on a range of analy

83 have attracted considerable interest because fluorescence signals can provide real-time guidance to a

84 each step shows that although changes in the fluorescence signal cease 10 s after the initiation of t

85 hat the antagonist induced the intrinsic Trp fluorescence signal change more than the agonist.

86 As such, based on the fluorescence signal change, a label-free fluorescence as

87 Fluorescence signals change effectively in response to t

88 These fluorescence signal changes are often subtle, so the sta

89 is the first demonstration of in vivo, local fluorescence signal collection on the sub-organelle leve

90 Microscopic fluorescence signal colocalized with immunoreactive stai

91 Osteogenic near-infrared fluorescence signals colocalized with alkaline phosphata

92 aging in mice confirmed that the nuclear and fluorescence signals colocalized.

93 The fluorescence signal comigrated with pDNA on acrylamide g

94 oduced only a mild (<30%) attenuation of the fluorescence signal compared with saline, affirming the

95 Within 1 h, the fluorescence signal concentrated throughout tumors to ex

96 choice of background can affect the measured fluorescence signal considerably.

97 CN(-) signals overlapped DAPI fluorescence signals corresponding to nuclei.

98 eting agents consistently yielded diminished fluorescence signals corresponding to the reduction obse

99 of the target protein these sensors produce fluorescence signal derived from target-dependent anneal

100 ds to IRDye 800CW, we extended the effective fluorescence signal detection to the NIR region without

101 Fluorescence signals display two distinct phases; an ini

102 Structure-switching, fluorescence-signaling DNA and RNA aptamers have been re

103 matic hydrolysis of the DNA strands yields a fluorescence signal due to diffusion of the fluorophores

104 n of Pan800QC was detected by an increase in fluorescence signal due to enzymatic digestion of the an

105 between the two, resulting in an increase in fluorescence signal due to the separation of the quenche

106 fails because of excessive surface Raman or fluorescence signals emanating from the packaging, capsu

107 effectively decrease without diminishing the fluorescence signals emitted from the cells.

108 When a green fluorescent protein fluorescence signal encoded by a DR5:green fluorescent p

109 efluor-2 (SF2) respond to H(2)S by a turn-on fluorescence signal enhancement and display high selecti

110 Protein deposition and fluorescence signal evaluation on these substrates are p

111 nanoparticles was confirmed by reduction in fluorescence signal following MSN-UPA nanoparticle treat

112 The green fluorescence signal for each bead set is resolved, and s

113 issolution of MnO2 nanosheets, can provide a fluorescence signal for monitoring the efficacy of deliv

114 Using the 2-AP fluorescence signal for nucleotide flipping, kon and kof

115 h the addition of GO in the second step, the fluorescence signal for perfectly matched and random DNA

116 The probes not only offer high fluorescence signal for use in flow cytometry, but also

117 ent based on quantitative detection of X-ray fluorescence signals for 3879 purified proteins from sev

118 mediated DNA strand displacement to generate fluorescence signals for the real-time monitoring of PiD

119 rate constant (based on the decrease in NIR fluorescence signals) for all SWCNT chiral species react

120 7 azide in vitro showed significantly higher fluorescence signal from (18)F-FDG-treated than untreate

121 inase pathway could significantly reduce the fluorescence signal from 2'-deoxy molecular beacons (MBs

122 n contrast, scanning FCS (SFCS) collects the fluorescence signal from a moving observation volume by

123 e nanorod is 58 times that of the two-photon fluorescence signal from a single rhodamine molecule.

124 ic and equilibrium methods by monitoring the fluorescence signal from a Trp residue that is incorpora

125 Additionally, fluorescence signal from cleaved CNIR800 reaches maximal

126 tly labeled DNA at which half of the maximum fluorescence signal from DNA-bound cells is reached).

127 The combined fluorescence signal from individual pores exhibits the s

128 We found that fluorescence signal from MBs depends critically on targe

129 However, the intensity and localization of fluorescence signal from MBs targeting nontranslated 28S

130 er the injection, approximately 6-10% of the fluorescence signal from the larger nanoparticles in the

131 wed that radioactivity count correlated with fluorescence signal from the nanoparticles, and both sig

132 e ability of a colored product to quench the fluorescence signal from the plate by absorbing either t

133 Fluorescence signal from the reporter gene was detected

134 Optical sectioning minimizes the fluorescence signal from the subphase, whereas convoluti

135 We assigned the tryptophan fluorescence signal from Y162W by removing two native tr

136 ated resistive heater and monitors real-time fluorescence signals from 60 individual reaction chamber

137 Fluorescence signals from all independently targeted sit

138 have developed the means to isolate specific fluorescence signals from background by using lock-in de

139 Quantitative analysis of fluorescence signals from cells reacted with fluorescent

140 viability was determined using the ratio of fluorescence signals from membrane permeant (calcein) an

141 utomated measurements of microbial cells and fluorescence signals from microscopy images.

