ライフサイエンスコーパス: fluorescence spectroscopy

1 on of different techniques (NMR, ESI-MS, and fluorescence spectroscopy).

2 ADPH cycle can be monitored in real time by fluorescence spectroscopy.

3 dband transient absorption and time-resolved fluorescence spectroscopy.

4 ino acids and their analysis by steady-state fluorescence spectroscopy.

5 , and calculate its loading efficiency using fluorescence spectroscopy.

6 onstituted channels and intrinsic tryptophan fluorescence spectroscopy.

7 n be enhanced by using synchronously scanned fluorescence spectroscopy.

8 ty to become molecular imaging agents, using fluorescence spectroscopy.

9 roscopy (cryo-TEM), UV-vis spectroscopy, and fluorescence spectroscopy.

10 y, with the use of conventional steady-state fluorescence spectroscopy.

11 characterized in solution by absorbance and fluorescence spectroscopy.

12 and a chlorophyllic compound) by front face fluorescence spectroscopy.

13 ranscripts could be followed in real time by fluorescence spectroscopy.

14 erties of selected examples were examined by fluorescence spectroscopy.

15 Binding experiments were conducted by fluorescence spectroscopy.

16 n in DMSO, enabling its selective sensing by fluorescence spectroscopy.

17 ulation was also confirmed by time-dependent fluorescence spectroscopy.

18 mapped this remodeling using single-molecule fluorescence spectroscopy.

19 in 6.9-12.8 ns, as measured by time-resolved fluorescence spectroscopy.

20 with N,N'-ethylenebis(iodoacetamide) and by fluorescence spectroscopy.

21 DNA cross-linking and photoreversibility via fluorescence spectroscopy.

22 TI)] with several experimental techniques of fluorescence spectroscopy.

23 rmaceutical, and this is usually measured by fluorescence spectroscopy.

24 performance characteristics of BSW-enhanced fluorescence spectroscopy.

25 roism, transmission electron microscopy, and fluorescence spectroscopy.

26 is as well as steady state and time-resolved fluorescence spectroscopy.

27 were further characterised using UV-Vis and fluorescence spectroscopy.

28 spheres were characterized by absorbance and fluorescence spectroscopy.

29 lmost exclusively on optical methods such as fluorescence spectroscopy.

30 ap and the cargo release was monitored using fluorescence spectroscopy.

31 ompounds were evaluated by potentiometry and fluorescence spectroscopy.

32 LUV) model biomembrane system was studied by fluorescence spectroscopy.

33 Ab1 binding to HT was measured by fluorescence spectroscopy.

34 red by both circular dichroism and intrinsic fluorescence spectroscopy.

35 calf thymus DNA is studied by time-resolved fluorescence spectroscopy.

36 l release were measured using UV/visible and fluorescence spectroscopy.

37 al residues fails to bind CaM as assessed by fluorescence spectroscopy.

38 tigated using steady-state and time-resolved fluorescence spectroscopy.

39 d 14-3-3 protein binding using time-resolved fluorescence spectroscopy.

40 rene groups at the chain ends was studied by fluorescence spectroscopy.

41 gated by cyclic voltammetry, absorption, and fluorescence spectroscopy.

42 gment (VCOP) in 0.1% dodecyl maltoside using fluorescence spectroscopy.

43 nalized particle content (cellular dose) via fluorescence spectroscopy.

44 lcium transients was examined using Fura-2AM fluorescence spectroscopy.

45 uantified by direct and tryptophan quenching fluorescence spectroscopy.

46 tigated using steady-state and time-resolved fluorescence spectroscopy.

47 ng electron paramagnetic resonance (EPR) and fluorescence spectroscopy.

48 teady-state and time-resolved absorption and fluorescence spectroscopy.

49 ut by Raman spectroscopy, TG-MS, UV/vis, and fluorescence spectroscopy.

50 onitor cleavage in real time by steady state fluorescence spectroscopy.

51 l properties were evaluated using UV-Vis and fluorescence spectroscopy.

52 were studied by using UV-Vis absorption and fluorescence spectroscopy.

53 inspired and validated using single-molecule fluorescence spectroscopy.

54 o Pimphales promelas using bile analysis via fluorescence spectroscopy.

55 ty around the TM3 C terminus as confirmed by fluorescence spectroscopy.

56 ata and identified interacting domains using fluorescence spectroscopy.

57 P3A4) by electron paramagnetic resonance and fluorescence spectroscopy.

58 uelva", were analyzed by excitation-emission fluorescence spectroscopy.

