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 data revealed that GM1, GM2, and GM3 were up-regu

3 ESI-MS, NMR, and DFT mechanistic studies reveal that the

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

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

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

7 he variation of the catalyst composition and ESI-MS analysis of the resulting products provided infor

8 ents with radical scavengers and DMSO-d6 and ESI-MS observations.

9 trene species 3(P2)(Ns) according to EPR and ESI-MS spectroscopic studies.

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

11 HPLC and ESI-MS analysis proved the presence of a mixture of acyl

12 HPLC and ESI-MS/MS results indicated the presence of vanillic, sy

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

14 aging, electrospray current measurement, and ESI-MS detection of a model analyte all confirm the MES

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

16 chromatography online coupled to ESI-MS and ESI-MS(n).

17 d sequences were determined using ESI-MS and ESI-MS/MS, respectively.

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

19 tion of phenO2 was confirmed by (1)H NMR and ESI-MS methods.

20 Monitoring the reaction with NMR and ESI-MS provided strong evidence for the nitrogen extrusi

21 aryl phosphoimidazoles was probed by NMR and ESI-MS techniques.

22 l X-ray diffraction, FT-IR, UV/Vis, NMR, and ESI-MS spectrometry.

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

24 s used to stain for GM1 and GM3 species, and ESI-MS was used to quantify the ganglioside species expr

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

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

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

28 Product analysis by ESI-MS revealed that the [(13)CU]glucose unit was added

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

30 C6(glc) sucrose and lactose were analyzed by ESI-MS(n), and the fragmentation patterns of these compo

31 that an older report of "MbO2" detection by ESI-MS may involve the misassignment of oxidation artifa

32 xed aggregate, which is observed directly by ESI-MS.

33 ure of the heteroleptic cage was examined by ESI-MS, COSY, DOSY, and NOESY methods, the latter of whi

34 ology to perform CZE separation, followed by ESI-MS infusion of the different fractions using the cap

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

36 he peptide sequence was obtained manually by ESI-MS spectra of GMPH (KGYSSYICDK) and F-II (SSYCIVKICD

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

38 s in the relative abundances (as measured by ESI-MS) of the carbohydrate complexes of a proxy protein

39 of protein-glycolipid complexes observed by ESI-MS reflect the relative concentrations in solution.

40 these ligand-bound forms can be observed by ESI-MS.

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

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

43 L and La(3+), and the same was supported by ESI-MS.

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

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

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

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

48 sent results with data obtained with the CaR-ESI-MS assay implemented using nanodiscs (NDs) revealed

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

50 th sheathless capillary electrophoresis (CE)-ESI-MS was evaluated for glycopeptide analysis.

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

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

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

54 asurements, similar values were found for CE-ESI-MS with DEN-gas.

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

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

57 ity fosters the use of DEN-gas sheathless CE-ESI-MS in protein glycosylation analysis, where precisio

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

59 ophoresis-electrospray mass spectrometry (CE-ESI-MS) for separation and simultaneous quantification.

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

61 The CE-ESI-MS methodology described here is a rapid and generic

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

63 DNA models have been analyzed by a combined ESI MS and X-ray diffraction (XRD) approach.

64 Using HPLC-coupled ESI-MS/MS, quercetin metabolites, including methylated a

65 zene were examined by X-ray crystallography, ESI MS, and NMR techniques.

66 tively, capillary zone electrophoresis (CZE)-ESI-MS/MS has great potential for phosphoproteome analys

67 an original strategy to perform off-line CZE-ESI-MS using CZE-UV/fraction collection technology to pe

68 the background electrolyte (BGE), online CZE-ESI-MS coupling is difficult to implement for mAbs isofo

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

70 for their quantitative profiles by HPLC-DAD-ESI-MS analyses.

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

72 HPLC-DAD-ESI-MS(n) analyses allowed the identification of sixteen

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

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

75 berry extracts, were studied using HPLC-DAD-ESI-MS/MS and CUPRAC assays, respectively.

76 onents of sumac fruit epicarp using HPLC-DAD-ESI-MS/MS in two different ionisation modes.

