ライフサイエンスコーパス: mass spectrometry analysis

1 as an interacting partner for IAV HA through mass spectrometry analysis.

2 verified it with chemical cross-linking and mass spectrometry analysis.

3 ous food samples prior to gas chromatography-mass spectrometry analysis.

4 ommon electrospray ionization time-of-flight mass spectrometry analysis.

5 digestion model combined to high resolution mass spectrometry analysis.

6 Hall effect and time-of-flight secondary ion mass spectrometry analysis.

7 ed through oxidation reactions of Trolox via mass spectrometry analysis.

8 uctural information available through native mass spectrometry analysis.

9 ed by affinity purification and quantitative mass spectrometry analysis.

10 ward their protein targets in vitro based on mass spectrometry analysis.

11 nsuming using traditional gas chromatography mass spectrometry analysis.

12 and liquid chromatography coupled to tandem mass spectrometry analysis.

13 urification time from 3.5 h to 30 min before mass spectrometry analysis.

14 cid content obtained from gas chromatography-mass spectrometry analysis.

15 en bromide cleavage to facilitate subsequent mass spectrometry analysis.

16 and enabled compatible sample processing for mass spectrometry analysis.

17 on and nanoflow liquid chromatography-tandem mass spectrometry analysis.

18 k of UV detection and as a result a need for mass spectrometry analysis.

19 on the basis of pyrolysis-gas chromatography/mass spectrometry analysis.

20 complex in planta by immunoprecipitation and mass spectrometry analysis.

21 ction and dissociation prior to ion mobility/mass spectrometry analysis.

22 leasing from glycoproteins/glycopeptides for mass spectrometry analysis.

23 ctionate the complex protein extracts before mass spectrometry analysis.

24 1 using chemical cross-linking combined with mass spectrometry analysis.

25 of the sea star, and identified dysferlin by mass spectrometry analysis.

26 ve fluorophotometry, electron microscopy and mass spectrometry analysis.

27 wise gradient elution and electrosprayed for mass spectrometry analysis.

28 h pressure using label-free quantitation and mass spectrometry analysis.

29 d VOCs were determined by gas chromatography-mass spectrometry analysis.

30 mented mice were characterized by lipidomics mass spectrometry analysis.

31 ts, demonstrating complementary detection by mass spectrometry analysis.

32 labeling and click chemistry with subsequent mass spectrometry analysis.

33 suspensions were analyzed by time of flight mass spectrometry analysis.

34 ormed via data-independent acquisition (DIA) mass spectrometry analysis.

35 es) prior to their gas chromatography tandem mass spectrometry analysis.

36 tification with liquid chromatography tandem mass spectrometry analysis.

37 nfirmation of their nuclear origin shown via mass spectrometry analysis.

38 her normal tissues, as determined by in vivo mass spectrometry analysis.

39 bulin as was observed by electrophoresis and mass spectrometry analysis.

40 studies, mass analysis, and high-resolution mass spectrometry analysis.

41 plex mixture (UCM) during gas-chromatography mass-spectrometry analysis.

42 id chromatography (UHPLC) and time-of-flight mass spectrometry analysis, allowing the acquisition of

43 Mass spectrometry analysis also enabled the identificati

44 Sulfhydration sites are identified by mass spectrometry analysis and are investigated by site-

45 rat brain utilizing immunohistochemistry and mass spectrometry analysis and assessed the effect of ag

46 Mass spectrometry analysis and coimmunoprecipitation (co

47 By using mass spectrometry analysis and coimmunoprecipitation ass

48 how that VolA is a canonical lipoprotein via mass spectrometry analysis and demonstrate the in vitro

49 46 in human IRF5 isoform 1), as evidenced by mass spectrometry analysis and detection with a phosphos

50 n studies with the OXA-24/40 enzyme, protein mass spectrometry analysis and docking studies allowed u

51 -Perchloric acid-soluble protein) by shotgun mass spectrometry analysis and gene identification, and

52 electrophoresis and major spots subjected to mass spectrometry analysis and identification.