142 intracellular processes, we analyzed sparse fluorescence signals from single-molecule time-lapse ima

143 onventional dyes in the skin "shadowed" real fluorescence signals from the kidneys and prevented noni

144 in vivo is primarily monitored by measuring fluorescence signals from the small fraction of excitati

145 of dye molecules bound to proteins (and the fluorescence signals from these protein complexes) were

146 iter plates in a multiplexed manner, and the fluorescence signals generated were able to quantitative

147 -valued function of concentration, as when a fluorescence signal goes into the self-quenched domain.

148 ted that Cu NCs showed strong blue and green fluorescence signals, good permeability and minimum toxi

149 ydrodynamically focused cells based on their fluorescence signal in a microfluidic device.

150 w cytometric measurements, an enhancement in fluorescence signal in excess of 300-fold is obtained fo

151 reduced--resulting in an enhancement of the fluorescence signal in fluorescence correlation spectros

152 expression dynamics and effectively reduces fluorescence signal in growing cells.

153 ligonucleotide results in the restoration of fluorescence signal in increments relative to the fluore

154 proposed mixture is engendered by changes in fluorescence signal in response to changes in environmen

155 urface of our analysis channel, the measured fluorescence signal in the preconcentration zone increas

156 eacting nucleic acid probes that give strong fluorescence signal in the presence of fully complementa

157 ence signal of DCFH, but it did not decrease fluorescence signal in the presence of the reactive oxyg

158 FP11-tags allows proportional enhancement of fluorescence signal in tracking intraflagellar transport

159 nfirmed PET/CT data by showing near-infrared fluorescence signal in tumors and a tumor-to-muscle rati

160 argeting is an effective method of enhancing fluorescence signal in tumors for optical imaging.

161 The distribution of IAA fluorescence signals in root tips was disturbed, and the

162 ide and gibberrellic acid) evoked pronounced fluorescence signals in single cells and in root tissues

163 ion, brighten encapsulated RNAs, and amplify fluorescence signals in situ in a single step.

164 NIRF images showed strong SWCNT-derived fluorescence signals in whole fish and excised intestina

165 On average, fluorescence signal increased 722%+/-117% (Mean+/-SD) fr

166 be quantified using the microarray, as their fluorescence signals increased linearly with GMO concent

167 Kinetic analysis of fluorescence signals indicate that P259R decelerates a c

168 After washing, the strength of the fluorescence signal indicates the extent of DNA binding.

169 ethyl arginine citrate inhibited the ROS/RNS fluorescence signal induced by methamphetamine, which su

170 As fluorescence signal intensities can vary significantly f

171 The fluorescence signal intensities of arthritic and normal

172 be used for more than 40 runs, although the fluorescence signal intensities of the DNA peaks decreas

173 Shifts in fluorescence signal intensity between the beta-actin LNA

174 size, which results in a large variation in fluorescence signal intensity from the dye-labeled DNA m

175 he TSA method led to a >100-fold increase in fluorescence signal intensity in comparison to an unampl

176 n wavelength of Cy5, was used to amplify the fluorescence signal intensity measured from a multiplexe

177 of Cyanines 5 (Cy5), was used to amplify the fluorescence signal intensity measured from a multiplexe

178 r to increase the light absorption and hence fluorescence signal intensity when bound to duplex RNA.

179 and there is a large and coincident loss of fluorescence-signal intensity in the labeled protein sub

180 edures and algorithms developed to transform fluorescence signals into changes in cell water volume (

181 grazing emission angle under which the X-ray fluorescence signal is detected, the probed depth range

182 The intracellular fluorescence signal is directly proportional to the 19F

183 ites are separated by two base pairs and the fluorescence signal is linear to 5 pmol of methylated ta

184 to the downstream pure-buffer zone where the fluorescence signal is monitored, providing a direct qua

185 ta clearly demonstrate that this upconverted fluorescence signal is produced via Pyr(1)RuPZn(2)-sensi

186 Approximately 40% of the E2-Crimson fluorescence signal is remarkably photostable.

187 The fluorescence signal is stable for >4 days and is approxi

188 rimination between synaptic and non-synaptic fluorescence signals is challenging.

