ライフサイエンスコーパス: electrospray

1 loading substrate and an emitter to generate electrospray.

2 be mandatory for the generation of a stable electrospray.

3 llary and the resulting shape of the primary electrospray.

4 tes molecules within evaporating droplets in electrosprays.

5 nanoparticles were synthesized via co-axial electrospraying.

6 incorporation of curcumin microcrystals upon electrospraying.

7 AuNPs) and targeted their delivery using the electrospray aerosol generator.

8 , operating in negative polarity with heated electrospray, allowed to detect over eighty free and gly

9 es and animal cells are disintegrated during electrospray, and the constituent lipids are ionized.

10 Electrospray- and atmospheric pressure photoionization (

11 n mechanisms, including corona discharge and electrospray, are involved in the ionization of analytes

12 Except in limited circumstances, electrospray based aerosolization has proven difficult t

13 LDTD could also be coupled with plasma- or electrospray-based ionization for the analysis of a vari

14 t amount of sample and from that same tip an electrospray can be directed into a mass spectrometer.

15 Using native-like incubation and electrospray conditions together with an automated tool

16 response of monomeric proteins under native electrospray conditions.

17 We evaluated electrospray deposition of liquid-phase derivatization a

18 ation, such as corona discharge, arcing, and electrospray destabilization, because of the presence of

19 This study presents an upgraded electrospray differential mobility analysis (ES-DMA) set

20 The novel hyphenation of electrospray-differential mobility analysis with single

21 s unfold before or during evaporation of the electrospray droplet and ionization occurs by the Chain

22 tivation of the intact complex in either the electrospray droplet or the gas phase produced c-type fr

23 tions for the evolution of a salt-containing electrospray droplet, this study provides a more complet

24 protein and detergent/lipid micelles in the electrospray droplet.

25 separation to prescribe different fates for electrosprayed droplets based on their size.

26 ained via vortex-induced inertial sorting of electrosprayed droplets/ions: one possible mode of DRILL

27 approach to measure flow rates at the tip of electrospray emitters when the ionization voltage is tur

28 with mass spectrometry via fully integrated electrospray emitters.

29 r intact protein complexes typically require electrospray (ES) ionization and have not been achieved

30 The extraction method combined with electrospray (ESI)-FTICR is supported by the significant

31 ted at a mass resolution of 100 000 to allow electrospray-generated ions of the deprotonated glucose

32 ropolymerized aniline deposited on top of an electrosprayed graphene/polyaniline (G/PANI) modified sc

33 d as an additive to the sheath liquid of the electrospray interface (ESI), generated a highly efficie

34 and low proton affinity which results in low electrospray interface (ESI)-MS sensitivity.

35 ays the analyte ions can rearrange following electrospray into kinetically stable gas-phase conformat

36 PCO(-), and PCS(-) anions were successfully electrosprayed into a vacuum, and these three ECX(-) ani

37 nding graphene were prepared by soft-landing electrospray ion beam deposition, which allows chemical-

38 n-evaporation process that occurs during the electrospray ion generation process.

39 Ions are generated in an electrospray ion source with a sampling cone interface a

40 A strategy based on electrospray ionisation (ESI) in negative mode coupled w

41 Electrospray ionisation mass spectrometry (ESI-MS) sugge

42 termination of their amino acid sequences by electrospray ionisation mass spectrometry (ESI-MS/MS).

43 equence comparisons, homology modelling, and electrospray ionisation mass spectrometry.

44 liquid chromatography-diode array detection-electrospray ionisation multistage mass spectrometry.

45 id chromatography combined with negative-ion electrospray ionisation quadrupole mass spectrometry.

46 ed on high-performance liquid chromatography/electrospray ionisation source/mass spectrometry (HPLC-E

47 ion (MALDI) MS and capillary electrophoresis electrospray ionization (CE-ESI)-MS are complementary an

48 e integration and optimization of desorption electrospray ionization (DESI) and liquid-microjunction

49 Desorption electrospray ionization (DESI) has emerged as a powerful

50 Here, we used desorption electrospray ionization (DESI) mass spectrometry (MS) to

51 ect analysis in real time (DART), desorption electrospray ionization (DESI), or low-temperature plasm

52 mination of tissue sections using desorption electrospray ionization (DESI)-MS revealed phospholipid-

53 ass spectrometric techniques like desorption electrospray ionization (DESI).

