ライフサイエンスコーパス: ion mobility

1 Eight conformers are observed using ion mobility.

2 products were activated immediately prior to ion mobility.

3 ncluding nominal precursor ion mass, product ion mobility, accurate mass of product ion, and ion abun

4 Here, both ion mobility and capillary electrophoresis are used to f

5 precursor or product ions to be separated by ion mobility and independent fragmentation spectra to be

6 approach will greatly facilitate analysis of ion mobility and mass spectra.

7 Ion mobility and mass spectrometry techniques are couple

8 Further, we have incorporated ion mobility and subsequent drift time gating into the U

9 We use ion mobility and tandem mass spectrometry to investigate

10 edictions are confirmed experimentally using ion mobility and TEM measurements.

11 potential difference, due to alterations on ion-mobility and also by changes in the pore structure.

12 s, (ii) to separate the generated species by ion mobility, and (iii) to characterize the species usin

13 oteins directly via both changes in mass and ion mobility, and assesses the effects of these interact

14 y penalty for oxygen vacancy formation, high ion mobility, and high water uptake.

15 ty advantages of classic gas chromatography, ion mobility, and mass spectrometry instruments are canc

16 a were examined by native mass spectrometry, ion mobility, and quantitative peptide mapping.

17 The resulting ion mobilities are directly correlated to the average li

18 Super-ionic solids, which exhibit ion mobilities as high as those in liquids or molten sal

19 (FAIMS) separate them by the change of their ion mobility at high fields.

20 S analyzer allowed the identification of new ion mobility bands, yielding a total of 63 mobility band

21 copy measurements that substantial magnesium ion mobility can indeed be achieved in close-packed fram

22 addition, ligated water clusters transit the ion mobility cell but (often) dissociate before detectio

23 ounds, a good separation was achieved in the ion mobility cell under the optimized conditions, which

24 tural differences that are not apparent from ion mobility characterization of the activated precursor

25 +)) in the gas phase by combining drift tube ion mobility, cold-ion spectroscopy, and first-principle

26 Ion mobility collision cross section (CCS) measurements

27 al cross sections (CCS), we created the PNNL Ion Mobility Cross Section Extractor (PIXiE).

28 method and software required to extract from ion mobility data the parameters that enable a quantitat

29 pha from existing field dependent drift tube ion mobility data.

30 mass spectrometry of all precursor ions with ion mobility determinations of all product ions, was app

31 In general, the addition of ion mobility dimension has increased the separation of c

32 The ion-mobility distribution of BK[1-5](2+) consists of two

33 However, analysis of ion mobility distributions reveals the two-state transit

34 annotated peptides occupied just 23% of the ion mobility drift space, yet inclusion of ion mobility

35 once Fourier transformed, reveals a standard ion mobility drift spectrum that corresponds to the stan

36 Historically, high pressure ion mobility drift tubes have suffered from low ion duty

37 lamines (PEs) in nitrogen using a drift tube ion mobility (DTIM) instrument and an evaluation of the

38 e ion mobility spectrum agree with the basic ion mobility equation when using nitrogen as drift gas a

39 on addition of dispersion co-solvents limits ion mobility, even while electronic conductivity improve

40 cids using low-pressure, ambient-temperature ion mobility experiments performed in a radio frequency-

41 (Pyr) are characterized using mass-selected ion mobility experiments.

42 -like oligomers to be formed and detected in ion-mobility experiments.

43 und those envelopes to split in differential ion mobility (FAIMS) spectra in a manner dependent on th

44 ions makes it possible to directly determine ion mobilities for unknown species and collision cross s

45 mination of the application of uniform field ion mobility for a narrow scope of isomers with variatio

46 de interfaces, with a critical transition in ion mobility for films thicker than three monolayers.

47 This allows us to distinguish the local Li-ion mobility from the long-range Li-ion motional process

48 ision cross-section (CCS) values obtained by ion mobility high-resolution mass spectrometry has added

49 w variable temperature (VT), high resolution ion mobility (IM) drift tube coupled to a commercial mas

50 ion (CCS) for compounds analyzed in previous ion mobility (IM) experiments representing a wide variet

51 Ion mobility (IM) is a gas-phase separation technique th

52 Ion mobility (IM) is now a well-established and fast ana

53 extended routing (SUPER) traveling wave (TW) ion mobility (IM) module in conjunction with mass spectr

54 Ion mobility (IM) separates ions based on their response

55 performance liquid chromatography (UPLC) and ion mobility (IM) separation to characterize a complex n

56 We report on ion mobility (IM) separations achievable using traveling

57 Ion mobility (IM) separations have a broad range of anal

58 on, wherein we collapse ion distributions in ion mobility (IM) separations into tighter packets provi

59 The initial use of traveling waves (TW) for ion mobility (IM) separations using structures for lossl

60 icient ion population compression for use in ion mobility (IM) separations.

