ライフサイエンスコーパス: ESI-MS

1 ESI MS measurements confirmed formation of stable adduct

2 ESI-MS/MS results showed that the isolated mannan oligom

3 Kinetics in the pH range 1.50-6.40, ESI-MS, (1)H NMR titration, and ROESY experiments were p

4 using acid hydrolysis, methylation analysis, ESI-MS/MS and 1D/2D NMR.

5 SAXS, NMR, and ESI MS differentiate beta-NaSn13 , Sn12 , and other clus

6 it in combination with IR laser ablation and ESI-MS for quantitative analysis.

7 studied various competition experiments and ESI-MS and 3D Mid-IR-ATR spectral analyses of the ongoin

8 etitive reactions, furoindole formation, and ESI-MS analyses of the ongoing cyclization reaction.

9 fit the requirements of both affinity LC and ESI-MS.

10 heric pressure photoionization (APPI) MS and ESI-MS were used for detection of (2)D.

11 cted by electrospray ionization (ESI-MS) and ESI-MS coupled to hydrophilic interaction liquid chromat

12 mechanistic studies including online-NMR and ESI-MS measurements were conducted to identify relevant

13 Metabolite profiling using NMR and ESI-MS provided evidences for metabolic reprograming in

14 A thorough analysis by (19)F NMR and ESI-MS revealed the nature of this reagent in solution.

15 ndary amines, as supported by FTIR, NMR, and ESI-MS studies.

16 (3+) was determined as 1:2 by Job's plot and ESI-MS as well as (1)H NMR titration.

17 IR laser ablation sampling and ESI-MS were used to quantify the rate of penetration of

18 X-ray scattering and ESI-MS revealed that Hf(18) is completely insoluble in t

19 action, (31)P NMR and IR spectroscopies, and ESI-MS.

20 d by (1)H NMR and (13)C NMR spectroscopy and ESI-MS.

21 Here, we apply ESI-MS to investigate the factors that govern complex fo

22 that the use of "in solution" assays such as ESI-MS and ITC is to be preferred.

23 ion mechanisms, and strong synergies between ESI-MS defined SAC sites and electronic structure theory

24 se extraction cartridge prior to analysis by ESI-MS/MS in negative ion mode.

25 oplets are split, one portion is analyzed by ESI-MS, and the second portion is sorted based on the MS

26 and identification of the active compound by ESI-MS, (1)H-NMR, and (13)C-NMR identified beta-rubromyc

27 th H(2) S to form superoxide, as detected by ESI-MS, a hydroethidine fluorescence assay, and EPR spin

28 ot remain intact in solution as evidenced by ESI-MS.

29 and small Au(I)SR species was identified by ESI-MS and UV-vis spectroscopy.

30 uble B3-peptide complexes were identified by ESI-MS.

31 hrome P450scc (C. macropomum), identified by ESI-MS/MS and showing the highest values of mercury conc

32 r weight (MW) of single proteins measured by ESI-MS is simple; however, algorithmic deconvolution is

33 relative affinities (of 14 HMOs) measured by ESI-MS with the reported specificities of hGal-1, hGal-3

34 i)Pr2O and was also confirmed in solution by ESI-MS and NMR.

35 This fact is supported by ESI-MS data, which showed mass peaks up to the pentameri

36 First, the catch-and-release (CaR)-ESI-MS assay, carried with ion mobility separation prior

37 Notably, for each lectin, CaR-ESI-MS screening required <1 h to complete and consumed

38 ectrospray ionization-mass spectrometry (CaR-ESI-MS) assay, implemented using picodiscs (complexes co

39 ectrospray ionization mass spectrometry (CaR-ESI-MS) for screening libraries of N-glycans derived fro

40 ectrospray ionization mass spectrometry (CaR-ESI-MS), capable of simultaneously screening mixtures of

41 ectrospray ionization mass spectrometry (CaR-ESI-MS)-based screening, implemented with nanodiscs, for

42 an equimolar concentration library, the CaR-ESI-MS assay identified 100% of ligands with affinities

43 The CaR-ESI-MS results revealed that CTB5 binds to six of the ga

44 s serve to highlight the ease with which CaR-ESI-MS can screen complex mixtures of N-glycans for inte

