ライフサイエンスコーパス: absorbance

1 een uptake (1.87-fold increase in normalized absorbance).

2 raw sugar colour contributed to starch-I3(-) absorbance.

3 iabetic retinas, as shown by a difference in absorbance.

4 constants in natural waters of any depth and absorbance.

5 thermal stability and an unmatched spectral absorbance.

6 a, and a finite detection time for measuring absorbance.

7 ration of pollutants can affect the infrared absorbance.

8 r, F5 registered the highest reducing power (absorbance 0.366) and hydroxyl-radical-scavenging activi

9 Al(3+) chelation increased absorbance 2-42x and lambdamax greater, similar40nm (pH

10 extracted using the microchip was pure with absorbance (260/280) ratio of 1.77+/-0.04, as compared t

11 vs -0.52 (-1.07, 0.00) kg day(-1)), and 24 h absorbance (35 (18, 60) vs 36 (22, 50) x 10(-6) m(-1));

12 th the TBARS spectrophotometric method with (absorbance) = 532 nm.

13 with a diode array detector (UPLC-DAD) with (absorbance) = 532 nm.

14 10 mum, and between 2.5 and 10 mum; PM(2.5) absorbance (a measurement of the blackness of PM(2.5) fi

15 ank was obtained by using the square root of absorbance (Abs) in order to adjust the residues of the

16 we describe a highly efficient microfluidic absorbance-activated droplet sorter (AADS) that extends

17 ntities of purified protein for intrinsic UV absorbance analysis and is amenable to medium throughput

18 Ultraviolet visible (UV-Vis) absorbance and 3-dimensional excitation emission matrix

19 Measurements show up to a 30% higher light absorbance and a factor of 2 larger photoemission during

20 The technique's sensitivity to anisotropic absorbance and birefringence provides rapid assessment o

21 in raft fractions, as revealed by increased absorbance and by mass fingerprint.

22 cted for light screening incorporating water absorbance and depth, suggesting endogenous photoinactiv

23 junction with real-time monitors, such as UV absorbance and dynamic light scattering (DLS), and an ar

24 o tags labeled with fluorophores of discrete absorbance and emission bands exhibited significantly re

25 significantly brighter dyes with red-shifted absorbance and emission maxima.

26 id state, unusually large blue-shifts in the absorbance and emission spectra, and higher fluorescence

27 Additionally, we report UV absorbance and emission T-jump results with improved sig

28 on exposure to visible light as indicated by absorbance and fluorescence features, second-order harmo

29 This model was evaluated by measuring the absorbance and fluorescence response of organic matter i

30 Absorbance and fluorescence spectral shape were largely

31 urce and composition was characterized using absorbance and fluorescence spectroscopies and high-reso

32 terized using cyclic voltammetry, UV-visible absorbance and fluorescence spectroscopy, spectroelectro

33 ed high fluorescent quantum yields where the absorbance and fluorescence spectrum of the fluorophore

34 (K(+) NS) modulates its optical properties (absorbance and fluorescence) according to the potassium

35 reduction on the optical properties of DOM (absorbance and fluorescence) and the formation of single

36 Solid-material absorbance and flux measurements differentiated light ab

37 analyzed by oxygen consumption measurements, absorbance and mass spectrometry.

38 tive associations with turbidity and UV(254) absorbance and negative associations with baseflow index

39 The influence of absorbance and reactivity has critical consequences for

40 in the visible spectrum due to reduced light absorbance and scatter by tissues.

41 nds were observed, including decreases in UV absorbance and shifts in the molecular composition of NO

42 The use of fluorescence data from an absorbance and transmission excitation-emission matrix (

43 he simultaneous measurement of optoacoustic, absorbance, and fluorescence spectra.

44 structures reveal CD spectra at the plasmon absorbance, and the NPs are imaged by HR-TEM.

45 lecular absorbance spectroscopy to determine absorbance as a function of molecular size.

46 n addition, we have converted an existing UV absorbance assay for FabA, the bifunctional dehydration/

47 content was determined by measurement of the absorbance at 252nm.

48 ky Mountains was strongly correlated with UV absorbance at 254 nm (Abs254, r = 0.88 p < 0.01) and org

49 y, the cladding polymer Cytop had negligible absorbance at 265 nm wavelength.

50 molecular solutes, and characteristic light absorbance at 270 nm.

51 mmer are correlated with the coumarin UV-vis absorbance at 274 nm.

52 mmer are correlated with the coumarin UV-vis absorbance at 274nm.