61 In our laboratory, an ion mobility (IM) shift strategy was employed to improve

62 Ion current measurements and ion mobility (IM) spectrometry analysis illustrated that

63 separations using traveling waves (TW) with ion mobility (IM) spectrometry.

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

65 et was used to evaluate the value of product ion mobility in identifying lipids in a complex mixture.

66 redictions also indicate that high magnesium ion mobility is possible in other chalcogenide spinels,

67 IMS conformers; this is strong evidence that ion mobility is sampling solution-phase structures.

68 on of four substances with similar low field ion mobility is shown: phosgene (K0 = 2.33 cm(2)/(V s)),

69 his study, we present a reference drift tube ion mobility mass spectrometer (DTIM-MS) where improveme

70 onstrate the capabilities of a laser-coupled ion mobility mass spectrometer for analysis of peptide s

71 ft time measurements, made on traveling wave ion mobility mass spectrometers, which have to be calibr

72 Concerted tandem and traveling wave ion mobility mass spectrometry (CTS analysis) is a uniqu

73 One attractive feature of ion mobility mass spectrometry (IM-MS) lies in its abili

74 Ion mobility mass spectrometry (IM-MS) showed that the t

75 pectrometry, collision-induced dissociation, ion mobility mass spectrometry (IM-MS), and density func

76 (ESI), tandem mass spectrometry (MS(2)), and ion mobility mass spectrometry (IM-MS).

77 Using traveling wave ion mobility mass spectrometry (MS), we measured the CCS

78 trometry and variable-temperature drift time ion mobility mass spectrometry (VT-DT-IM-MS).

79 Here, we apply variable temperature ion mobility mass spectrometry (VT-IM-MS) to study the e

80 complementary, multistep approach involving ion mobility mass spectrometry and high-performance liqu

81 Here we combine ion mobility mass spectrometry and molecular dynamics si

82 Comparison of the ion mobility mass spectrometry data of the lasso and bra

83 Ion mobility mass spectrometry data were collected on a

84 Our data demonstrate the utility of ion mobility mass spectrometry for probing the structure

85 orption electrospray ionization coupled with ion mobility mass spectrometry imaging (DiBT-IMMS).

86 In this study, we applied ion mobility mass spectrometry in conjunction with chemi

87 Ion mobility mass spectrometry of integral membrane prot

88 ertain the potential of utilizing drift tube ion mobility mass spectrometry to aid in the separation

89 Overall, ion mobility mass spectrometry together with molecular m

90 ogies: for example native mass spectrometry, ion mobility mass spectrometry, and FRET.

91 calorimetry, (1)H, NOESY, and ROESY NMR, and ion mobility mass spectrometry, clearly indicating a bin

92 Using ion mobility mass spectrometry, we demonstrate that isom

93 Using ion mobility mass spectrometry, we show that both inhibi

94 ng mutations that mimic phosphorylation, and ion mobility mass spectrometry, we show that successive

95 ng data-independent acquisition coupled with ion mobility mass spectrometry-mass spectrometry (DIA-IM

96 ere considered and analyzed using drift time ion mobility mass spectrometry.

97 y charge-reduced complexes by traveling wave ion mobility mass spectrometry.

98 Herein, a combination of ion-mobility mass spectrometry (IM-MS) and hydrogen/deut

99 COSY, NOESY, DOSY) NMR spectroscopy, ESI-MS, ion-mobility mass spectrometry (IM-MS), AFM, and TEM.

100 of a protein-surfactant assembly studied by ion-mobility mass spectrometry (IMS) and vacuum molecula

101 oli Hsp70 DnaK by two complementary methods, ion-mobility mass spectrometry and double electron-elect

102 We have developed an ion-mobility mass spectrometry approach, which discerns

103 Crystallographic and native ion-mobility mass spectrometry data show that the TIH-bo

104 Ion-mobility mass spectrometry is utilized to examine th

105 Here, we use novel ion-mobility mass spectrometry methods to probe the earl

106 A combination of ion-mobility mass spectrometry with infrared spectroscop

107 Our research, using ion-mobility mass spectrometry, challenges the notion th

108 Here we use ion-mobility mass spectrometry, in combination with elec

109 energy transfer, atomic force microscopy and ion-mobility mass spectrometry.