45 strated using capillary electrophoresis (CE)-ESI-MS in the analysis of aminopyrene-trisulfonate label

46 CE-ESI-MS allows quantitative measurements of cellular meta

47 of optical microscopy-guided MALDI MS and CE-ESI-MS for sequential chemical profiling of individual,

48 Last, we used microprobe single-cell CE-ESI-MS to uncover previously unknown reorganization of t

49 Microprobe CE-ESI-MS of <0.02% of the single-cell content allowed us t

50 w avenues for highly sensitive sheathless CE-ESI-MS approaches in glycoproteomics research, by signif

51 erved compared to conventional sheathless CE-ESI-MS.

52 SIL-CE-ESI-MS enables the accurate monitoring of InsPs and PP-I

53 lectrospray ionization mass spectrometry (CE-ESI-MS) to enable direct metabolic analysis of identifie

54 e alpha and beta cells were analyzed with CE-ESI-MS to obtain qualitative information on metabolites,

55 Depending on the conditions, ESI-MS of lipid extracts in negative ion mode can give r

56 y, compared to the operation of conventional ESI-MS.

57 utors that are unresolved using conventional ESI-MS/MS.

58 ate via a new C-N bond, as detected via cryo-ESI-MS.

59 ray ionization-tandem mass spectrometry (CZE-ESI-MS/MS) has been recognized as an invaluable platform

60 HLPC-DAD-ESI-MS(n) allowed the evaluation of the quantitative and

61 An HPLC-DAD-ESI-MS method was developed to investigate the distribut

62 in lentil hulls were studied using HPLC-DAD-ESI-MS(n) and their antioxidant potential determined usi

63 Phenolic compounds were analyzed by HPLC-DAD-ESI-MS(n).

64 e found only in PS as identified by HPLC-DAD-ESI-MS(n).

65 ere tentatively characterized using HPLC-DAD-ESI-MS(n).

66 bush and Rabbiteye blueberry, using HPLC-DAD-ESI-MS(n).

67 unds were tentatively identified by HPLC-DAD-ESI-MS(n).

68 ods, and (ii) identify compounds by HPLC-DAD-ESI-MS.

69 HPLC-DAD-ESI-MS/MS analysis identified cyanidine glycosides as th

70 BZF was identified (HPLC-DAD-ESI-MS/MS) only in the dry outer scales of onions and sh

71 onization tandem mass spectrometry (HPLC-DAD-ESI-MS/MS) over two consecutive vintages (2016 and 2017)

72 and HMF analyses were performed with LC-DAD-ESI-MS/MS and LC-DAD-RID was used for the sugar analyses

73 d in cactus pear juice using a single LC-DAD-ESI-MS/MS method.

74 ionization tandem mass spectrometry (LC-DAD-ESI-MS/MS) in multiple reaction monitoring mode (MRM).

75 the MRC as compared to the DRC using LC-DAD-ESI-MS/MS.

76 as developed for the extraction and UFLC-DAD-ESI-MS analysis of carbonyl compounds (CCs) in oils heat

77 One-/two-dimensional NMR and UPLC-DAD-ESI-MS(n) measurements were used to monitor the synthesi

78 h aqueous ethanol and analyzed with UPLC-DAD-ESI-MS, HPLC-DAD, and NMR.

79 UPLC-DAD-ESI-MS/MS analyses disclosed phenolic acids and tannins

80 Spectrophotometry and UPLC-DAD-ESI-MS/MS systems were utilized for quantitative analysi

81 The HPLC-DAD/ESI-MS profiles allowed the tentative identification of

82 Chromatographic analysis (HPLC-DAD/ESI-MS) of blue maize extracts showed the presence of se

83 hocyanins adducts, were analyzed by HPLC-DAD/ESI-MS.