53 Quantitative mass spectrometry analysis and the 5-6 A resolution cryo

54 onstrated using liquid chromatography-tandem mass spectrometry analysis, and a total of 106 S-sulfhyd

55 vitro reconstruction of CTD phosphorylation, mass spectrometry analysis, and chromatin immunoprecipit

56 luding EV isolation, PTM/peptide enrichment, mass spectrometry analysis, and data quantification.

57 hromatography-electrospray ionization-tandem mass spectrometry analysis, and enzyme kinetic studies u

58 captured protein, tryptic digestion, tandem mass spectrometry analysis, and label-free quantificatio

59 he key events (sample desorption/ionization, mass spectrometry analysis, and sample translation) nece

60 ers are additionally acetylated, as shown by mass spectrometry analysis, and their binding to PARP-1

61 se 1 and 2 (PYCR1, PYCR2) were identified by mass spectrometry analysis as components of RRM2B comple

62 RNA affinity pull-down followed by mass spectrometry analysis as well as RNA coimmunoprecip

63 Using mass spectrometry analysis based on capturing endophilin

64 protein identification and quantification in mass spectrometry analysis by blocking peptide amino gro

65 he GC-O/FID system with GCxGC-time-of-flight mass spectrometry analysis by means of retention indices

66 of biological extracts coupled to precision mass spectrometry analysis (chromatographic fractionatio

67 data from top-down and bottom-up proteomics mass spectrometry analysis combined with NEM labeling re

68 Triple quadrupole mass spectrometry analysis conducted during the reaction

69 Liquid chromatography-mass spectrometry analysis confirmed successful coupling

70 Mass spectrometry analysis confirmed that all Arg residu

71 ion experiments in liquid media coupled with mass spectrometry analysis confirmed that biogenic cyani

72 Further mass spectrometry analysis confirmed that the isolated F

73 spectroscopy and hydrogen/deuterium exchange mass spectrometry analysis coupled to activity assays re

74 Mass spectrometry analysis demonstrated that cytoplasmic

75 Mass-spectrometry analysis demonstrated blood from plate

76 Mass spectrometry analysis detected 2.67 ng/mL of Ro5-33

77 Mass spectrometry analysis detected a 4.6-fold increase

78 tion and rapid, single-run, data-independent mass spectrometry analysis (DIA).

79 yrosine phosphatase PTPN14 was identified by mass spectrometry analysis exclusively in co-immunopreci

80 Using tandem mass spectrometry analysis followed by immunoblotting, w

81 Here we conducted mass spectrometry analysis for brain-derived interactors

82 ed GC-IRMS (gas chromatography-isotope-ratio mass-spectrometry) analysis for carbon and nitrogen isot

83 Enabled by a shotgun mass spectrometry analysis founded on tissue culture mod

84 Gas chromatography-mass spectrometry analysis further indicated that OlvA(B

85 gas chromatography combustion isotope ratio mass spectrometry analysis (GC-C-IRMS).

86 drop of whole blood using gas chromatography-mass spectrometry analysis (GC-MS) of their per-O-methyl

87 Our mass spectrometry analysis has independently identified

88 labeling of surface residues, combined with mass spectrometry analysis, has increasingly played an i

89 After mass spectrometry analysis, higher amounts of low molecu

90 We used hydrogen exchange mass spectrometry analysis (HX MS) to resolve and charac

91 Independent mass spectrometry analysis identified 40 of the 48 prote

92 Mass spectrometry analysis identified a 3 kDa peptide, H

93 Tandem mass spectrometry analysis identified a novel phosphoryl

94 Mass spectrometry analysis identified a peptide specific

95 Mass spectrometry analysis identified a total of 181 pro

96 Quantitative mass spectrometry analysis identified all core desmosoma

97 Mass spectrometry analysis identified five phosphosites,

98 Mass spectrometry analysis identified GLP-1R-dependent u

99 Our mass spectrometry analysis identified INSL6 as a novel C

100 CIEF immunoassay and immunoprecipitation mass spectrometry analysis identified peptides starting

101 key pathways affected by ATG treatment, and mass spectrometry analysis identified protein phosphatas