59 aureus were compared using minimal RNAs and fluorescence spectroscopy.

60 mass spectrometry (hydrophilic fraction) and fluorescence spectroscopy.

61 ay absorption spectroscopy and laser-induced fluorescence spectroscopy.

62 rized in vivo and in vitro by absorption and fluorescence spectroscopies.

63 gomers were studied by UV-vis absorption and fluorescence spectroscopies.

64 racterized by Fourier transform infrared and fluorescence spectroscopies.

65 jump coupled with time-resolved infrared and fluorescence spectroscopies.

66 mid-IR and visible transient absorption and fluorescence spectroscopies.

67 Two-dimensional fluorescence spectroscopy (2D FS) provides a non-invasiv

68 laser ablation plumes using two-dimensional fluorescence spectroscopy (2DFS).

69 opy is developed by combining 3D Micro X-ray Fluorescence Spectroscopy (3D Micro-XRF) and conventiona

70 angle geometry three-dimensional synchronous fluorescence spectroscopy (3D-SFS) for the differentiati

71 itu X-ray absorption (XRF/XANES), Raman, and fluorescence spectroscopy, along with imaging of Li(x)Ni

72 s different metal ions was investigated with fluorescence spectroscopy, amongst them Fe(3+) ions show

73 destabilize its structure utilizing NMR and fluorescence spectroscopies, analytical ultracentrifugat

74 usly characterized by circular dichroism and fluorescence spectroscopy, analytical ultracentrifugatio

75 ition was characterized using absorbance and fluorescence spectroscopies and high-resolution mass spe

76 e followed by steady-state and time-resolved fluorescence spectroscopy and by excitation spectra for

77 in buffered aqueous media by absorbance and fluorescence spectroscopy and by isothermal titration ca

78 e in an intact bacterium was demonstrated by fluorescence spectroscopy and checkerboard assays, the l

79 reactivity were evaluated by absorption and fluorescence spectroscopy and chlorination-based DBP for

80 nd SDBP-FP were quantified by absorption and fluorescence spectroscopy and chlorination-based DBP-FP

81 DOM was characterized by absorption and fluorescence spectroscopy and chlorination/chloraminatio

82 ronic properties was performed by UV-vis and fluorescence spectroscopy and cyclic voltammetry.

83 prepared and characterized using UV-vis and fluorescence spectroscopy and cyclic voltammetry.

84 in vitro using steady state and time domain fluorescence spectroscopy and density functional theory.

85 te nanoparticles (NaCas) at pH 7 and pH 2 by fluorescence spectroscopy and dynamic light scattering.

86 I (AnsA) and II (AnsB), which are shown via fluorescence spectroscopy and dynamics in combination wi

87 ted single-photon counting with steady-state fluorescence spectroscopy and femtosecond transient abso

88 Fluorescence spectroscopy and fluorescence quenching met

89 ng stations using excitation emission matrix fluorescence spectroscopy and further separated DOM into

90 e, and monitoring the recognition process by fluorescence spectroscopy and gel electrophoresis.

91 In this work, fluorescence spectroscopy and HPLC techniques were used

92 mal subunits, and tRNA using single-molecule fluorescence spectroscopy and identified multiple parall

93 ototautomerization reactions investigated by fluorescence spectroscopy and laser flash photolysis (LF

94 Fluorescence spectroscopy and lifetime imaging microscop

95 oups and aromatic side chains was studied by fluorescence spectroscopy and liposome leakage assays.

96 on by electron paramagnetic resonance (EPR), fluorescence spectroscopy and medical imaging.

97 Herein, using a combination of fluorescence spectroscopy and microscopy, we studied fou

98 Biochemical analysis using NMR, fluorescence spectroscopy and mutagenesis identified key

99 f the MPER sequence (residues 662-683) using fluorescence spectroscopy and oriented circular dichrois

100 strategy for the detection of methanol using fluorescence spectroscopy and photoelectrochemical (PEC)

101 rmined using cyclic voltammetry, UV/vis, and fluorescence spectroscopy and quantum chemistry.