84 and electrospray-mass spectrometry (HPLC/DAD/ESI-MS); nineteen different phenolic compounds and six d

85 tion pathway of eosin in linseed oil, and DI-ESI-MS provided additional information on the native con

86 lectrospray ionization mass spectrometry (DI-ESI-MS) were used to characterize the degradation pathwa

87 A direct ESI-MS comparison of lipid binding to the soluble protei

88 protein ESI-MS method, which combines direct ESI-MS protein-ligand binding measurements and competiti

89 No direct ESI-MS evidence of CTB(5) binding to the other five gang

90 es improved up to 19-fold compared to direct ESI-MS of single-phase droplets (aqueous plugs segmented

91 the magnitudes of these templation effects, ESI-MS was used to gauge the effect of each template upo

92 The rapid UHPLC-ELSD-ESI-MS(2) method does not require labeling steps or addi

93 ementation in a fully automated platform for ESI-MS-based high-throughput screening.

94 Label-free ESI-MS droplet screening expands the toolbox for droplet

95 The final HILIC/ESI-MS/MS method is applied for the analysis of porcine

96 cinolysis and thioglycolysis coupled to HLPC-ESI-MS were applied for the characterization of the nati

97 Products were identified by HPLC, ESI-MS, FT-IR, and [Formula: see text] spectroscopy.

98 HPLC-ESI-MS of procyanidins-rich fraction without any reactio

99 nols were identified using HPLC-PDA and HPLC-ESI-MS(n) analyses.

100 The polyphenol profile was studied by HPLC-ESI-MS/MS, while the antioxidant capacity was measured b

101 phenolic metabolites were quantified by HPLC-ESI-MS/MS.

102 ls using combined laser microdissection/HPLC-ESI-MS analysis.

103 rst time, and characterized by means of HPLC-ESI-MS data.

104 Further characterization via RP-HPLC-ESI-MS identified the main phenolics as hydroxycinnamate

105 ther chromatographed and examined by RP-HPLC-ESI-MS.

106 ctrospray ionization mass spectrometry (HPLC-ESI-MS) method was developed for analyzing triolein and

107 ctrospray ionization-mass spectrometry (HPLC-ESI-MS) to be epi(catechin) dimers and trimers.

108 ay ionization-tandem mass spectrometry (HPLC-ESI-MS/MS) are commonly employed for ascaroside detectio

109 ay-ionization tandem mass spectrometry (HPLC-ESI-MS/MS) to simultaneously quantify adenine nucleotide

110 The HPLC-ESI-MS/MS analysis of the fractions enriched in phenolic

111 Thioglycolysis-HPLC-ESI-MS identified five oxidation markers of PCs with [M-

112 phloroglucinolysis- and thioglycolysis-HPLC-ESI-MS/MS, respectively.

113 time characterized and quantified using HPLC-ESI-MS/MS.

114 re we describe a novel method utilizing HPLC-ESI-MS/MS to identify and quantify multiple full-length

115 Fractions were subjected to HPLC/ESI-MS/MS and (1)H NMR analysis.

116 FT-IR monitoring and HR-ESI-MS spectra point to a stable coordination of the ace

117 idated by 1D- and 2D-NMR spectroscopy and HR-ESI-MS/MS spectrometry, while a combination of chemical

118 e crab shells and their identification by HR-ESI-MS technique.

119 esolution electrospray mass spectrometry (HR-ESI-MS) allowed the identification of water-soluble Fe(I

120 The HR-ESI-MS identified 23 compounds, depending on the adopted

121 The proposed 2D-IC-ESI-MS method developed for a QExactive MS instrument wi

122 ion high-resolution mass spectrometry (2D-IC-ESI-MS) allowed isotope dilution quantitation of phospha

123 ation prior to GBP "release" (i.e., CaR(IMS)-ESI-MS), is employed to rapidly identify GBP-GP binding

124 ach GP was successfully detected by CaR(IMS)-ESI-MS; no binding was detected for a noninteracting ref

125 Direct-infusion ESI-MS showed that the tested volatile eluent salts seem

126 produced a specific spectrum in negative ion ESI-MS(n).

127 action, (1)H and (13)C NMR, and negative-ion ESI-MS.

128 re then detected by electrospray ionization (ESI-MS) and ESI-MS coupled to hydrophilic interaction li

129 ATR-FTIR) analysis, electrospray ionization (ESI-MS), direct analysis in real time mass spectrometry

130 s spectrometry with electrospray ionization (ESI-MS).

