ライフサイエンスコーパス: mass spectrometer

1 sequenced via Shotgun proteomics (Q-Exactive mass spectrometer).

2 tion directly infused into a high-resolution mass spectrometer.

3 er transform ion cyclotron resonance (FTICR) mass spectrometer.

4 nization region of an ambient pressure inlet mass spectrometer.

5 hin-layer cell connected to a membrane inlet mass spectrometer.

6 ation of an ultrasensitive latest generation mass spectrometer.

7 n of the technology to a Bruker timsTOF fleX mass spectrometer.

8 lizer and the inlet capillary of an Orbitrap mass spectrometer.

9 n-small-molecule interactions on an Orbitrap mass spectrometer.

10 ly activated by laser irradiation inside the mass spectrometer.

11 lites using a hybrid triple quadrupole (QQQ) mass spectrometer.

12 gmentation of intact protein ions inside the mass spectrometer.

13 ns in vacuum in a linear quadrupole ion trap mass spectrometer.

14 zed using a gas chromatograph coupled with a mass spectrometer.

15 ghput of 100 000 samples per day on a single mass spectrometer.

16 or integrated in a quadrupole/time-of-flight mass spectrometer.

17 tudied by using a linear quadrupole ion trap mass spectrometer.

18 hromatography coupled to a triple quadrupole mass spectrometer.

19 s in an electrostatic linear ion trap (ELIT) mass spectrometer.

20 ae lysate digest on an Orbitrap Fusion Lumos mass spectrometer.

21 accurately measured with a triple quadrupole mass spectrometer.

22 cations, and subsequently analyzed using the mass spectrometer.

23 rce of a linear quadrupole ion trap/orbitrap mass spectrometer.

24 ed high-mass-range, high-resolution Orbitrap mass spectrometer.

25 tegrated electrospray ionization needle to a mass spectrometer.

26 t atmospheric pressure, to a linear ion trap mass spectrometer.

27 ase ion-molecule reactions (IMRs) inside the mass spectrometer.

28 induced fragmentation of each glycan in the mass spectrometer.

29 at nanoliter/min flows to an LEI-interfaced mass spectrometer.

30 sing a Q-Exactive Hybrid Quadrupole-Orbitrap mass spectrometer.

31 their overall topology was preserved in the mass spectrometer.

32 ning of >1000 samples per day using a single mass spectrometer.

33 ation (IMS) quadrupole-time-of-flight (QTOF) mass spectrometer.

34 ansform electrostatic linear ion trap (ELIT) mass spectrometer.

35 ny biochemical laboratory having access to a mass spectrometer.

36 rformance liquid chromatography coupled to a mass spectrometer.

37 ode on a quadrupole-Orbitrap high resolution mass spectrometer.

38 pressure chemical ionization source on this mass spectrometer.

39 e tip an electrospray can be directed into a mass spectrometer.

40 coupled to a high resolution Orbitrap Fusion mass spectrometer.

41 ap/Fourier transform ion cyclotron resonance mass spectrometer.

42 ctrometry (LC-MS/MS) using a high-resolution mass spectrometer.

43 pectrometry (MS/MS) with a triple quadrupole mass spectrometer.

44 l coulometric detector and a high-resolution mass spectrometer.

45 onitoring mode and using a triple quadrupole mass spectrometer.

46 PE-UVPD for peptide analysis in an ion trap mass spectrometer.

47 ylamide capillary coupled to a Q Exactive HF mass spectrometer.

48 pressure and the initial vacuum stage of the mass spectrometer.

49 lipid extracts into a high resolution tandem mass spectrometer.

50 ation source for subsequent measurement by a mass spectrometer.

51 optics was designed to conduct ions into the mass spectrometer.

52 the high mass accuracy and resolution of the mass spectrometer.

53 l traveling-wave ion mobility time-of-flight mass spectrometer.

54 n application programming interface with the mass spectrometer.

55 analyzed by HPLC combined with DAD and QTOF mass spectrometer.

56 andem mass spectrometry on a 6600 Triple-TOF mass spectrometer.

57 achieved using the Orbitrap Eclipse Tribrid mass spectrometer.

58 ide to those obtained on a commercial tandem mass spectrometer.

59 e with a gas chromatograph hyphenated with a mass spectrometer.

60 a previous-generation Orbitrap Fusion Lumos mass spectrometer.

61 tocol, and metabolites were screened using a mass spectrometer.

62 ich are finally analyzed by LC-HRMS on a TOF mass spectrometer.