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

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

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

80 ionization tandem mass spectrometry (LC-DAD-ESI-MS/MS), whereby the two purine alkaloids were detect

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

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

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

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

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

86 HPLC-DAD/ESI-MS(n) measurements in the fruits' peel and pulp show

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

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

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

90 Using a newly developed ESI-MS assay, the proxy ligand method, the association c

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

92 were compared with those obtained by direct ESI-MS detection as well as LC-ESI-MS.

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

94 Ligand loss during ESI-MS is around 20%.

95 term electrostatic precipitation-ESI-MS (EP-ESI-MS), is shown to enable analysis of nanogram quantit

96 We additionally show that EP-ESI-MS has a dynamic range of close to 5 orders of magni

97 With EP-ESI-MS, the integrated mass spectrometric signals are fo

98 combination of several methods such as EPR, ESI-MS, X-ray, in situ IR kinetics, and DFT calculations

99 by UV-vis absorption, resonance Raman, EPR, ESI-MS, and XAS analyses.

100 ectrospray ionization mass spectrometry (FIA-ESI-MS).We used series dilutions of HL-60 cell extracts

101 hod is described herein using time-of-flight ESI-MS/MS to effectively fragment and identify short pep

102 molecular weight protein, cytochrome-c, for ESI-MS detection.

103 The situation is more favorable for ESI-MS studies on Hb.

104 IPS addresses two major drawbacks of IPC for ESI-MS: it avoids both ion suppression and ion source co

105 e ratios are approximately 10x higher in HDC-ESI-MS than in direct infusion ESI-MS experiments (with

106 We suggest that HDC-ESI-MS can be used in quality control analyses of biopar

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

108 However, ESI-MS is incompatible with nonvolatile solution additiv

109 HPLC-ESI-MS/MS analysis showed that levels of indole-3-acetic

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

111 intact N-glycopeptidome and analyzed by HPLC-ESI-MS together to enable the identification of peptide

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

113 e application and modification of a new HPLC-ESI-MS/MS sum parameter method to quantitate PA content

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

115 RP-HPLC-ESI-MS/MS results showed different peptides occurring in

116 roducts were analyzed by RP-HPLC and RP-HPLC-ESI-MS/MS.

117 ay ionisation source/mass spectrometry (HPLC-ESI-MS).

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

119 ay ionisation tandem mass spectrometry (HPLC-ESI-MS/MS) method was used for the phenolic compounds an

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

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

122 s that were extracted and quantified by HPLC/ESI-MS/MS measurements.

123 Comparison of HPLC/ESI-MS and HPLC/DAD indicated that HPLC/ESI-MS is more s

124 HPLC/ESI-MS and HPLC/DAD indicated that HPLC/ESI-MS is more sensitive, reliable and selective.

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

126 using an elution head-based interface (HPTLC-ESI-MS).

127 trospray ionization mass spectrometry (HPTLC-ESI-MS) via the elution-head-based TLC-MS Interface.

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

129 ting efficient analyte ionization desired in ESI-MS analysis.

130 higher in HDC-ESI-MS than in direct infusion ESI-MS experiments (with or without dilution).

131 compared favorably to results from infusion-ESI-MS and imaging CE (iCE) analysis of the ADC, techniq

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

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

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

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

136 The IXC/ESI MS measurements allow protein conjugates to be profi

137 enoids were analyzed and characterized by LC-ESI MS.

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

139 LC-ESI-MS (liquid chromatography-electrospray ionization-ma

140 LC-ESI-MS mass spectra were successfully obtained and used

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

142 gation, the analysis with conventional 1D-LC-ESI-MS/MS approaches can lead to incomplete glycosylatio

143 2D LC-ESI-MS/MS showed that the expression of neurotrimin (NTM

144 coupled to a tandem mass spectrometry (2D LC-ESI-MS/MS) in high definition mode (HDMS(E)) to identify

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

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

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

148 s kappa-casein, analysed by Urea-PAGE and LC-ESI-MS, whereas the degradation of alpha and beta-casein

149 ned by direct ESI-MS detection as well as LC-ESI-MS.

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

151 nm which were separated and identified by LC-ESI-MS as catechol-diglycine adduct that undergoes polym

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

153 ssues, especially liver, as determined by LC-ESI-MS/MS.

