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1 at least 24 h under the vacuum of our MALDI mass spectrometer.
2 controlled by a laser source external to the mass spectrometer.
3 urements made using an ion-molecule reaction mass spectrometer.
4 rete water samples run on a laboratory-based mass spectrometer.
5 resolution achievable using a given imaging mass spectrometer.
6 ny biochemical laboratory having access to a mass spectrometer.
7 chromatography coupled with high resolution mass spectrometer.
8 rectly into the trapping cell of an Orbitrap mass spectrometer.
9 ( approximately 100 cm) and a Q Exactive HF mass spectrometer.
10 agnetic sector field gas-phase isotope ratio mass spectrometer.
11 d laser desorption/ionization time-of-flight mass spectrometer.
12 ionization interface of a triple quadrupole mass spectrometer.
13 terferences in an inductively coupled plasma mass spectrometer.
14 r transform-ion cyclotron resonance (FT-ICR) mass spectrometer.
15 rformance liquid chromatography coupled to a mass spectrometer.
16 orous acid-treated hemoglobin by an accurate mass spectrometer.
17 diode array detector and a triple-quadrupole mass spectrometer.
18 ay ionization (ESI) interface to an ion-trap mass spectrometer.
19 ode on a quadrupole-Orbitrap high resolution mass spectrometer.
20 ion (UVPD) implemented on an Orbitrap Fusion mass spectrometer.
21 r of the Raman spectroscope and the inlet of mass spectrometer.
22 he instrument-in this case, a time-of-flight mass spectrometer.
23 ult by the need of programmatic control of a mass spectrometer.
24 pressure chemical ionization source on this mass spectrometer.
25 ng a proton-transfer-reaction time-of-flight mass spectrometer.
26 located prior to a quadrupole time-of-flight mass spectrometer.
27 DDA algorithms prior to implementation on a mass spectrometer.
28 alyses prior to analysis in a field portable mass spectrometer.
29 e tip an electrospray can be directed into a mass spectrometer.
30 surface by the high mass-resolution Orbitrap mass spectrometer.
31 are directed to the inlet and analyzed by a mass spectrometer.
32 on a low pumping capacity, single-quadrupole mass spectrometer.
33 actions (PTR) and ion parking on an Orbitrap mass spectrometer.
34 coupled to a high resolution Orbitrap Fusion mass spectrometer.
35 ion reactions on an ion trap-Orbitrap hybrid mass spectrometer.
36 a gas chromatography:pyrolysis:isotope ratio mass spectrometer.
37 quadrupole-based inductively coupled plasma mass spectrometer.
38 on the front-end of a linear ion trap (LIT) mass spectrometer.
39 ligosaccharides were performed on an AccuTOF mass spectrometer.
40 ive phosphoproteomics on the Orbitrap Fusion mass spectrometer.
41 ectron transfer dissociation on the Orbitrap mass spectrometer.
42 he recently introduced Orbitrap Exactive EMR mass spectrometer.
43 ing a high-resolution time-of-flight aerosol mass spectrometer.
44 h an existing single-particle time-of-flight mass spectrometer.
45 in positive-ion mode on an orbital trapping mass spectrometer.
46 erture of an atmospheric pressure ionization mass spectrometer.
47 her a Waters SYNAPT G2 or a Thermo LTQ Velos mass spectrometer.
48 conversion elemental analyzer:isotope ratio mass spectrometer.
49 eactor coupled to an electrospray ionization mass spectrometer.
50 chronizing parallel HPLC systems to a single mass spectrometer.
51 then accumulated and isolated in an ion trap mass spectrometer.
52 upled to a quadrupole/time-of-flight (Q/ToF) mass spectrometer.
53 ansform electrostatic linear ion trap (ELIT) mass spectrometer.
54 ap/Fourier transform ion cyclotron resonance mass spectrometer.
55 ctrometry (LC-MS/MS) using a high-resolution mass spectrometer.
56 pectrometry (MS/MS) with a triple quadrupole mass spectrometer.
57 l coulometric detector and a high-resolution mass spectrometer.
58 onitoring mode and using a triple quadrupole mass spectrometer.