63 quadrupole time-of-flight (QTOF) part of the mass spectrometer.

64 deflector, backed by a static, magnet-based, mass spectrometer.

65 hin a quadrupole/ion mobility/time-of-flight mass spectrometer.

66 he reproducibility of data acquired from any mass spectrometer.

67 onization (ESI)-MS/MS in a triple quadrupole mass spectrometer.

68 cleotide (ASO) impurities using a Q-Exactive mass spectrometer.

69 , outside the high vacuum environment of the mass spectrometer.

70 -nanoelectrospray ionization high-resolution mass spectrometer.

71 d into a LEI/CI interfaced triple quadrupole mass spectrometer.

72 as chromatograph coupled to an isotope ratio mass spectrometer.

73 otein samples at different flow rates into a mass spectrometer.

74 relying on high-resolution and fast-response mass spectrometers.

75 y used for CK profiling on triple quadrupole mass spectrometers.

76 cal devices such as electron microscopes and mass spectrometers.

77 th multicollector inductively coupled plasma mass spectrometers.

78 nd fragmentation behavior of peroxy acids in mass spectrometers.

79 etry (FAIMS) coupled to the Orbitrap Tribrid mass spectrometers.

80 nt interfaces for coupling the CE devices to mass spectrometers.

81 on wide-scan data sets from high resolution mass spectrometers.

82 T-ICR) and linear quadrupole ion trap (LQIT) mass spectrometers.

83 particular ease of hyphenation to a range of mass spectrometers.

84 the utility of the Orbitrap Eclipse Tribrid mass spectrometer (advanced quadrupole filter, optimized

85 ompounds using a prototype acoustic ejection mass spectrometer (AEMS) platform.

86 ns and protein complexes are detected by the mass spectrometer after electrospray ionization.

87 yanions are measured by isotope-ratio sector mass spectrometers after conversion into gases.

88 The introduction of more sensitive mass spectrometers allows researchers to adapt front-end

89 show that the combination of a miniaturized mass spectrometer, ambient ionization, and statistical a

90 d laser desorption/ionization time-of-flight mass spectrometer analyses.

91 n with dichloromethane and gas chromatograph-mass spectrometer analysis.

92 cs (linear trap quadrupole-Fourier transform mass spectrometer) analysis.

93 The pen-like interface is connected to the mass spectrometer and a separate control unit via a bund

94 roach was implemented on an Orbitrap Tribrid mass spectrometer and begins with selection of a parent

95 ccharides are dissociated in an ion mobility mass spectrometer and collision cross section values of

96 y, we developed FAIMS at 15-30 Torr within a mass spectrometer and demonstrated it for small and medi

97 vesicles are concentrated, introduced into a mass spectrometer and ionized.

98 ways of fragmentation available on a tribrid mass spectrometer and optimized their collision energies

99 tion process increases the duty cycle of the mass spectrometer and reduces the number of points colle

100 Science Langmuir Probe, the Ion and Neutral Mass Spectrometer and the fluxgate magnetometer.

101 s using advanced instruments such as Aerosol Mass Spectrometer and the major contributor to organic s

102 o modify the desolvation gas on a Q-Exactive mass spectrometer and to demonstrate the utility in impr

103 coupled to a high-resolution time-of-flight mass spectrometer and was applied to 149 edible fish fil

104 6.3 mDa mass differences in high resolution mass spectrometers and a set of 9 reagents with 1 Da spa

105 ementation of AI-ETD and IRMPD on commercial mass spectrometers and broadening the accessibility of t

106 ompatible with both high- and low-resolution mass spectrometers and different levels of endogenous pe

107 instrumentation including thermal ionization mass spectrometers and inductively coupled plasma mass s

108 plied to hyperspectral images from different mass spectrometers and integrated with other established

109 by an online high-resolution time-of-flight mass spectrometer) and dissolved organic matter in the o

110 -performance liquid chromatography, accurate mass spectrometer, and an Orbitrap mass analyzer.

111 e tested the ESA and deflector, magnet-based mass spectrometer, and anode in the laboratory to demons

112 ted without FAIMS on this higher performance mass spectrometer, approaching the same order of magnitu

113 To that end, contemporary mass spectrometers are outfitted with multiple analyzers

114 ssociation (UVPD) implemented on an Orbitrap mass spectrometer as another option for structural chara

115 les directly from microtiter plates into the mass spectrometer at subsecond per well sampling rates.

