ライフサイエンスコーパス: fluorescence intensity

1 specific HLA antibodies (DSA) below 500 mean fluorescence intensity.

2 s was accurately quantified as a function of fluorescence intensity.

3 olution, leading to a sizable enhancement of fluorescence intensity.

4 ween sub-regions determined from nanocluster fluorescence intensity.

5 ntibodies had worse eGFR and higher DSA mean fluorescence intensity.

6 blue to green and a 10-fold increase in the fluorescence intensity.

7 additional 51-fold amplification of the net fluorescence intensity.

8 on (Cu(2+))-facilitated amplification of the fluorescence intensity.

9 ti-Ab fluorochrome-conjugated Abs to amplify fluorescence intensity.

10 ed which results in a decrease of the Ag NCs fluorescence intensity.

11 induces quenching of about 90% of the tubes' fluorescence intensity.

12 by a greater than 100% increase in IgG mean fluorescence intensity.

13 with clustered fluorophores showing reduced fluorescence intensity.

14 endrimers and an exponential increase in the fluorescence intensity.

15 he polymerization and induced an increase of fluorescence intensity.

16 rse relationship between gene expression and fluorescence intensity.

17 hanges or through ratiometric differences in fluorescence intensity.

18 ssayed all lymph nodes for radioactivity and fluorescence intensity.

19 nm) of the wavelength of maximum tryptophan fluorescence intensity.

20 17A (IL-17A) production, as measured by mean fluorescence intensity.

21 ed the orientation by a three-fold change in fluorescence intensity.

22 lds net more than tenfold enhancement of the fluorescence intensity.

23 the probes leads to a large increase in the fluorescence intensity.

24 s (EPS) and deoxyribonucleic acid (DNA), and fluorescence intensities.

25 ationship between apoptotic cell numbers and fluorescence intensities.

26 t eliminate alloantibody responses (IgG mean fluorescence intensity, 486 T 153 vs. control 792 T 193,

27 The median fluorescence intensity, a proxy of HLA-C expression, was

28 ination of H2S was based on the quenching of fluorescence intensity after direct selective reaction b

29 cation within the channel of the increase in fluorescence intensity after electroporation.

30 ed, in 4 (36%) of 11 DSA were below 500 mean fluorescence intensity after treatment.

31 Fluorescence intensity analysis reveals that the total n

32 ular traffic jams at filopodial tips amplify fluorescence intensities and allow PPIs to be interrogat

33 H site, the variable and anomalous levels of fluorescence intensities and DOC concentrations three ye

34 ent, and quasi-simultaneous determination of fluorescence intensities and lifetimes of different fluo

35 to quantify telomere length by means of the fluorescence intensity and area of each telomere within

36 tiomers, rendering them large differences in fluorescence intensity and chemical reactivity.

37 Furthermore, linearly increased fluorescence intensity and deeper color were observed wi

38 issue sarcomas were labeled with the highest fluorescence intensity and greatest tumor-to-background

39 Optical metabolic imaging quantifies the fluorescence intensity and lifetime of NADH and FAD, coe

40 serve strong polarization dependences of the fluorescence intensity and line broadening for both tran

41 ast and reliable automated method to analyze fluorescence intensity and localization, cell morphology

42 with MAN-LIP had significantly higher brain fluorescence intensity and MAN-LIP relatively concentrat

43 urately counted by applying filters based on fluorescence intensity and nuclear size.

44 d the subsequent spatiotemporal evolution in fluorescence intensity and observed the collective parti

45 In eGFP transfections in vitro both the mean fluorescence intensity and percentage of cells transfect

46 found that seven of them display sufficient fluorescence intensity and photostability to visualize m

47 reomeric iminoboronates that differ in their fluorescence intensity and polarization.

48 tantly it leads to an initial increase in GO fluorescence intensity and significant (100 nm) blue shi

49 haviour enables correlation of MRI contrast, fluorescence intensity and spin concentration with tissu

50 distinct populations that differed in their fluorescence intensity and velocity.