59 PE-UVPD for peptide analysis in an ion trap mass spectrometer.
60 ylamide capillary coupled to a Q Exactive HF mass spectrometer.
61 pressure and the initial vacuum stage of the mass spectrometer.
62 lipid extracts into a high resolution tandem mass spectrometer.
63 ation source for subsequent measurement by a mass spectrometer.
64 optics was designed to conduct ions into the mass spectrometer.
65 the high mass accuracy and resolution of the mass spectrometer.
66 l traveling-wave ion mobility time-of-flight mass spectrometer.
67 analyzed by HPLC combined with DAD and QTOF mass spectrometer.
68 andem mass spectrometry on a 6600 Triple-TOF mass spectrometer.
69 th multicollector inductively coupled plasma mass spectrometers.
70 uch instrumentation is coupled with ion trap mass spectrometers.
71 xpensive and more robust than other types of mass spectrometers.
72 on, thus making MAI ideal for field-portable mass spectrometers.
73 etection limits are required, or on portable mass spectrometers.
74 with high-resolution and high mass accuracy mass spectrometers.
75 coupled between quadupole and time-of-flight mass spectrometers.
76 nt interfaces for coupling the CE devices to mass spectrometers.
77 nd fragmentation behavior of peroxy acids in mass spectrometers.
78 on wide-scan data sets from high resolution mass spectrometers.
79 similar ions in various types of widely used mass spectrometers.
80 s using CZE coupled to an LTQ-Orbitrap Velos mass spectrometer; 799 protein groups and 3381 peptides
81 )D separation in LC x LC and to use multiple mass spectrometers across both dimensions to perform con
82 nological advances have made high-resolution mass spectrometers affordable to many laboratories, thus
83 tor cartridge and measured with a quadrupole mass spectrometer, after in-line purification with react
84 show that the combination of a miniaturized mass spectrometer, ambient ionization, and statistical a
87 ganic Aerosol (OOA) determined by an aerosol mass spectrometer (AMS) at two locations in Houston, Tex
88 sol (OA) components identified by an aerosol mass spectrometer (AMS) based on their ability to genera
90 ts are consistent with those from an aerosol mass spectrometer (AMS) with a thermal denuder, implying
91 mber of field observations employing aerosol mass spectrometers (AMS) have demonstrated that organic
94 er-transform ion cyclotron resonance (FTICR) mass spectrometer and a time-of-flight (TOF) instrument
95 oupled to a nanoelectrospray high-resolution mass spectrometer and applied for the separation of the
96 on-induced dissociation (CID) on a miniature mass spectrometer and emphasize useful applications.
97 ways of fragmentation available on a tribrid mass spectrometer and optimized their collision energies
98 ements were obtained using a high-resolution mass spectrometer and the quantitative proteomic softwar
99 ween the emitter and the heated inlet to the mass spectrometer and the voltage applied to the emitter
100 ently mass isolated in a quadrupole ion trap mass spectrometer and then irradiated by the tunable inf
101 to increase the fraction that can enter the mass spectrometer and with minimum loss of material towa
102 rapid scanning high-resolution high accuracy mass spectrometers and the desire for high throughput sc
103 by an online high-resolution time-of-flight mass spectrometer) and dissolved organic matter in the o
104 and proteins within the ICR cell of a FT-ICR mass spectrometer are accomplished through appropriate m
105 activated dissociation (CAD) in an ion trap mass spectrometer are demonstrated to allow the identifi
106 e introduction of labile biomolecules into a mass spectrometer are of fundamental importance to biomo
109 aration efficiencies were observed with both mass spectrometers as detectors, with about 6 times bett
110 rosol particle measurements with two aerosol mass spectrometers at different heights on a meteorologi
111 In this study, an aerosol time-of-flight mass spectrometer (ATOFMS) was used for rapid analysis o
113 ntation of peptides and proteins in ion trap mass spectrometers, but the spectral signal-to-noise rat
114 ed carbene was generated in situ in a tandem mass spectrometer by decarboxylation of oxo[4-(trimethyl
115 fragmentation capabilities of the Q Exactive mass spectrometer can be extended with ultraviolet photo
117 Multistage fragmentation (MS(n)) in the mass spectrometer can provide sufficient evidence for Il
118 Our approach relies on the advanced Orbitrap mass spectrometer capable of multistage MS analysis acro
119 using a high-resolution chemical ionization mass spectrometer (CIMS) equipped with an "inlet-less" N
122 ve methodology employing a tandem quadrupole mass spectrometer coupled to a gas chromatograph with he
123 highly sensitive inductively coupled plasma mass spectrometer coupled to a scanning flow cell, the a