131 aration orthogonality for 16 different 2D LC-ESI MS systems has been evaluated.

132 c analysis in Camponotus floridanus, nano-LC-ESI MS/MS was used to identify these neuropeptides bioch

133 LC-ESI-MS/MS analysis led to identification of 14-17 compon

134 A LC-ESI-MS method was optimized and 41 different compounds w

135 Native FcRn affinity LC-ESI-MS can tremendously reduce the time required to asse

136 Native FcRn affinity LC-ESI-MS was performed on a therapeutic mAb undergoing var

137 multiplex glycomic analysis method on an LC-ESI-MS platform.

138 oteins (FPOP) followed by proteolysis and LC-ESI-MS/MS analyses.

139 of other small molecules using trap-based LC-ESI-MS/MS detection.

140 n-up, and detection and quantification by LC-ESI-MS/MS of phylloquinone (PK), menaquinone-4 (MK-4), m

141 eight between 148 and 624 m/z detected by LC-ESI-MS/MS.

142 rude extract and further characterized by LC-ESI-MS/MS.

143 ion to its individual phenolic compounds (LC-ESI-MS/MS), antioxidant capacity, total monomeric anthoc

144 The DLLME-LC-ESI-MS/MS method was successfully applied to the determi

145 nation of phenolic compounds in extracts, LC-ESI-MS/MS method was used.

146 methodology based on high resolution nano-LC-ESI-MS/MS for LAB identification at genus, species and s

147 ionization-tandem mass spectrometry (nano-LC-ESI-MS/MS) is currently one of the most sensitive analyt

148 pistachios, and walnuts) using a QuEChERS-LC-ESI-MS-Triple Quadrupole approach was set up.

149 etry with electrospray ionization source (LC-ESI-MS/MS).

150 w-through elution coupled with online SPE-LC-ESI-MS/MS for the quantitative determination of four rep

151 liquid chromatography-mass spectrometry (LC-ESI-MS) experiments of biological samples remain unident

152 lectrospray ionization mass spectrometry (LC-ESI-MS) for estimating and correcting blood volume varia

153 lectrospray ionization mass spectrometry (LC-ESI-MS) method was used to simultaneously estimate the b

154 lectrospray ionization-mass spectrometry (LC-ESI-MS) via unmediated sampling by MMS DESI-IMS.

155 hy-electrospray-tandem mass spectrometry (LC-ESI-MS/MS) method recently developed in our lab.

156 pray ionization tandem mass spectrometry (LC-ESI-MS/MS) methodology employing high-resolution/accurat

157 pray ionisation tandem mass spectrometry (LC-ESI-MS/MS).

158 We report the LC-ESI-MS/MS determination of betaines in commercial flours

159 In the phenolic fraction obtained by the LC-ESI-MS/MS method, a total of 12 phenolic compounds was f

160 Samples were analyzed using LC-ESI-MS/MS in combination with online extraction.

161 individual compo3unds were detected using LC-ESI-MS/MS.

162 genic SOA systems analyzed via (-) or (+) LC/ESI-MS under various LC conditions, and demonstrates tha

163 tantial systematic errors in quantitative LC/ESI-MS analyses of SOA.

164 that molecular products measureable by LC/(-)ESI-MS account for only 21.8 +/- 2.6% and 18.9 +/- 3.2%

165 trospray ionization mass spectrometry [LC/(-)ESI-MS] is routinely employed to characterize the identi

166 emonstrate the potential of the proxy ligand ESI-MS approach for comprehensive and quantitative studi

167 urements, carried out using the proxy ligand ESI-MS binding assay, confirmed that GD1b binding to CTB

168 measured using the competitive proxy ligand-ESI-MS binding assay.

169 The K(a) measured by proxy ligand-ESI-MS for AGP, Hp1-1 and alpha2M (4 x 10(5) M(-1), 2 x

170 on of the samples by GC-MS, NMR and off-line ESI-MS showed that it was possible to obtain inulin mole

171 However, most ESI-MS based analyses require no more than 25 mug of pro

172 Application of MALDI-MS, ESI-MS, and IM-MS to the polymer-peptide biomaterial con

173 Here we present a quantitative NACE-ESI-MS/MS method for separating and determining physcion

174 are obtained using the reported GC-DBD-nano-ESI-MS.

