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

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

4 mass spectrometry (hydrophilic fraction) and fluorescence spectroscopy.

5 anonical genetic structures using UV-Vis and fluorescence spectroscopy.

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

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

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

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

10 inspired and validated using single-molecule fluorescence spectroscopy.

11 o Pimphales promelas using bile analysis via fluorescence spectroscopy.

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

13 t also includes Raman, photoluminescence, or fluorescence spectroscopy.

14 ata and identified interacting domains using fluorescence spectroscopy.

15 P3A4) by electron paramagnetic resonance and fluorescence spectroscopy.

16 aureus were compared using minimal RNAs and fluorescence spectroscopy.

17 ay absorption spectroscopy and laser-induced fluorescence spectroscopy.

18 dband transient absorption and time-resolved fluorescence spectroscopy.

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

20 ed PM using excitation-emission matrix (EEM) fluorescence spectroscopy.

21 , and calculate its loading efficiency using fluorescence spectroscopy.

22 onstituted channels and intrinsic tryptophan fluorescence spectroscopy.

23 n be enhanced by using synchronously scanned fluorescence spectroscopy.

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

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

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

27 characterized in solution by absorbance and fluorescence spectroscopy.

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

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

30 erties of selected examples were examined by fluorescence spectroscopy.

31 Binding experiments were conducted by fluorescence spectroscopy.

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

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

34 mapped this remodeling using single-molecule fluorescence spectroscopy.

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

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

37 DNA cross-linking and photoreversibility via fluorescence spectroscopy.

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

39 trope, on BSA/lutein binding at pH 7.4 using fluorescence spectroscopy.

40 nanomaterials, and compare it with ensemble fluorescence spectroscopy.

41 nvestigated these interactions using NMR and fluorescence spectroscopy.

42 lity for assessment of gut function based on fluorescence spectroscopy.

43 resis, macromolecule biosynthesis assays and fluorescence spectroscopy.

44 es used to characterize oligomeric stages is fluorescence spectroscopy.

45 udied by surface plasmon resonance (SPR) and fluorescence spectroscopy.

46 r, Energy-Dispersive X-ray (EDX), Raman, and fluorescence spectroscopy.

47 ing circular dichroism and intrinsic protein fluorescence spectroscopy.

48 e to the presence of saponin was observed by fluorescence spectroscopy.

49 S was observed by low-temperature ESI-MS and fluorescence spectroscopy.

50 the time of deposition of semen stains using fluorescence spectroscopy.

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

52 racterized by Fourier transform infrared and fluorescence spectroscopies.

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

54 using resonant ionization and laser-induced fluorescence spectroscopies.

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

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

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

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

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

60 les as demonstrated by (1)H NMR, UV-vis, and fluorescence spectroscopies and electrospray ionization

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

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

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

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

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

66 of MOF-1s with fibrinogen also studied using fluorescence spectroscopy and corresponding data were pl

67 Fluorescence spectroscopy and cyclic voltammetry investi

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

69 graphitic cone were elucidated by UV/vis and fluorescence spectroscopy and cyclic voltammetry.

70 ordering, as was suggested by microscopy and fluorescence spectroscopy and demonstrated by computer s

71 olyacrylamide gel electrophoresis (PAGE) and fluorescence spectroscopy and demonstrated their applica

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

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

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

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

76 Fluorescence spectroscopy and fluorescence quenching met

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

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

79 lculations support the results obtained from fluorescence spectroscopy and give insights into the int

80 chniques (oxidative stress, surface tension, fluorescence spectroscopy and HPLC) were used to investi

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

82 P3EHT outer core which was characterized by fluorescence spectroscopy and laser confocal scanning fl

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

84 Fluorescence spectroscopy and lifetime imaging microscop

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

86 were guided by findings from single-molecule fluorescence spectroscopy and molecular dynamics simulat

87 for polyphenol quantification, 3D front face fluorescence Spectroscopy and Near Infrared Spectroscopy

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

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

90 C in the presence of Gsp was demonstrated by fluorescence spectroscopy and PXRD analysis, respectivel

91 Fluorescence spectroscopy and SDS-PAGE techniques were e

92 The products were examined with UV-vis/fluorescence spectroscopy and showed interesting halochr

93 ation of anomalous diffusion by the means of fluorescence spectroscopy and simulation.