125 sitive matrix factorization (PMF) of aerosol mass spectrometer data collected in areas dominated by i
126 tion of a novel differential electrochemical mass spectrometer (DEMS) cell geometry that enables the
129 present a reference drift tube ion mobility mass spectrometer (DTIM-MS) where improvements on the me
130 are directly infused into a high-resolution mass spectrometer (e.g., Orbitrap) using a chip-based nE
131 s accuracy data obtained by state-of-the-art mass spectrometers (e.g., Orbitraps) can significantly i
132 s directly coupled to an electron ionization mass spectrometer (EI-MS) without any interface or modif
133 ace, which was coupled to different Orbitrap mass spectrometers (Elite and Q Exactive Plus) and exten
135 We describe modifications to an Orbitrap mass spectrometer, enabling high-resolution native MS an
137 sensor and by gas chromatograph coupled with mass spectrometer exhibited the correlation coefficient
138 as developed on a Thermo Q-Exactive orbitrap mass spectrometer for (1) accurate mass measurements of
139 capabilities of a laser-coupled ion mobility mass spectrometer for analysis of peptide sequence and s
140 uctively coupled plasma (ICP) tine-of-flight mass spectrometer for detection and quantitation using e
141 ase extraction that is directly coupled to a mass spectrometer for the quantitative screening of 12 d
143 tion methods available on an Orbitrap Fusion mass spectrometer for three proteins and an E. coli cell
144 ual detection (flame ionisation detector and mass spectrometer) for quantitative and qualitative purp
145 escribe a field-deployable gas equilibration mass spectrometer (GEMS) that provides continuous, real-
147 e ion injection period (IT)of low-duty cycle mass spectrometers has been previously shown to improve
148 on the popular benchtop Q Exactive Orbitrap mass spectrometer have so far relied exclusively on high
150 ion microscope coupled with a secondary ion mass spectrometer (HIM-SIMS) with Kelvin probe force mic
152 tly developed high-resolution time-of-flight mass spectrometer (HR TOF MS), under the challenging con
155 nization, and a tribrid ultrahigh-resolution mass spectrometer (HRMS) to enable untargeted (discovery
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
160 detector like an inductively coupled plasma mass spectrometer (ICPMS), but this is rarely practical
162 ection system coupled to a gas chromatograph-mass spectrometer (ILR-CIS-GC-MS) has been explored for
163 on of DESI with the IT of an LTQ Orbitrap-XL mass spectrometer improves spatial resolution by factors
165 on system and analyze a single sample on the mass spectrometer in approximately 20 s, with minimal sa
167 ntenance) and wider availability of Orbitrap mass spectrometers in university departments means that
168 h directly to the electrospray source of the mass spectrometer, in order to provide an extremely sens
169 ng matrix:analyte samples to the vacuum of a mass spectrometer, including common laboratory materials
170 ir space between the DART ion source and the mass spectrometer inlet, with the entire observed mass s
171 a high-sensitivity proton-transfer reaction mass spectrometer installed at a suburban site in Mohali
172 ce in a Tedlar bag, which was connected to a mass spectrometer ionization source via a short deactiva
174 rfacing the microfluidic cell culture to the mass spectrometer is challenging because of geometric an
178 ssociation (UVPD) implemented on an Orbitrap mass spectrometer is used to localize double bond positi
179 the CF-MIMS (Continuous Flow Membrane Inlet Mass Spectrometer) is an innovative tool allowing the in
180 hod hyphenated to an ion-trap time-of-flight mass spectrometer (IT-TOF-MS) for the separation and ide
181 e extract to the liquid chromatograph-tandem mass spectrometer (LC-MS/MS) or direct coupling of the i
182 raphy coupled to a quadrupole-time-of-flight mass spectrometer (LC-QTOF-MS) was developed and applied
183 iquid chromatography/drift tube ion mobility-mass spectrometer (LC/IM-MS) was evaluated for its utili
185 lity spectrometer (IMS) to a linear ion trap mass spectrometer (LIT-MS) via modulation of the ion bea
186 stigated the application of the LTQ-Orbitrap mass spectrometer (LTQ-Velos Pro, Thermo Fisher) for res
187 mass spectrometry but collected outside the mass spectrometer, making the subsequent NMR measurement
190 rix factorization analyses, based on aerosol mass spectrometer measurements, resolved organic carbon
191 stem with a negative-ion chemical ionization mass spectrometer (methane reagent gas) was used for dir
193 SPIN) coupled to a membrane inlet quadrupole mass spectrometer (MIMS) was developed for automated and
194 or the analysis of clinical samples with the mass spectrometer (MS) can be extensive and expensive.