175 Native ESI-MS and NMR spectroscopic analyses corroborated the s

176 ns obtained during offline and online native ESI-MS were used to monitor alterations in protein struc

177 branching points by direct-infusion negative ESI-MS(n).

178 tide ligand libraries (CPLLs), SDS-PAGE, nLC-ESI-MS/MS, and database search, permitted identifying 17

179 the formation of [hmim]PTS as probed by NMR, ESI-MS, DART-MS, and HPLC studies.

180 lecular complexes were characterized by NMR, ESI-MS, UV-vis, ITC, and cyclic voltammetric studies.

181 The observed ESI-MS signals were shifted to a "clearer" lower-mass re

182 Additionally, the coupling of ESI-MS with online laser irradiation has been successful

183 Results of ESI-MS(n) analysis can be explained by the presence of t

184 sperm whale Mb at up to five sites based on ESI-MS analysis.

185 upled to either charged aerosol detection or ESI-MS.

186 e catalysis is predicted on the basis of our ESI-MS study of the ongoing reaction and literature.

187 ing result combinations: BC positive and PCR/ESI-MS negative, 4.3%; BC positive and PCR/ESI-MS positi

188 -MS positive, 15.3%; and BC negative and PCR/ESI-MS negative, 70.1%.

189 ted sepsis (sepsis-2 definition), BC and PCR/ESI-MS on whole blood were positive in 14.6% and 25.6% o

190 R/ESI-MS negative, 4.3%; BC positive and PCR/ESI-MS positive, 10.3%; BC negative and PCR/ESI-MS posit

191 /ESI-MS positive, 10.3%; BC negative and PCR/ESI-MS positive, 15.3%; and BC negative and PCR/ESI-MS n

192 Compared with BC, PCR/ESI-MS showed the following sensitivities (coagulase-neg

193 In conclusion, PCR/ESI-MS showed excellent performance on contrived samples

194 re 82% (74%, 89%) and 92% (85%, 97%) for PCR/ESI-MS and MB, respectively.

195 re 95% (88%, 98%) and 88% (80%, 94%) for PCR/ESI-MS and MB, respectively.

196 tions (n = 603) had significantly higher PCR/ESI-MS positivity rates than patients without prior anti

197 , with or without spiked microorganisms, PCR/ESI-MS produced 99.1% true-positive and 97.2% true-negat

198 ectrospray ionization mass spectrometry (PCR/ESI-MS) and molecular beacons (MB), for detecting genes

199 ectrospray ionization-mass spectrometry (PCR/ESI-MS) can detect DNA from hundreds of different microo

200 rospray ionization mass detectors (UHPLC/PDA/ESI-MS).

201 The assay is based on the proxy protein ESI-MS method, which combines direct ESI-MS protein-liga

202 n of UHPLC with ion trap and high resolution ESI-MS.

203 Using high-resolution ESI-MS, multiangle laser light scattering (MALLS), and m

204 , and cytochrome c) could be analyzed by SEC-ESI-MS using different column chemistries without compro

205 ectrospray-ionization mass spectrometry (SEC-ESI-MS) is a useful tool to study proteins in their nati

206 Overall, with SEC-ESI-MS, the effect of nonspecific interactions between p

207 rospray ionization mass spectrometry signal (ESI-MS) was observed relative to ammonia and triethylami

208 diction of electrospray tandem mass spectra (ESI-MS/MS), but unlike CFM-ESI, CFM-EI can handle odd-el

209 onfirmed by electrospray mass spectrometric (ESI MS) experiments.

210 electrospray ionization mass spectrometric (ESI-MS) analysis.

211 n electrospray ionization mass spectrometry (ESI MS) coupled with size exclusion chromatography.

212 d electrospray ionization-mass spectrometry (ESI-MS) allowed a more detailed characterization of the

213 Electrospray ionization mass spectrometry (ESI-MS) analysis of filter-collected particles indicates

214 o-electrospray ionization-mass spectrometry (ESI-MS) and nano-ESI-ion mobility (IM)-MS with collision

215 y electrospray ionization mass spectrometry (ESI-MS) and their great importance in API synthesis.