54 rmance liquid chromatography (UPLC)/negative electrospray ionization (ESI(-))/quadrupole time-of-flig

55 Electrospray ionization (ESI) allows the production of i

56 (FF-APPI) source was evaluated against both electrospray ionization (ESI) and atmospheric pressure c

57 A comparison of electrospray ionization (ESI) and LDI spectra showed tha

58 arity makes them difficult to ionize by both electrospray ionization (ESI) and matrix-assisted laser

59 on inlet (ESII) combines positive aspects of electrospray ionization (ESI) and solvent-assisted ioniz

60 L) leads to increased uniformity in positive electrospray ionization (ESI) efficiencies across the va

61 Electrospray ionization (ESI) Fourier transform ion cycl

62 Electrospray ionization (ESI) high resolution accurate m

63 ) has been coupled online with the aid of an electrospray ionization (ESI) interface to an ion-trap m

64 Electrospray ionization (ESI) is widely used in liquid c

65 DESI MS system, in angled LS DESI MS, and in electrospray ionization (ESI) MS, which produced the mos

66 d phenomena influence microflow and nanoflow electrospray ionization (ESI) of peptides in a way that

67 Electrospray ionization (ESI) of solution mixtures often

68 Electrospray ionization (ESI) of ubiquitin from acidifie

69 nately, TAA is not easily ionized by regular electrospray ionization (ESI) or MALDI.

70 chromatography (LC) coupled to the negative electrospray ionization (ESI) quadrupole tandem mass spe

71 ries at the same time that the efficiency of electrospray ionization (ESI) remained unaltered between

72 ins from rates of H/D exchange) coupled with electrospray ionization (ESI), allowed us to obtain deta

73 mass (and size) cluster ions when ionized by electrospray ionization (ESI), detection of AN/UN using

74 ionization efficiency and spray stability in electrospray ionization (ESI), in particular for nanospr

75 ssisted laser desorption ionization (MALDI), electrospray ionization (ESI), tandem mass spectrometry

76 Subsequent intact protein analysis by electrospray ionization (ESI)-collision-induced dissocia

77 ocomotion) device, which is an interface for electrospray ionization (ESI)-mass spectrometry (MS) tha

78 d ammonia containing buffers compatible with electrospray ionization (ESI)-MS can compromise the inte

79 High-resolution electrospray ionization (ESI)-Orbitrap MS analyses ident

80 (RP-HPLC) separation and parallel ICPMS and electrospray ionization (ESI)-Orbitrap-MS to determine s

81 mentation mode in both positive and negative electrospray ionization (ESI).

82 detection using mass spectrometry (MS) with electrospray ionization (ESI).

83 clusters and weakly bound species created by electrospray ionization (ESI).

84 nhancement effects as compared with standard electrospray ionization (ESI).

85 The NO2-PLs were then detected by electrospray ionization (ESI-MS) and ESI-MS coupled to h

86 urier transfer infrared (ATR-FTIR) analysis, electrospray ionization (ESI-MS), direct analysis in rea

87 its aza-version using mass spectrometry with electrospray ionization (ESI-MS).

88 de array detection (RP-UHPLC-PDA) and heated electrospray ionization (HESI) multistage mass spectrome

89 ng infrared matrix-assisted laser desorption electrospray ionization (IR-MALDESI) mass spectrometry i

90 nt infrared matrix-assisted laser desorption electrospray ionization (IR-MALDESI) mode, allowed the d

91 Laser ablation electrospray ionization (LAESI) is an ambient ionization

92 iological samples using nanospray desorption electrospray ionization (nano-DESI) was developed by int

93 ient ionization source, nanospray desorption electrospray ionization (nanoDESI), interfaced with ligh

94 ng that lipids have a low propensity to form electrospray ionization adducts.

95 ent monosaccharide isomers) are generated by electrospray ionization and analyzed by combined ion mob

96 e) were transferred to the gas phase by nano-electrospray ionization and characterized using UVPD.

97 ity of the ion source operated in desorption electrospray ionization and desorption atmospheric press

98 populating EEIs with POM anions generated by electrospray ionization and gas-phase dissociation.