102 Furthermore, mass spectrometry analysis identified protein S-glutathi

103 Interestingly, mass spectrometry analysis identified the DEAD-box RNA h

104 Mass spectrometry analysis identified the magenta-colour

105 Mass spectrometry analysis identified the pol II subunit

106 Mass spectrometry analysis identified this protein as ad

107 Mass spectrometry analysis identified two asparagine res

108 strains by liquid chromatography, coupled to mass spectrometry analysis, identified a total of 2161 p

109 psilon is acetylated, which was confirmed by mass spectrometry analysis, identifying 4 acetylated lys

110 Affinity pull-down mass spectrometry analysis in human plasma demonstrated

111 RNA precipitation assays combined with mass spectrometry analysis indicate that LINC00346 inter

112 Furthermore, mass spectrometry analysis indicated Lys-72 as an acetyl

113 Mass spectrometry analysis indicated that the complex co

114 Mass spectrometry analysis indicated the TTSS motif is n

115 We report mass spectrometry analysis indicating that peroxynitrite

116 trating tumors, and were comparable to other mass spectrometry analysis interfaces.

117 Proteomic mass spectrometry analysis is becoming routine in clinic

118 des with cation-exchange beads followed with mass spectrometry analysis is presented.

119 degradation of cartilage was detected using mass spectrometry analysis (liquid chromatography-tandem

120 and multimodal liquid chromatography-tandem mass spectrometry analysis of >330,000 synthetic tryptic

121 archaeological pottery based on accelerator mass spectrometry analysis of (14)C in absorbed food res

122 The liquid chromatography-tandem mass spectrometry analysis of 45 phenolics resulted in q

123 Furthermore, mass spectrometry analysis of a cyclic S12 cluster, whic

124 vides a solution to the problem of real-time mass spectrometry analysis of a three-dimensional object

125 Combined gas chromatography-mass spectrometry analysis of acid hydrolysates of the f

126 s were quantified through gas chromatography/mass spectrometry analysis of adsorbent samples collecte

127 s was accomplished by the comparative tandem mass spectrometry analysis of authentic TA derivatives f

128 extraction method for the Gas Chromatography-Mass Spectrometry analysis of blackberry (Rubus sp.) vol

129 The f-AuNPs allow for the mass spectrometry analysis of both lipophilic and polar

130 lly restricted enzymatic tagging followed by mass spectrometry analysis of Caenorhabditis elegans inf

131 Mass spectrometry analysis of Calvarial-CM identified 13

132 Using mass spectrometry analysis of complex HLA-bound peptide

133 CI) source was developed that allowed direct mass spectrometry analysis of complex mixtures at a samp

134 Mass spectrometry analysis of conditioned medium derived

135 Mass spectrometry analysis of CSB identified lysine (K)

136 Here we report that mass spectrometry analysis of dual-affinity purification

137 hromatography electrospray ionization tandem mass spectrometry analysis of eighteen water-soluble art

138 Mass spectrometry analysis of extensively fractionated N

139 cattering imaging of single living cells and mass spectrometry analysis of extracted lipids, we repor

140 Mass spectrometry analysis of fibrinogen proteolytic rea

141 Single particle microscopy and mass spectrometry analysis of field and laboratory-gener

142 Mass spectrometry analysis of FliI immunoprecipitates sh

143 Untargeted mass spectrometry analysis of food samples has the poten

144 rdeum vulgare) plants and gas chromatography-mass spectrometry analysis of free amino acids and liqui

145 have not been investigated in ADPKD yet, and mass spectrometry analysis of Gb4Cer from tissue extract