216 d electrospray ionization mass spectrometry (ESI-MS) approach for investigating glycan-mediated inter

217 d electrospray ionization mass spectrometry (ESI-MS) assay and model membranes of defined composition

218 e electrospray ionization mass spectrometry (ESI-MS) assay for measuring the kinetic parameters of CA

219 n electrospray ionization mass spectrometry (ESI-MS) assay for screening carbohydrate libraries again

220 y electrospray ionization mass spectrometry (ESI-MS) at pH 5.

221 t electrospray ionization mass spectrometry (ESI-MS) data suggest that the size and composition of 1-

222 h electrospray ionization mass spectrometry (ESI-MS) for the in vivo analysis of xylem sap directly f

223 n electrospray ionization mass spectrometry (ESI-MS) identified several key intermediates in the cata

224 y electrospray ionization mass spectrometry (ESI-MS) in combination with online laser irradiation of

225 h electrospray ionization mass spectrometry (ESI-MS) in native conditions to study the influence of m

226 Electrospray ionization mass spectrometry (ESI-MS) is a ubiquitously used analytical method applied

227 t electrospray ionization mass spectrometry (ESI-MS) is capable of capturing transient interactions b

228 o electrospray ionization mass spectrometry (ESI-MS) is implemented to analyze complex mixtures of In

229 h electrospray ionization mass spectrometry (ESI-MS) is routinely used in proteomics research.

230 e electrospray ionization mass spectrometry (ESI-MS) is the most widely used technology in lipidomics

231 d electrospray ionization mass spectrometry (ESI-MS) revealed the cluster formula to be [Ag67(SPhMe2)

232 e electrospray ionization mass spectrometry (ESI-MS) spectra of selected biochemical species were obt

233 s electrospray ionization-mass spectrometry (ESI-MS) studies.

234 Electrospray ionisation mass spectrometry (ESI-MS) suggested 2 to be a Mn(II) Mn(III) -peroxide com

235 f electrospray ionization mass spectrometry (ESI-MS) to study molecularly defined SACs supported on p

236 f electrospray ionization mass spectrometry (ESI-MS) to the mitoxantrone conjugate was improved by an

237 e electrospray ionization mass spectrometry (ESI-MS) was used to determine the distribution of the fu

238 h electrospray ionization mass spectrometry (ESI-MS), a BGE composed of NH(4)Ac, 1.0 mM, pH 4.0, in 7

239 electron-spray ionization mass spectrometry (ESI-MS), Carr-Purcell-Meiboom-Gill relaxation dispersion

240 Electrospray ionization mass spectrometry (ESI-MS), on the other hand, while revealing important st

241 s electrospray ionization mass spectrometry (ESI-MS)-based sample injection at a sampling rate faster

242 d electrospray ionization mass spectrometry (ESI-MS).

243 g electrospray ionization mass spectrometry (ESI-MS).

244 n electrospray ionization-mass spectrometry (ESI-MS).

245 d electrospray ionization mass spectrometry (ESI-MS).

246 g electrospray ionization mass spectrometry (ESI-MS).

247 y electrospray ionization mass spectrometry (ESI-MS).

248 s electrospray ionization mass spectrometry (ESI-MS).

249 y electrospray ionization mass spectrometry (ESI-MS).

250 d electrospray ionization mass spectrometry (ESI-MS).

251 rospray ionization-tandem mass spectrometry (ESI-MS/MS) at a rate of 6 s per sample, allowing for sim

252 rospray ionization tandem mass spectrometry (ESI-MS/MS) method has been developed for the identificat

253 rospray ionization tandem mass spectrometry (ESI-MS/MS) provides glycerophospholipid (GPL) class (i.e

254 tification of mercury and Mass Spectrometry (ESI-MS/MS) were used for the identification of proteins.

255 rospray ionization tandem mass spectrometry (ESI-MS/MS).

256 -mass electrospray tandem mass spectrometry (ESI-MS/MS).

257 rospray ionization-tandem mass spectrometry (ESI-MS/MS).