110 -to-anion proton-transfer reactions (CAPTR), ion mobility, mass spectrometry, and complementary energ

111 d flexible deconvolution of mass spectra and ion mobility-mass spectra with minimal user intervention

112 commercial liquid chromatography/drift tube ion mobility-mass spectrometer (LC/IM-MS) was evaluated

113 ent with the results obtained from cryogenic ion mobility-mass spectrometry (cryo-IM-MS) measurements

114 Experimental data obtained by cryogenic ion mobility-mass spectrometry (cryo-IM-MS) show that de

115 e report results for electrospray ionization ion mobility-mass spectrometry (ESI-IM-MS) and collision

116 ), when coupled with electrospray ionization-ion mobility-mass spectrometry (ESI-IM-MS), successfully

117 ombined mass spectrometry approach utilizing ion mobility-mass spectrometry (IM-MS) and tandem mass s

118 Ion mobility-mass spectrometry (IM-MS) can provide ortho

119 ss section (CCS) measurements resulting from ion mobility-mass spectrometry (IM-MS) experiments provi

120 Ion mobility-mass spectrometry (IM-MS) has gained consid

121 Ion mobility-mass spectrometry (IM-MS) in combination wi

122 Ion mobility-mass spectrometry (IM-MS) is a powerful tec

123 Ion mobility-mass spectrometry (IM-MS) is a technology o

124 show using collision-induced unfolding (CIU) ion mobility-mass spectrometry (IM-MS) that ncUbq exhibi

125 Ion mobility-mass spectrometry (IM-MS), tandem mass spec

126 The use of ion mobility-mass spectrometry (IM-MS), which separates

127 the analysis of the intact proteins based on ion mobility-mass spectrometry (IM-MS).

128 as monitored by nanoelectrospray ionization-ion mobility-mass spectrometry (nESI-IM-MS).

129 ) measurement of lipids using traveling wave ion mobility-mass spectrometry (TWIM-MS) is of high inte

130 that it resembled the complex formed in vivo Ion mobility-mass spectrometry analysis resulted in an o

131 transmission electron microscopy, as well as ion mobility-mass spectrometry coupled to infrared (IR)

132 High resolution ion mobility-mass spectrometry data revealed two peaks i

133 Analysis of protein complexes by ion mobility-mass spectrometry is a valuable method for

134 Furthermore, ion mobility-mass spectrometry measurements of complexes

135 Overall, variable-velocity traveling-wave ion mobility-mass spectrometry significantly enhances pr

136 e, we show using collision-induced unfolding ion mobility-mass spectrometry that the recently reporte

137 we combine IR-vibrational spectroscopy with ion mobility-mass spectrometry to yield gas-phase IR spe

138 es by ultraperformance liquid chromatography ion mobility-mass spectrometry.

139 eferences of the complex were analyzed using ion mobility-mass spectrometry.

140 gs to stabilize intact protein complexes for ion mobility-mass spectrometry.

141 were investigated by electrospray ionization-ion mobility-mass spectrometry.

142 ism of supercharging were investigated using ion mobility-mass spectrometry.

143 port defined slices of liquid chromatography/ion mobility/mass spectrometry (LC-IM-MS) data, providin

144 density lipoprotein subfractions but not for ion mobility-measured HDL subfractions.

145 atherogenic particles: apolipoprotein B and ion mobility-measured non-HDL particles, LDL particles,

146 tested whether lipids, apolipoproteins, and ion mobility-measured particle concentrations at baselin

147 Incorporation of ion mobility measurements in the experimental workflow a

148 is demonstrated with mass spectrometric and ion mobility measurements of acetone, eucalyptol, and di

149 ecursor-product relationships, combined with ion mobility measurements of all products, enables data

150 Utilization of ion mobility measurements of the product ions is a novel

151 Ion mobility measurements were carried out at temperatur

152 The latter is supported by Ion Mobility measurements.

153 y coupled to mass spectrometry and gas-phase ion-mobility measurements.