102 Here, we combine kinetics assays using fluorescence spectroscopy and single actin filament obse

103 ce of dithiolthreitol is measured using both fluorescence spectroscopy and single droplet paper spray

104 he two proteins was also examined using both fluorescence spectroscopy and specific biochemical assay

105 combination with time-resolved laser-induced fluorescence spectroscopy and thermodynamic modeling, we

106 Here, we used single-molecule fluorescence spectroscopy and two-focus correlation spec

107 een C2alpha and phospholipid membranes using fluorescence spectroscopy and ultracentrifugation experi

108 Using electron microscopy coupled with fluorescence spectroscopy and X-Ray diffraction, we repo

109 (15)N, and (19)F NMR, electronic absorption, fluorescence spectroscopies, and first-principle calcula

110 eagents, peptide array analysis, chemotaxis, fluorescence spectroscopy, and circular dichroism, we pr

111 theory computations, gas sorption analysis, fluorescence spectroscopy, and cyclic voltammetry were e

112 tion-emission spectroscopy and time-resolved fluorescence spectroscopy, and demonstrate that autolumi

113 of thermodynamic parameters, absorption and fluorescence spectroscopy, and DNA recognition experimen

114 by NMR ((1)H, (11)B, and (13)C), IR, UV/vis, fluorescence spectroscopy, and high-resolution mass spec

115 ography (SD-OCT), infrared reflectance (IR), fluorescence spectroscopy, and histologic analysis.

116 small angle x-ray scattering, time-resolved fluorescence spectroscopy, and hydrogen-deuterium exchan

117 grammed domain deletion, expression, in vivo fluorescence spectroscopy, and in vitro reconstitution e

118 re we have combined NMR line shape analysis, fluorescence spectroscopy, and isothermal titration calo

119 was investigated by preparative photolyses, fluorescence spectroscopy, and laser flash photolysis (L

120 energy dispersive X-ray spectroscopy (EDS), fluorescence spectroscopy, and mass spectrometry, wherea

121 NMR spectroscopy, surface plasmon resonance, fluorescence spectroscopy, and molecular dynamics simula

122 on electron microscopy, UV-Vis spectroscopy, fluorescence spectroscopy, and NMR spectroscopy.

123 Using a systematic alanine scan approach, fluorescence spectroscopy, and other biophysical methods

124 Nuclear Overhauser effect analysis, fluorescence spectroscopy, and paramagnetic relaxation e

125 G-quadruplex folding by circular dichroism, fluorescence spectroscopy, and photodynamic techniques.

126 es in red wine were identified by Front-Face fluorescence spectroscopy, and the emission intensity tr

127 zed dendrimers were determined by UV/vis and fluorescence spectroscopy, and the influence of the gene

128 mbly using size-exclusion chromatography and fluorescence spectroscopy, and the unfolding using circu

129 e diffuse-reflectance infrared spectroscopy, fluorescence spectroscopy, and X-ray crystallography are

130 of the common techniques for single-molecule fluorescence spectroscopy applied to photosynthetic syst

131 The optical properties (UV-visible and fluorescence spectroscopy) are described.

132 scale were investigated by temperature-jump fluorescence spectroscopy as a function of temperature i

133 throughput format, here we sought to exploit fluorescence spectroscopy as a tool to develop a novel m

134 When employing fluorescence spectroscopy as the detection tool, quantit

135 l properties (steady-state and time-resolved fluorescence spectroscopy as well as anisotropy decay an

136 ination of X-ray crystallography, UV-vis and fluorescence spectroscopy as well as cyclic voltammetry,

137 were characterized by UV-vis absorption and fluorescence spectroscopy as well as cyclic voltammetry.

138 teady-state and time-resolved absorption and fluorescence spectroscopy as well as femtosecond stimula

139 ed using both steady-state and time-resolved fluorescence spectroscopy as well as transient absorbanc

140 Here we present a fluorescence-spectroscopy-based method for estimating th

141 bility of a protein network was evaluated by fluorescence spectroscopy, by protein solubility studies

142 cterized by UV melting temperature analysis, fluorescence spectroscopy, collisional fluorescence quen

143 k assesses the potential of multidimensional fluorescence spectroscopy combined with chemometrics for

144 s assessed by the use of excitation-emission fluorescence spectroscopy combined with PARAllel FACtor

145 mined using excitation emission matrix (EEM) fluorescence spectroscopy combined with parallel-factor

146 The potential of front-face fluorescence spectroscopy combined with second-order che

147 lowed by UV-visible, circular dichroism, and fluorescence spectroscopy combined with site-directed mu

