ライフサイエンスコーパス: visible absorption

1 gas chromatography-mass spectrometry, and UV-visible absorption.

2 ore that exhibits force-dependent changes in visible absorption.

3 m peroxidase-mediated oxidation based on its visible absorption.

4 ing experiments, but remain limited by their visible absorption.

5 , are stable in aqueous solution with strong visible absorption.

6 to explore other metal clusters with broader visible absorption.

7 lting" of opal films even in the absence of "visible" absorption.

8 no-naphthalene-1-sulfonic acid fluorescence, visible absorption, activity, and differential scanning

9 l and spectroscopic techniques, including UV-visible absorption and 57Fe Mossbauer spectroscopies, ha

10 ers can be produced at 20 degrees C and have visible absorption and CD spectra identical to the dimer

11 Visible absorption and CD spectra suggest the cobalt exi

12 Cluster transfer reactions, monitored by UV-visible absorption and CD spectroscopy, showed that a [4

13 UV-visible absorption and CD, resonance Raman, EPR, ENDOR,

14 Enzyme kinetics coupled to UV/visible absorption and electron paramagnetic resonance (

15 center in azurin has been investigated by UV-visible absorption and electron paramagnetic resonance s

16 Using ultraviolet-visible absorption and electron paramagnetic resonance s

17 a characteristic bathochromic shift of their visible absorption and emission bands by ca. 200 nm comp

18 ay absorption spectroscopy, together with UV-visible absorption and emission spectroscopy, indicates

19 , cyclic voltammetry, 1H and 19F NMR, and UV visible absorption and emission spectroscopy.

20 e electrochemical scan cycles as shown by UV-visible absorption and energy dispersive X-ray spectrosc

21 ned stopped-flow injection device to collect visible absorption and fluorescence EEM spectra of react

22 action can be combined with high-pressure UV-visible absorption and fluorescence emission spectroscop

23 Besides, the UV/visible absorption and fluorescence properties of the en

24 a and 1s were investigated using ultraviolet-visible absorption and fluorescence spectroscopies, cycl

25 Stopped-flow UV-visible absorption and freeze-quench Mossbauer experimen

26 dialysate and retentate were analyzed by UV-visible absorption and high-resolution Orbitrap mass spe

27 fraction, cyclic voltammetry and NMR, and UV-visible absorption and low-temperature luminescence spec

28 0-100%) have been studied by steady state UV/visible absorption and luminescence spectroscopic method

29 litting parameters, respectively) and the UV-visible absorption and magnetic CD spectra are dominated

30 UV-visible absorption and magnetic circular dichroism (MCD)

31 The UV--visible absorption and magnetic circular dichroism spect

32 d II) or Compound ES] is characterized by UV-visible absorption and magnetic circular dichroism spect

33 Visible absorption and multipeaked fluorescence excitati

34 smission Electron Microscopy (TEM), FTIR, UV-Visible absorption and Photoluminiscence (PL) techniques

35 UV-visible absorption and powder X-ray diffraction measurem

36 Using stopped-flow UV/visible absorption and rapid freeze-quench electron para

37 The visible absorption and resonance Raman spectroscopic pro

38 d a [Fe(4)S(4)](2+,+) cluster as shown by UV-visible absorption and resonance Raman studies of the ox

39 atic polycyclic compounds resulted in strong visible absorption and sharp fluorescence with efficient

40 Characterization with ultraviolet visible absorption and ultraviolet resonance Raman spect

41 -reduced samples using the combination of UV-visible absorption and variable-temperature magnetic cir

42 -modified forms, using the combination of UV-visible absorption and variable-temperature magnetic cir

43 UV/visible absorption and VTMCD studies facilitate resoluti

44 itration in proteins was detected by UV/Vis (visible) absorption and Western blot analysis.

45 03 mm/s, DeltaE(Q) = 0.58 +/- 0.03 mm/s), UV-visible absorption, and circular dichroism studies of th

46 g high-performance liquid chromatography, UV-visible absorption, and electron spin resonance spectros

47 ctron microscopy (HRTEM), zeta potential, UV-visible absorption, and photoluminescence spectroscopy.