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

155 able, we have now developed an efficient, LC-ESI-MS/MS-based protocol for the quantitative analysis o

156 When compared to previously reported nano-LC-ESI-MS measurements, similar values were found for CE-ES

157 id chromatography-mass spectrometry (nano-LC-ESI-MS), a better ESI performance has been observed when

158 ction unachieved by state-of-the-art nano-LC-ESI-MS.

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

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

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

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

163 lectrospray ionization-mass spectrometry (LC-ESI-MS) is a versatile and robust platform for metabolom

164 lectrospray ionization mass spectrometry (LC-ESI-MS), where the eluent does not contain any ion-pairi

165 hy-electrospray tandem mass spectrometry (LC-ESI-MS/MS) in the positive ion mode with DMA D6 as an in

166 to electrospray tandem mass spectrometry (LC-ESI-MS/MS) is widely used in proteomic and metabolomic w

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

168 pray ionization tandem mass spectrometry (LC-ESI-MS/MS) methods, based on data-dependent acquisition

169 hy-electrospray tandem mass spectrometry (LC-ESI-MS/MS) was developed to measure trace levels of sulf

170 pray ionization tandem mass spectrometry (LC-ESI-MS/MS).

171 ample-to-solvent dilution ratios) and the LC-ESI-MS data acquisition steps of the metabolomics workfl

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

173 The detection limit of the LC-ESI-MS/MS method was 0.03 muM InsP(n), which is superior

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

175 Changes in samples were monitored with LC-ESI-MS coupled with UV and fluorescence detectors.

176 PM2 samples were further inspected by LC/(-)ESI-MS/MS using commercial as well as de novo synthesize

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

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

179 ionization tandem mass spectrometry (LMD-LVC/ESI-MS/MS) system for online and absolute quantitation o

180 try (ESI-MS) and characterized by tandem MS (ESI-MS(n)).

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

182 ay ionization tandem-mass spectrometry (muLC-ESI MS/MS).

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

184 erated by nano-electrospray ionization (nano-ESI-MS-MS) and NMR techniques were utilized for the iden

185 ctrospray-ionization mass spectrometry (nano-ESI-MS), ion mobility (IM), and native top-down electron

186 rospray ionization-mass spectrometry (nanoLC-ESI-MS) detection.

187 lient protein carried out directly by native ESI MS without the need to use relatively homogeneous su

188 formation that can be provided by IXC/native ESI MS and tandem mass spectrometry (MS/MS) on protein-b

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

190 licited through the changes observed in NMR, ESI MS, emission, and absorption spectroscopy.

191 copic and spectrometric studies (1D, 2D NMR, ESI-MS, and MS/MS).

192 early demonstrated on the basis of (1)H NMR, ESI-MS, and absorption spectroscopy, and the heat change

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

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

195 f the transfer line removes the influence of ESI-MS on FFE, but creates a current leak from the ESI i

196 l, work from this study validates the use of ESI-MS for cell-derived gangliosides and supports the fu

197 tudy will further demonstrate the utility of ESI-MS and its applicability to process control monitori

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

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

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

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

202 duct formation was monitored by RP-UHPLC-PDA-ESI-MS.

203 isation mass spectrometric detection (LC/PDA/ESI-MS).

204 e, which we term electrostatic precipitation-ESI-MS (EP-ESI-MS), is shown to enable analysis of nanog

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

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

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

208 ay ultraviolet visible (PDA) UV-Vis spectra, ESI-MS spectrometric data and spiking experiments with a

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

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

211 rospray ionization-tandem mass spectrometry (ESI MS MS).

212 e electrospray ionization mass spectrometry (ESI MS) allows characterization of complex and heterogen

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

214 e electrospray ionization mass spectrometry (ESI MS) in combination with limited charge reduction in

215 g electrospray ionization mass spectrometry (ESI MS) to find out the mechanism of fluorescent quenchi

216 Electrospray ionization-mass spectrometry (ESI-MS) analysis combined with the use of nanodiscs (NDs

217 r electrospray ionization mass spectrometry (ESI-MS) analysis of biological samples.