148 CD and fluorescence spectroscopy confirmed that denaturation of

149 Depth profiling with confocal micro-X-ray fluorescence spectroscopy (confocal micro-XRF) is a nond

150 Single protein fluorescence spectroscopy constitutes an approach of cho

151 The results showed that fluorescence spectroscopy could be used as a powerful to

152 These findings suggest that fluorescence spectroscopy could offer a rapid and high-t

153 Front face fluorescence spectroscopy coupled with chemometric tools

154 Fluorescence spectroscopy coupled with parallel factor a

155 Fluorescence spectroscopy coupled with parallel factor a

156 alyses of data obtained using absorbance and fluorescence spectroscopies, cyclic voltammetry, and DFT

157 Fourier-transform infrared and fluorescence spectroscopy data revealed important change

158 gether with small-angle X-ray scattering and fluorescence spectroscopy data, our findings are consist

159 Ultrafast fluorescence spectroscopy demonstrates extensive excited

160 Near-infrared fluorescence spectroscopy demonstrates that the SWNTs ex

161 ase expression assay and laser fragmentation fluorescence spectroscopy; demonstration that PCBs can c

162 albumin (BSA) at pH 3.5, 5.0, and 7.4 using fluorescence spectroscopy, differential scanning nanocal

163 cer detection system that combines intrinsic fluorescence spectroscopy, diffuse reflectance spectrosc

164 vary protein interactions were studied using fluorescence spectroscopy, dynamic light scattering and

165 terization measurements by NMR spectroscopy, fluorescence spectroscopy, dynamic light scattering, ato

166 temperature is demonstrated by infrared and fluorescence spectroscopy, dynamic light scattering, sma

167 erization methods, including NMR, UV-vis and fluorescence spectroscopy, electrospray ionization mass

168 ory, recently used for the interpretation of fluorescence spectroscopy experiments on disordered prot

169 Fluorescence spectroscopy experiments showed that among

170 ple Molecular Dynamics (MD) simulations with fluorescence spectroscopy experiments to characterize th

171 Fluorescence spectroscopy facilitates the detection of v

172 Front face fluorescence spectroscopy (FFFS) emission spectra were a

173 apefruit juice were studied by 3D-front-face fluorescence spectroscopy followed by Independent Compon

174 ation, and circular dichroism and tryptophan fluorescence spectroscopies for conformational character

175 These results show the potential use of fluorescence spectroscopy for screening apple juices for

176 ual dairy proteins was investigated by using fluorescence spectroscopy, Fourier transform infrared sp

177 ion, X-ray photoelectron spectroscopy, X-ray fluorescence spectroscopy, Fourier transform infrared sp

178 Time-resolved fluorescence spectroscopy furnishes radiative and nonrad

179 Circular dichroism and tryptophan fluorescence spectroscopy further show that the expansio

180 Grazing incidence and grazing emission X-ray fluorescence spectroscopy (GI/GE-XRF) are techniques tha

181 mental imaging that combines radiography and fluorescence spectroscopy has been developed and applied

182 Single-molecule fluorescence spectroscopy has been used to image and cha

183 Recently, single-molecule fluorescence spectroscopy has provided new insights into

184 Fluorescence spectroscopy has the potential to be used i

185 ism spectroscopy to atomic force microscopy, fluorescence spectroscopy, immunoblot studies, solubilit

186 Fluorescence spectroscopy implicates interprotein dityro

187 Time-resolved fluorescence spectroscopy in combination with CLSM revea

188 Excitation emission matrix (EEM) fluorescence spectroscopy in combination with Parallel F

189 a biologically relevant sequence by NMR and fluorescence spectroscopy in highly competitive media.

190 ata to the equivalent samples analyzed using fluorescence spectroscopy in order to validate the Raman

191 fic introduction of chromophores for NMR and fluorescence spectroscopy in the human kappa-opioid rece

192 e (HD) by combining in vitro single molecule fluorescence spectroscopy, in silico molecular docking s

193 These reactions can be monitored by fluorescence spectroscopy, in stark contrast to the corr

194 UV-vis and fluorescence spectroscopies indicate limited interaction

195 The results of fluorescence spectroscopy indicated that the fluorescenc

196 Fluorescence spectroscopy indicates that the bottom of t

197 Single-molecule fluorescence spectroscopy is a powerful technique that m

198 is species in the catalytic pathway, whereas fluorescence spectroscopy is used to obtain the binding

199 Thus, combining multivariate analyses and fluorescence spectroscopy is useful for monitoring and p

200 Using fluorescence spectroscopy, isothermal calorimetry, and d

201 ated by preparative photolyses in CH3CN-D2O, fluorescence spectroscopy, LFP, and ab initio calculatio

202 Prior to the advent of single-molecule fluorescence spectroscopy, many of the fundamental optic

203 is method is demonstrated via absorption and fluorescence spectroscopy measurements as well as direct

204 Fluorescence spectroscopy methods can quantify and chara

205 luorescence intermittency in single-molecule fluorescence spectroscopy/microscopy, particularly for s

206 We have used fluorescence spectroscopy, molecular modeling, and limit

207 Insights from fluorescence spectroscopy, molecular modeling, and NMR s

208 entrations of 0.05 to 0.25 M, and UV-vis and fluorescence spectroscopy monitoring.