48 R, resonance Raman, Fourier transform IR, UV-visible absorption, and variable-temperature variable-fi

49 nsitions and accompanying blue-shifts of the visible absorptions, as the ligand pi-systems are extend

50 21G azurin resulted in a species with strong visible absorptions at 350 and 452 nm and a relatively l

51 and we show this species to have a distinct visible absorption band and a transition moment that we

52 A new visible absorption band appears in the presence of polar

53 For one of the anionic guests, a visible absorption band appears upon host-guest formatio

54 ads to a decrease in the magnitude of the UV-visible absorption band at approximately 400 nm that we

55 However, the visible absorption band does not match that of the monom

56 eaction is observed upon excitation into the visible absorption band of ethidium, higher-energy irrad

57 y toward p-nitrophenyl phosphate, exhibits a visible absorption band with lambda(max) at 570 nm.

58 7% of the observed spectral evolution in the visible absorption bands and 4% in the MORD.

59 and others lead to a model in which the two visible absorption bands correspond to GFP in two ground

60 The observed UV-visible absorption bands for the Fe(3+)-nitrile intermed

61 ts bathochromic shifts in both the Soret and visible absorption bands in the presence of Cc and an ab

62 e effect of nonplanar deformations on the UV-visible absorption bands is then probed experimentally w

63 contrast, time-resolved perturbations of the visible absorption bands of L29F and V68L deoxyMb genera

64 iew that the large red shifts seen in the UV-visible absorption bands of peripherally crowded nonplan

65 d or Co 3d --> corrin pi* transitions and by visible absorption bands similar to the corrin pi-->pi*

66 n the cytochrome Soret (gamma) and Q (alpha) visible absorption bands, respectively.

67 t a qualitative picture of the origin of the visible absorption based on molecular orbital perturbati

68 he switched state as indicated by an intense visible absorption (ca. 530 nm) and near-infrared (ca. 1

69 In this work, resonance Raman and UV-visible absorption/CD spectroscopies and MS were used to

70 +) cluster per homodimer as determined by UV-visible absorption/CD, resonance Raman and EPR spectrosc

71 uestions, in vitro spectroscopic studies (UV-visible absorption/CD, resonance Raman and Mossbauer) ha

72 6-N2 dihedral angle could be consistent with visible absorption changes and the chemical shift differ

73 re quantitated by simultaneous monitoring of visible absorption changes in the protein film.

74 We compared femtosecond transient visible absorption changes of normal, white-light (WL)-g

75 ist at C5 could satisfy the observed NMR and visible absorption changes.

76 was quantitated by simultaneously monitoring visible absorption changes.

77 sfolding of the opsins as observed by the UV/visible absorption characteristics and by separation of

78 catechuate 3,4-dioxygenase (3,4-PCD) with UV/visible absorption, circular dichroism (CD), magnetic CD

79 Visible absorption, circular dichroism, and electron par

80 Visible absorption, circular dichroism, and fluorescent

81 d forms have been characterized using the UV-visible absorption, circular dichroism, and variable-tem

82 Using elemental analysis and UV-visible absorption, circular dichroism, EXAFS, Mossbauer

83 In this study, UV-visible absorption, circular dichroism, resonance Raman

84 -anilinonaphthalene-1-sulfonic acid binding, visible absorption, copper content, and oxidase activity

85 ing a five points regression graph of the UV-visible absorption data collected at the wavelength of m

86 iquid chromatography (HPLC) with ultraviolet-visible absorption detection and tandem mass spectrometr

87 chromatograms generated with conventional UV-visible absorption detectors.