53 fference in molecular weight and specific UV absorbance at 280 nm (SUVA280) between the two solid pha

54 (DNPH) to form protein-bound hydrazones with absorbance at 370 nm.

55 with iodine forms followed by measurement of absorbance at 370 nm.

56 n, the decline of turbidity during time, the absorbance at 420 nm, the GRP (grape reaction products)

57 compared with other conventional parameters: absorbance at 420nm (A420) and the content of 5-hydroxym

58 med in alkaline media at pH 11.5 has maximum absorbance at 520nm and emittance at 600nm.

59 RIF binding was monitored using absorbance at 525 nm to determine a dissociation constan

60 nd epigallocatechin contents and with higher absorbance at 620nm and slower with higher levels of gal

61 mpound showed a strong reduction of its peak absorbance at 765 nm upon addition of calcium ions that

62 ith samples, different temperatures, and the absorbance at different wavelengths by applying PARAFAC

63 libration=45, nvalidation=20), including the absorbance at two wavelengths (257, 324nm), was obtained

64 ses, the spectra were red-shifted to maximum absorbance at wavelengths longer than 500 nm and emissio

65 Wine absorbances at 230 nm (A230) proved more suitable for as

66 t protection of the juices, reflected in low absorbances at 420 nm, remarkable increases in the polyf

67 Further, we identified two new NIR bone absorbances, at 6560 cm(-1) and 6688 cm(-1), associated

68 while adding 250 x 10(-5) M KMS whereas the absorbance band at 523 nm was decreased.

69 d, accompanied by a strong broadening of the absorbance band, tailing out to 850-950 nm.

70 Importantly, no transient absorbance bands could be assigned to CYP101[FeO(2+)por(

71 des (LEDs) are now widely used in analytical absorbance-based detectors; as compared to conventional

72 Here, we report a plasmonic fiber optic absorbance biosensor (P-FAB) strategy for mannosylated L

73 (SECT) to distinguish materials with similar absorbances but different elemental compositions.

74 etup due to limitations imposed by low light absorbance by protein monolayers and/or slow long-range

75 ng the dye-filled microstructure followed by absorbance calculation and the reconstruction of the opt

76 ) antioxidant activity by the Oxygen Radical Absorbance Capacity (27 mM Trolox equivalents).

77 ties according to hydrophilic-oxygen radical absorbance capacity (H-ORAC(FL)) and ferric reducing ant

78 vity (DPPH) (95.4+/-0.3%) and oxygen radical absorbance capacity (ORAC) (0.82+/-0.07g equivalent Trol

79 se IV (DPP-IV) inhibitory and oxygen radical absorbance capacity (ORAC) activities.

80 e radical savenging activity, oxygen radical absorbance capacity (ORAC) and beta-carotene bleaching.

81 dant capacity was measured by Oxygen Radical Absorbance Capacity (ORAC) and Folin Ciocalteau Reagent

82 The oxygen radical absorbance capacity (ORAC) assay confirmed that the phen

83 The oxygen radical absorbance capacity (ORAC) assay, frequently applied to

84 r antioxidant activity by the Oxygen Radical Absorbance Capacity (ORAC) assay.

85 antioxidant power (FRAP) and oxygen radical absorbance capacity (ORAC) assays with a measured half-m

86 antioxidant power (FRAP) and oxygen radical absorbance capacity (ORAC) compared to those generated w

87 total antioxidant capacity by Oxygen Radical Absorbance Capacity (ORAC) methods.

88 ated enzymatic digestion, the oxygen radical absorbance capacity (ORAC) of CPH obtained from germinat

89 The oxygen radical absorbance capacity (ORAC) of the obtained pure anthocya

90 A significantly higher oxygen radical absorbance capacity (ORAC) value was obtained for WP hyd

91 l-1-picrylhydrazyl (DPPH) and Oxygen radical absorbance capacity (ORAC), and biological model as 2,2'

92 dical scavenging activity and oxygen radical absorbance capacity (ORAC).

93 ivalent antioxidant capacity, oxygen radical absorbance capacity and nitric oxide scavenging assays.

94 The Oxygen radical absorbance capacity assay indicated 5 of the Kombucha be

95 ommon foods analysed with the oxygen radical absorbance capacity method.

96 tioxidant assays (hydrophilic-oxygen radical absorbance capacity {H-ORAC(FL)} and ferric reducing ant

97 l-1-picrylhydrazyl) and ORAC (oxygen radical absorbance capacity) assays.

98 or total antioxidant intake (oxygen radical absorbance capacity).