209 luding chromatography, UV-Vis absorption and fluorescence spectroscopy, MS and (1)H NMR spectrometry.

210 olding kinetics of a model OMP (tOmpA) using fluorescence spectroscopy, native mass spectrometry, and

211 taining lysine or arginine residues by using fluorescence spectroscopy, NMR spectroscopy, and isother

212 Using fluorescence spectroscopy of engineered tyrosines, we sh

213 l information on the electrical mobility and fluorescence spectroscopy of gas-phase ions.

214 Intrinsic fluorescence spectroscopy of purified proteins confirmed

215 Sequential extractions and laser-induced fluorescence spectroscopy of sediments from the columns

216 combined molecular dynamics simulations with fluorescence spectroscopy of the prokaryotic homolog Glt

217 ptical properties (as measured by UV-vis and fluorescence spectroscopies) of the novel oxa- and dioxa

218 We performed fluorescence spectroscopy on Arch and its photogenerated

219 Here, we demonstrate with picosecond-fluorescence spectroscopy on C. reinhardtii cells that,

220 ance energy transfer (spFRET) using confocal fluorescence spectroscopy on molecules traveling at spee

221 Rather than using fluorescence spectroscopy or magnetic resonance imaging,

222 Fluorescence spectroscopy results show that the quenchin

223 The biophysical data collected by CD and fluorescence spectroscopies reveal a three-state equilib

224 ctively coupled plasma mass spectrometry and fluorescence spectroscopy revealed that DMAV, like Cu,Zn

225 tron microscopy with energy dispersive X-ray fluorescence spectroscopy revealed that the newly formed

226 TFA titration study of 4c using UV-vis and fluorescence spectroscopy reveals that the fluorescence

227 rode were evaluated by UV-vis absorption and fluorescence spectroscopy, scanning electron microscopy,

228 grees C) determined by rheology, synchronous fluorescence spectroscopy (SFS) and turbiscan measuremen

229 ns of naphthenic acids (NAs) and synchronous fluorescence spectroscopy (SFS).

230 with neutral PC/PE/cholesterol membranes by fluorescence spectroscopy show that tryptophan-labeled K

231 Fluorescence spectroscopy showed that HHP treatment, as

232 Single-molecule fluorescence spectroscopy showed that, contrary to previ

233 ent dyes, which were characterized by UV-vis/fluorescence spectroscopy, single-crystal X-ray diffract

234 Here we employ a combination of NMR, fluorescence spectroscopy, site-directed mutagenesis, an

235 nities for ATP, ADP, and AMPPCP according to fluorescence spectroscopy, small angle x-ray scattering

236 d in individual complexes by single-molecule fluorescence spectroscopy (SMS).

237 yclic voltammetry, UV-visible absorbance and fluorescence spectroscopy, spectroelectrochemistry, and

238 t exclusively been focused on Stokes-shifted fluorescence spectroscopy (SSF) in which the emitted pho

239 urements, (13)C CP MAS NMR spectroscopy, and fluorescence spectroscopy strongly supported the observe

240 Fluorescence spectroscopy studies confirmed that resvera

241 ay be useful for future crystallographic and fluorescence spectroscopy studies.

242 Results from absorption and fluorescence spectroscopy suggest that the duplex stabil

243 othermal titration calorimetry and intrinsic fluorescence spectroscopy suggests that YKL-39 binds to

244 tion, along with results from absorption and fluorescence spectroscopy, suggests that the pyrene moie

245 enesis, circular dichroism, and a variety of fluorescence spectroscopy techniques, we determined that

246 We have studied by fluorescence spectroscopy the specific binding of HSA wi

247 trapping mass spectrometry and laser-induced fluorescence spectroscopy, the structure of a fluorescen

248 rameters using time-resolved single-molecule fluorescence spectroscopy thus yields direct access to t

249 pments in the application of single molecule fluorescence spectroscopy to (bio)catalysis research.

