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 rse relationship between gene expression and fluorescence intensity.

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

4 aused an increase in Hoechst-stained nuclear fluorescence intensity.

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

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

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

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

9 ween sub-regions determined from nanocluster fluorescence intensity.

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

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

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

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

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

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

16 rance by lactose and partially recovered the fluorescence intensity.

17 that transforms effector concentration into fluorescence intensity.

18 bilayer regions with more than two levels of fluorescence intensity.

19 erium data, including cell length, area, and fluorescence intensity.

20 ationship between apoptotic cell numbers and fluorescence intensities.

21 y mapping each epithelial cell and recording fluorescence intensities.

22 stain is added to the eluted product and the fluorescence intensity accurately quantifies the amount

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

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

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

26 antibodies against ARHGDIB (adjusted median fluorescence intensity [aMFI] >= 1000), a minor histocom

27 Single-molecule fluorescence intensity analysis of CaMKII-alpha expresse

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

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

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

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

32 g correlation among single antigen bead mean fluorescence intensity and complement assays positivity,

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

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

35 Significant changes in the fluorescence intensity and emission wavelengths, between

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

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

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

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

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

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

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

43 Our data suggest that DSA mean fluorescence intensity and presence of gDSA might provid

44 asurements are robustly independent of total fluorescence intensity and scatter.

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

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

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

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

49 imately 210 IRDye 800CW fluorophores (with a fluorescence intensity approximately 6,700-fold that of

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

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

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

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

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

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

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

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

58 The reaction was monitored by measuring the fluorescence intensity at lambda(660nm) for resorufin, a

59 s and living organisms based on the ratio of fluorescence intensities between the cell nucleus and cy

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

61 C3G decreased PD-L1 fluorescence intensity by 39%.

62 harides release (p < 0.001), and reduced the fluorescence intensity by 47% after staining with Calcof

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

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

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

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

67 using electrophoretic mobility shift assays, fluorescence intensity changes and fluorescence anisotro

68 Fluorescence intensity changes upon addition of MgCl2 we

69 one cell of a pair, or to a monolayer while fluorescence intensity changes were recorded.

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

71 Here, by analyzing fluorescence intensities collected using a polarization

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

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

74 EB-NS fluoresce at 910 nm and the fluorescence intensity correlates with the number of Cu(

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

76 -fixed tissue slices yielded an optimal mean fluorescence intensity cutoff value for tumor detection

77 evacizumab-800CW for tumor detection, a mean fluorescence intensity cutoff value was determined from

78 One can also compare the fluorescence intensity data from two different microarra

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

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

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

82 However, the fluorescence intensity doubled during the festival.

83 1476), 3 of 6 patients with AMR and low mean fluorescence intensity DSA (<3000) had DSA-M.

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

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

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

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

88 Fluorescence intensity emitted by hydrolyzed fluorescein

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

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

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

92 The EBOV sensor exhibits substantial fluorescence intensity enhancement in immunoassays compa

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

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

95 Here, we introduce fluorescence intensity fluctuation spectrometry for dete

96 Forster resonance energy transfer (FRET) and fluorescence intensity fluctuation spectroscopy to asses

97 We also monitored by fluorescence intensity fluctuation-based methods (scanni

98 tablished technique based on the analysis of fluorescence intensity fluctuations detected in a confoc

99 sent at higher pH values (7-9) showed higher fluorescence intensity for both anthocyanins, with an op

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

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

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

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

104 Positivity criteria for DSA was mean fluorescence intensity greater than 500 for test 1, wher

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

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

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

108 ctly identified a tumor-positive CRM by high fluorescence intensities in 1 of 2 patients (50%) with a

109 Temporal sequences of fluorescence intensities in single-molecule experiments

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

111 otoisomerization behavior along with tunable fluorescence intensity in both isotropic and anisotropic

112 We observed significant shifts in fluorescence intensity in CHO cell culture fluid spiked

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

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

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

116 and found that mKate2 yields the highest red fluorescence intensity in our assay.