154 e ion mobility drift space, yet inclusion of ion mobility nearly doubled the overall peak capacity.

155 Reduced ion mobilities of TAA cations (C2-C8) were calculated at

156 The effect of humidity on reduced ion mobilities of TAA cations is discussed.

157 in ions can be indirectly investigated using ion mobility of their CAPTR product ions, even for subtl

158 ording to their characteristic dependence of ion mobility on electric field strength.

159 We initially derived the differential ion mobility parameter, alpha, from classic empirical IM

160 Using standard traveling-wave ion mobility parameters (600 m/s, 40 V), 90% of the anno

161 available low pressure IMS platforms and an ion mobility peak capacity of approximately 32 for TW sp

162 ll multiply protonated molecules, and narrow ion mobility peak widths associated with the coexistence

163 e was originally separated by HPLC, multiple ion mobility peaks due to structural isomers were observ

164 This compression ratio ion mobility programming (CRIMP) approach has been imple

165 traveling wave (TW) based compression ratio ion mobility programming (CRIMP) approach within structu

166 An ion mobility quadrupole time-of-flight mass spectrometer

167 C-IM-MS) data, providing a route to quantify ion mobility resolution from a commercial traveling-wave

168 s, there has been no quantitative measure of ion mobility resolution in a complex proteomic sample.

169 The ion mobility resolution was characterized at different p

170 s developed in order to predict the required ion mobility resolving power needed to separate the vari

171 The high ion mobility resolving power of the TIMS analyzer allowe

172 Sulfolane was shown not to affect ion mobility results and to allow the formation of highl

173 trospray ionization (LAESI) MS combined with ion mobility separation (IMS) can analyze complex format

174 The utilization of ion mobility separation (IMS) improved the molecular cov

175 ation relies on the molecular weights (MWs), ion mobility separation arrival times, and collision-ind

176 Ion mobility separation can add an orthogonal analytical

177 tion cells located in front of and after the ion mobility separation device enabled oligosaccharide p

178 ectrospray ionization mass spectrometry with ion mobility separation for nontargeted analysis of sing

179 Despite the advantages of ion mobility separation in complex proteomics analyses,

180 Ion mobility separation of native-like protein and prote

181 e that the combination of mass spectrometry, ion mobility separation, and collision-induced dissociat

182 The influence of main factors affecting the ion mobility separation, such as modifier types and conc

183 o yield an additional dimension of gas-phase ion mobility separation.

184 ctivity provided by a postsampling gas-phase ion mobility separation.

185 raphy coupled to mass spectrometry employing ion mobility separation.

186 e PMP labeling technique in conjunction with ion-mobility separation and tandem mass spectrometry.

187 e used in combination with chromatography or ion-mobility separation.

188 sless Ion Manipulations (TW-SLIM) module for ion mobility separations (IMS).

189 dvantageously applied to the applications of ion mobility separations and gas phase reactions, ion in

190 first time that the current state-of-the-art ion mobility separations benchmark at a CCS-based resolv

191 Here, we report on ion mobility separations in a structures for lossless io

192 Relative to fixed velocity traveling-wave ion mobility settings, ramping the traveling-wave veloci

193 e performance of a small, plastic drift tube ion mobility spectrometer (DT-IMS) is described.

194 This novel field asymmetric time of flight ion mobility spectrometer (FAT-IMS) allows high repetiti

195 n atmospheric pressure, dual-gate drift tube ion mobility spectrometer (IMS) to a linear ion trap mas

196 nvestigated using a Synapt G2 traveling wave ion mobility spectrometer coupled between quadupole and

197 esent for the first time an ambient pressure ion mobility spectrometer which is able to separate ions

198 e that using a compact ultra-high-resolution ion mobility spectrometer with a resolving power of 250

199 Drift tube ion mobility spectrometers (DT-IMS) separate ions by the

200 w field ion mobility, while field asymmetric ion mobility spectrometers (FAIMS) separate them by the

201 n have been the shortcomings of the previous ion mobility spectrometers, in particular (a) diffusiona

202 Atmospheric pressure drift tube ion mobility spectrometry (AP-DTIMS) was coupled with Fo

203 sed as an ionization source for differential ion mobility spectrometry (DMS) for the first time.

204 estion (PD) is demonstrated using drift tube ion mobility spectrometry (DTIMS) coupled with linear io

205 an electrospray ionization high-performance ion mobility spectrometry (ESI-HPIMS).