99 habitat; copepods had higher oxygen-reactive absorbance capacity, glutathione-S-transferase, and tota

100 The decrease in DOM absorbance caused by ozonation leads to an enhancement o

101 eat treatment increased particle size, light absorbance, centrifugal instability, iron expulsion from

102 We take advantage of the absorbance change in the POT film while being oxidized,

103 By monitoring the UV absorbance change of AuNPs, a sensitive dCO2 sensor with

104 In contrast, absorbance changes are negligible in a 25% Fe-doped cata

105 The colorimetric absorbance changes are simultaneously followed by a digi

106 UV absorbance, circular dichroism and fluorescence microsco

107 used to process the relationship between the absorbance data and the concentration of analytes.

108 ological refinement to correct [CO3(2-)]spec absorbance data for small but significant instrumental d

109 thod is designed for modeling multicomponent absorbance data with the presence of shifts or changes o

110 ephthalein dye absorbances) to the shipboard absorbance data, we fit the combined-cruise data set to

111 d by mathematical simulations of the angular absorbance dependence.

112 nce (e.g., different times, latitudes, water absorbances, depth).

113 sid proteins was achieved with convenient UV absorbance detection at 214 nm, equivalent to 20 pg of p

114 ed large signal drifts (1/f noise), allowing absorbance detection in a mere 27 mum optical path.

115 Absorbance detection in food microdevices has not been t

116 In this work, we demonstrate enhanced absorbance detection in glass microfluidic channels usin

117 A planar, chip-based flow cell for UV-vis absorbance detection in HPLC is presented.

118 Absorbance detection is often prohibited in microfluidic

119 Quantitative ELISAs employing the absorbance detection method were demonstrated on the not

120 and growth along with the unsupervised LSPR absorbance detection of AuNPs with a dynamic range for d

121 th a commercial capillary electrophoresis-UV absorbance detection system.

122 ometry and a commercial system that utilizes absorbance detection.

123 A new miniature deep UV absorbance detector has been developed using low-cost an

124 SC, R(2) = 0.96, RMSEP = 0.58%) and index of absorbance difference (I(AD), R(2) = 0.96, RMSEP = 0.08)

125 loyed to monitor changes in ultraviolet (UV) absorbance during CV and identify transient intermediate

126 ld nanoparticles (GNPs) enhance the damaging absorbance effects of high-energy photons in radiation t

127 the catalytic and spectroscopic (electronic absorbance, EPR) properties of KsHDH in comparison with

128 enuation coefficient and near-infrared (NIR) absorbance, excellent light-to-heat conversion efficienc

129 of the PB film is confirmed by colorimetric absorbance experiments as a function of applied potentia

130 fluoresence for vitamins A and E and visible absorbance for beta-carotene.

131 ry calculations demonstrated long-wavelength absorbance for both model DOM chromophores and their mol

132 ity induced by nanomaterials, scattering and absorbance from the nanomaterials act as interferences t

133 to large differences in the spectral peak of absorbance (i.e. the lambdamax value).

134 ion in mice, and that they have high optical absorbance in a broad near-infrared region spectral rang

135 es with low quantum yields, corresponding to absorbance in a ground state with a maximum at 389nm, an

136 , enabling up to 30% increase of the overall absorbance in semiconductor layer.

137 Strong absorbance in the near-infrared (NIR) region is observed

138 h measures and calculates the differences of absorbance in the test tube containing 10% sodium deoxyc

139 The seed oil showed absorbance in the ultraviolet ranges, thus it can be use

140 Goldenberry waste oil exhibited absorbance in the UV range at 100-400nm.

141 The shock energy absorbance in ZIF-8 is proportional to ZIF-8 thickness,

142 ing ethanol are correlated with the coumarin absorbances in summer, winter and spring whereas mixture

143 vertheless, silicon coatings allow up to 64% absorbance increase in the narrow band spectral range be

144 sorption provided by the nanoprobes, with an absorbance increase up to two orders of magnitude, allow

145 The absorbance intensities of LP-hCy7 nanoprobe at 690 and 8

146 ut signals were recorded through reading the absorbance intensity transition, dynamic light scatterin

147 Using measurements of absorbance intensity, the binding constants for the 4a +

148 ations according to AB significantly reduced absorbance interference from compounds other than pyruva

149 Identification of light-absorbance interfering compounds was performed by spectr

150 hnique enables simultaneous fluorescence and absorbance interrogation of rapidly moving droplets in a