88 We show that the shift of the main visible absorption edge does not constrain the point of

89 UV-visible absorption, electron paramagnetic resonance, and

90 behavior as identified and quantified via UV-visible absorption, emission, (1)H DOSY, and NMR spectro

91 Combining UV-visible absorption, EPR, and enzyme activity measurement

92 ctively coupled plasma mass spectrometry, UV-visible absorption, EPR, and Mossbauer spectroscopies, w

93 esults, in combination with complementary UV-visible absorption, EPR, and resonance Raman spectroscop

94 Analyses using UV-visible absorption, far-UV circular dichroism, and EPR s

95 The metal ion content coupled with the visible absorption feature is compatible with the presen

96 e transfer states to create multiple intense visible absorption features and the ability to fine-tune

97 transition of the solvent and the absence of visible absorption features associated with the Mn(II)2

98 edox properties were examined by ultraviolet-visible absorption, fluorescence, and cyclic voltammetri

99 and subunit size, amino-acid composition, UV-visible absorption, heme content, pH optimum, inhibitor

100 esonance, mass spectrometry, and ultraviolet-visible absorption identify the enhancer as lumichrome,

101 ow these results may relate to the origin of visible absorption in (Ga(1-x)Zn(x))(N(1-x)O(x)) and its

102 This product was characterized by visible absorption, infrared absorption, and mass and NM

103 We also find that the strength of the visible absorption is comparable to that of direct band

104 The visible absorption is determined to be dependent on mixi

105 In this work, we present visible absorption, light-scattering, and resonance Rama

106 he self-assembly of these molecules using UV/visible absorption, luminescence, and circular dichroism

107 The UV-visible absorption, magnetic circular dichroism (MCD) an

108 mparison with that of wild-type nNOS with UV-visible absorption, magnetic circular dichroism, and ele

109 BPR, respectively), on the basis of both the visible absorption maxima (530 versus 490 nm) and photoc

110 visible spectra suggested by the shift in UV-visible absorption maxima that correspond with a rise in

111 varying degrees of blue-shift in the flavin visible absorption maxima while visible CD spectra of th

112 rameters obtained from the wavelengths of UV/Visible absorption maxima with solute H-bond parameters

113 S oxygenase domain thus prepared exhibits UV-visible absorption (maxima at 419 and 553 nm, shoulder a

114 a slow light inactivation and a red-shifted visible absorption maximum as compared with the more ext

115 Transient infrared and visible absorption measurements along with density funct

116 ich are in excellent agreement with previous visible absorption measurements, showing the molecular m

117 found for the mutant D76N, in agreement with visible absorption measurements.

118 scaffold protein has been demonstrated by UV-visible absorption, Mossbauer, and resonance Raman spect

119 tical and spectroscopic methods including UV-visible absorption, Mossbauer, EPR, and HYSCORE spectros

120 ereof were shown to effectively modulate the visible absorption of anthocyanins from strawberry (Frag

121 ipates in proton transfers and regulates the visible absorption of bacteriorhodopsin and its photoint

122 UV-visible absorption of f-HupS has bands approximately 340

123 Under these circumstances, the visible absorption of K is expected to be more red-shift

124 EPR and UV-visible absorption of purified recombinant human ferroch

125 by direct observation of the characteristic visible absorption of the oxidized and inhibited states.

126 imately 1 micros) excited-state lifetime and visible absorption of the sensor simplifies measurements

127 tride (InN) nanocrystals that exhibit both a visible absorption onset ( approximately 1.8 eV) and a s

128 DNA precipitated is accurately determined by visible absorption or fluorescence spectroscopic analyse

129 in reduction was measured either directly by visible absorption or indirectly by coupling ferredoxin

130 ted at 85 degreesC for 2 h, as judged by its visible absorption properties.

131 rge-transfer interactions also determine the visible absorption properties.

132 We demonstrate with UV-visible absorption, resonance Raman, and magnetic circul

133 The two [4Fe-4S]2+ clusters have similar UV-visible absorption, resonance Raman, and Mossbauer prope

134 een investigated using the combination of UV-visible absorption, resonance Raman, and Mossbauer spect

135 Using UV-visible absorption, resonance Raman, and stopped-flow sp

136 Transient visible absorption reveals a high yield of the formation

137 This combination of strong broadband visible absorption, sharp near-infrared emission, and lo

138 The time-resolved infrared (TRIR) and visible absorption spectra (TA) of 1 following excitatio

139 upported by monitoring changes in XRD and UV/Visible absorption spectra across a range of infiltratio