196 specially effective for quantification and a mass spectrometer (MS) produces data that is especially
197 complexity and dynamic range and to utilize mass spectrometer (MS) time efficiently, high chromatogr
202 real time (DART) ion source with an ion trap mass spectrometer, native cholesterol in its free alcoho
205 a Fourier transform ion cyclotron resonance mass spectrometer only for situations when the prominent
206 asy handling and low-cost benchtop RGA-based mass spectrometer, opening a new strategy for CO2 captur
207 iature cylindrical ion trap (mini-CIT)-based mass spectrometer operated at >/=1 Torr with air as the
208 presented is based on the use of an Orbitrap mass spectrometer operated at a mass resolution of 100 0
210 olet photodissociation (UVPD) on an Orbitrap mass spectrometer optimized for native MS and benchmark
211 TIMS ion gating operation modes and Orbitrap mass spectrometer parameters with regard to sensitivity
212 collisional purification" inside an ion trap mass spectrometer paving the way for an improved analysi
215 3, a proton transfer reaction-time-of-flight mass spectrometer (PTR-TOF) using a new gas inlet and an
216 ng a proton transfer reaction time-of-flight mass spectrometer (PTR-ToF-MS) at an engine test facilit
217 of a proton transfer reaction-time-of-flight-mass spectrometer (PTR-ToF-MS) can be used to enhance sp
218 ng a proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS), we investigate the emiss
223 rformance liquid chromatography coupled to a mass spectrometer repetition and noncompartmental PKs we
224 analysis of OA mass spectra from an aerosol mass spectrometer resolved two types of biomass burning
225 droplets are aspirated into the inlet of the mass spectrometer, resulting in the facile formation of
226 ser desorption/ionization (LDI) in a bipolar mass spectrometer, revealing elemental constituents and
230 s-sampling valve and a soot particle aerosol mass spectrometer (SP-AMS) enabled online measurements o
233 ach precursor ion is isolated twice with the mass spectrometer switching between CID and UVPD activat
236 dvances in chemical sampling using miniature mass spectrometer technology are used to monitor slow re
239 However, to date, triple quadrupole tandem mass spectrometers, the workhorses of quantitative analy
240 g an inductively coupled plasma-sector field mass spectrometer, thereby reducing analysis time and in
241 lyzed by LC-HRMS on an Orbitrap Elite hybrid mass spectrometer (Thermo Fisher Scientific, CA, USA) at
243 ure regions (e.g., ion source interfaces) of mass spectrometers, thus providing increased sensitivity
244 etween mass-selected ions and ozone inside a mass spectrometer to assign sites of unsaturation in com
245 15 T solariX Fourier transform ion cyclotron mass spectrometer to characterize an IgG1 mAb molecule c
246 sing [(18)O]-labeled O2 and a membrane inlet mass spectrometer to characterize Chlamydomonas reinhard
247 evice was designed and fitted to a hand-held mass spectrometer to characterize its potential in direc
248 The DMS effluent was directly coupled to a mass spectrometer to confirm the elemental identity of t
249 pectroscopy has been carried out in a tandem mass spectrometer to determine the three-dimensional str
250 s in real time (DART) coupled to an Orbitrap mass spectrometer to identify the structure of the speci
251 e method utilizes the Orbitrap Fusion tribid mass spectrometer to rapidly assign multiple Xle residue
253 a framework to extend the application of QqQ mass spectrometers to large-scale metabolite profiling.