146 Ultra-high sensitivity mass spectrometry analysis of glycans released from such

147 Mass spectrometry analysis of histone modifications reve

148 l adenocarcinoma (PDAC), we performed tandem mass spectrometry analysis of HLA class I-bound peptides

149 In parallel, mass spectrometry analysis of HLA peptidome is increasin

150 n was confirmed by coimmunoprecipitation and mass spectrometry analysis of immunoprecipitation produc

151 We extend this approach with large-scale mass spectrometry analysis of immunoprecipitations of 50

152 Comparative mass spectrometry analysis of immunopurified FBXW11 prot

153 Mass spectrometry analysis of in vitro kinase assays sho

154 Mass spectrometry analysis of isolated proteolytic fragm

155 core components, based on cross-linking and mass spectrometry analysis of isolated, functional intac

156 Purification of Tls1 and mass spectrometry analysis of its interacting proteins s

157 Conclusion Targeted mass spectrometry analysis of just three cyst fluid biom

158 In recent years, new generation mass spectrometry analysis of lipids (termed lipidomics)

159 Mass spectrometry analysis of many phospholipids is pref

160 Mass spectrometry analysis of membrane proteins that wer

161 In contrast, mass spectrometry analysis of monoubiquitinated poliota

162 tease, (5) liquid chromatography with tandem mass spectrometry analysis of O-GalNAc glycopeptides, (6

163 Nevertheless, mass spectrometry analysis of oligosulfurs (S n ), which

164 Mass spectrometry analysis of one of these strains showe

165 Gas Chromatography and Mass Spectrometry analysis of P. halepensis Mill., P. pi

166 Mass spectrometry analysis of patient sera also revealed

167 has been probed using liquid chromatography-mass spectrometry analysis of peptide-lipid mixtures.

168 Electron transfer dissociation mass spectrometry analysis of peptides bearing this modi

169 led to accurate-mass, high-resolution tandem mass spectrometry analysis of peptides fractionated off-

170 Mass spectrometry analysis of phosphospecific immunoprec

171 Mass spectrometry analysis of plasma and brain samples i

172 uxes using a combined NMR/gas chromatography-mass spectrometry analysis of plasma following infusion

173 PLEKHA7 by yeast two-hybrid screening and by mass spectrometry analysis of PLEKHA7 immunoprecipitates

174 n of the seed followed by gas chromatography-mass spectrometry analysis of polar metabolites also rev

175 vidence from immunolabel, RNA expression and mass spectrometry analysis of postmortem samples that hu

176 d RT-qPCR, Western blot, flow cytometry, and mass spectrometry analysis of precisely dissected NR-lab

177 e new method demonstrates utility for native mass spectrometry analysis of proteins and G-quadruplex

178 Using liquid chromatography-tandem mass spectrometry analysis of proteins extracted from th

179 Mass spectrometry analysis of proteins that co-immunopre

180 f free amino acids and liquid chromatography-mass spectrometry analysis of proteins to track the enri

181 Mass spectrometry analysis of purified KIF3A showed that

182 Mass spectrometry analysis of purified mutant LPS was us

183 Using mass spectrometry analysis of recombinant human PRC2, we

184 Mass spectrometry analysis of recombinant STAT3 protein

185 Here, we report the mass spectrometry analysis of serine and threonine pyrop

186 re profiled via liquid chromatography tandem mass spectrometry analysis of serum from 161 patients wi

187 on-chromatography coupled to high resolution mass spectrometry analysis of the 105 samples did not sh

188 Moreover, using O-GlcNAc-specific mass spectrometry analysis of the aging hippocampus, tog

189 Mass spectrometry analysis of the biotinylated proteins

190 Combining mass spectrometry analysis of the dUTPase-catalyzed reac

191 sis with a phosphoprotein-specific stain and mass spectrometry analysis of the enriched phosphoprotei

192 Here, using twin ion mass spectrometry analysis of the extracts of whole Dros

193 Mass spectrometry analysis of the fractions obtained at

194 validated using hydrogen-deuterium-exchange mass spectrometry analysis of the full-length protein an

195 trolysis experiments, gas chromatography and mass spectrometry analysis of the headspace in the elect

196 Mass spectrometry analysis of the in vitro methyltransfe

197 Mass spectrometry analysis of the native protein confirm

198 thods and allows for a successful downstream mass spectrometry analysis of the reaction products.