218 n electrospray ionization mass spectrometry (ESI-MS) analysis showed characteristic and similar TAG p

219 r electrospray ionization-mass spectrometry (ESI-MS) analysis via a simple liquid-liquid extraction p

220 y electrospray ionization mass spectrometry (ESI-MS) and capillary isoelectric focusing (cIEF), which

221 y electrospray ionization mass spectrometry (ESI-MS) and characterized by tandem MS (ESI-MS(n)).

222 e electrospray ionization mass spectrometry (ESI-MS) and immunohistochemistry to evaluate the tempora

223 e electrospray ionization mass spectrometry (ESI-MS) and IR spectroscopy; nu(N-O) absorptions at 1520

224 y electrospray ionization mass spectrometry (ESI-MS) and measurements of worn surfaces by time-of-fli

225 s electrospray ionization mass spectrometry (ESI-MS) and picodiscs, which are composed of human sphin

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

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

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

229 t electrospray ionization mass spectrometry (ESI-MS) experimental results reflect the situation in so

230 o electrospray ionization-mass spectrometry (ESI-MS) for rapid extraction and real time analysis of v

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

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

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

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

235 h electrospray ionization-mass spectrometry (ESI-MS) is presented in this work as an alternative appr

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

237 e electrospray ionization mass spectrometry (ESI-MS) of low molecular weight cationic samples prepare

238 y electrospray ionization-mass spectrometry (ESI-MS) owing especially to the low polarity of the func

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

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

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

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

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

244 Electrospray ionization-mass spectrometry (ESI-MS) was tested for its use in monitoring spent nucle

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

246 y electrospray ionization-mass spectrometry (ESI-MS), proton nuclear magnetic resonance ((1)H-NMR), a

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

248 y or nanospray ionization mass spectrometry (ESI-MS).

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

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

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

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

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

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

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

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

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

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

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

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

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

262 ere, we describe the results of a systematic ESI-MS study aimed at elucidating the processes that inf

263 ass spectrometry, challenges the notion that ESI-MS results directly reflect solution-phase structure

264 The isotopic peak pattern observed in the ESI MS confirmed the presence of Zn(2+) or Cu(2+) presen

265 The ESI-MS and MALLS data revealed that POPC-PDs consist pre

266 The ESI-MS protocols used in this study will further demonst

267 The ESI-MS spectra showed a molecular mass shift between 183

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 The results of the ESI-MS measurements reveal that proteins bind reversibly

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

272 ctrophoresis (FFZE) technique prior to their ESI-MS analysis.

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

274 d by liquid chromatography online coupled to ESI-MS and ESI-MS(n).

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

276 using high resolution mass analysis (HR-ToF-ESI-MS).

277 foundational technology piece for transient ESI-MS measurements of complex biological liquid specime

278 diffusivities between salts and the typical ESI-MS target bioanalytes, e.g., peptides and proteins.

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

280 hroughput, comprehensive and accurate UHPSFC/ESI-MS method is suitable for the lipidomic analysis of

281 Developed UHPSFC/ESI-MS method is applied for the analysis of porcine bra

282 The final UHPSFC/ESI-MS method enables a fast separation of 30 nonpolar a

283 were studied using EPR, UV-vis, IR, VCD, UHR-ESI-MS, and XANES/XAFS measurements.

284 CN, while MbCO and MbO2 do not survive under ESI-MS conditions.

285 or purified alpha-CN was assessed using UPLC ESI MS/MS.

286 ide sequences were identified following UPLC-ESI MS/MS analysis of SP RP-HPLC 25_F28.

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

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

289 cterized and quantified by HPLC-MWD and UPLC-ESI-MS.

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

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

292 Furthermore, the UPLC-ESI-MS/MS analysis showed an increase of several nutrace

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

294 Oligopeptides were determined by UPLC/ESI-MS and 35 low-molecular weight peptides were identif

295 d amino acid sequences were determined using ESI-MS and ESI-MS/MS, respectively.

296 nents in the juice was made using an HPLC-UV-ESI-MS method.

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

298 ale FFE (using a highly conductive BGE) with ESI-MS.

299 c resolution and complete compatibility with ESI-MS without sample treatment, hydroxypropylcellulose

300 ction configuration was further studied with ESI-MS, FTIR, XPS and XANES characterizations.