99 Mass spectrometric measurements both by electrospray ionization and matrix assisted laser desorp

100 are fragile and prone to fragmentation under electrospray ionization and matrix-assisted laser desorp

101 nt ionization techniques, namely, desorption electrospray ionization and paper spray, both coupled to

102 yoglobin, and bovine serum albumin formed by electrospray ionization are measured using charge detect

103 Supercharging electrospray ionization can be a powerful tool for incre

104 formations in live colonies using desorption electrospray ionization coupled with ion mobility mass s

105 For the first time, the electrospray ionization efficiency (IE) scales in positi

106 izes this high Pu affinity subfraction using electrospray ionization Fourier transform ion cyclotron

107 WEOM was determined by ultrahigh resolution electrospray ionization Fourier transform ion cyclotron

108 We used ultra-high-resolution electrospray ionization Fourier transform ion cyclotron

109 otonation site of p-hydroxybenzoic acid upon electrospray ionization has been a subject of fervent de

110 Experiments have been carried out in which electrospray ionization has been used to generate ionic

111 d explosives are detected is reported for an electrospray ionization high-performance ion mobility sp

112 d chromatography, detected via negative mode electrospray ionization high-resolution MS, and their fr

113 Upon elution and electrospray ionization in the negative mode, ultraviole

114 Electrospray ionization inlet (ESII) combines positive a

115 In this paper, laser ablation electrospray ionization ion mobility time-of-flight mass

116 Here, we report results for electrospray ionization ion mobility-mass spectrometry (

117 rformance liquid chromatography coupled with electrospray ionization ion-trap multistage mass spectro

118 -2-propyl) phosphate (BCIPP)] using negative electrospray ionization liquid chromatography tandem mas

119 MR methods (including DOSY, EXSY, and COSY), electrospray ionization mass and UV-vis spectroscopies,

120 (13)C NMR spectra, thermograms, aerosol and electrospray ionization mass spectra, surface activity,

121 n, but the presence of the DS(-) hampers the electrospray ionization mass spectrometric (ESI-MS) anal

122 ation-free assay, based on catch-and-release electrospray ionization mass spectrometry (CaR-ESI-MS),

123 te extraction, and capillary electrophoresis electrospray ionization mass spectrometry (CE-ESI-MS) to

124 ification membranes, we have used desorption electrospray ionization mass spectrometry (DESI MS), whe

125 In this paper, desorption electrospray ionization mass spectrometry (DESI MS)-base

126 ucosal metabolome profiling using desorption electrospray ionization mass spectrometry (DESI-MS) anal

127 rine xenografts were subjected to desorption electrospray ionization mass spectrometry (DESI-MS) imag

128 le of necrotic breast cancer with Desorption Electrospray Ionization Mass Spectrometry (DESI-MS) imag

129 tence and composition of the CEI, desorption electrospray ionization mass spectrometry (DESI-MS) is a

130 gn and geometry on performance in desorption electrospray ionization mass spectrometry (DESI-MS) is a

131 Here, we used desorption electrospray ionization mass spectrometry (DESI-MS) to i

132 tion products from the surface by desorption electrospray ionization mass spectrometry (DESI-MS).

133 oparticle (SCNP) folding via high-resolution electrospray ionization mass spectrometry (ESI MS) coupl

134 In this work we use native electrospray ionization mass spectrometry (ESI MS) in co

135 me monitoring of the hydrolysis of ACh using electrospray ionization mass spectrometry (ESI MS) to fi

136 tion profile of the ADC was characterized by electrospray ionization mass spectrometry (ESI-MS) and c

137 The purpose of this study is to use electrospray ionization mass spectrometry (ESI-MS) and i

138 al approach, which combines the proxy ligand electrospray ionization mass spectrometry (ESI-MS) assay

139 An electrospray ionization mass spectrometry (ESI-MS) assay

140 Recent electrospray ionization mass spectrometry (ESI-MS) data

141 General consensus is that electrospray ionization mass spectrometry (ESI-MS) exper

142 echanistic studies utilizing high-resolution electrospray ionization mass spectrometry (ESI-MS) ident

143 cyclopropylaniline (CPA, 1) and styrene 2 by electrospray ionization mass spectrometry (ESI-MS) in co

144 cRn affinity liquid chromatography (LC) with electrospray ionization mass spectrometry (ESI-MS) in na

145 It was recently established that electrospray ionization mass spectrometry (ESI-MS) is ca

146 Liquid chromatography coupled with electrospray ionization mass spectrometry (ESI-MS) is ro

147 Single crystal X-ray diffraction (SCXRD) and electrospray ionization mass spectrometry (ESI-MS) revea

148 4)D) electropherograms and interference-free electrospray ionization mass spectrometry (ESI-MS) spect

149 Sensitivity of electrospray ionization mass spectrometry (ESI-MS) to th

150 ent of hGal-9 (hGal-9N), were measured using electrospray ionization mass spectrometry (ESI-MS).