140 Here we present ultraviolet-visible absorption spectra and cross-sections of HgCl, H

141 la: see text] transition peak of ultraviolet-visible absorption spectra and exhibit inherent magnetic

142 The elution profile, visible absorption spectra and mass spectra were compare

143 Their visible absorption spectra are dominated by intense pi -

144 The differences in visible absorption spectra between the most common grape

145 UV-Visible absorption spectra demonstrate distinct optical

146 ctroelectrochemical measurements afforded UV-visible absorption spectra for both the radical cations

147 Kinetic analysis and UV-visible absorption spectra indicate that the ability of

148 UV-visible absorption spectra indicated that the catalase i

149 ces, core volumes, (57)Fe isomer shifts, and visible absorption spectra make evident the high degree

150 The UV-visible absorption spectra obtained from freshly purifie

151 The static ultraviolet-visible absorption spectra of holo-EAL and ternary compl

152 room temperature was determined from the UV/visible absorption spectra of several pH indicators.

153 The visible absorption spectra of such strains indicate a hi

154 ation that is clearly evident in the EPR and visible absorption spectra of the protein and suggests t

155 ured electrochemical redox potentials and UV-visible absorption spectra reveal little or no ground-st

156 In addition, the UV-visible absorption spectra show a maximum at 258 nm.

157 Resonance Raman and UV-visible absorption spectra show that nickel(II) microper

158 EPR and UV-visible absorption spectra show that protonation of the

159 Indeed, the visible absorption spectra show the photoinduced reducti

160 Mn(III)SOD from Thermus thermophilus and by visible absorption spectra showing that azide binding to

161 These both had ultraviolet-visible absorption spectra similar to milk xanthine oxid

162 d Schiff base, and the pH-independence of UV-visible absorption spectra suggests that the protonated

163 re biologically benign portion of the flavin visible absorption spectra that has not previously been

164 The change in the UV--visible absorption spectra upon modification indicated t

165 to contain [2Fe-2S] clusters of which the UV-visible absorption spectra were identical to that of the

166 homolog purified as a homodimer, and the UV-visible absorption spectra were nearly identical to that

167 UV-visible absorption spectra were obtained for the oxidize

168 PP, however, TCPP aggregates below pH 1 have visible absorption spectra which depend on the counterio

169 rhodopsin by the following criteria: (i) UV-visible absorption spectra, (ii) the formation of metarh

170 ncreased rhombicity evident from its EPR and visible absorption spectra, and an increase in distance

171 The molecular masses, UV-visible absorption spectra, and cofactor contents of the

172 thalene-reacted ISPNAP gave almost identical visible absorption spectra.

173 e site and resulted in significantly shifted visible absorption spectra.

174 Visible-absorption spectra of purified recombinant TcAPx

175 Partition binding and visible absorption spectral measurements on the gel were

176 The ultraviolet-visible absorption spectrometry (UV-vis), transmission e

177 n both crystal and solution using EPR and UV-visible absorption spectrometry as a function of tempera

178 scopy, electron impact mass spectroscopy, UV visible absorption spectrometry, GC and high pressure li

179 nce liquid chromatography (HPLC)-ultraviolet/visible absorption spectrophotometry (UV/Vis)-mass spect

180 Browning was monitored by UV-visible absorption spectrophotometry and UHPLC-DAD.

181 ed by HRTEM, SEM, XRD, EDX, fluorescence, UV-Visible absorption spectrophotometry, and FTIR.

182 voltammetry, atomic force microscopy, and UV-visible absorption spectrophotometry.

183 oteins also makes it possible to observe its visible absorption spectroscopic features more clearly.

184 r confirmed by site-directed mutagenesis and visible absorption spectroscopic studies.

185 Femtosecond transient IR and visible absorption spectroscopies have been employed to

186 onal theory, nuclear magnetic resonance, and visible absorption spectroscopies provide valuable insig

187 Here we report Stark and visible absorption spectroscopies that interrogate the F

188 From X-ray absorption, EPR, and UV/visible absorption spectroscopies, we have shown that al

189 etic parameters with the aid of (1)H NMR and visible absorption spectroscopies.