51 These included mass, fluorescence intensity, and absorbance measurements and

52 and 300 nm in ultraviolet spectra, declined fluorescence intensity, and decolored performance of HA-

53 (DMA)C's fluorescence intensity, anisotropy, and energy transfer

54 The IFE-corrected fluorescence intensities are linearly correlated to fluo

55 ional states, correlated with characteristic fluorescence intensities, are extracted from the images

56 The fluorescence intensity arising from the virus-bound anti

57 uent measurements of the individual particle fluorescence intensities as a function of the applied el

58 Using a novel method to calibrate the Cy3 fluorescence intensity as a function of hRPA position on

59 re found to display periodic patterns in the fluorescence intensity as a function of sample number fo

60 in parallel, monitoring changing patterns of fluorescence intensity as N-terminal amino acids are seq

61 an be easily measured through an increase in fluorescence intensity as the potential is manipulated.

62 Here we describe a novel homogeneous fluorescence intensity assay for circulating FAP activit

63 ve-state model with a unique set of apparent fluorescence intensities assigned to each state accordin

64 owever, there were order-of-magnitude higher fluorescence intensities associated with these component

65 (EEMs) by PARAFAC analysis and by selecting fluorescence intensities at a priori defined excitation/

66 The fluorescence intensity at 410nm was observed to be propo

67 biopsy needle demonstrated a sharp margin of fluorescence intensity at the tumor-liver interface.

68 Differences in distribution of fluorescence intensity between cells originated from the

69 DNA sensors present more than 50% change in fluorescence intensity between complementary DNA and 1 b

70 transducer resulted in an enhancement of the fluorescence intensity by 1 order of magnitude, when com

71 proteins was determined by normalizing their fluorescence intensity by the brightness of a tBid monom

72 During immunosensing, fluorescence intensity can be doubled by the application

73 Chang of fluorescence intensity can be magnified by SIFs.

74 ons that, with calibrated donor and acceptor fluorescence intensities, can yield dissociation constan

75 ignificant changes in 2h: reduced tryptophan fluorescence intensity, carbonyl formation, and extensiv

76 ting photomultiplier voltage while measuring fluorescence intensity changed all three parameters (0 <

77 Moreover, the averaged fluorescence intensity changes across a population of ce

78 e relaxations were similar for each, whereas fluorescence intensity changes differed significantly.

79 Fluorescence intensity changes upon addition of MgCl2 we

80 ime by Forster resonance energy transfer and fluorescence-intensity changes.

81 zation, and achieved 10-fold enhancement in fluorescence intensity compared to a bare glass substrat

82 In all three cases, it is observed that the fluorescence intensity consistently increases with resin

83 The fluorescence intensity correlated linearly with the seco

84 MERTK expression (mean fluorescence intensity) correlated with the severity of

85 should be assessed with a bead-specific mean fluorescence intensity cutoff based on TFL-006 reactivit

86 on efficiency (E) from least-squares fits of fluorescence intensity data for cycles near the onset of

87 Fluorescence intensity decay curves emulated on the basi

88 The fluorescence intensity decay, in particular, is a powerf

89 mit of 1.2 x 10(-16)M and on the other hand, fluorescence intensity declined linearly with concentrat

90 on, leading to QDs getting closer along with fluorescence intensity decreasing.

91 Changes in fluorescence intensity (DeltaF) in response to membrane

92 We further investigated whether the fluorescence intensity depended on np-Au feature size, c

93 d complementary oligonucleotides resulted in fluorescence intensities dependent on ethanolamine conce

94 The fluorescence intensities detected from the C-Dots on the

95 Compared with DSA mean fluorescence intensity, DSA IgG3 positivity and C1q bind

96 labelled with Cy3 results in an increase in fluorescence intensity due to protein-induced fluorescen

97 measure changes in either FRET efficiency or fluorescence intensity during PRE complex formation.

98 nanoparticles (NP-UCNPs) creates changes in fluorescence intensity during rotational motion.

99 deration is the change in the macromolecular fluorescence intensity during the course of the experime

100 cite GOx-FS, which undergoes a change in the fluorescence intensity during the enzymatic reaction wit

101 Fluorescence intensity emitted by hydrolyzed fluorescein

102 e evaluated by gel electrophoresis, relative fluorescence intensity, emulsifying properties, light mi

103 is probe exhibited a significant ratiometric fluorescence intensity enhancement as solvent viscosity

104 It exhibited approximately 16-fold fluorescence intensity enhancement at 435 nm after react

105 ein probe, AcroB, that undergoes a >350-fold fluorescence intensity enhancement concomitant with prot

106 ysis assessed CD66b, CD69, and CD203c median fluorescence intensity expression.