189 actomyosinV-ADP-Pi does not itself produce a fluorescence signal, it produces a lag in the signal for

190 When compared to the simultaneously acquired fluorescence signals, it appears that the signal change

191 imately 10-fold amplification of the optical fluorescence signal, leading to high tumor-to-background

192 n the following two observations: first, the fluorescence signal length (FL time-of-flight [ToF]) dec

193 -forming sequences and demonstrated that ThT fluorescence signal may be used to predict G4 formation.

194 we have established a spatial correlation of fluorescence signal obtained by non-invasive, tomographi

195 Here, we use growth rates of fluorescence signals obtained from short CCS intensity t

196 dose dependent decrease of total pancreatic fluorescence signal occurred upon administration of know

197 in ambient atmosphere markedly improves the fluorescence signal of a plasmonic-based DNA detection s

198 ects of light absorption for quantifying the fluorescence signal of aluminum phthalocyanine tetrasulf

199 re nonfluorescent dyes that can modulate the fluorescence signal of an appropriate fluorophore donor

200 green provided a significant increase in the fluorescence signal of arthritic joints compared with ba

201 The fluorescence signal of arthritic joints was significantl

202 Magnetite caused a decrease in fluorescence signal of DCFH, but it did not decrease flu

203 In this study, we used the tryptophan fluorescence signal of Escherichia coli RecQ helicase to

204 The fluorescence signal of FlAsH on the tetra-Cys-containing

205 Using the MCF, we show that the fluorescence signal of IBPs conjugated to green fluoresc

206 In direct binding studies, the internal fluorescence signal of KU675 was used to determine the b

207 By imaging the fluorescence signal of molecular beacons, the spread of

208 In addition, fluorescence signal of oxyresveratrol increased when Mbe

209 ce enhancement process which can elevate the fluorescence signal of single fluorescent dyes by severa

210 umn addition of a reagent which quenches the fluorescence signal of the analytes.

211 iles resulted in a proportional reduction in fluorescence signal of the honeys at the marker waveleng

212 th malathion results in switching off of the fluorescence signal of the probe due to the availability

213 ylates significantly influenced the absolute fluorescence signal of the thiol-qBBr complex.

214 The fluorescence signal of the variant was also sensitive to

215 a specific, binding-induced increase in the fluorescence signal of up to 30-fold.

216 sion in mammalian cells provides the highest fluorescence signals of all jellyfish GFP or coral RFP d

217 we simultaneously measure cell mechanics and fluorescence signals of cells that overexpress the GFP-t

218 The fluorescence signals of each FP were detectable in whole

219 of simultaneously monitoring scattering and fluorescence signals of individual particles separated b

220 in target RNAs are readily identified by the fluorescence signals of MBs.

221 mulated and analyzed orthogonally decomposed fluorescence signals of single molecules undergoing rota

222 ver, the quenching effect of Hg(2)(+) on the fluorescence signals of the NC(IL-130) was distinctively

223 The fluorescence signals of the newly developed probes were

224 The emitted fluorescence signals of the spots are independently and

225 during stable and unstable propagation from fluorescence signals of Vm at thousands of sites (3 kHz)

226 Examples of the fluorescence signals one can expect are described.

227 ides excitation light into the brain and the fluorescence signal out of the brain.

228 Challenges exist because green fluorescence signals overlap with endogenous activity-de

229 lied to obtain quantitative information from fluorescence signals, particularly using Forster Resonan

230 o be contained and to contribute to a single fluorescence signal, preserving the selectivity of CZE s

231 h as cell segmentation, lineage tracking and fluorescence signal quantification.

232 between CDs and AuNPs as nanoquenchers, the fluorescence signal quenched during sandwich complex for

233 ts with respect to glass (spot to background fluorescence signal ratios 30:1 to 40:1) was demonstrate

234 escence labeling we show a voltage-dependent fluorescence signal, reflecting a conformational change,

235 Fluorescence signal related to mitochondrial membrane po

236 residues 2-9 of melittin (bee venom)], three fluorescence signals report oxidative stress in the cyto

237 ace, generating on-and-off fluctuations in a fluorescence signal representing a very low noise two-st

238 al neural network to the pattern of relative fluorescence signals resulted in correct lineage assignm

239 icroscope was used to detect a laser-induced fluorescence signal resulting from both encapsulated and

240 rm for immobilization of structure-switching fluorescence-signaling RNA aptamer reporters, using both

241 s, Mie scatter conditions were observed, and fluorescence signals show a similar trend to light scatt

242 The fluorescence signal shows an intensity increasing with t

243 The single vector and nuclear localized fluorescence signals simplify delivery into cells and al

244 ied out and proved that our unique "turn-on" fluorescence signalling strategy was highly effective an

245 Under the assay conditions used, the fluorescence signal strength was dependent on type of su

246 echanism for the substantial increase in the fluorescence signal strength.

