ライフサイエンスコーパス: absorbance

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

2 xides (NOx), particulate matter (PM) mass or absorbance).

3 constants in natural waters of any depth and absorbance.

4 a sample and its corresponding RGB-resolved absorbance.

5 emically, and to the loss of DOM ultraviolet absorbance.

6 ble oxide semiconductor with strong infrared absorbance.

7 rface, which resulted in changes in the LSPR absorbance.

8 ple and therefore increase the corresponding absorbance.

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

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

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

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

13 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));

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

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

16 The cell acts as a nonlinear absorbance amplifier, improving both the limit of detect

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

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

19 hifted SPR along with continuous increase in absorbance and also through AFM.

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

21 -p38/JNK, TNFalpha, Caspase-8, mitochondrial absorbance and Cyt-c were all similar in Lac + Hyd and M

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

23 xclusion chromatography, in combination with absorbance and emission matrix fluorometry, was applied

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

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

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

27 Absorbance and fluorescence measurement confirmed the oc

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

29 Absorbance and fluorescence spectral shape were largely

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

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

32 lsification and characterized in solution by absorbance and fluorescence spectroscopy.

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 Other parameters such as pH, temperature, UV-absorbance and free chlorine were measured concurrently,

37 was accompanied by decreases in specific UV absorbance and increases in the E2/E3 ratio (254 nm abso

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

39 re associated with total trihalomethanes, UV-absorbance and pH.

40 The influence of absorbance and reactivity has critical consequences for

41 howed improved solubility, as measured by UV absorbance and reverse-phase HPLC experiments.

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

43 nce regardless of mirror reflectivity or the absorbance and show that in the limit of high reflectivi

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 l measurements, such as specific ultraviolet absorbance at 254 nm (SUVA254), show promise for use as

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

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

52 Sulphur dioxide (SO2) proved to increase absorbance at 280 nm of grape skin and seed extracts con

53 Additional absorbance at 280 nm was also observed in acetone:H2O ex

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

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

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

57 UHPLC-UV-MS(E) information (retention time, absorbance at 450 nm, and accurate masses of precursors

58 cavity ring-down measurements of gaseous NO absorbance at 5.2 mum.

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

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

61 Absorbance at 600 nm, particle size, and zeta potential

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

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

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

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

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

67 The small size of GAF-FP and its additional absorbance band in the violet range has allowed for desi

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

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

70 ffold exhibiting two spectrally resolved NIR absorbance bands which correspond to the 2-picolinic est

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

72 dent light in the broadband spectrum and the absorbance by Si nanocone arrays is higher than 95% over

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

74 aces that display near-ideal electromagnetic absorbance can be tuned from the visible into the mid-in

75 roadband absorbance of samples (RGB-resolved absorbance) can be calculated using the RGB color values

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

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

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

79 for Malbec GPE determined by oxygen radical absorbance capacity (ORAC) assay was 2,756 mumol TEg(-1)

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

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

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

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

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

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

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

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

88 Oxygen radical absorbance capacity (ORAC) values of selected short chai

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

90 ing antioxidant power (FRAP), oxygen radical absorbance capacity (ORAC), total phenolic content (TPC)

91 residue contributes to a high oxygen radical absorbance capacity (ORAC).

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

93 antioxidant power (FRAP) and Oxygen radical absorbance capacity (ORAC)] and antioxidant groups: phen

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

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

96 ts were evaluated by using an oxygen radical absorbance capacity method (ORAC).

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

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

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

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

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

102 Here, we have recorded transient absorbance changes of ChR2 from Chlamydomonas reinhardti

103 pth of metals and employing the natural bulk absorbance characteristics of the semiconductors in thos

104 Plastics with defined absorbance characteristics provided protection with this

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

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

107 r that permitted the acquisition of accurate absorbance data in suspensions of cells that scattered l

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

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

110 and by the 2D correlation analysis of FT-IR absorbance data, we were able to identify a common sudde

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

117 lary (MWC) was developed for ultra-sensitive absorbance detection.