107 he sensors triggered concentration-dependent fluorescence intensity (FI) changes that strictly correl

108 migrating cells, the normalized FAK/Paxillin fluorescence intensity (FI) ratio is > 1 ( approximately

109 At pH 3.0 and 5.0, the fluorescence intensity (FI) was greater than values obta

110 with the alum/MNrgp120 vaccine (gp120 median fluorescence intensities [FIs] in infants = 7,118 and in

111 l cytokine importance using Z scores of mean fluorescence intensity for individual cytokines.

112 fied according to ratio between the measured fluorescence intensity for treated and nontreated beads.

113 mune encephalomyelitis mice, with the higher fluorescence intensity found in CD4(+) cells.

114 Measurement of the ratio of fluorescence intensities from coumarin and the NBD-Cys o

115 The real-time fluorescence intensity from 8HQ/Ca(2+)/PA complexes can

116 was shown that after reaching a maximum, the fluorescence intensity gradually decreased toward longer

117 De novo DSA mean fluorescence intensity >6237 and >10,000 at 2 and 5 year

118 ver, the effect of nanostructured surface on fluorescence intensity has largely been ignored, which l

119 nd large surface area, SNPs as amplifiers of fluorescence intensity, higher affinity of Apt toward it

120 sus dexamethasone: 504+/-263 versus 194+/-77 fluorescence intensities in hearts; P=0.002).

121 Temporal sequences of fluorescence intensities in single-molecule experiments

122 Mapping the fluorescence intensity in 3D by CLSM enables us to recon

123 olved 3D colocalization information, and the fluorescence intensity in both channels.

124 ium and copper showed a negligible change in fluorescence intensity in comparison to zinc ions.

125 -gene read depth in RNA-Seq than they are on fluorescence intensity in microarrays.

126 Comparison of cytosolic fluorescence intensity in positive cells versus backgrou

127 ulum of BAs and displayed a marked change in fluorescence intensity in response to adrenergic stimula

128 ation wavelength = 500 nm) revealed that the fluorescence intensity in surface laser-treated tumors 2

129 rescence intensity in the lesion by the mean fluorescence intensity in the adjacent liver parenchyma.

130 meter by approximately 30% and increases the fluorescence intensity in the center of the domain mouth

131 cal microscopy was performed to quantify the fluorescence intensity in the cornea according to the di

132 (TBRs) were calculated by dividing the mean fluorescence intensity in the lesion by the mean fluores

133 -active molecules due to a modulation of the fluorescence intensity in the vicinity of a bipolar elec

134 measured as an increase in their CD11b mean fluorescence intensity in whole blood and after isolatio

135 The fluorescence intensity increased in dose dependent manne

136 arget unmethylated and methylated ssDNA, the fluorescence intensity increased in linear range by conc

137 on of 3 in 2:1 water/methanol with NaCl, the fluorescence intensity increased.

138 he interpretation of evanescent-wave excited fluorescence intensities is the undetermined cell refrac

139 n the addition of target methylated DNA, the fluorescence intensity is decreased in a linear range wh

140 r accurately the droplets flow even if their fluorescence intensity is negligible.

141 An increase in TPE-TPP fluorescence intensity is observed only with ordered pro

142 ected in the G-quadruplex structure and high fluorescence intensity is observed.

143 Following addition of SYBR Gold, a strong fluorescence intensity is obtained.

144 In the absence of STR, the fluorescence intensity is weak.

145 By performing simultaneous measurements of fluorescence intensity, lifetime, and spectra of single

146 Spdo: cargoes exhibiting high GFP/low Cherry fluorescence intensities localized mostly at the plasma

147 hter than Cyanine5 free dye and the measured fluorescence intensity matched a homo-Forster Resonance

148 However, intratumoral heterogeneity of fluorescence intensity may reflect different onco-metabo

149 ric read-out and self-referenced ratiometric fluorescence intensity measurements.