117 show that the presence of GNPs increase the fluorescence intensity in platelets treated with GNPs-an

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

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

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

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

122 sed in human cells, both FRET efficiency and fluorescence intensity in the nucleus increased followin

123 ion of the TPE moiety was confirmed when its fluorescence intensity increased by the addition of wate

124 The fluorescence intensity increased in dose dependent manne

125 As an ICT sensor, fluorescence intensity increased upon diol recognition,

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

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

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

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

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

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

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

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

134 lood cultures yielded essentially background fluorescence intensity levels for cultures with Gram-neg

135 tive bacteria, and only ~ 3.5-fold increased fluorescence intensity levels over background for cultur

136 the P2&3TT probe resulted in 50-fold higher fluorescence intensity levels than incubation with cultu

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

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

139 Besides, fluorescence intensity measurements indicated a signific

140 f field-effect experiments were supported by fluorescence-intensity measurements of the PAH- or DNA-m

141 served a strong correlation between SAB mean fluorescence intensity (MFI) and complement assays posit

142 G subclass profile was characterized by mean fluorescence intensity (MFI) and normalized subclass com

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

144 7%) and 194 (37%) transplanted with DSA mean fluorescence intensity (MFI) of 500 to 1000 and greater

145 Change in mean fluorescence intensity (MFI) value did not correlate wit

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

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

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

149 Among positive responders, bAb net mean fluorescence intensity (MFI) was significantly higher wi

150 s in PRF and GrB percent expression and mean fluorescence intensity (MFI) were highly correlated with

151 was increased incrementally from nevi [mean fluorescence intensity (MFI), 48.1; interquartile range,

152 16 patients, of which 11/19 were <1000 mean fluorescence intensity (MFI), 7/19 were between 1000 and

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

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

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

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

157 e of the presence of dnDSA (One Lambda, mean fluorescence intensity [MFI], >1000).

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

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

160 l ecology indices and immune-mediator median fluorescence intensities (MFIs) between sample types.

161 background ratios instead of absolute median fluorescence intensities (MFIs).

162 erating characteristic curve analysis of the fluorescence intensities of formalin-fixed tissue slices

163 We calibrate the fluorescence intensities of individual compact quantum d

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

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

166 In this study, we measured the fluorescence intensities of recombinant green fluorescen

167 The fluorescence intensities of the 5-aza-7-deazaguanine nuc

168 onstruction were quantified via the relative fluorescence intensities of the respective probes.

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

170 rotein age to be estimated from the ratio of fluorescence intensities of the two fluorescent proteins

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

172 7.4 s(-1), KM of 15 muM, and an increase in fluorescence intensity of 104-fold upon cleavage, thus p

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

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

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

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

177 The fluorescence intensity of ADD probe was drastically quen

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

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

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

181 Mean fluorescence intensity of CD203c on MPs was increased in

182 Fluorescence intensity of DHRh 123 in bulk increased at

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

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

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

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

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

188 Fluorescence intensity of GFP at the tumor surface decre

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

190 pending on the surfactant identity, the blue fluorescence intensity of GO at 440 nm increases with th

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

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

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

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

195 Increase in Atg16 protein expression and fluorescence intensity of LC3 was also observed in IAP-t

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

197 ated with different drugs by quantifying the fluorescence intensity of nuclei stained with Hoechst DN

198 The mean-fluorescence intensity of peptide-MHC-tetramer binding w

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

200 e of the sensing method is a decrease in the fluorescence intensity of PTCDI in the presence of free

201 er/CS-modified AuNPs releases CS and so, the fluorescence intensity of PTCDI is reduced.