151 B capsules in the gas phase was confirmed by electrospray ionization mass spectrometry (ESI-MS).

152 ee-flow electrophoresis (FFE) and sheathless electrospray ionization mass spectrometry (ESI-MS).

153 via small-angle X-ray scattering (SAXS) and electrospray ionization mass spectrometry (ESI-MS).

154 roscopies, elemental (C H N S) analysis, and electrospray ionization mass spectrometry (ESI-MS).

155 Laser-ablation electrospray ionization mass spectrometry (LAESI-MS) is

156 d (PCI-IS) method with liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) fo

157 phy (IPC) approach for liquid chromatography electrospray ionization mass spectrometry (LC-ESI-MS), w

158 (AMS), high-resolution nanospray desorption electrospray ionization mass spectrometry (nano-DESI/HRM

159 Two RMD platforms, PCR combined with electrospray ionization mass spectrometry (PCR/ESI-MS) a

160 Moreover, electrospray ionization mass spectrometry and (1)H as we

161 Analysis of a complex of ICL1:2-VIC by electrospray ionization mass spectrometry and X-ray crys

162 drive allostery, we performed time-resolved electrospray ionization mass spectrometry coupled to hyd

163 We applied an approach combining desorption electrospray ionization mass spectrometry imaging (DESI-

164 We performed desorption electrospray ionization mass spectrometry imaging (DESI-

165 In situ nanospray desorption electrospray ionization mass spectrometry imaging (nano-

166 Electrospray ionization mass spectrometry indicates that

167 Electrospray ionization mass spectrometry is used extens

168 sing online and subsequent offline secondary electrospray ionization mass spectrometry of exhaled bre

169 he yeast Kluyveromyces lactis, with nanoflow electrospray ionization mass spectrometry, and mapped in

170 intermediates were observed by gas-phase and electrospray ionization mass spectrometry, as well as by

171 ucts that are observed using high-resolution electrospray ionization mass spectrometry, but these pro

172 ltracentrifugation, electron microscopy, and electrospray ionization mass spectrometry, with a molecu

173 rformance liquid chromatography coupled with electrospray ionization mass spectrometry.

174 ster conversion reaction using time-resolved electrospray ionization mass spectrometry.

175 user effect spectroscopy and high-resolution electrospray ionization mass spectrometry.

176 One, the cluster size was determined via electrospray ionization mass spectrometry.

177 soft drinks based upon liquid chromatography-electrospray ionization mass spectrometry.

178 tides were analyzed by liquid chromatography electrospray ionization mass spectrometry.

179 a handheld laser source is coupled with nano-electrospray ionization mass spectrometry.

180 complex samples analyzed by direct infusion electrospray ionization mass spectrometry.

181 Through desorption electrospray ionization MS imaging (DESI-MSI), specific

182 ge-state distributions are not resolved from electrospray ionization MS using 1.6 mum diameter emitte

183 eparated by reversed phase LC and ionized by electrospray ionization MS.

184 sed approaches such as liquid chromatography/electrospray ionization multiple reaction monitoring mas

185 Negative-mode electrospray ionization of aqueous solutions of host-gue

186 phenoxide (P(-)) ions (m/z 137) generated by electrospray ionization of p-hydroxybenzoic acid.

187 cationized by the attachment of Na(+) during electrospray ionization operated in the positive ion mod

188 performance liquid chromatography coupled to electrospray ionization Orbitrap mass spectrometry.

189 dditives were tested in order to improve the electrospray ionization process and to detect as many me

190 eduction (ISR) of disulfide bonds during the electrospray ionization process to facilitate disulfide

191 In this study electrospray ionization quadrupole time-of-flight (ESI-Q

192 ygen-18 isotope-labeling, HPLC combined with electrospray ionization quadrupole time-of-flight and hi

193 ultrahigh-performance liquid chromatography-electrospray ionization quadrupole time-of-flight tandem

194 chromatography-tandem mass spectrometry with electrospray ionization source (LC-ESI-MS/MS).

195 using an interchangeable thermal desorption/electrospray ionization source (TD-ESI) is a relatively

196 p (IFT) to accumulate ions from a continuous electrospray ionization source and was limited to inject

197 We have deployed an efficient secondary electrospray ionization source coupled to an Orbitrap ma

198 graphy and tandem mass spectrometry using an electrospray ionization source operating in negative and

199 es are coupled with a temperature-controlled electrospray ionization source to follow the structural

200 A microchip electrospray ionization source was coupled with high pre

201 imately 5 x 10(9) charges introduced from an electrospray ionization source were trapped for a 40 s a

202 lytes in preparation for ionization using an electrospray ionization source.