206 miniaturized high-field asymmetric waveform ion mobility spectrometry (FAIMS) and mass spectrometry

207 Full scan field asymmetric waveform ion mobility spectrometry (FAIMS) combined with liquid c

208 a chip-based high-field asymmetric waveform ion mobility spectrometry (FAIMS) device to image metabo

209 coupled with high field asymmetric waveform ion mobility spectrometry (FAIMS) for top-down protein a

210 High-field asymmetric waveform ion mobility spectrometry (FAIMS) is an atmospheric pres

211 Using high-definition differential ion mobility spectrometry (FAIMS) with electron transfer

212 t coupling of high field asymmetric waveform ion mobility spectrometry (FAIMS), also known as differe

213 to study the potential of gas chromatography-ion mobility spectrometry (GC-IMS) to differentiate lact

214 findings allow for integration of MS(2) with ion mobility spectrometry (IM-MS(2)) and lead to a strat

215 e analytical separation techniques including ion mobility spectrometry (IMS) and liquid chromatograph

216 rrival time distributions (ATDs) recorded by ion mobility spectrometry (IMS) can often be interpreted

217 ar gas chromatography (GC) column coupled to ion mobility spectrometry (IMS) has been explored to cla

218 Ion mobility spectrometry (IMS) has been shown to be a v

219 Recently, ion mobility spectrometry (IMS) has been shown to effect

220 Recently, ion mobility spectrometry (IMS) has been used to support

221 Ion mobility spectrometry (IMS) has proven to be useful

222 Although ion mobility spectrometry (IMS) has shown great promise

223 Ion mobility spectrometry (IMS) in conjunction with mass

224 developed for detecting heavy metals via the ion mobility spectrometry (IMS) in the negative mode.

225 Ion mobility spectrometry (IMS) is a fast and sensitive

226 Ion mobility spectrometry (IMS) is a gas phase separatio

227 Ion mobility spectrometry (IMS) is increasingly used to

228 Detection by mass spectrometry (MS) and/or ion mobility spectrometry (IMS) is traditionally difficu

229 Ion mobility spectrometry (IMS) may be used to show sepa

230 Conversely, gas phase ion mobility spectrometry (IMS) techniques can be used t

231 Separation of d/l-peptides using ion mobility spectrometry (IMS) was impeded by small col

232 es (extra virgin, virgin and lampante) using Ion Mobility Spectrometry (IMS) was improved by replacin

233 The integration of ion mobility spectrometry (IMS) with mass spectrometry (

234 The progress of ion mobility spectrometry (IMS), together with its assoc

235 MAIV-MS coupled with ion mobility spectrometry (IMS)-MS and tandem mass spect

236 d in baby formula samples and detected using ion mobility spectrometry (IMS).

237 e for direct liquid sampling and analysis by ion mobility spectrometry (IMS).

238 Oversampling Selective Accumulation Trapped Ion Mobility Spectrometry (OSA-TIMS) when coupled to ult

239 present work, selected accumulation trapped ion mobility spectrometry (SA-TIMS) is coupled to Fourie

240 the Traveling Wave (TWIMS), and the Trapped Ion Mobility Spectrometry (TIMS) coupled to mass spectro

241 For the first time, trapped ion mobility spectrometry (TIMS) in tandem with Fourier

242 The recent development of trapped ion mobility spectrometry (TIMS) provides a promising ne

243 The potential of a Transversal Modulation Ion Mobility Spectrometry (TMIMS) instrument for protein

244 troduced based on the transversal modulation ion mobility spectrometry (TMIMS) technique, which provi

245 While the coupling of traveling wave ion mobility spectrometry (TWIMS) and mass spectrometry

246 we describe how to integrate traveling-wave ion mobility spectrometry (TWIMS) into traditional LC-MS

247 Traveling wave ion mobility spectrometry (TWIMS) isomer separation was

248 rift time determination using traveling wave ion mobility spectrometry (TWIMS) of poorly resolved or

249 Although the hyphenation of traveling-wave ion mobility spectrometry (TWIMS) with high-resolution q

250 (UPLC-IM-TOFMS), integrating traveling wave ion mobility spectrometry (TWIMS) with negative electros

251 Ion mobility spectrometry allows for the measurement of

252 Ion mobility spectrometry allows one to determine ion co

253 imination of oligosaccharide isomers by both ion mobility spectrometry and tandem mass spectrometry.