116 ptember 2016 using an aerosol time-of-flight mass spectrometer (ATOFMS) and a time-of-flight aerosol

117 ntation of peptides and proteins in ion trap mass spectrometers, but the spectral signal-to-noise rat

118 ed carbene was generated in situ in a tandem mass spectrometer by decarboxylation of oxo[4-(trimethyl

119 dditionally, the isolation efficiency of the mass spectrometer can be taken into account.

120 Multistage fragmentation (MS(n)) in the mass spectrometer can provide sufficient evidence for Il

121 Our approach relies on the advanced Orbitrap mass spectrometer capable of multistage MS analysis acro

122 coupled to an ultrahigh-resolution Orbitrap mass spectrometer (CI-Orbitrap).

123 ess than 15 min but is not optimized for the mass spectrometers commonly found in clinical microbiolo

124 highly sensitive inductively coupled plasma mass spectrometer coupled to a scanning flow cell, the a

125 nd lightweight laser desorption ionization - mass spectrometer designed and developed for in situ spa

126 A quadrupole-time-of-flight mass spectrometer detector (QTOF-MS) operating in full s

127 present a reference drift tube ion mobility mass spectrometer (DTIM-MS) where improvements on the me

128 ty and HFIP can affect the robustness of the mass spectrometer due to its corrosive nature.

129 mirrors in an electrostatic linear ion trap mass spectrometer (ELIT).

130 ace, which was coupled to different Orbitrap mass spectrometers (Elite and Q Exactive Plus) and exten

131 Recent work has demonstrated that for mass spectrometers employing analog-to-digital converter

132 We describe modifications to an Orbitrap mass spectrometer, enabling high-resolution native MS an

133 P1 (HHHHHHIIKIIK) using an Orbitrap tribrid mass spectrometer equipped with a solid-state 213 nm UV

134 Using a time-of-flight secondary ion mass spectrometer equipped with an argon cluster ion for

135 esolution time-of-flight chemical ionization mass spectrometer equipped with iodide reagent ion chemi

136 esolution time-of-flight chemical ionization mass spectrometer (FIGAERO-HR-ToF-CIMS) was used to anal

137 th samples were analyzed on an isotope ratio mass spectrometer for 13C enrichment.

138 nt systems into a linear quadrupole ion trap mass spectrometer for diagnostic gas-phase ion/molecule

139 h a Q Exactive HF hybrid quadrupole-orbitrap mass spectrometer for in situ imaging of N-linked glycan

140 AIMS Pro) coupled with a Thermo Fusion Lumos mass spectrometer for liquid extraction surface analysis

141 trospray interface of a trapped ion mobility-mass spectrometer for rapid diastereomer separation in t

142 cable to couple an infrared (IR) laser to a mass spectrometer for robust, efficient, and safe photoa

143 rgical aerosol, which was transferred into a mass spectrometer for subsequent chemical analysis.

144 ase extraction that is directly coupled to a mass spectrometer for the quantitative screening of 12 d

145 on a commercial dual source, hybrid QhFT-ICR mass spectrometer for use during imaging mass spectromet

146 spectrometers and inductively coupled plasma mass spectrometers for isotopic abundance measurements.

147 a simple tool, extensible to Orbitrap-based mass spectrometers, for postdetection data processing th

148 up to 66 kDa on three commercially available mass spectrometers from salty solutions to mimic cellula

149 ss-resolution electron ionization quadrupole mass spectrometer (GC/EI-MS), a standard and widely avai

150 mentation of such methods on high-resolution mass spectrometers has aided the interpretation of the c

151 High-resolution mass spectrometers have become increasingly adapted to t

152 Ion trap mass spectrometers have emerged as powerful on-site anal

153 the availability of high-resolution benchtop mass spectrometers have made it possible to use high-thr

154 logies utilized to couple these workflows to mass spectrometers have significant limitations that for

155 to a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS).

156 rom a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS).

157 esolution time-of-flight chemical ionization mass spectrometer (HRToF-CIMS) equipped with an acetate

158 esolution chemical ionization time-of-flight mass spectrometer (HRToF-CIMS), operated with two differ

159 nfiguration of an inductively coupled plasma mass spectrometer (ICPMS) allowing the sample introducti

160 y HPLC coupled with diode array detector and mass spectrometer if required.

161 come less reliable as the accuracy of modern mass spectrometers improved.