203 and stoichiometric tests performed using an electrospray ionization spectrometer, revealed the possi

204 matography (HILIC) coupled to a negative-ion electrospray ionization tandem mass spectrometry (ESI-MS

205 ography coupled to diode array detection and electrospray ionization tandem mass spectrometry (LC-DAD

206 ography coupled to diode array detection and electrospray ionization tandem mass spectrometry (LC-DAD

207 n mind, we developed a liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI

208 laser microdissection-liquid vortex capture electrospray ionization tandem mass spectrometry (LMD-LV

209 oped and compared with liquid chromatography electrospray ionization tandem mass spectrometry analysi

210 y and high-performance liquid chromatography electrospray ionization tandem mass spectrometry.

211 detected by microbore liquid chromatography-electrospray ionization tandem-mass spectrometry (muLC-E

212 ra-performance liquid chromatography-coupled electrospray ionization tandem-MS/MS and NMR to determin

213 critical conditions (UP-LCCC) combined with electrospray ionization time-of flight mass spectrometry

214 ethods were studied photometrically and with electrospray ionization time-of-flight mass spectrometry

215 clusters are exclusively detected by common electrospray ionization time-of-flight mass spectrometry

216 y characterized by multinuclear NMR, 2D NMR, electrospray ionization time-of-flight mass, and UV-vis

217 mples using liquid chromatography coupled to electrospray ionization ultrahigh-resolution mass spectr

218 us morphologies were tested using desorption electrospray ionization with plastic objects coated by 2

219 nvironment (charged nanodroplet generated by electrospray ionization) to the solvent-free peptide ion

220 array detection, and mass spectrometry with electrospray ionization); and fatty acids (using gas-liq

221 ed using electrospray ionization, desorption electrospray ionization, and low temperature plasma ioni

222 drophilic interaction liquid chromatography, electrospray ionization, and tandem mass spectrometry in

223 es, and two coffee types were measured using electrospray ionization, desorption electrospray ionizat

224 extremely acidic species can be generated in electrospray ionization, in the presence of not just N2

225 Using electrospray ionization, oligo(triazole amide)s were bes

226 His-2Cys motif peptides were investigated by electrospray ionization-ion mobility-mass spectrometry.

227 bes the application of the catch-and-release electrospray ionization-mass spectrometry (CaR-ESI-MS) a

228 Intraoperative desorption electrospray ionization-mass spectrometry (DESI-MS) is u

229 o be recovered by swabbing and extracted for electrospray ionization-mass spectrometry (ESI-MS) analy

230 t typically do not provide strong signals by electrospray ionization-mass spectrometry (ESI-MS) owing

231 aring MALDI results to those of our previous electrospray ionization-mass spectrometry (ESI-MS) studi

232 Electrospray ionization-mass spectrometry (ESI-MS) was t

233 fluorescence change and it was confirmed by electrospray ionization-mass spectrometry (ESI-MS), prot

234 Liquid chromatography coupled to electrospray ionization-mass spectrometry (LC-ESI-MS) is

235 ultrahigh-performance liquid chromatography-electrospray ionization-mass spectrometry (UHPLC-ESI-MS)

236 ma was objectively detected using desorption electrospray ionization-mass spectrometry imaging (DESI-

237 Desorption electrospray ionization-mass spectrometry imaging (DESI-

238 Electrospray ionization-mass spectrometry independently

239 LC-ESI-MS (liquid chromatography-electrospray ionization-mass spectrometry) with the righ

240 Chelator conjugation was confirmed by electrospray ionization-mass spectrometry, and radiolabe

241 Using liquid chromatography-electrospray ionization-mass spectrometry, we identified

242 d by ultra-performance liquid chromatography/electrospray ionization-quadruple time of flight mass sp

243 owed by light chain analysis by microflow-LC-electrospray ionization-quadrupole-time-of-flight mass s

244 Capillary zone electrophoresis-electrospray ionization-tandem mass spectrometry (CZE-ES

245 trophenylhydrazine (DNPH) derivatization and electrospray ionization-tandem mass spectrometry (ESI-MS

246 ed on high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (HPLC-E

247 tion, high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry analysi

248 gle-run reversed-phase liquid chromatography-electrospray ionization-tandem mass spectrometry from si

249 ipidomic analysis with liquid chromatography electrospray ionization-tandem mass spectrometry on a ca

250 ) and then analyzed by liquid chromatography-electrospray ionization-triple quadrupole-tandem mass sp

251 di Sarconi beans performed by flow injection-electrospray ionization-ultrahigh resolution mass spectr

252 E (Bio-SPME) fibers to MS systems for direct electrospray ionization.

253 ganic solvent to desorb analytes and perform electrospray ionization.

