ライフサイエンスコーパス: ESI

1 ESI >3.7 g/day is associated with adverse cardiac remode

2 ESI >3.7 g/day was associated with larger left atrial an

3 ESI MS measurements confirmed formation of stable adduct

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

5 ong subjects) with linear splines (spline 1: ESI </=3.7 g/day, spline 2: ESI >3.7 g/day based on visu

6 lines (spline 1: ESI </=3.7 g/day, spline 2: ESI >3.7 g/day based on visual inspection of fractional

7 were created for both modes of acquisition (ESI-/ESI+) and red meat intake classes (YES/NO).

8 We evaluated the associations among ESI and LS, circumferential strain, and e' velocity usin

9 An ESI ion trap mass spectrometer was designed for high-thr

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

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

12 7, and 12 patients had combined EEG-fMRI and ESI that was correct in 11.

13 e highest EC (87.91%), EAI (87.18m(2)/g) and ESI (12.51min) compared to the other protein concentrate

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

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

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

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

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

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

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

21 sing both EEG-fMRI hemodynamic responses and ESI.

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

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

24 iminates the requirement for adding acids as ESI(+) additives, which are normally used to favor proto

25 ation with other ionization methods, such as ESI, for FTICR MS studies of NOM.

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

27 ion we used a low conductivity, silica-based ESI probe with withdrawn inner capillary.

28 polynomial plots of the association between ESI and indices of strain and e' velocity).

29 14% and 20% of the indirect effects between ESI and LS and e' velocity, respectively, whereas serum

30 xplained 19% of the indirect effects between ESI and LS.

31 erum aldosterone on the relationship between ESI and strain and e' velocity.

32 ures, appears to have the attributes of both ESI and SAI.

33 velocity (p < 0.05 for all comparisons), but ESI </=3.7 g/day was not (p > 0.05 for all comparisons).

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

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

36 s C for 3h and the residues were analyzed by ESI/qTOF/MS using MS/MS and isotope labeling techniques.

37 egrees C for 2h and subsequently analyzed by ESI/qTOF/MS/MS in addition to isotope labelling techniqu

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

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

40 s (reagents, intermediates, and products) by ESI(+)-MS.

41 tes were successfully ionized in solution by ESI and directly from steel surfaces using DESI ambient

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

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

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

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

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

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

52 electrophoresis electrospray ionization (CE-ESI)-MS are complementary analytical platforms frequentl

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

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

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

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

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

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

59 The tool extends CFM-ESI, a recently developed method for computational predi

60 dem mass spectra (ESI-MS/MS), but unlike CFM-ESI, CFM-EI can handle odd-electron ions and isotopes an

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

62 gnitude to that observed with a conventional ESI source on the same instrument.

63 ching to a TD-ESI source from a conventional ESI source.

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

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

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

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

68 cs (measured by Folin Ciocalteu and HPLC-DAD-ESI/MS(n)) at harvest and during storage for 21days at 2

69 ization/ion trap mass spectrometry (HPLC-DAD-ESI/MS(n)).

70 nd 4 betacyanins were identified by HPLC-DAD-ESI/MS(n), 23 and 15 new compounds being described in ye

71 y detector and a mass spectrometer (HPLC-DAD-ESI/MS).

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

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

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

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

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

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

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

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

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

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

85 xtraction method combined with electrospray (ESI)-FTICR is supported by the significant reduction of

86 often a matter of trial and error to enhance ESI efficiency and, hence, the response of a given set o

87 created for both modes of acquisition (ESI-/ESI+) and red meat intake classes (YES/NO).

88 ospray ionization quadrupole time-of-flight (ESI-Q-TOF) mass spectrometry was used to investigate pro

89 The combined EEG-fMRI/ESI region entirely predicted outcome in 9 of 9 patients

90 from the combination of both maps (EEG-fMRI/ESI spatial intersection).

91 nt maps: 47 of 53 for EEG-fMRI, 44 of 53 for ESI, and 34 of 53 for both.

92 The use of FAIMS improved selectivity for ESI generated analyte ions through reduction in the chem

93 individual test (EEG-fMRI global maxima [GM]/ESI maximum) and from the combination of both maps (EEG-

94 tion that was correct in 11, 22 patients had ESI localization that was correct in 17, and 12 patients

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

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

97 HPLC-ESI-ITMS/MS results highly correlated with those obtaine

98 HPLC-ESI-Q-TOF allowed the detection of 25 different raw form

99 ship between CM determined by ELISA and HPLC-ESI-ITMS/MS and therefore supports the implementation of

100 mpares three different ELISA assays and HPLC-ESI-ITMS/MS for the analysis of CML in several food item

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

102 treatment were clearly distinguished by HPLC-ESI-ITMS/MS, but could not always be detected by ELISA.

103 he first characterisation of shellac by HPLC-ESI-Q-ToF and an atlas of MS/MS spectra of shellac compo

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

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

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

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

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

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

110 epicarp of this fruit was studied using HPLC/ESI-TOF-MS.