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

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

96 We used stopped-flow fluorescence spectroscopy and single-molecule motility a

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

98 Transport was monitored by fluorescence spectroscopy and the presence of the differ

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

100 f pirimiphos-methyl (PMM) in maize grains by fluorescence spectroscopy and three-way calibration was

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

102 d-type and Nrf2(-/-) mice, by combination of fluorescence spectroscopy and wavelet transform processi

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

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

105 Using fluorescence microscopy, fluorescence spectroscopy, and cell fractionation experi

106 ion-Fourier transform infrared spectroscopy, fluorescence spectroscopy, and circular dichroism spectr

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

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

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

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

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

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

113 a-crystallin using UV/vis and IR absorption, fluorescence spectroscopy, and light microscopy to chara

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

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

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

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

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

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

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

121 als where the common UV-vis spectrometry and fluorescence spectroscopy are inadequate.

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

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

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

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

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

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

128 Using steady-state fluorescence spectroscopy, CD spectroscopy, and time-cor

129 c tools such as steady-state & time-resolved fluorescence spectroscopy, Circular Dichroism (CD) and F

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

131 n faster is excitation-emission matrix (EEM) fluorescence spectroscopy combined with multivariate cla

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

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

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

135 Here, using ultrafast fluorescence spectroscopy, computational methods and ext

136 CD and fluorescence spectroscopy confirmed that denaturation of

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

138 Single protein fluorescence spectroscopy constitutes an approach of cho

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

140 Fluorescence spectroscopy coupled with parallel factor a

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

142 tom identity were investigated by UV-vis and fluorescence spectroscopy, cyclic and differential pulse

143 the products were investigated by UV-vis and fluorescence spectroscopy, cyclic voltammetry, and DFT c

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

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

146 Steady-state intrinsic fluorescence spectroscopy demonstrated that phosphoinosi

147 Ultrafast fluorescence spectroscopy demonstrates extensive excited

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

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

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

151 Moreover, in-cell fluorescence spectroscopy disclosed that the intracellul

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

153 try, on the basis of energy dispersive X-ray fluorescence spectroscopy (EDXRF).

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

155 Fluorescence spectroscopy experiments showed that among

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

157 potential for multiparameter monitoring via fluorescence spectroscopy, extending previous work on pr

158 Fluorescence spectroscopy facilitates the detection of v

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

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

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

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

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

164 NS were well characterized by UV-Visible and Fluorescence spectroscopy, FT-IR, XRD and HR-TEM.

165 Time-resolved fluorescence spectroscopy furnishes radiative and nonrad

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

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

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

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

170 Time-resolved and single-molecule fluorescence spectroscopy have been chosen to monitor th

171 Fluorescence microscopy and time-resolved fluorescence spectroscopy have been employed to uncover

172 By pairing mass spectrometry and fluorescence spectroscopy, here we show that hydrology a

173 Utilizing fluorescence spectroscopy, high-resolution confocal imag

174 Fluorescence spectroscopy implicates interprotein dityro

175 ameter single-fiber reflectance/single-fiber fluorescence spectroscopy in 15 patients with a dysplast

176 Time-resolved fluorescence spectroscopy in combination with CLSM revea

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

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

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

180 Kinetic unfolding experiments monitored by fluorescence spectroscopy in varying concentrations of g

181 supercomplexes complemented by time-resolved fluorescence spectroscopy in vivo.

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

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

184 UV-vis and fluorescence spectroscopies indicate limited interaction

185 The results of fluorescence spectroscopy indicated that the fluorescenc

186 Excitation-emission matrix fluorescence spectroscopy indicated that the origin of t

187 Time-resolved fluorescence spectroscopy indicated that the PSI antenna

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

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

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

191 Using fluorescence spectroscopy, isothermal calorimetry, and d

192 ent and enables DNA detection in solution by fluorescence spectroscopy (limit of detection 3 pM) and

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

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

195 Also, steady state fluorescence spectroscopy measurements highlighted the s

196 Here, by a combination of NMR and fluorescence spectroscopy methods, we find that vesicula

197 ed by data from multispectral imaging, X-ray fluorescence spectroscopy, micro-FTIR, and SEM-EDS.