258 y electrospray ionisation mass spectrometry (ESI-MS/MS).

259 E fractioning followed by mass spectrometry (ESI-MS/MS).

260 unds were characterized by NMR spectroscopy, ESI-MS spectrometry, and X-ray single-crystal diffractom

261 sional (COSY, NOESY, DOSY) NMR spectroscopy, ESI-MS, ion-mobility mass spectrometry (IM-MS), AFM, and

262 cterized by NOESY and DOSY NMR spectroscopy, ESI-MS, TWIM-MS, and transmission electron microscopy.

263 ansient absorption, and UV-vis spectroscopy; ESI-MS; X-ray crystallography; DFT calculations; reactiv

264 idinemia was demonstrated by the IEF syringe-ESI-MS system with accuracy from 88.25% to 102.16% and a

265 ed by H(2) S was observed by low-temperature ESI-MS and fluorescence spectroscopy.

266 The ESI-MS measurements confirmed the presence of glutathion

267 Additionally, the ESI-MS/MS(QTOF) analysis has allowed the tentative ident

268 blished from the agreement found between the ESI-MS data and affinities of a small number of HMOs for

269 The reliability of the ESI-MS assay for quantifying the affinities of HMOs for

270 icular, for the imidazoline catalyst, the (+)ESI-MS/(MS) detection of the genuine Breslow intermediat

271 size-exclusion chromatography (SEC)-cIEF to ESI-MS/MS enabled the identification of nearly 2000 prot

272 strated using the DRILL interface coupled to ESI-MS along with an improved limit of detection (10-fol

273 ation by off-line injections of fractions to ESI-MS/MS.

274 d increased to -400 V during the infusion to ESI-MS at a flow rate of 4.0 muL/min.

275 eptide and digested protein samples prior to ESI-MS.

276 sion-induced dissociation (CID), traditional ESI-MS/MS fails to define fatty acyl regiochemistry alon

277 sure stable solvent conditions for transient ESI-MS signals.

278 -box fermentation method and employing UHPLC-ESI MS/MS for the analysis of peptides and proteins extr

279 Using a newly developed UHPLC-ESI-MS/MS method to monitor beer production, we demonstr

280 trometry with electrospray ionization (UHPLC-ESI-MS/MS) method has been developed for the quantificat

281 trospray ionization-mass spectrometry (UHPLC-ESI-MS), and partial least-squares regression (PLSR).

282 y ionization-tandem mass spectrometry (UHPLC-ESI-MS/MS) method was developed for the analysis of AAB

283 suitable for high-throughput targeted UHPLC-ESI-MS/MS metabolomic analysis in large-scale clinical a

284 of the fractions was performed using a UPLC-ESI-MS(n) method.

285 In this report, a UPLC-ESI-MS/MS method for the simultaneous determination of a

286 A UPLC-ESI-MS/MS methodology based on the precursor ion scan of

287 This was confirmed by UPLC-ESI-MS/MS analyses.

288 romatography and analyze them by nanoRP-UPLC-ESI-MS.

289 t suitable for high-throughput targeted UPLC-ESI-MS/MS metabonomic analysis in clinical and epidemiol

290 in full scan mode was combined with the UPLC-ESI-MS/MS system to confirm the identity of detected myc

291 The utility of F-TD/CIMS + UPLC/ESI-MS is demonstrated by application to alpha-pinene oz

292 The complementary F-TD/CIMS + UPLC/ESI-MS method offers previously inaccessible insight int

293 ctrospray ionization mass spectrometry (UPLC/ESI-MS).

294 ne oxidation products on the filter via UPLC/ESI-MS.

295 m the GP, are screened against the GBP using ESI-MS to identify the glycans that are recognized by th

296 olymer and the SCNPs can be well ionized via ESI MS, and the strong covalent cross-links are stable d

297 for cyclopeptide alkaloids was proposed via ESI-MS.

298 characterized at cryogenic temperatures via ESI-MS and UV-vis, (2)H NMR, and EPR spectroscopies.

299 Combining capillary microsampling with ESI-MS enabled targeted sampling of the xylem sap and si

300 For simpler and improved quantitation with ESI-MS, laser-induced fluorescent images were collected