254 owing liquid extraction surface analysis and electrospray ionization.

255 eration in charged microdroplets produced by electrospray ionization.

256 e of 5.88+; whereupon, liquid chromatography/electrospray ionization/charge reduction/mass spectromet

257 hy coupled to photodiode-array detection and electrospray ionization/ion trap mass spectrometry (HPLC

258 ultrahigh-performance liquid chromatography-electrospray ionization/quadrupole-time-of-flight mass s

259 ta samples by a liquid chromatography-heated electrospray ionization/tandem mass spectrometry (LC-HES

260 metimes can exhibit the same exact mass upon electrospray ionization; this presents an analytical cha

261 action and show by (27) Al NMR spectroscopy, electrospray-ionization mass spectrometry, and small- an

262 When compared with airbrush application, electrospray led to a 3-fold improvement in detection li

263 ent analysis and discrimination of the laser electrospray mass spectral (LEMS) measurements resulted

264 the CB7.FcG(+) complex was also confirmed by electrospray mass spectrometric (ESI MS) experiments.

265 ic extracts of the chips were analysed using electrospray mass spectrometry and 28 phenolic and furan

266 MR and electronic absorption spectroscopies, electrospray mass spectrometry and DFT computations.

267 Desorption electrospray mass spectrometry imaging (DESI-MSI) genera

268 on of analytical ultracentrifugation, native electrospray mass spectrometry, and negative stain and c

269 1)H NMR, diffusion-ordered spectroscopy NMR, electrospray mass spectrometry, transmission electron mi

270 Its presence in solution is corroborated by electrospray mass spectrometry.

271 rm polymers, as evidenced by high-resolution electrospray mass spectrometry.

272 dimension fingerprint), which is measured by electrospray mass spectrometry.

273 lowing more effective subsequent analysis by electrospray mass spectrometry.

274 raphy coupled with diode array detection and electrospray-mass spectrometry (HPLC/DAD/ESI-MS); ninete

275 consists of highly-textured superhydrophobic electrosprayed microparticle coatings, composed of biode

276 Forty-two metabolites were measured using electrospray MS/MS and multivariate regression models we

277 A variety of electrospray-MS strategies using Q-TOF technology were u

278 and high drug encapsulation efficacy of the electrosprayed nanoparticles.

279 Electrospray of a solution containing hexose and a lithi

280 Electrospraying of G/PANI increases the electrode surfac

281 laser irradiation followed by generation of electrospray on the edge of the paper for MS analysis.

282 Electrosprays operate in several modes depending on the

283 e complementary nature of cLC flow rates and electrospray or nanospray ionization mass spectrometry (

284 Electrospray produces at least one structure that reacts

285 The ion landing of electrosprayed protein molecules is performed under atmo

286 ch bound metal ions modulate the response of electrosprayed proteins and protein complexes to collisi

287 The electrosprayed proteins are immobilized on dry metal and

288 signatures are detected using water-methanol electrospray solution.

289 pillary liquid chromatograph directly to the electrospray source of the mass spectrometer, in order t

290 loped method for computational prediction of electrospray tandem mass spectra (ESI-MS/MS), but unlike

291 s species, was investigated by accurate-mass electrospray tandem mass spectrometry (ESI-MS/MS).

292 Liquid chromatography coupled to electrospray tandem mass spectrometry (LC-ESI-MS/MS) is

293 d and tyrosine phosphorylated peptides using electrospray tandem mass spectrometry.

294 An opposite-polarity electrospray technique is developed to synthesize Mn3 O4

295 oduced by employing a simple and inexpensive electrospraying technique, with their sizes well control

296 r vaporization combined with high-resolution electrospray time-of-flight mass spectrometry enables an

297 Most studies have used electrospray to generate a polydisperse source of highly

298 rum samples implies daily calculation of the electrospray transmission efficiency (E) of the system w

299 ncentration measurement uncertainties is the electrospray transmission efficiency.

300 oline liposomes, within a WPC matrix through electrospraying, were developed and used as delivery veh