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

199 ically varied, were thoroughly studied using fluorescence spectroscopy, molecular dynamics simulation

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

201 multiwavelength anomalous diffraction, X-ray fluorescence spectroscopy, Mossbauer spectroscopy, and g

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

203 on in earthworms was examined by micro-X-ray fluorescence spectroscopy (muXRF), after epoxy resin emb

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

205 Intrinsic fluorescence spectroscopy of purified proteins confirmed

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

207 of weak scattered light over long distances, fluorescence spectroscopy of single trapped atoms or mol

208 Fluorescence spectroscopy of the LSPH/CUR complex confir

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

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

211 highly effective sensor using time-resolved fluorescence spectroscopy on live-cell suspensions, whic

212 agreement between results of HS-SPME/GC and fluorescence spectroscopy regarding the safranal binding

213 Fluorescence spectroscopy results show that the quenchin

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

215 nalysis by gel permeation chromatography and fluorescence spectroscopy revealed a cooperative self-as

216 Solution fluorescence spectroscopy revealed that the COF crystall

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

218 UV/vis and fluorescence spectroscopy reveals that the anthracene-su

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

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

221 In this study, synchronous fluorescence spectroscopy (SFS) method was developed for

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

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

224 Fluorescence spectroscopy showed that HHP treatment, as

225 Tryptophan fluorescence spectroscopy showed that MatC, the periplas

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

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

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

229 lecular dynamics simulations with tryptophan fluorescence spectroscopy, site-directed mutagenesis, an

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

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

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

233 radiation induced micro- and submicro-X-ray fluorescence spectroscopy (SR-XRF), gadolinium was detec

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

235 by performing single-molecule multiparameter fluorescence spectroscopy, stopped-flow experiments, and

236 Fluorescence spectroscopy studies confirmed that resvera

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

238 r the first time, a comprehensive UV-Vis and fluorescence spectroscopy study has been carried out to

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

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

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

242 se and N-acetyl-lactosamine using tryptophan fluorescence spectroscopy (TFS) and, as a comparison, is

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

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

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

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

247 Moreover, we used fluorescence spectroscopy to assay their aggregation pro

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

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

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

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

252 Here, we used single-molecule fluorescence spectroscopy to track the conformational ch

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

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

255 Here we demonstrate time-resolved fluorescence spectroscopy (TRFS) as a novel technique to

256 has been demonstrated by temporally resolved fluorescence spectroscopy (TRFS) techniques.

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

258 Additionally, time-resolved laser-induced fluorescence spectroscopy (TRLFS) identified phosphoryl

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

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

261 Fluorescence spectroscopy using tryptophans (Trp) insert

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

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

264 Our results demonstrated that fluorescence spectroscopy was more sensitive than IR in

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

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

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

268 Synchronous fluorescence spectroscopy was used in combination with p

269 Fluorescence spectroscopy was used to analyze the impact

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

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

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

273 highly sensitive wavelength-dispersive X-ray fluorescence spectroscopy (WD-XRF) technique is designed

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

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

276 Using single-molecule fluorescence spectroscopy, we find that this positively

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

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

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

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

281 ession, along with light-scattering, CD, and fluorescence spectroscopy, we report that HN and BAX can

282 Using intrinsic tryptophan fluorescence spectroscopy, we reveal clear distinctions

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

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

285 Using NMR and fluorescence spectroscopy, we show that Thr55 phosphoryl

286 Using fluorescence spectroscopy, we show that, contrary to ear

287 For that, ultraviolet-visible and fluorescence spectroscopies were applied together with p

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

289 Molecular modeling and tryptophan fluorescence spectroscopy were consistent with the inter

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

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

292 NMR and fluorescence spectroscopy were used to address the effec

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

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

295 mbination of time- and polarization-resolved fluorescence spectroscopy with molecular dynamics simula

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

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

298 Recent advances in handheld X-Ray Fluorescence spectroscopy (XRF) systems have enabled non

299 nt were evaluated using synchrotron mu-X-ray fluorescence spectroscopy (XRF), nano-XRF, and mu-X-ray

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