118 nce and increases in the E2/E3 ratio (254 nm absorbance divided by that at 365 nm).

119 Hence, an absorbance drop at 528 nm gives evidence of the co-local

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

121 These probes had absorbance/emission maxima ranging from 367/454 to 546/5

122 r a given amount of dye with and without the absorbance-enhancing inserts in the wells.

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

124 decreased peroxide and iodine values, and UV absorbance extinction coefficients, of the oil.

125 difficult to detect, owing to the lack of UV absorbance, fluorescence, or facile ionization.

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

127 data collected at the wavelength of maximum absorbance for each analyte.

128 Interestingly, the ratio of absorbance for these two bands is found to be extremely

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

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

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

132 red resistive losses with the useful optical absorbance in the active semiconductors.

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

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

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

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

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

138 accumulation of P700(+*) was followed by the absorbance increase at 826 nm.

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

140 We attribute such a drastic absorbance increase to ground-state ligand/QD orbital mi

141 fferent time points to measure mitochondrial absorbance, infarct size, serum markers and apoptotic in

142 silico and experimental evidence support the absorbance-inhibition mechanism proposed for KHI binding

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

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

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

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

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

148 Fatty sample absorbance is easily followed by the absorption band of

149 For opaque pillars, we show that absorbance is linearly related to platinum concentration

150 High absorbance is maintained over a wide incident angle rang

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

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

153 in the limit of high reflectivities and low absorbances it predicts the same numerical values as tha

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

155 exposure increased the wavelength of maximum absorbance (lambdamax ) of the rod and the medium (M, gr

156 ck carbon, using a temporally adjusted PM2.5 absorbance land use regression (LUR) model.

157 leads to a broadband increase of the optical absorbance larger than 300% for colloidal PbS QDs also a

158 ution, excellent band separation between the absorbance maxima of (E)- and (Z)-isomers in the UV or v

159 01[FeO2](2+) Judging by the appearance of an absorbance maximum at 440 nm, we conclude that CYP101[Fe

160 HPLC of underivatized nectar and showed a UV absorbance maximum of 258 nm.

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

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

163 the labeled metabolites and ultraviolet (UV) absorbance measurement using a microplate reader.

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

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

166 By combining absorbance measurements with flow cytometry, we quantifi

167 with time), much more sensitive than single absorbance measurements, allowed for direct and fast tox

168 ation step to remove latex aggregates before absorbance measurements, eliminating aggregate interfere

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

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

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

172 ods with two possible configurations as high-absorbance nanomaterials from various gold multipods usi

173 .5, PM10, and PMcoarse, respectively); PM2.5 absorbance; nitrogen oxides (NO2 and NOx); traffic inten

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

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

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

177 ate in the extracellular region, the maximum absorbance of BR proteins shifts markedly to the longer

178 The UV absorbance of browning products of immature kumquat drie

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 f DPPH. by polyphenols, and on the change in absorbance of DPPH. when reduced/oxidised.

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

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

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

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

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

187 extend the spectral region up to 750 nm for absorbance of light that drives photochemistry.

188 High absorbance of melanin suppresses multiple scattering, ca

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

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

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

192 The absorbance of quercetin autooxidation products at 320nm

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

194 The broadband absorbance of samples (RGB-resolved absorbance) can be c

195 ral laboratories for parallel measurement of absorbance of samples can be replaced by photometers bas

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

197 neath the skin, owing to hemoglobin-specific absorbance of the light.

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

199 Spectral absorbance of the photoreceptor cells in these sharks re

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

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

202 w trout, zebrafish, and killifish and on the absorbance of visual pigments in rainbow trout and zebra

203 colored DMPD(+) radical cation, the optical absorbance of which was measured at a wavelength of 554

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

205 Intensities and absorbances of red, green and blue (RGB) were obtained w

206 ability to perform accurate measurements of absorbance on liquid samples, in parallel and at low cos

207 ide for evaluation of forthcoming commercial absorbance optics.