199 eration sequencing and liquid chromatography-mass spectrometry analysis of the secretomes of encapsul

200 ted clickable NAD(+) precursor, quantitative mass spectrometry analysis of the two probes in MDA-MB-2

201 Mass spectrometry analysis of these polypeptides resulte

202 Mass spectrometry analysis of Tr-OxPL species in young (

203 Fast atom bombardment-mass spectrometry analysis of urine and bile at baseline

204 netic defect that causes this disorder using mass spectrometry analysis of urine, bile, and serum sam

205 a tubular furnace and subsequent ICP-MS (ICP Mass Spectrometry) analysis of the obtained residues all

206 n based technique that enables the direct-to-mass-spectrometry analysis of extracted compounds via th

207 ombination with liquid chromatography/tandem mass spectrometry analysis, of which 22 exhibited signif

208 r cross-linking were distinguished by tandem mass spectrometry analysis on fibers seeded from solutio

209 uid chromatography-mass spectrometry, tandem mass spectrometry analysis on individual arterial sample

210 e retrocycloaddition reaction as revealed by mass spectrometry analysis on quasi-enantiomeric pyrroli

211 Liquid chromatography-mass spectrometry/mass spectrometry analysis on the tryptic peptide fragme

212 Mass spectrometry analysis provided a description of cho

213 nserine, as confirmed by chromatographic and mass spectrometry analysis, rat UPF0586 was more active

214 bled the complex formed in vivo Ion mobility-mass spectrometry analysis resulted in an observed mass

215 The liquid chromatography-tandem mass spectrometry analysis resulted in quantification of

216 Mass spectrometry analysis revealed a reducing terminal

217 Coimmunoprecipitation and mass spectrometry analysis revealed an interaction betwe

218 Mass spectrometry analysis revealed eight sites of O-Glc

219 Liquid chromatography-tandem mass spectrometry analysis revealed marked differences b

220 Mass spectrometry analysis revealed R25 to be the subuni

221 Mass spectrometry analysis revealed that ADA and Piccolo

222 Mass spectrometry analysis revealed that AvrPtoB phospho

223 A coimmunoprecipitation assay followed by mass spectrometry analysis revealed that dCRY interacts

224 Mass spectrometry analysis revealed that DPP4 (dipeptidy

225 ase-associated mutations, lectin binding and mass spectrometry analysis revealed that GNE deficiency

226 Mass spectrometry analysis revealed that in vivo the occ

227 target protein was purified, and subsequent mass spectrometry analysis revealed that Mup44 is the cy

228 Mass spectrometry analysis revealed that non-muscle myos

229 Mass spectrometry analysis revealed that Scabin labels t

230 Mass spectrometry analysis revealed that the CSF proteom

231 Gas chromatography-mass spectrometry analysis revealed that the mutant has

232 raperitoneal (IP) administration of SBI-425, mass spectrometry analysis revealed that the SBI-425 doe

233 Mass spectrometry analysis revealed that treatment of di

234 Liquid chromatography-tandem mass spectrometry analysis revealed that various anti-in

235 Mass spectrometry analysis revealed that wild-type B. pa

236 YFP followed by liquid chromatography-tandem mass spectrometry analysis revealed the presence of prot

237 Mass spectrometry analysis revealed wild-type EPC-derive

238 Mass spectrometry analysis reveals that NAD simultaneous

239 Mass spectrometry analysis reveals that Pol gamma exo do

240 ure of gammaTuRC, combined with crosslinking mass spectrometry analysis, reveals an asymmetric confor