254 -HCD MS(3) analysis using an Orbitrap Fusion mass spectrometer, to reliably identify Leu and Ile resi
255 etection was performed with a time-of-flight mass spectrometer (TOF-MS) to allow for a comprehensive
256 nanocalorimeter sensor into a time-of-flight mass spectrometer (TOFMS) for simultaneous thermal and s
257 Philae's initial comet touchdown, the COSAC mass spectrometer took a spectrum in sniffing mode, whic
258 Ultra High Performance Liquid Chromatography-Mass Spectrometer (UHPLC-HR-MS), we demonstrated that mo
260 rchers use a wide variety of high-resolution mass spectrometers under different operating conditions,
262 coupled to an ion trap with a time-of-flight mass spectrometer (UPLC-IT-TOF-MS) that allowed the char
263 d to a diode array detector (HPLC-DAD) and a mass spectrometer (UPLC-MS), was used to compare the dir
264 an ultra-high pressure liquid chromatography-mass spectrometer (UPLC-MS/MS) analytical method has bee
265 r was analyzed using a Thermo Fusion Tribrid mass spectrometer using a multistage top down MS approac
266 s integrated in a SLIM and coupled to a QTOF mass spectrometer using an ion funnel interface to evalu
267 tection is achieved with a triple quadrupole mass spectrometer using atmospheric pressure photoioniza
268 evice coupled to a quadrupole time-of-flight mass spectrometer using novel branched radio frequency i
269 ella enterica were directly infused into the mass spectrometer using static source nanoelectrospray i
270 chromatography (LC) ESII/MS on two different mass spectrometers using a mixture of drugs, a peptide s
272 The fragmentation patterns of molecules in mass spectrometers using electron impact ionization at 7
273 was coupled with an electrospray ionization mass spectrometer via a low profile liquid vortex captur
277 eal-time ( approximately 1 s) vapor analysis mass spectrometer was developed to provide tools, techni
278 ovel proton transfer reaction time-of-flight mass spectrometer was employed for the aroma compounds a
279 romatograph coupled with a triple quadrupole mass spectrometer was employed to quantify BMAA and its
280 of an IMS-capable quadrupole time-of-flight mass spectrometer was undertaken to allow the introducti
281 In this study, an aerosol time-of-flight mass spectrometer was used to analyze laboratory generat
282 An ion mobility quadrupole time-of-flight mass spectrometer was used to examine the gas-phase stru
283 nce of the recently produced Orbitrap hybrid mass spectrometer, we have developed a protocol that com
285 ion scanning features of the Orbitrap Fusion mass spectrometer were employed to biomonitor PhIP in dy
286 ard laboratory and with a classical ion trap mass spectrometer were other remarkable characteristics
287 er transform ion cyclotron resonance (FTICR) mass spectrometers when operated under the selected accu
288 's native structure and its structure in the mass spectrometer (where it is gaseous) remains unclear.
289 n proteomics studies utilize high-throughput mass spectrometers which can produce data at an astonish
290 rements, made on traveling wave ion mobility mass spectrometers, which have to be calibrated to extra
291 , where they are analyzed using a quadrupole mass spectrometer with a time resolution of less, simila
293 imension for separation, a benchtop Orbitrap mass spectrometer with HCD-MS/MS for peptide sequencing,
294 es have been revolutionized by the advent of mass spectrometers with detectors that afford high mass
295 (SDI) was previously developed for hand-held mass spectrometers with discontinuous atmospheric pressu
297 Feature article we argue that development of mass spectrometers with increasingly high resolution and
299 facilitating a path toward compact/hand-held mass spectrometers with numerous potential applications.
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