111 assigned as [8]- and [10]-gingerol via HPTLC-ESI-HRMS.

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

113 ts for both steps are provided based on HRMS-ESI(+) studies.

114 rive EEG-fMRI and electrical source imaging (ESI) maps.

115 In ESI, 2-ring MDA isomers formed single unique [M + H](+)

116 ization efficiency of different compounds in ESI source differs by orders of magnitude.

117 ly predicting the ionization efficiencies in ESI source based on a model, which uses physicochemical

118 lene glycol units led to the largest gain in ESI response.

119 iochemically profiled using UHPLC-QTof-MS in ESI+ mode of acquisition.

120 ions of interest explained the variation in ESI+.

121 ty index (EAI) and emulsion stability index (ESI), water absorption capacity (WAC) and fat absorption

122 ction fraction, and wall motion score index, ESI >3.7 g/day was associated with both strain parameter

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

124 on of Epac1 with an Epac specific inhibitor, ESI-09, phenocopied the effects of Epac1 null by suppres

125 rimental effects of estimated sodium intake (ESI) on subclinical cardiovascular disease.

126 sheath liquid of the electrospray interface (ESI), generated a highly efficient and sensitive method.

127 which results in low electrospray interface (ESI)-MS sensitivity.

128 s bias in its 2008 early-stage investigator (ESI) policy to fund young PIs at higher rates.

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

130 A strategy based on electrospray ionisation (ESI) in negative mode coupled with quadrupole-time of fl

131 phy (UPLC)/negative electrospray ionization (ESI(-))/quadrupole time-of-flight mass spectrometry (qTO

132 Electrospray ionization (ESI) allows the production of intact gas-phase ions from

133 luated against both electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI)

134 A comparison of electrospray ionization (ESI) and LDI spectra showed that different types of comp

135 t to ionize by both electrospray ionization (ESI) and matrix-assisted laser desorption ionization (MA

136 positive aspects of electrospray ionization (ESI) and solvent-assisted ionization (SAI).

137 formity in positive electrospray ionization (ESI) efficiencies across the various PL subclasses.

138 Electrospray ionization (ESI) high resolution accurate mass (HRAM) mass spectrome

139 Electrospray ionization (ESI) is widely used in liquid chromatography coupled to

140 LS DESI MS, and in electrospray ionization (ESI) MS, which produced the most intense ion signals fro

141 roflow and nanoflow electrospray ionization (ESI) of peptides in a way that prevents the formation of

142 Electrospray ionization (ESI) of solution mixtures often generates complex mass s

143 Electrospray ionization (ESI) of ubiquitin from acidified (0.1%) aqueous solution

144 led to the negative electrospray ionization (ESI) quadrupole tandem mass spectrometry (MS/MS) was use

145 hange) coupled with electrospray ionization (ESI), allowed us to obtain detailed understanding about

146 spray stability in electrospray ionization (ESI), in particular for nanospray applications.

147 ionization (MALDI), electrospray ionization (ESI), tandem mass spectrometry (MS(2)), and ion mobility

148 protein analysis by electrospray ionization (ESI)-collision-induced dissociation (CID)-FTICR MS was a

149 is an interface for electrospray ionization (ESI)-mass spectrometry (MS) that exploits a swirling flo

150 High-resolution electrospray ionization (ESI)-Orbitrap MS analyses identified pyrimidine photohyd

151 ctrometry (MS) with electrospray ionization (ESI).

152 sitive and negative electrospray ionization (ESI).

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

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

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

156 zing negative mode Electro Spray Ionization (ESI).

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

158 LC-ESI/MS/MS was also used to tentatively identify the CPA

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

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

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

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

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

164 17, respectively, were not identified by LC-ESI-QTOF-MS.

165 cation of phytochemicals was performed by LC-ESI/MS and the correlation between the phytochemical com

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

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

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

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

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

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

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

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

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

175 The LC-ESI/LTQOrbitrap/MS profile of the methanolic extract of

176 d MW 214 Da (C10H14O5) was confirmed with LC-ESI/MS/MS.

177 n in field conditions using a validated LC-(+ESI)MS/MS method.

178 LC/ESI/MS is a technique widely used for qualitative and qu

179 nd their metabolites were investigated by LC/ESI-Orbitrap-MS in urine and finger nails collected from

180 ntially long analysis times per sample of LC/ESI-MRM-MS.

181 r we present an approach for quantitative LC/ESI/MS analysis without standard substances.

182 le reaction monitoring mass spectrometry (LC/ESI-MRM-MS) are more commonly used in clinical research.

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

184 m the human embryonic stem cell (hESC), line ESI-017.

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

186 is work, we report on a novel combined MALDI/ESI interface, which was coupled to different Orbitrap m

187 In tissue imaging experiments, the MALDI/ESI interface has been employed in experiments with rat

188 The median ESI was 3.73 (interquartile range: 3.24, 4.25) g/day.

189 ted and deprotonated using negative-ion mode ESI in a linear quadrupole ion trap/Fourier transform io

190 )/UPLC-MS/MS (positive and negative ion mode ESI) and HILIC/UPLC-MS/MS with negative ion mode ESI.