151 biocontaminants by decomposing their optical absorbance into two physically measurable components and

152 nducting polymer with a strong near-infrared absorbance is synthesized and its water-dispersed nanopa

153 onset potential for bleaching of the FA-PVSK absorbance is used to estimate the CBM, which provides v

154 curve was generated by plotting the ratio of absorbance (lambda515 nm/lambda482 nm) against the HRP-I

155 a green copper-binding protein that displays absorbance maxima near 411, 581, and 721 nm and is monom

156 01[FeO2](2+) Judging by the appearance of an absorbance maximum at 440 nm, we conclude that CYP101[Fe

157 transfer complex NAD(+):beta-FADH(-) with an absorbance maximum at 650 nm.

158 ders of magnitude, along with a shift of the absorbance maximum from 416 to 398 nm.

159 ucing an astonishing 200 nm red shift in the absorbance maximum.

160 x was collected in a CH2Cl2 organic drop and absorbance measured at 435nm.

161 Signal quantification was carried out by absorbance measurement.

162 e included mass, fluorescence intensity, and absorbance measurements and specifications for classes o

163 ible with our design, the sensitivity of our absorbance measurements in a 30 mum-deep channel was imp

164 evaluation of circular dichroism and visible absorbance measurements of guanidine-hydrochloride-induc

165 h surface plasmon resonance measurements and absorbance measurements of the experimental multivalent

166 By combining absorbance measurements with flow cytometry, we quantifi

167 formation on the surface was followed using absorbance measurements, showing maximum signal increase

168 lity by size-exclusion chromatography and UV absorbance measurements.

169 essing future (and historical) [CO3(2-)]spec absorbance measurements.

170 er, the results were less sensitive than the absorbance measurements.

171 dology composed of quantitative bright-field absorbance microscopy (QBAM) and deep neural networks (D

172 ptide sequence-encoded properties such as UV absorbance, morphology, coloration, and electrochemical

173 idation testing of a broad-spectrum and high-absorbance near-infrared optoacoustic contrast agent, E4

174 .5, PM10, and PMcoarse, respectively); PM2.5 absorbance; nitrogen oxides (NO2 and NOx); traffic inten

175 phaloscyllium ventriosum exhibited a maximum absorbance of 484 +/- 3 nm and an absorbance range at ha

176 Furthermore the absorbance of assay reaction was approximately constant

177 relatively free from interference due to the absorbance of biomolecules.

178 Using this approach, we have measured the absorbance of both the unstructured and structured nucle

179 of Ca(2+) lead to a robust blueshift of the absorbance of CaSPA, which translated into an accompanyi

180 In UV method, the absorbance of chlorpyrifos and prophenofos was measured

181 The exceptional absorbance of DASAs in solution, uniquely controllable r

182 urface plasmon resonances alters the visible absorbance of dried, printed sensor spots made from inks

183 uced the lowest cell proliferation (relative absorbance of formazan: 23.4% +/- 7, 44.6% +/- 7.5, 95.8

184 uced the lowest cell proliferation (relative absorbance of formazan: 23.4% +/- 7, 44.6% +/- 7.5, 95.8

185 Wavelengths related to absorbance of green, yellow and orange colour indicated

186 Similarly, significantly decreased absorbance of HA-AAAs between 250 and 300 nm in ultravio

187 The value of logK (ratio of absorbance of humic acids at 400 and 600 nm) was cedar >

188 High absorbance of melanin suppresses multiple scattering, ca

189 opy is a powerful technique that detects the absorbance of molecular vibrations and is perfectly suit

190 to thermal gradients generated by plasmonic absorbance of NIR irradiation, with velocities ranging u

191 e only amino acid that exhibited specific UV absorbance of nitrosamines at 335nm, supporting the assu

192 nic acid supplementation generally increased absorbance of non-acylated anthocyanins by up to 97.9 an

193 lot permeability [Ks]) and 4% higher maximum absorbance of plasma clots that displayed impaired fibri

194 lead to increased yields (i) the red-shifted absorbance of polynuclear photosensitizers, (ii) the mor

195 the tissues overlap with the regions of high absorbance of predominantly the phosphate (1143-1100 cm(

196 The absorbance of quercetin autooxidation products at 320nm

197 formed in order to compare spectra in pseudo-absorbance of Saffron samples with different geographica

198 LC/MS-based approach, leveraging the high IR absorbance of sulfoxides at 10.6 mum, for selective diss

199 The absorbance of the Fe(II)-(Br-PADAP)(2) complex was measu

200 The UV/visible light absorbance of the Ni-only catalyst depends on the applie

201 photolysis lifetimes for the ONs and for the absorbance of the NO(3)(*)-aged aerosols are on the orde

202 mical images showing the distribution of the absorbance of the nu(as) OH spectral band.