190 ant visible light absorption was shown by UV-visible absorption spectroscopy (UV-Vis), which confirme

191 EM), X-ray diffraction (XRD) and ultraviolet-visible absorption spectroscopy (UV-vis).

192 UV-visible absorption spectroscopy also revealed the presen

193 oscopy (TEM) was used in conjunction with UV-visible absorption spectroscopy and DLS to identify the

194 d from purified NirS and characterized by UV-visible absorption spectroscopy and finally identified b

195 ted with pH-dependent resonance Raman and UV-visible absorption spectroscopy and molecular mechanics

196 the acrylic double bond, as indicated by UV-visible absorption spectroscopy and resonance Raman spec

197 Finally, visible absorption spectroscopy and small-angle X-ray sc

198 UV-visible absorption spectroscopy and transmission electro

199 inic acid in n-dodecane have been studied by visible absorption spectroscopy and X-ray absorption fin

200 Exponential fits of stopped-flow UV-visible absorption spectroscopy data supported multiple-

201 by 1H and 19F NMR for 4 and by 1H NMR and UV-visible absorption spectroscopy for 3.

202 first excited singlet state is confirmed by visible absorption spectroscopy in an argon matrix at 20

203 ymes with magnetic circular dichroism and UV-visible absorption spectroscopy in order to determine th

204 ) nanocrystal formation was studied using UV-visible absorption spectroscopy integrated with an autom

205 UV-visible absorption spectroscopy of both human and murine

206 e photoproduct dynamics by using ultraviolet-visible absorption spectroscopy on the 10(-7)-10(-1) s t

207 UV-visible absorption spectroscopy reveals enantiomer sensi

208 UV/visible absorption spectroscopy showed that the pKa is >

209 UV-visible absorption spectroscopy shows two prominent abso

210 extraction followed by HPLC analysis and UV-visible absorption spectroscopy support the above model

211 In this report, using visible absorption spectroscopy we show that the electro

212 e exclusion chromatography, (1)H NMR, and UV/visible absorption spectroscopy with cobalt(II) as a spe

213 ated the feasibility of coupling ultraviolet-visible absorption spectroscopy with MS by using the met

214 ingle-crystal x-ray diffraction, ultraviolet-visible absorption spectroscopy, and scanning electron m

215 R) spectroscopy, X-ray diffraction (XRD), UV-visible absorption spectroscopy, Fluorescence emission s

216 With the aid of UV-visible absorption spectroscopy, fluorescence spectrosco

217 This compound was characterized by visible absorption spectroscopy, infrared spectroscopy,

218 orm IR difference spectroscopy combined with visible absorption spectroscopy, isotope labeling, and e

219 By combining HP-SANS and HP-ultraviolet/visible absorption spectroscopy, our strategy highlights

220 yl)porphyrins have been investigated with UV-visible absorption spectroscopy, resonance Raman spectro

221 Characterization with ultraviolet-visible absorption spectroscopy, solid-state nuclear mag

222 compared against gravimetric analysis and UV-visible absorption spectroscopy, spICP-MS quantification

223 The nanocrystals are characterized using UV-visible absorption spectroscopy, transmission electron m

224 neutron scattering (SANS) and HP-ultraviolet/visible absorption spectroscopy, we report the specific

225 fluorescence microscopy, fluorescence and UV-visible absorption spectroscopy, zeta potential analysis

226 xidase has been investigated by Raman and UV-visible absorption spectroscopy.

227 mine, and tyramine was carried out, using UV-visible absorption spectroscopy.

228 etal binding site and probed by EXAFS and UV-visible absorption spectroscopy.

229 rystal lattice is confirmed by time-resolved visible absorption spectroscopy.

230 otoactivity are determined using ultraviolet-visible absorption spectroscopy.

231 of the modified HBC were investigated by UV/visible absorption spectroscopy.

232 nant human CBS by static and stopped-flow UV-visible absorption spectroscopy.