150 33 vs. 0.84, 0.15-2.37 years) and lower mean fluorescence intensity (MFI) (2658, 1573-3819 vs. 7820,

151 off admission nCD64 expression of 230 median fluorescence intensity (MFI) identified sepsis with a se

152 endent cytotoxicity XM results with the mean fluorescence intensity (MFI) in Luminex class I single a

153 Mean fluorescence intensity (MFI) of 70 total DSA decreased b

154 Only DSAs with a mean fluorescence intensity (MFI) of greater 999 were include

155 The dnDSA mean fluorescence intensity (MFI) of the stable function pati

156 or recipients with no DSA or with a DSA mean fluorescence intensity (MFI) value of 500 or less, scree

157 For undiluted sera, Luminex mean fluorescence intensity (MFI) values for IgG-SAB and C1q-

158 Anti-HLA antibodies mean fluorescence intensity (MFI) values were stable prior to

159 -binding activity, presence of AMR, DSA mean fluorescence intensity (MFI) values, and immunoglobulin

160 complement-fixation, in parallel to IgG mean fluorescence intensity (MFI), allows for improved predic

161 ing specificity, HLA class specificity, mean fluorescence intensity (MFI), C1q-binding, and IgG subcl

162 x, and antibodies were quantified using mean fluorescence intensity (MFI).

163 nts with high peak or day 0 DSA levels (mean fluorescence intensity [MFI] > 3000) with a complement-d

164 in controls (n=3) (median difference in mean fluorescence intensity [MFI] 703 arbitrary units [p=0.06

165 ,665 SABs with positive IgGpan results (mean fluorescence intensity [MFI]>500), strong complement-bin

166 on in relation to DSA binding strength (mean fluorescence intensity [MFI]_max).

167 of OPA-tryptophan adduct, the difference in fluorescence intensity obtained at 280 and 300 nm excita

168 s and of PNNs were not altered; however, the fluorescence intensities of PV immunoreactivity in cell

169 microscopy, we quantified the densities and fluorescence intensities of PV neurons and PNNs labeled

170 of metal ions was examined by comparing the fluorescence intensities of the solutions before and aft

171 The fluorescence intensities of the two apt-DAR NPs are both

172 canalography method that uses slope-adjusted fluorescence intensities of two different chromophores t

173 7.4 s(-1), KM of 15 muM, and an increase in fluorescence intensity of 104-fold upon cleavage, thus p

174 nce of weak de novo DSA or non-DSA at a mean fluorescence intensity of 500 or higher was higher in th

175 ian donor-specific antibody level was a mean fluorescence intensity of 710 (interquartile range, 328-

176 on was also monitored by the fluctuations in fluorescence intensity of a Cy3 fluorophore attached to

177 the axoneme's ATP consumption by monitoring fluorescence intensity of a fluorophore-coupled reporter

178 enumeration of mitochondrial nucleoids, and fluorescence intensity of a genetically encoded mitochon

179 Fluorescence intensity of a humic-like fluorophore (i.e.

180 Our technique measures the local fluorescence intensity of a neutrally charged fluorescen

181 When immobilized on a surface, the fluorescence intensity of a single DNA- or RNA-wrapped S

182 In 24 patients, decrease in mean fluorescence intensity of antibodies by more than 50% wa

183 gic gate fabrication was discussed using the fluorescence intensity of Au-NCs as output.

184 quenching analysis showed an increase in the fluorescence intensity of BSA upon increasing the amount

185 fluorescence spectroscopy indicated that the fluorescence intensity of BSA was decreased considerably

186 asophil activation was evaluated by the mean fluorescence intensity of CD203c on basophil MPs.

187 Mean fluorescence intensity of CD203c on MPs was increased in

188 was not significant (P = .052), but the mean fluorescence intensity of CD69 increased significantly o

189 Fluorescence intensity of DHRh 123 in bulk increased at

190 n absolute quantification for thiols because fluorescence intensity of different thiol adducts varies

191 Relationships between the specific fluorescence intensity of DOM and its radiocarbon age we

192 Both groups showed decreased mean fluorescence intensity of donor-specific antibodies as s

193 The sum of mean fluorescence intensity of DSA (DSA MFI-Sum) of 6,000 or

194 et molecules to be detected by measuring the fluorescence intensity of each droplet.

195 ggest that nanostructured surfaces alter the fluorescence intensity of fluorophores by modulating bot

196 eta were similar between IT groups, the mean fluorescence intensity of Foxp3 was highest in the SCIT

197 In CCI-vehicle, sham and CCI-SR49059 groups, fluorescence intensity of GFAP was 349+/-38, 56+/-5, and

198 Fluorescence intensity of GFP at the tumor surface decre

199 , there was no significant difference in the fluorescence intensity of GFP in the tumors among all gr

200 sed to record the mAb-IR700 distribution and fluorescence intensity of green fluorescent protein (GFP

201 High fluorescence intensity of HDTA in mice came from the ile

202 L-5- and IL-13-expressing ILC2s and the mean fluorescence intensity of IL-5 and IL-13 staining.

203 IL-13-expressing ILC2s, as well as the mean fluorescence intensity of IL-5 and IL-13 staining.

204 ), with a concomitant increase in the median fluorescence intensity of interleukin 4 (IL-4; P < .05)

205 n RNA (shRNA) to reduce vimentin by 90%, the fluorescence intensity of mitochondria decreases by 20%.