191 and HILIC/UPLC-MS/MS with negative ion mode ESI.

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

193 e betacyanins quantification (by HPLC-PDA-MS/ESI and spectrophotometric analysis), the extraction-yie

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

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

196 Currently, nano-ESI is typically done at capillary LC flow rates ranging

197 monstrate the application of the pulsed nano-ESI AP-IM-MS with enhanced ion sampling for detection of

198 soft ion generation, we report a pulsed nano-ESI source to introduce a packet of ions into the room-t

199 psin and chymotrypsin and analyzed by nanoLC-ESI-IT-MS/MS.

200 e highest activity were identified by nanoLC-ESI-QTOF-MS and thirteen peptides were selected for synt

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

202 has been unequivocally characterized by NMR, ESI-IM-MS, and TEM techniques.

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

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

205 s to examine how SCAs affect the behavior of ESI nanodroplets.

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

207 on the basis of the additional dimension of ESI-TOF-MS.

208 an ionization selectivity similar to that of ESI but, at higher inlet temperatures, appears to have t

209 our knowledge for the first time, the use of ESI-FTICR MS and MALDI-FTICR MS is described in a comple

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

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

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

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

214 compounds which were identified by HPLC-PDA-ESI/MS(n) as the biflavonoids morelloflavone, Gb-2a and

215 atoms or nitro groups gave a lower predicted ESI response.

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

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

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

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

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

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

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

223 performed via both tandem mass spectrometry (ESI(+)-MS/MS) and accurate m/z measurements.

224 m ion cyclotron resonance mass spectrometry (ESI-FTICRMS) and discovers additional substructural comp

225 y ionization ion mobility-mass spectrometry (ESI-IM-MS) and collision-induced unfolding (CIU) analysi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

249 ionization time-of flight mass spectrometry (ESI-TOF-MS).

250 high-performance ion mobility spectrometry (ESI-HPIMS).

251 d X-ray absorption (near-edge) spectroscopy, ESI mass spectrometry, and DFT methods.

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

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

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

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

256 , emulsifying activity (EAI), and stability (ESI) indexes) properties of alkali-(A-FPC), enzymatic-(E

257 r the higher biotin-load when using standard ESI conditions as opposed to nanoESI native-MS condition

258 tative confirmation) after switching to a TD-ESI source from a conventional ESI source.

259 d challenges associated with the use of a TD-ESI source to detect adulterants on traditional Chinese

260 equate sensitivity within 30s, the use of TD-ESI for semi-quantification is applicable only for homog

261 esorption/electrospray ionization source (TD-ESI) is a relatively new technique that has had only a l

262 While TD-ESI can offer direct (i.e., without any sample preparati

263 ve protein conformation is conserved in TENG-ESI, and that patterned ion deposition on conductive and

264 ween the calculated molecular volume and the ESI response, while correlation with hydrophobicity (log

265 re are attributed to differences between the ESI and DESI ionization processes.

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

267 EEG-fMRI GM in 8 of 20 patients, and by the ESI maximum in 13 of 16.

268 By comparing the ESI response of 70 derivatives, we found that there was

269 ure, while aliphatic compounds dominated the ESI spectra of SRFA.

270 The estimated resolving power for the ESI-HPIMS used in this study was 61 +/- 0.22.

271 However, the ESI process is still not completely understood, and it i

272 re ionized in the APCI source but not in the ESI source.

273 lets while accelerating the remainder of the ESI plume, producing a high velocity stream of gas-enric

274 omplex formation occurs independently of the ESI process.

275 work we performed a systematic study of the ESI response of 14 amino acids that were acylated with o

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

277 physicochemical descriptors relating to the ESI response from molecular structures using the amino a

278 During transport to the ESI source drug related material was completely extracte

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

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

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

282 al background ions were observed relative to ESI for all drugs and peptides tested at flow rates from

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

284 me-of-flight tandem mass spectrometry (UHPLC-ESI-QTOF-MS/MS) metabolite profiling data of saponins an

285 o tandem mass spectrometry detection (UHPLC-(ESI)MS/MS).

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

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

288 Compounds were identified by UPLC-ESI-qTOF-MS/MS in negative ion mode.

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

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

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

292 Using ESI-qToF, we observed that the ligand was a derivative o

293 sine cross-linked dimer of Abeta(1-16) using ESI tandem mass spectrometry.

294 By using ESI-QTOF-MS technique, formation of glycated cytochrome

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

296 istance to matrix suppression effects, while ESI performance was impacted the most dramatically.

297 at a spatial resolution of 15-30 mum, while ESI-generated ions are injected orthogonally to the inte

298 (maximum number of species for O7-O9), while ESI compounds belong to higher oxygen classes (maximum n

299 INTERPRETATION: EEG-fMRI combined with ESI provides a simple unbiased localization that may pre

300 , explaining why they were not observed with ESI.