162 N-Glycans are detected with a MALDI FT-ICR mass spectrometer in a concentration-dependent manner wh

163 on system and analyze a single sample on the mass spectrometer in approximately 20 s, with minimal sa

164 In this study, a miniaturized mass spectrometer in combination with three ambient ioni

165 tification method using a QExactive Orbitrap mass spectrometer in high-resolution with a parallel rea

166 s to an Agilent 6560 drift tube ion mobility-mass spectrometer in order to perform robust, simultaneo

167 liquid chromatographic system connected to a mass spectrometer in order to test the specific retentio

168 upole-ion mobility-time-of-flight (Q-IM-TOF) mass spectrometer in particular, by exploiting the full

169 Further separation of proteoforms inside the mass spectrometer (in-MS) allowed for isolation of indiv

170 new design for the FT ICR cell and the whole mass spectrometer, in which an open, dynamically harmoni

171 Aside from mass spectrometer instrumentation advancement, a single-

172 analytical techniques evaluated used modern mass spectrometer instrumentation including thermal ioni

173 analyses in modern chemical ionization (CI) mass spectrometer instruments, which are increasingly be

174 s to the electrospray ionization source of a mass spectrometer is automated using a multiposition val

175 E) fiber, and the inlet of a high-resolution mass spectrometer is described.

176 issolved (noble) gases with a field portable mass spectrometer is presented.

177 the CF-MIMS (Continuous Flow Membrane Inlet Mass Spectrometer) is an innovative tool allowing the in

178 a laser ablation inductively coupled plasma mass spectrometer (LA-ICP-MS) setup allows for high-reso

179 iquid chromatography/drift tube ion mobility-mass spectrometer (LC/IM-MS) was evaluated for its utili

180 a multicollector inductively coupled plasma mass spectrometer (MC-ICPMS).

181 In addition, quadrupole mass spectrometer measurements of emitted D-containing s

182 SPIN) coupled to a membrane inlet quadrupole mass spectrometer (MIMS) was developed for automated and

183 limited availability of ultrahigh-resolution mass spectrometers, most studies cannot afford analyzing

184 adsorbed bioassay medium is eluted into the mass spectrometer (MS) and interfering with evaluation.

185 or the analysis of clinical samples with the mass spectrometer (MS) can be extensive and expensive.

186 complexity and dynamic range and to utilize mass spectrometer (MS) time efficiently, high chromatogr

187 ce allows users to upload baseline corrected mass spectrometer (MS) tracing data and correct for natu

188 zation (LARESI) platform coupled to a tandem mass spectrometer (MS/MS) operated in selected reaction

189 real time (DART) ion source with an ion trap mass spectrometer, native cholesterol in its free alcoho

190 ll apart after exiting the drift cell of the mass spectrometer, novel features that have shorter (a l

191 Recent improvements in the sensitivity of mass spectrometers offered us the ability to quantify th

192 ng observations from the Neutral Gas and Ion Mass Spectrometer on the Mars Atmosphere and Volatile Ev

193 a Fourier transform ion cyclotron resonance mass spectrometer only for situations when the prominent

194 iature cylindrical ion trap (mini-CIT)-based mass spectrometer operated at >/=1 Torr with air as the

195 presented is based on the use of an Orbitrap mass spectrometer operated at a mass resolution of 100 0

196 gas chromatography-quadrupole time-of-flight mass spectrometer operated in positive and negative mode

197 Replicates are run on six mass spectrometers operating continuously with varying m

198 hat obstructed coupling to Fourier transform mass spectrometers operating under ultrahigh vacuum, but

199 is in Real Time, DART) and a high-resolution mass spectrometer (Orbitrap) has enabled the rapid and e

200 TIMS ion gating operation modes and Orbitrap mass spectrometer parameters with regard to sensitivity

201 d more than the signal-to-noise ratio of the mass spectrometer peaks.

202 We use the high-precision Penning trap mass spectrometer PENTATRAP to measure the cyclotron fre

203 t its implementation on the Orbitrap Tribrid mass spectrometer platform.

204 cell groups were acquired on three different mass spectrometer platforms representing thousands of in

205 Secondary Ion Mass Spectrometer profiles into the (13)C-labeled solids

206 3, a proton transfer reaction-time-of-flight mass spectrometer (PTR-TOF) using a new gas inlet and an

207 ng a proton transfer reaction time-of-flight mass spectrometer (PTR-ToF-MS) at an engine test facilit

208 nd a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS).

