ライフサイエンスコーパス: fluorescence signal

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

2 quenchers and thus a significant increase in fluorescence signal.

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

4 -catalyzed phosphorylation can switch on the fluorescence signal.

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

6 lecules due to the overwhelming isoenergetic fluorescence signal.

7 e (DSB-3), whose reaction with PE produces a fluorescence signal.

8 , the DNA/RNA NFs produced a higher-contrast fluorescence signal.

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

10 he scattered Raman signal from the competing fluorescence signal.

11 ccount for technical variation in background fluorescence signal.

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

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

14 he dye cargo with detectable enhancements of fluorescence signal.

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

16 uld accelerate the elimination to generate a fluorescence signal.

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

18 re accurate quantitative measurements of the fluorescence signal.

19 uisition speed and signal/noise ratio of the fluorescence signal.

20 and excitation light, as well as collect the fluorescence signal.

21 results in emission of a readily detectable fluorescence signal.

22 d spectral information in the time dependent fluorescence signal.

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

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

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

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

27 on sequence to simplify quantitative nuclear fluorescence signal.

28 the binding event directly into an enhanced fluorescence signal.

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

30 agreement was observed between ripeness and fluorescence signals.

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

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

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

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

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

36 an express reporter genes and produce strong fluorescence signals.

37 in pairs and thus activate multiple Broccoli fluorescence signals.

38 relationships between E(app) and measurable fluorescence signals.

39 inserted into the dsDNA, generating enhanced fluorescence signals.

40 er ablation plume and saturation behavior of fluorescence signals.

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

42 itiate DNA amplification and generate strong fluorescence signals.

43 ne encounter events into readable cumulative fluorescence signals.

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

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

46 ing nicking endonuclease-assisted isothermal fluorescence signal amplification.

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

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

49 For the inkjet and pin printing, the largest fluorescence signal and contrast with the background was

50 They display a bright NAD(P)H fluorescence signal and low uptake of voltage-dependent

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

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

53 available probes suffer from relatively weak fluorescence signals and are not suitable for simple, af

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

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

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

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

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

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

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

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

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

63 Encoding and detection fluorescence signals are distinguishable by nonoverlappi

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

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

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

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

68 behavioral events, as well as analyzed brain fluorescence signals as they relate to spontaneous and/o

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

70 On the basis of the emergence of the fluorescence signal at 480 nm and its signal strength, t

71 100 s later, BTBM-CN(2) emitted a new green fluorescence signal at 480 nm, which is mainly due to th

72 s, and BTBM-CN(2) presented a "turn-on" red fluorescence signal at 598 nm.

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

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

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

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

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

78 atop Ag(111) shows both phosphorescence and fluorescence signals at high applied voltage.

79 Fluorescence-signal-averaging is performed on each tempo

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

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

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

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

84 Fluorescence signals (blips) arising from single functio

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

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

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

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

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

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

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

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

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

94 Fluorescence signals change effectively in response to t

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

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

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

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

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

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

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

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

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

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

108 Fluorescence signal enhancement via isothermal nucleic a

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

110 essing or color science and does not require fluorescence signals, expensive imaging equipment or cus

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

112 In the measured conditions, there was no fluorescence signal for carmoisine due to a strong quenc

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

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

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 es selective biorecognition and quenching of fluorescence signals for rapid and sensitive quantificat

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

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

121 7 azide in vitro showed significantly higher fluorescence signal from (18)F-FDG-treated than untreate

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

123 Additionally, fluorescence signal from cleaved CNIR800 reaches maximal

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

125 The combined fluorescence signal from individual pores exhibits the s

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

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

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

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

130 Fluorescence signal from the reporter gene was detected

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

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

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

134 Fluorescence signals from all independently targeted sit

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

136 Quantitative analysis of fluorescence signals from cells reacted with fluorescent

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

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

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

140 s recording of the produced photocurrent and fluorescence signals from the photosynthetic chain.

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

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

143 loop-mediated isothermal amplification with fluorescence signal generation.

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

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

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

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

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

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

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

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

152 ing demonstrates a significantly higher mean fluorescence signal in metastatic LNs compared to benign

153 It is also observed a clear tendency of the fluorescence signal in platelets treated with the conjug

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

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

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

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

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

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

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

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

164 dified glass slides, whereas for the uCP the fluorescence signal increased with increasing hydrophili

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

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

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

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

169 As fluorescence signal intensities can vary significantly f

170 The fluorescence signal intensities of arthritic and normal

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

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

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

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

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

176 B (gB) of MDV, and cholesterol (filipin III) fluorescence signal intensity peaks.

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

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

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

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

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

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

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

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

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

186 ous cellular autofluorescence masks a useful fluorescence signal, limiting the ability to reliably vi

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

188 Moreover, the amplification of both the fluorescence signal, modulated by vertically-nano-calibr

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

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

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

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

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

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

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

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

197 The fluorescence signal of arthritic joints was significantl

198 this colorant also led to a decrease of the fluorescence signal of cochineal.

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

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

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

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

203 In addition, fluorescence signal of oxyresveratrol increased when Mbe

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

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

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

207 s, their shape, and the contrast between the fluorescence signal of the pattern and the background, c

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

209 The fluorescence signal of the sample is excited by a laser

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

211 The fluorescence signal of the variant was also sensitive to

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

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

214 The fluorescence signals of each FP were detectable in whole

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

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

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

218 The fluorescence signals of the newly developed probes were

219 The emitted fluorescence signals of the spots are independently and

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

221 e observation of a quartic dependence of the fluorescence signal on the excitation light intensity.

222 al confocal imaging when local intracellular fluorescence signals originating from Ca(2+) release fro

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

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

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

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

227 covered that formaldehyde fixation makes the fluorescence signal, photoconversion rate, and photoblea

228 ssays on neuronal cultures (i.e., suboptimal fluorescence signals, phototoxicity, and unphysiological

229 ensitivity equivalent to Voltron but flipped fluorescence signal polarity.

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

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

236 Fluorescence signal related to mitochondrial membrane po

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

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

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

240 nge, a stringent requirement arises that the fluorescence signal should be efficiently differentiated

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 assays on synthetic paper provide a stronger fluorescence signal, similar or better reproducibility,

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

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

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 ion either as discrete signals or an average fluorescence signal, thus being compatible with both hig

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

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 to account for the experimental current and fluorescence signals, to analyze their degree of correla

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

266 DNAzymes conjugated to the constituents, the fluorescence signals upon the cocaine-induced separation

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

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

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

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

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

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

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

274 In contrast, no fluorescence signal was detected in the capsule body.

275 Almost no fluorescence signal was detected when specimens were pre

276 Fluorescence signal was imaged over time.

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

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

279 The green fluorescence signal was most intense after treatment wit

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

281 Fluorescence signal was present in TLR2 expressing pancr

282 The fluorescence signal was quantified as signal-to-backgrou

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

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

285 This fluorescence signal was then further enhanced with the u

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

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

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

289 Fluorescence signals were detected in LAD coronary, thym

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 hat both the transcript level of gfp and its fluorescence signals were more than 2-fold higher in the

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

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

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

297 ntifies an individual dNTP based on a robust fluorescence signal, with the detection chemistry extend

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