203 The peak absorbance of the OH functional group increased while th

204 Spectral absorbance of the photoreceptor cells in these sharks re

205 Imaging studies showed that the absorbance of the protein bands was linear with the amou

206 results in an up to 10-nm red-shifted light absorbance of the receptor.

207 of layered materials in NMP and the optical absorbance of the solvent in the dispersion.

208 ealed significant peak shifts and changes in absorbance of the spectral bands that correspond to the

209 The spread of the absorbance of the stable FADH(*) radical (300-700 nm) al

210 The regions of high absorbance of this band in the tissues overlap with the

211 inguish primary ZIKV infection; the ratio of absorbance of ZIKV-NS1 to DENV1-NS1 IgG ELISA can distin

212 ide for evaluation of forthcoming commercial absorbance optics.

213 riation of the protocol applying traditional absorbance or an interference optical system can be used

214 For cation-selective electrodes, the absorbance or blue intensity of the connected PB film is

215 wheat gluten powder and aqueous suspension (absorbance, particle size and microstructure, free sulfh

216 Cy7 nanoprobe displays unique dual-shift NIR absorbance peaks and produces a normalized turn-on respo

217 tions are complemented by intensification of absorbance peaks in FTIR spectra and a systematic change

218 d then analyzed for acrylamide content, MRPs absorbance, pH, color, antioxidant capacity, antibacteri

219 tion at 310-410 nm, due to differences in UV absorbance properties of components.

220 lms leads to a dramatic shift in the optical absorbance properties, which correlates with the band ed

221 Further testing evaluated its handle of absorbance, quenching, and relative scattering intensity

222 a maximum absorbance of 484 +/- 3 nm and an absorbance range at half maximum (lambda1/2max) of 440-5

223 um absorbance was 488 +/- 3 nm with the same absorbance range.

224 of photoreceptor visual pigments, with peak absorbance ranging from 369 to 557 nm.

225 and blue-pigmented chromoproteins (CPs) with absorbances ranging from green to far-red, including 2 t

226 ce intensity at lambda(660nm) for resorufin, absorbance ratio (lambda(570nm)/lambda(605nm)), and chan

227 e calculated from direct measurements of the absorbance ratio R of the dye in natural samples as[Form

228 This technology was combined with automated absorbance readings and data analysis to determine MICs.

229 The hundreds of absorbance readings collected simultaneously for hundred

230 ng conditions of these assays and the use of absorbance readings make them suitable for application b

231 module, microdroplets can be sorted based on absorbance readout at rates of up to 300 droplets per se

232 Poly(cyclosilane) has red-shifted optical absorbance relative to the monomer.

233 s used to obtain the profiles of antioxidant absorbance's as a function of time due to uv-vis absorpt

234 The change in UV absorbance showed loss of protein solubility depending o

235 e analytical sensitivity, measurement of the absorbance signal was obtained by summing molecular tran

236 rst effort in the determination of terahertz absorbance signals, investigation of real-time dye perme

237 wavelengths that is unexpected based on bulk absorbance spectra and selection rules for nonlinear hyp

238 enzymes are challenging, as the ultraviolet absorbance spectra for reactant MTA and product adenine

239 Absorbance spectra have been plotted and peak absorbance

240 ec) derived from observations of ultraviolet absorbance spectra in lead-enriched seawater.

241 Captured images and resulting absorbance spectra of the gold nanoparticle, glutathione

242 not detected by sensors continuously logging absorbance spectra, thereby challenging their applicabil

243 UV absorbance spectrophotometry is widely used for the quan

244 Pressurized absorbance spectroscopy is used to characterize their me

245 onfirmed by microsphere exclusion and UV-VIS absorbance spectroscopy of samples flanking the fat, may

246 xclusion chromatography coupled to molecular absorbance spectroscopy to determine absorbance as a fun

247 We use optical absorbance spectroscopy to quantify the densities of red

248 gas exchange, chlorophyll fluorescence, and absorbance spectroscopy under different light intensitie

249 RS9916 using recombinant protein expression, absorbance spectroscopy, and tandem mass spectrometry.

250 Existing bulk methods, such as absorbance spectroscopy, can quantify sp(2) carbon based

251 The degradation, traced through absorbance spectroscopy, is well fit to first-order kine

252 d molecules, which are amenable to transient absorbance spectroscopy, the study of (3)CDOM* is hamper

253 To this end we have used ultrafast transient absorbance spectroscopy, to define heme-heme electron tr

254 ration microscopy, and femtosecond transient absorbance spectroscopy.