209 ve UHMR Hybrid Quadrupole-Orbitrap (QE-UHMR) mass spectrometer, pushing the upper mass limit of prote

210 uadrupole-cyclic ion mobility-time-of-flight mass spectrometer (Q-cIM-ToF) for the analysis of protei

211 using Q-exactive hybrid quadrupole-orbitrap mass spectrometer (Q-OT-MS).

212 th dual-channel detection using a quadrupole mass spectrometer (qMS) and a flame ionization detector

213 analysis of gas chromatograph time-of-flight mass spectrometer results could be a novel tool to help

214 cted by an online inductively coupled plasma mass spectrometer revealed a low-molecular-mass (LMM) Fe

215 ane protein complex with bound lipids in the mass spectrometer revealed enrichment of specific lipids

216 ser desorption/ionization (LDI) in a bipolar mass spectrometer, revealing elemental constituents and

217 ser desorption/ionization (LDI) in a bipolar mass spectrometer reveals the inorganic constituents and

218 Fourier transform mass spectrometers routinely provide high mass resolutio

219 ls (species, tissues, etc), instrumentation (mass spectrometer, sequencer), keywords and other provid

220 ied using liquid chromatography coupled to a mass spectrometer, show both similarities and difference

221 s-sampling valve and a soot particle aerosol mass spectrometer (SP-AMS) enabled online measurements o

222 ionization drift tube ion mobility-Orbitrap mass spectrometer specifically designed to enhance sensi

223 Single particle mass spectrometers (SPMSs), which generate in situ singl

224 ach precursor ion is isolated twice with the mass spectrometer switching between CID and UVPD activat

225 nd laser ablation-inductively coupled plasma-mass spectrometer system, are reported.

226 ercome these limitations by using a portable mass spectrometer system, which enables a fast and effic

227 cluding the use of versatile, reduced-format mass spectrometer systems.

228 ) and online (compact time-of-flight aerosol mass spectrometer) techniques.

229 dvances in chemical sampling using miniature mass spectrometer technology are used to monitor slow re

230 T Fourier transform ion cyclotron resonance mass spectrometer that can analyze a mixture of agrochem

231 vailable quadrupole-Orbitrap-linear ion trap mass spectrometer that uses a front-end glow discharge s

232 Orbitraps are high-resolution ion-trap mass spectrometers that are widely used in metabolomics.

233 ology using an Orbitrap Fusion Lumos Tribrid mass spectrometer, the Mascot search engine, the weighte

234 When these droplets enter the mass spectrometer through a heated inlet, rapid vaporiza

235 The ejected material is transferred to the mass spectrometer through an atmospheric interface and a

236 apped ion mobility quadrupole time-of-flight mass spectrometer (timsTOF fleX MALDI-2, Bruker Daltonic

237 apped ion mobility quadrupole time-of-flight mass spectrometer (timsTOF Pro).

238 (HRMS) by using a quadrupole time-of flight mass spectrometer to assess glycosylation of etanercept

239 etween mass-selected ions and ozone inside a mass spectrometer to assign sites of unsaturation in com

240 15 T solariX Fourier transform ion cyclotron mass spectrometer to characterize an IgG1 mAb molecule c

241 sing [(18)O]-labeled O2 and a membrane inlet mass spectrometer to characterize Chlamydomonas reinhard

242 e, we modified a traveling wave ion mobility mass spectrometer to enable IMRs in the trapping region

243 and a fast-response proton transfer reaction mass spectrometer to make direct measurements of VOC emi

244 e sampling using an advanced single-particle mass spectrometer to measure the spatial variability of

245 own using a ketone mixture introduced to the mass spectrometer to optimize atmospheric conditions.

246 drupole mass filter of a commercial QhFT-ICR mass spectrometer to perform selected ion ejection prior

247 croplasma ionization source with an Orbitrap mass spectrometer to perform uranium isotopic analyses o

248 e method utilizes the Orbitrap Fusion tribid mass spectrometer to rapidly assign multiple Xle residue

249 These abilities allow ion trapping mass spectrometers to be filled to capacity with only io

250 coupled to a high-resolution time-of-flight mass spectrometer (TOF-MS).

251 an inductively coupled plasma time-of-flight mass spectrometer (TOFMS) to a traditional CFA system.

252 techniques coupled to ultra-high-resolution mass spectrometers (UHRMS) allows screening of thousands

253 sampling and ionization device, coupled to a mass spectrometer under ambient conditions.