206 is detected by quantitatively comparing the fluorescence intensity of mitochondria stained with the

207 ructure switching, leading to a reduction of fluorescence intensity of PG.

208 f is longer than that of ReAsH-EDT2, and the fluorescence intensity of ReAsH-EDT2 increases in solven

209 relation between the simultaneously recorded fluorescence intensity of resorufin and electrochemical

210 The average fluorescence intensity of riboflavin at a depth of 100,

211 Forest to learn the relationship between the fluorescence intensity of sets of microarray probes and

212 th filamin A or alpha-actinin2, the membrane fluorescence intensity of SK2 channels increased signifi

213 e nuclearization of Smad3, and intracellular fluorescence intensity of Smad7 and the corneal crystall

214 The fluorescence intensity of suspension of these UAPs was f

215 The fluorescence intensity of the aluminum-DEMAX complex rem

216 The decreases in fluorescence intensity of the BSAGNCs allow sensitive de

217 Although mean fluorescence intensity of the immunodominant DSA diagnos

218 amount of the analytes present based on the fluorescence intensity of the lines (quantitative analys

219 al background intensity, especially when the fluorescence intensity of the molecule is used quantitat

220 g, the TNV-polythiophene complex changes the fluorescence intensity of the nanofilm.

221 get antibiotics were realized by imaging the fluorescence intensity of the near-infrared label captur

222 to shift the UCNP emission color, since the fluorescence intensity of the organic dyes excited by FR

223 Thus, the fluorescence intensity of the quantum dots was enhanced

224 avage sequence, a consequent decrease in the fluorescence intensity of the sample could be observed.

225 Under optimal conditions, the fluorescence intensity of the sensing system displayed a

226 The normalized fluorescence intensity of the Streptococcus pyogenes gav

227 ntracellular structures and leads to reduced fluorescence intensity of the targets of interest.

228 The fluorescence intensity of this probe using the three tar

229 of the emission spectra of these PTMs to the fluorescence intensity of Trp, to determine semi-quantit

230 using a novel approach based on the overall fluorescence intensity (OFI) of PARAFAC components.

231 ons, and those results are used to calibrate fluorescence intensities on the same sample at much high

232 per and fluorophore emission spectra and the fluorescence intensity on an imaging system of interest

233 sion of the transducer, yielding increase in fluorescence intensity on analyte concentration increase

234 tion in the sample resulted in dependence of fluorescence intensity on logarithm of zinc ions concent

235 y was determined by the dependence of the QD fluorescence intensity on the distances between them in

236 chlorin dyads exhibit a strong dependence of fluorescence intensity on the solvent polarity, which re

237 cular infections, with ~3.4 x enhancement in fluorescence intensity over background.

238 phoresis (CE) and quantitated by integrating fluorescence intensity over respective CE peaks.

239 some genus showing a decreasing proportional fluorescence intensity over time were still actively res

240 ivity (ROA) spectrometer, which ensured high fluorescence intensity owing to the strong 532 nm laser

241 s (p < 0.05) were observed as were lower DCF fluorescence intensity (p < 0.05) in FABP1 cDNA transfec

242 llaritis Banff score (P=0.002), and DSA mean fluorescence intensity (P<0.001) after treatment.

243 An axial scan through the cell generates a fluorescence intensity profile that is analyzed to deter

244 Simulation of the resulting fluorescence intensity profiles is achieved on the basis

245 Fluorescence intensity profiles measured along the optic

246 ERthermAC fluorescence intensity profiles were congruent with mito

247 vides global and individual calcium-reporter fluorescence intensity profiles.

248 gainst donor DQ antigens, often of high mean fluorescence intensity, rarely of the IgG3 subclass, and

249 Red/green fluorescence intensity ratios from individual mitochondr

250 emission spectra, thermal quenching ratios, fluorescence intensity ratios, and sensitivity.