255 ive inhibition experiments; fluorescence and absorbance spectroscopy; circular dichroism; and electro

256 ncing, subcellular fractionation, and atomic absorbance spectroscopy] and report a previously unappre

257 ugation, leads to a >200 nm red-shift in the absorbance spectrum and injects a charge into a helical

258 individual vibrational bands within an FTIR absorbance spectrum by curve fitting, which leads to a v

259 are evident in the 550-750 nm region of the absorbance spectrum of [Os(bpy)(3)](2+), yet are poorly

260 This threshold, where absorbance starts to dominate the signal, exactly matche

261 ticity, as indicated by specific ultraviolet absorbance (SUVA), while Cu uptake rate constants of bot

262 muM), DOM aromaticity (specific ultraviolet absorbance (SUVA254)), and Hg(II)-DOM and Hg(II)-DOM-sul

263 llows us to determine the relative amount of absorbance that can be attributed to each species in ord

264 cattering that depends on morphology and not absorbance that largely depends on the volume of materia

265 ption path length can give rise to such high absorbance that the sample becomes opaque around the tra

266 and the localized surface plasmon resonance absorbance through the sample was measured after exposur

267 The absorbance titration of 1 with CN(-) revealed a new band

268 pH determinations from sulfonephthalein dye absorbances) to the shipboard absorbance data, we fit th

269 on optical assays, such as luminescence and absorbance, to probe the viability of the bacteria.

270 For intervention homes, absorbance-to-mass ratios suggest a higher proportion of

271 A low-absorbance transition formerly ignored in classical phot

272 ts with significant differences observed for absorbance, trapping, and electron transport.

273 lue observed were respectively of 41.8+/-0.8 Absorbance Unit (AU)/g oil and 254.3+/-5.8meq.O2/kg oil

274 then collected continuously and converted to absorbance units relative to the initial reference spect

275 uals were JCV antibody seropositive based on absorbance units.

276 electronic applications, the absorber yields absorbance up to ~ 70% even with the incidence obliquity

277 Bathochromic shifts were observed for both absorbance (up to 37 nm) and emission (up to 60 nm) in d

278 Ps-ALD) were analyzed by ultraviolet-visible absorbance (UV-vis) spectrophotometer, Attenuated total

279 measurements, we examine fluorescence, X-ray absorbance, UV/vis, and IR spectra, complex refractive i

280 The absorbance value of oxidized TMB is linearly associated

281 Applying a calculated optimal cut-off absorbance-value of 2.1, differentiated S. pneumoniae fr

282 iodictyol, luteolin, and quercetin increased absorbance values (without substrate) in the DNS assay a

283 public interfering substances had no obvious absorbance values and it was less than 0.1.

284 mide content has a positive correlation with absorbance values at OD294 and OD420 but a negative corr

285 Infrared absorbance values of the different spectral bands, hiera

286 ar discriminant analysis based on 8 selected absorbance values, concentrated near 279, 305 and 328nm,

287 ons of intact PSA yielded higher immunoassay absorbance values, even between lots from the same manuf

288 f 440-540 nm, whereas for S. retifer maximum absorbance was 488 +/- 3 nm with the same absorbance ran

289 With no metal ions, lambdamax and absorbance was greatest for cyanidin with diacylation>mo

290 Absorbance was measured at 510 nm.

291 Upon ozonation, a decrease in DOM absorbance was observed in parallel with an increase in

292 S-SDME procedure, and the analytical signal (absorbance) was monitored online during the extraction p

293 Notable exceptions are the higher UV/visible absorbance wavelength dependence (Angstrom coefficients)

294 xplain the bathochromic shift in the maximal absorbance wavelength when CR is bound to amyloids.

295 bsorbance spectra have been plotted and peak absorbance wavelengths have been extracted for each conc

296 ments of fine particulate matter (PM2.5) and absorbance were conducted in cooking areas, village cent

297 Fast imaging (several characteristic absorbances were selected for every substance of interes

298 tion to a spectral region with greater water absorbance, which results in greater heating-induced sig

299 e Er-PVDF film due to its excellent infrared absorbance, which, leads to rapid and large temperature

300 des, that allows the accurate measurement of absorbance within individual pL-volume droplets moving w