233 as A2E levels were quantified by HPLC and UV-visible absorption spectroscopy.

234 cale at 295 K by using transient ultraviolet-visible absorption spectroscopy.

235 gives rise to a shoulder at 391 nm in the UV/visible absorption spectrum and indicates that the hydro

236 of SRFA in the dialysate had a different UV-visible absorption spectrum and was enriched in low mole

237 litatively similar perturbations of the MTOX visible absorption spectrum are observed for complexes f

238 Co-TrzN showed a visible absorption spectrum characteristic of other memb

239 This double mutant had a UV-visible absorption spectrum consistent with a protonated

240 environmental sensitivity of quercetin's UV-visible absorption spectrum gave information about querc

241 The visible absorption spectrum in solution is characteristi

242 The peak of the excited-state visible absorption spectrum is shifted to ca. 490 nm, an

243 ATATGGCCATATAT)] have been examined by using visible absorption spectrum methods.

244 n of the DHOase secondary structure, but the visible absorption spectrum of a Co(2+)-substituted DHOa

245 The PAS instrument is used to measure the UV-visible absorption spectrum of ambient aerosol demonstra

246 The ultraviolet/visible absorption spectrum of E.NAD+ from denaturation-

247 The visible absorption spectrum of FeIIMb-CN has a split alp

248 In addition, the UV-visible absorption spectrum of H77Y Fe(II) CooA without

249 We also report that the maximum of the visible absorption spectrum of human MnSOD (epsilon480 =

250 the UV-visible absorption spectrum of L-Arg-bound ferric full l

251 h a positively charged Arg did not shift the visible absorption spectrum of PR.

252 llamine (SNAP), indicate a rapid loss of the visible absorption spectrum of the [2Fe-2S] cluster.

253 The visible absorption spectrum of the cobalt(II) complex is

254 ed by a bathochromically shifted band in the visible absorption spectrum of the DASA.

255 This yields a significant change in the visible absorption spectrum of the film, with a decrease

256 alently attached to the polypeptide, and the visible absorption spectrum of the mutant protein is ide

257 The dependence of the visible absorption spectrum of the oxy-ferrous complex o

258 sfer (PT*) products by the difference in the visible absorption spectrum of the species emerging from

259 The visible absorption spectrum of this intermediate closely

260 The visible absorption spectrum of W161F MnSOD in the inhibi

261 The UV-visible absorption spectrum reveals that the mutation of

262 mol of S (2-) per ApbC monomer and had a UV-visible absorption spectrum similar to known [4Fe-4S] cl

263 n of the C9-linked perylene wire) exhibits a visible absorption spectrum that is the sum of the spect

264 Levenberg-Marquardt algorithm fitting of UV-visible absorption spectrum to calculate the precise con

265 rified N-terminal domain has an identical UV/visible absorption spectrum to the wild-type protein and

266 Q143N MnSOD lacked the visible absorption spectrum typical of wild-type Mn(III)

267 The UV-visible absorption spectrum was characteristic of iron-s

268 chromatography (HPTLC) and a characteristic visible absorption spectrum with a peak near 450 nm.

269 ectrum of the chromophores was compared with visible absorption spectrum, and both were deconvoluted.

270 concentrations is in agreement with CPO-II's visible absorption spectrum, which shows no change over

271 UV-visible absorption, steady-state, and time-resolved fluo

272 ibit intense metal-to-ligand charge-transfer visible absorptions that are red-shifted and more intens

273 buted to the broad, high oscillator strength visible absorption, the ordered molecular packing, and a

274 Further, we investigate the nature of this visible absorption using electron attachment/detachment

275 were investigated using a combination of UV-visible absorption, variable temperature magnetic circul

276 results, taken together with the previous UV-visible absorption, variable temperature magnetic circul

277 ty of methods including electrochemistry, UV-visible absorption, variable temperature photoluminescen

278 e been investigated by the combination of UV/visible absorption, variable-temperature magnetic circul

279 Visible absorption, visible circular dichroism, and elec

280 The UV-visible absorption, X- and Q-band EPR, and Cu EXAFS spec