251 ependent fluorescence assays showed that the fluorescence intensity reached a plateau within 20s afte

252 The fluorescence intensity recorded from the DNA sample is p

253 The average IR700 fluorescence intensity recovery after PIT to the tumor s

254 In contrast, class I-II HLA-DSA mean fluorescence intensity remained unchanged in groups II a

255 Regardless of calcium ion presence, the fluorescence intensity results suggest that tyrosinase t

256 cence spectra of PCS revealed lower relative fluorescence intensity (RFI 112) compared to 'free' sesa

257 l tumor types demonstrated that GFP relative fluorescence intensity (RFI) in s-tumor was significantl

258 Th17/Treg ratio and the IL-17 relative mean fluorescence intensity (rMFI of IL-17) were also positiv

259 ults from pi-pi stacking and by the enhanced fluorescence intensity seen in the green fluorescent pro

260 lated [Ca2+]i transient and of the simulated fluorescence intensity signal, F/F0, reached values simi

261 hly correlated with cell viability; when the fluorescence intensity still increased 120s after openin

262 ssDNA constructs, together with increases in fluorescence intensity, suggest that gp32 binding direct

263 pliteal nodes had higher (P < 0.050) optical fluorescence intensity than the paraaortic nodes at the

264 match location near the 5' end led to higher fluorescence intensity than those near the 3' end when t

265 energy from donor Coumarin 2 emitted higher fluorescence intensity than when directly excited, indic

266 ce images by applying empirically determined fluorescence intensity thresholds.

267 asts is unique in producing an intracellular fluorescence intensity time curve that increases in a si

268 , the aged SOA particles may have sufficient fluorescence intensities to interfere with the fluoresce

269 AM addresses core questions of how to relate fluorescence intensity to tumor tissue and how to quanti

270 by monocytes increased from 530 to 1306 mean fluorescence intensity units (P = 0.016).

271 rils is signified by large reductions in the fluorescence intensity upon either fully protonating, or

272 ng fluorescein, a fluorescent dye that loses fluorescence intensity upon reaction with oxidative spec

273 mean number of 1.6 +/- 0.8 DSAs with a mean fluorescence intensity value of 2,815 +/- 2,550.

274 lass I, a higher frequency and a higher mean fluorescence intensity value of C1q-dnDSA at all time-po

275 g Luminex single antigen beads, where a mean fluorescence intensity value of more than 1500 was consi

276 e SAP(-), 2 expressed SAP with mean relative fluorescence intensity values below the range of healthy

277 Although we found a high correlation of mean fluorescence intensity values between C1q- and C4d-Lumin

278 A disparity between antigen density and mean fluorescence intensity values for some alleles within an

279 hannels are rendered simultaneously, whereas fluorescence intensity values from each channel need to

280 s within an eplet group was noted, with mean fluorescence intensity values of the lowest fluorescence

281 Our method also preserves original fluorescence intensity values on graphics hardware, a cr

282 Anti-HLA antibodies with mean fluorescence intensity values over 5,000 for HLA-A, HLA-

283 , donor-specific antibody frequency, or mean fluorescence intensity values.

284 glion, the numbers of stained DPANs, and the fluorescence intensity via 1) conventional crystalline D

285 UV range (between 350 and 405 nm) and (iii) fluorescence intensity wanes as the emission wavelength

286 The maximal fluorescence intensity was achieved with a pulp to AO/LD

287 among all groups, however the highest IR700 fluorescence intensity was consistently shown in group 5

288 etween C1q- and C4d-Luminex assays, IgG mean fluorescence intensity was not a suitable surrogate mark

289 the intracellular actin network and rise in fluorescence intensity was observed.

290 Fluorescence intensity was quantified using integrated i

291 The fluorescence intensity was recorded as the mutants were

292 Values of mean fluorescence intensity were comparable in both groups.

293 relaxation and the time course of change in fluorescence intensity were described by single exponent

294 was determined from image analysis of their fluorescence intensity when diffusing across the monolay

295 The composite AO/LDH reaches the highest fluorescence intensity when the AO initial concentration

296 eously a 2,300-fold enhancement in the total fluorescence intensity, which indicates a high radiative

297 3 types of GBM tissues on the basis of their fluorescence intensity, which was characterized as stron

298 g staining resulted in considerably improved fluorescence intensity with both pMHC tetramers and dext

299 of tryptophan to NADH and the change rate of fluorescence intensity with respect to wavelength also i

300 d lower limit of detection and 4-fold higher fluorescence intensity with the "papaya particles" compa

301 oliter effective volume) detecting increased fluorescence intensity within seconds after initiation o