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

203 On the other hand, fluorescence intensity of samples containing the DPPP pr

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

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

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

207 NF-kappaB may be visualized and measured by fluorescence intensity of specific near-infrared (NIR) f

208 The fluorescence intensity of suspension of these UAPs was f

209 Although the near-infrared (NIR) fluorescence intensity of SWCNTs at 998 nm is either unc

210 The fluorescence intensity of the aluminum-DEMAX complex rem

211 The fluorescence intensity of the cell was linearly proporti

212 DiBs' unique properties: strong increase in fluorescence intensity of the chromophore upon binding,

213 Although mean fluorescence intensity of the immunodominant DSA diagnos

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

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

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

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

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

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

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

221 The normalized fluorescence intensity of the Streptococcus pyogenes gav

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

223 GEC (dim(tdT) and bright(tdT)) based on the fluorescence intensity of the Tek(tdT) signal.

224 onal motion of the DEB while diminishing the fluorescence intensity of the TPE.

225 The fluorescence intensity of this probe using the three tar

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

227 ed soluble proteins are routinely assayed as fluorescence intensities on the Luminex (Luminex, Austin

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

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

230 -3(+) T lymphocytes as well as CEACAM-1 mean fluorescence intensity on CD4(+) T lymphocytes were sign

231 esults in a linear increase of red bead ring fluorescence intensity over a period of 5 h.

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

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

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

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

236 polarization by simultaneously detecting the fluorescence intensities parallel and perpendicular to t

237 data on the cells and targets geometric and fluorescence intensity parameters, automatically discrim

238 emoves plate/batch/lot artifacts from median fluorescence intensities prior to correction for nonspec

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

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

241 Fluorescence intensity profiles measured along the optic

242 orescence-activated cell sorting (FACS) from fluorescence intensity profiles of cells to multidimensi

243 In this work, we studied fluorescence intensity profiles of one of the three mamm

244 ERthermAC fluorescence intensity profiles were congruent with mito

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

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

247 The fluorescence intensity ratio from individual green, and

248 monstrate diminishing green/red (550/630 nm) fluorescence intensity ratios for HeLa and MCF-7 cancer

249 ing qPCR amplification efficiency E analyzes fluorescence intensity ratios from pairs of points deeme

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

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

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

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

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

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

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

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

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

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

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

261 es have relied on binding-induced changes in fluorescence intensity that are prone to excitation sour

262 ing is manifest through bright spots of high fluorescence intensity that can be observed when the bil

263 ed proteins because of an enhancement of Cy3 fluorescence intensity that results when the protein con

264 Apart from the response in the fluorescence intensity, the optodes show pH-dependent li

265 ce images by applying empirically determined fluorescence intensity thresholds.

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

267 ysis, we were able to assign the increase in fluorescence intensity to the chemically stable UV-B fil

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

269 The increase in fluorescence intensity upon 0.1% breakthrough of an 1 g/

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

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

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

273 taset, we analyzed potential changes in mean fluorescence intensity values (reflecting bound anti-HLA

274 IgG-isolated supernatants showed higher mean fluorescence intensity values compared with concentrated

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

276 While median mean fluorescence intensity values of DSA with concurrent DSA

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

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

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

280 The excitation ratio of fluorescence intensities was demonstrated to faithfully

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

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

283 Fluorescence intensity was quantified using integrated i

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

285 The fluorescence intensity was recorded as the mutants were

286 Fluorescence intensity was recorded as the number of cel

287 Importantly, the measured fluorescence intensities were dose-dependent, and a posi

288 For the other patient, low fluorescence intensities were shown, although (sub)milli

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

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

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

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

293 3 types of GBM tissues on the basis of their fluorescence intensity, which was characterized as stron

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

295 5 healthy controls, with good concordance in fluorescence intensity with standard RT-qPCR (Pearson co

296 A decrease in fluorescence intensity with the age of the vesicles sugg

297 The change in SGQDs fluorescence intensity with varying quercetin content re

298 ptide release events as real-time changes in fluorescence intensity, with sub-second temporal resolut

299 rm, accompanied by a 10-fold decrease in its fluorescence intensity within 60 seconds when exposed to

300 ize tetracycline (TC) in milk, enhancing the fluorescence intensity without interference from other c