254 Ion mobility spectrometry combined with multicapillary c

255 rk explores the capabilities of differential ion mobility spectrometry coupled to tandem mass spectro

256 Drift tube ion mobility spectrometry coupled with mass spectrometry

257 predict separation efficiency for drift tube ion mobility spectrometry experiments.

258 Ion mobility spectrometry is a powerful and low-cost tec

259 Ion mobility spectrometry provides ion separation in the

260 A combination of CID and ion mobility spectrometry was applied for the first time

261 isomers separated by both chromatography and ion mobility spectrometry were studied.

262 We combine ion mobility spectrometry with cryogenic, messenger-tagg

263 The combination of field asymmetric waveform ion mobility spectrometry with liquid chromatography-mas

264 alpha-pinene are investigated using coupled ion mobility spectrometry with mass spectrometry.

265 for interrogation by electrospray ionization-ion mobility spectrometry-mass spectrometry (ESI-IMS-MS)

266 A recent ion mobility spectrometry-mass spectrometry (IMS-MS) stu

267 trospray ionization and analyzed by combined ion mobility spectrometry-mass spectrometry (IMS-MS) tec

268 we report a high-throughput method based on ion mobility spectrometry-mass spectrometry (IMS-MS) tha

269 en/deuterium back exchange (HDX) and trapped ion mobility spectrometry-mass spectrometry (TIMS-MS).

270 shown here experimentally by traveling wave ion mobility spectrometry-mass spectrometry (TWIMS-MS) o

271 amyloid intermediates using a combination of ion mobility spectrometry-mass spectrometry and gas-phas

272 loride ions using a novel technique coupling ion mobility spectrometry-mass spectrometry with infrare

273 s challenge, we developed a drift tube-based ion mobility spectrometry-Orbitrap mass spectrometer (IM

274 e high-performance liquid chromatography and ion mobility spectrometry.

275 enables the separation of isotopologues with ion mobility spectrometry.

276 y can be accurately calibrated against other ion-mobility spectrometry (IMS) techniques.

277 oices include liquid chromatography (LC) and ion-mobility spectrometry (IMS), in which separation tak

278 ation of OzID in a high-pressure region, the ion-mobility spectrometry cell, of a contemporary quadru

279 es of molecular species using traveling wave ion-mobility spectrometry-mass spectrometry (TWIMS-MS) i

280 ctrospray ionization (ESI) with differential ion mobility spectroscopy (FAIMS) and "soft" mass spectr

281 The observed peak shifts in the ion mobility spectrum agree with the basic ion mobility

282 aphy coupled to electrospray high-definition ion mobility tandem mass spectrometry.

283 ctrometry (FAIMS) is an atmospheric pressure ion mobility technique that separates gas phase ions acc

284 resolution from a commercial traveling-wave ion mobility time-of-flight mass spectrometer.

285 aper, laser ablation electrospray ionization ion mobility time-of-flight mass spectrometry (LAESI-IMS

286 sing ultra performance liquid chromatography ion mobility time-of-flight mass spectrometry (UPLC-IM-T

287 Ultraperformance liquid chromatography ion mobility time-of-flight mass spectrometry (UPLC-IM-T

288 natured ubiquitin ions in the gas phase, and ion mobility to probe their structures.

289 ques evaluated (i.e., uniform field, trapped ion mobility, traveling wave, cyclic, and overtone instr

290 fferent peak broadening phenomenon inside an ion mobility tube.

291 rometry (MS(E)) workflow with traveling wave ion mobility (TWIM) and UV detection, to improve the cha

292 Traveling wave ion mobility (TWIM) mass spectrometry (MS) is a powerful

293 sional data set (precursor ion, product ion, ion mobility value, and intensity) was found to be usefu

294 Indeed, differential ion mobility was able to resolve (resolution >4) nicotin

295 For drift tube ion mobility, we describe a new method, coined "FWHMstep

296 CCS values derived from ion mobility were not affected by instrument settings or

297 but no significant difference in the sodium ion mobility were obtained.

298 rotein particle concentrations determined by ion mobility, were made at the end of each experimental

299 ons by the absolute value of their low field ion mobility, while field asymmetric ion mobility spectr

300 trometry (FAIMS), also known as differential ion mobility, with liquid extraction surface analysis (L