247 As expected, the fluorescence signal suggested the primary localization o

248 nm x 56 nm NR, resulting in a much stronger fluorescence signal than that of an individual dye-label

249 oth short and long targets led to much lower fluorescence signals than the perfectly complementary ta

250 We identify fluctuation patterns in the fluorescence signal that can be rationalized in terms of

251 beads, generating a clearly distinguishable fluorescence signal that enables droplet sorting at appr

252 ncentration of Ca(2+), we observed transient fluorescence signals that probably represented action po

253 tial to report by direct visualization via a fluorescence signal the intimate association of minimall

254 The drop in the fluorescence signal thereby indicates the phase of the t

255 nitrobenzofurazan-based reagents reduced the fluorescence signal, thus establishing the incompatibili

256 al level, permitting the nature of recovered fluorescence signal to be studied at greater resolution

257 o the gel, cleaved the peptide, and caused a fluorescence signal to come on.

258 conjugation step effectively constrains the fluorescence signal to the locale of interest, thus impr

259 Calibration allows conversion of relative fluorescence signals to absolute mole fractions.

260 illustrate a quantitative approach to relate fluorescence signals to malignant tissues and improve th

261 , which enables isolation of plasma membrane fluorescence signals, to determine the limiting subunit

262 This increase in fluorescence signal, together with the observed resembla

263 Fluorescence signal transformations of all the component

264 Although this distribution affects the fluorescence signal under polarized-light excitation, it

265 esonance energy transfer (FRET) into a large fluorescence signal (up to 34% change per 100 mV) with a

266 Using a pSi microcavity biosensor, the fluorescence signal upon detection of LDH was amplified

267 Certain tethers typically lead to a superior fluorescence signal upon RNA folding, as demonstrated by

268 e system, one can measure forces and collect fluorescence signals upon biological systems simultaneou

269 , with the amplitude of quantum beats in the fluorescence signal used as an easily measured surrogate

270 t concentration was accurately measured from fluorescence signals using a linear calibration curve, w

271 ratiometric sensing to discriminate the two fluorescence signals using minimal optics and power requ

272 itory effect was confirmed by the background fluorescence signal values under LD and SD, which were h

273 The ICG fluorescence signal was analyzed with Ad Hoc imaging sof

274 ard to intraoperative navigation, a specific fluorescence signal was detected in PSMA-expressing tiss

275 Little DsRed fluorescence signal was detected in skin under steady-st

276 Almost no fluorescence signal was detected when specimens were pre

277 Fluorescence signal was imaged over time.

278 The fluorescence signal was measured from the glass-fractal'

279 T assay led to contradictory results, as low fluorescence signal was measured in the presence of all

280 thus eliminating the need for fixation, and fluorescence signal was monitored both by microscopy and

281 The green fluorescence signal was most intense after treatment wit

282 With the other species tested fluorescence signal was not detected or Ct was significa

283 Fluorescence signal was present in TLR2 expressing pancr

284 The frequency dependence of the fluorescence signal was sensitive to pharmacological blo

285 The fluorescein amine fluorescence signal was significantly quenched and the r

286 This fluorescence signal was then further enhanced with the u

287 work, in which the increase in the intrinsic fluorescence signal was used to monitor iron release fro

288 The highest intensity of fluorescence signals was detected in the apical meristem

289 To provide the capability of activatable fluorescence signaling, we conjugated a fluorescent dye

290 Intense NIR fluorescence signals were detected in osteosarcoma xenog

291 ing and ultrafast spectroscopic detection of fluorescence signals were developed for monitoring the r

292 Green fluorescence signals were found to express according to

293 Fluorescence signals were recorded with spatial resoluti

294 The GNP-ActFP can generate fluorescence signal when ActFP is cleaved by proteolytic

295 algorithm utilizing chromaticity to analyze fluorescence signals, which improves the discrimination

296 rge platelet samples and a decrease in total fluorescence signal with time due to photobleaching.

297 tive image analysis correlated near-infrared fluorescence signals with immunoreactive vascular cell a

298 e dissimilarities of the fluctuations of the fluorescence signals, with the dissimilarity being taken

299 ignal to noise ratio and localization of the fluorescence signal within cells, and possess the necess

300 h target is identified by its time-dependent fluorescence signal without the need for spectral demult