250 We used fluorescence spectroscopy to characterize the dissolved

251 ab initio molecular dynamics simulations and fluorescence spectroscopy to demonstrate that these intr

252 Here, we use NMR and 2-aminopurine fluorescence spectroscopy to examine how DMSO affects th

253 escein, was used in conjunction with in situ fluorescence spectroscopy to facilitate real-time monito

254 Here, we used single-molecule force and fluorescence spectroscopy to investigate E. coli SSB bin

255 Here we use single-molecule fluorescence spectroscopy to investigate how the DnaJ-Dn

256 Using stopped-flow fluorescence spectroscopy to measure association and dis

257 in the duplex, and suggested the utility of fluorescence spectroscopy to monitor probe conformation.

258 The suitability of using fluorescence spectroscopy to rapidly assay drug release

259 Hence, excitation-emission fluorescence spectroscopy, together with PARAFAC, provid

260 The Time-resolved fluorescence spectroscopy (TR-FS) has the potential to d

261 investigated by time-resolved laser-induced fluorescence spectroscopy (TRLFS) and a variety of physi

262 lium temperature time-resolved laser-induced fluorescence spectroscopy (TRLFS).

263 h spectroscopic (time-resolved laser-induced fluorescence spectroscopy, TRLIFS, and X-ray absorption

264 ing ultraviolet-visible (UV-vis) absorption, fluorescence spectroscopies under simulated physiologica

265 Fluorescence spectroscopy, urea denaturation, and limite

266 hydrophobicity of the polymers determined by fluorescence spectroscopy using pyrene as the probe.

267 were adsorbed by GAC and characterized using fluorescence spectroscopy, UV-absorption, and size exclu

268 Mutagenesis studies and fluorescence spectroscopy validated the identification o

269 first time, Excitation Emission Matrix (EEM) fluorescence spectroscopy was combined with parallel fac

270 The LOD was reduced to 400nM when fluorescence spectroscopy was used as the detection tool

271 The LOD was reduced to ~400nM when fluorescence spectroscopy was used as the detection tool

272 In this study, label-free fluorescence spectroscopy was used for the first time to

273 Synchronous fluorescence spectroscopy was used in combination with p

274 Fluorescence spectroscopy was used to analyze the impact

275 Here, steady-state and time-resolved fluorescence spectroscopy was used to compare the abilit

276 In this study, real-time fluorescence spectroscopy was used to determine the rate

277 Steady-state fluorescence spectroscopy was used to monitor a change i

278 By using pico- and femtosecond fluorescence spectroscopy we demonstrate herein that the

279 By using surface plasmon resonance and fluorescence spectroscopy we here show that short peptid

280 ng circular dichroism, X-ray absorption, and fluorescence spectroscopy, we found that a high Au-S coo

281 Using differential scanning calorimetry and fluorescence spectroscopy, we found that the size of the

282 By using single-molecule fluorescence spectroscopy, we have determined that phosp

283 Using fluorescence spectroscopy, we have examined the associat

284 Using femtosecond time-resolved fluorescence spectroscopy, we have studied the conformat

285 Therefore, using time-resolved fluorescence spectroscopy, we interrogate these emitters

286 electron microscopy, circular dichroism, and fluorescence spectroscopy, we monitored fibril formation

287 Using intrinsic tryptophan fluorescence spectroscopy, we reveal clear distinctions

288 Using ensemble and single molecule fluorescence spectroscopy, we show that sigmaNS also bin

289 cs." Using circular dichroism and tryptophan fluorescence spectroscopy, we show that the conformation

290 form infrared and high-pressure stopped-flow fluorescence spectroscopies were applied.

291 crystal X-ray diffraction, and time-resolved fluorescence spectroscopy were employed.

292 oscopy, X-ray diffraction, and time-resolved fluorescence spectroscopy were performed for comprehensi

293 NMR and fluorescence spectroscopy were used to address the effec

294 ophoresis and steady state and time-resolved fluorescence spectroscopy were used to investigate the e

295 cs were monitored by serial AFM scanning and fluorescence spectroscopy, which revealed faster kinetic

296 ents help elucidate DOM properties for which fluorescence spectroscopy with PARAFAC may be a weak pre

297 emonstrate that femtosecond resolution X-ray fluorescence spectroscopy, with its sensitivity to spin

298 fraction, X-ray reflectivity (XR), and X-ray fluorescence spectroscopy (XFS).

299 echniques based on Raman spectroscopy, X-ray fluorescence spectroscopy (XRF), and scanning electron m

300 e electronic structure, while absorption and fluorescence spectroscopies yielded information about th