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

209 ticles, where dimensions are used to control absorbance or emission.

210 different analytical methodologies based on absorbance or fluorescence measurements were used to dem

211 form) that is measured by changes in either absorbance or fluorescence.

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

213 ation PTL, L-MAG0460, to have a favorable 2P absorbance peak at 850 nm, enabling efficient 2P activat

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

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

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

217 displayed highly bathochromic and broadened absorbance profiles spanning 400-900 nm with molar absor

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

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

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

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

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

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

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

225 The hundreds of absorbance readings collected simultaneously for hundred

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

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

228 We develop the general expression for absorbance regardless of mirror reflectivity or the abso

229 ence intensity and by shifts in the broad IR absorbance region for electron trap sites, which is also

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

231 advances will result from synthesizing high-absorbance resist materials using heavier atoms.

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

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

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

235 uch as depth, solar irradiance, water matrix absorbance, singlet oxygen concentration, and the virus-

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

237 Absorbance spectra have been plotted and peak absorbance

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

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

240 ents after charge screening led to different absorbance spectra, despite the identical electronic pro

241 of solid-state structures and EPR, NMR, and absorbance spectra.

242 UV absorbance spectrophotometry is widely used for the quan

243 to nanosecond transient infrared and visible absorbance spectroscopy afforded direct observation of i

244 Further analysis by absorbance spectroscopy and hemin-agarose pulldown assay

245 Pressurized absorbance spectroscopy is used to characterize their me

246 ue and transparent pillars can be applied to absorbance spectroscopy of high absorptivity, microliter

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

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

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

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

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

252 roduct or can be quantified using UV-visible absorbance spectroscopy.

253 ration microscopy, and femtosecond transient absorbance spectroscopy.

254 anthocyanins were identified by means of the absorbance spectrum and fragmentation pattern by tandem

255 shes a well-defined relationship between the absorbance spectrum of a sample and its corresponding RG

256 ity, but the exponential slope of the UV-vis absorbance spectrum was a better surrogate for molecular

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

258 rties of NOM, including specific ultraviolet absorbance (SUVA), aromatic and carbonyl carbon contents

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

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

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

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

263 um(2), owing to the enhanced broadband light absorbance through strong plasmonic resonances in the ab

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

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

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

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

268 A low-absorbance transition formerly ignored in classical phot

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

270 ng LDL samples, the sigmoidal changes in the absorbance units vs. temperature curves corresponded wit

271 uals were JCV antibody seropositive based on absorbance units.

272 ne; and PLIN2 median [95% CI], 3.1 [2.4-3.7] absorbance units/mg creatinine) and the 720 patient scre

273 and PLIN2 median [95% CI], 37.8 [22.8-83.7] absorbance units/mg creatinine) than in the 80 healthy c

274 eatinine; and PLIN2 median [95% CI], 0 [0-0] absorbance units/mg creatinine).

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

276 The electrons are measured by their optical absorbance using a total internal reflection geometry.

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

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

279 demand and increased removal of effluent UV absorbance (UVA254), further establishing that ozone rea

280 gy coupling effect results in an increase in absorbance value at the plasmonic resonance wavelength.

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

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

283 different origins were compared to specific absorbance values measured according to the ISO Normativ

284 ement factor was calculated by comparing the absorbance values measured for a given amount of dye wit

285 n samples quantitated by GC and the specific absorbance values of safranal by the UV method did not c

286 Infrared absorbance values of the different spectral bands, hiera

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

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

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

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

291 Absorbance was measured at 510 nm.

292 ent or semitransparent pillars, the measured absorbance was successfully corrected for the fractional

293 e sigmoid/concentration at half value of the absorbance) was found to be the optimal parameter to rep

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

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

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

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

298 eir home and school exposure to PM2.5 filter absorbance, which is well-correlated with black carbon,

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

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

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