254 rchers use a wide variety of high-resolution mass spectrometers under different operating conditions,

255 coupled to an ion trap with a time-of-flight mass spectrometer (UPLC-IT-TOF-MS) that allowed the char

256 d to a diode array detector (HPLC-DAD) and a mass spectrometer (UPLC-MS), was used to compare the dir

257 to an electrospray quadrupole time-of-flight mass spectrometer (UPLC/ESI-HR-QTOFMS) was used for phyt

258 The high-resolution accurate mass spectrometers used for proteome dynamics studies ar

259 phere by connecting the plasma source to the mass spectrometer using a 2 mm ID closed reactant capill

260 tself connected to a gas chromatograph and a mass spectrometer using a borosilicate glass cross piece

261 s integrated in a SLIM and coupled to a QTOF mass spectrometer using an ion funnel interface to evalu

262 chromatography (LC) ESII/MS on two different mass spectrometers using a mixture of drugs, a peptide s

263 Five ion mobility mass spectrometers utilizing commercially available IMS

264 /molecule reactions can be introduced into a mass spectrometer via a continuous flow apparatus or thr

265 rboxylate ions, were then derivatized in the mass spectrometer via an ion/ion charge inversion reacti

266 e and introduction of said analytes into the mass spectrometer via electrospray ionization.

267 An ESI ion trap mass spectrometer was designed for high-throughput and r

268 eal-time ( approximately 1 s) vapor analysis mass spectrometer was developed to provide tools, techni

269 romatograph coupled with a triple quadrupole mass spectrometer was employed to quantify BMAA and its

270 nar FAIMS device coupled with a Thermo Elite mass spectrometer was employed.

271 of an IMS-capable quadrupole time-of-flight mass spectrometer was undertaken to allow the introducti

272 In this study, an aerosol time-of-flight mass spectrometer was used to analyze laboratory generat

273 An ion mobility quadrupole time-of-flight mass spectrometer was used to examine the gas-phase stru

274 An inductively coupled plasma mass spectrometer was utilized for ultrasensitive detect

275 s case by use of a modified Synapt G2-S QTOF mass spectrometer (Waters), we investigated the influenc

276 Here, using an Orbitrap Fusion Tribrid mass spectrometer, we present an optimized methodology t

277 omplexes directly from native membranes into mass spectrometers-we provided insights into association

278 iation (CAD) in a linear quadrupole ion trap mass spectrometer were demonstrated to enable the differ

279 Exactive(TM) Hybrid Quadrupole-Orbitrap(TM) Mass Spectrometer were matched with the BIOPEP database.

280 ard laboratory and with a classical ion trap mass spectrometer were other remarkable characteristics

281 ng nanoelectrospray and transferred into the mass spectrometer where the detergent molecules are stri

282 P is easy to operate and align in front of a mass spectrometer, which will facilitate broader use of

283 were then analyzed using a nanoLC-chip-QTOF mass spectrometer with a porous graphitized carbon (PGC)

284 Thermo Scientific Q Exactive high-resolution mass spectrometer with a rapid 30 s analytical method.

285 imension for separation, a benchtop Orbitrap mass spectrometer with HCD-MS/MS for peptide sequencing,

286 ta were obtained using a Q Exactive orbitrap mass spectrometer with moderate scanning speed (12 Hz) a

287 on and analysis using a GC-triple quadrupole mass spectrometer with multiple reaction monitoring, res

288 s were analyzed using a GC-single quadrupole mass spectrometer with selected ion monitoring, utilizin

289 be employed by every lab having access to a mass spectrometer with tandem mass spectrometry capabili

290 at a MALDI quadrupole time-of-flight (Q-TOF) mass spectrometer with trapped ion mobility spectrometry

291 an predict peptide fragmentation patterns in mass spectrometers with accuracy within the uncertainty

292 the factor of insufficient vacuum in FT ICR mass spectrometers with an ultrahigh magnetic field is e

293 es have been revolutionized by the advent of mass spectrometers with detectors that afford high mass

294 me nominal mass can be resolved using modern mass spectrometers with high mass resolution, the correc

295 Feature article we argue that development of mass spectrometers with increasingly high resolution and

296 We equipped precision mass spectrometers with laser-postionization (MALDI-2) m

297 stalled in the Q Exactive series of Orbitrap mass spectrometers with minimal disruption of standard f

298 quire complex chemical reactions or advanced mass spectrometers with special fragmentation techniques

299 fore increasing the apparent resolution of a mass spectrometer without any further instrument modific

300 g of biological C=C isomers using commercial mass spectrometers without any instrument modification.