241 Selected ion flow tube mass spectrometry analysis showed HCN was not elevated i

242 0 kDa on SDS-PAGE and did not contain Gbeta5 Mass spectrometry analysis showed no other proteins to b

243 Site-directed mutagenesis combined with mass spectrometry analysis showed that a disulfide bridg

244 Mass spectrometry analysis showed that CBP/p300 acetylat

245 Mass spectrometry analysis showed that H2A.Z.1 and H2A.Z

246 Immunoprecipitation followed by mass spectrometry analysis showed that several N-termina

247 Affinity chromatography followed by mass spectrometry analysis showed that the antibody reco

248 In contrast, mass spectrometry analysis showed that the majority of t

249 Mass spectrometry analysis showed that the wild type gly

250 Mass spectrometry analysis showed that these peptides ar

251 In addition, the factors involved in mass spectrometry analysis, such as MALDI matrix, plate,

252 -layer chromatography and gas chromatography-mass spectrometry analysis suggested the presence of ars

253 A systematic mass (and tandem mass) spectrometry analysis suggests that the SME reacti

254 We reveal by coimmunoprecipitation and mass spectrometry analysis that alpha-tubulin interacts

255 Now, we demonstrate by mass spectrometry analysis that P1N-PISPO is indeed prod

256 , and host-host protein interactions using a mass spectrometry analysis that takes just a few hours.

257 d by in vitro nuclear magnetic resonance and mass spectrometry analysis to assess intramyocardial lip

258 th its interactors, which were identified by mass spectrometry analysis to be mainly photosystem II a

259 sing laser capture methodology, we performed mass spectrometry analysis to compare T and NT protein e

260 We performed immunoprecipitation-mass spectrometry analysis to detect in vivo interactors

261 tudy, we performed affinity purification and mass spectrometry analysis to explore protein-protein in

262 applied chemical cross-linking coupled with mass spectrometry analysis to gain insight into interact

263 AGE gel and isolated bands are submitted for mass spectrometry analysis to identify drug targets.

264 We used mass spectrometry analysis to quantify free-iodide conta

265 s multiple dimensions of separation prior to mass spectrometry analysis to reduce sample complexity a

266 We performed membrane inlet mass spectrometry analysis to show that D. armatus has a

267 wn assays, with GGGGCC5, in conjunction with mass spectrometry analysis, to identify candidate bindin

268 RNA-affinity purification followed by mass spectrometry analysis uncovered that sfRNA specific

269 We show by spectroscopic techniques and mass spectrometry analysis under native conditions that

270 hly sensitive ( approximately 0.6 zeptomole) mass spectrometry analysis using minimal sample (18 pl p

271 ed a substrate trapping mutant combined with mass spectrometry analysis using Stable Isotope Labellin

272 Liquid chromatography-mass spectrometry analysis was employed for detection an

273 ure followed by liquid chromatography tandem mass spectrometry analysis was implemented and validated

274 Liquid chromatography mass spectrometry analysis was performed to confirm glyc

275 Mass spectrometry analysis was then performed to identif

276 Gas chromatography-mass spectrometry analysis was used for quantification o

277 Immunoprecipitation-mass spectrometry analysis was used to identify interact

278 Finally, inductively coupled plasma mass spectrometry analysis was used to quantify gadolini

279 Using co-immunoprecipitation and mass spectrometry analysis we identify unique FLCN bindi

280 olecular genetics, analytical chemistry, and mass spectrometry analysis, we demonstrated that GAC bio

281 nosine (dG) and liquid chromatography-tandem mass spectrometry analysis, we demonstrated unambiguousl

282 Using high-performance liquid chromatography-mass spectrometry analysis, we detected these flavonoids

283 In this study, using mass spectrometry analysis, we discovered a distinct pho

284 Using mass spectrometry analysis, we found that VLVs contained

285 Using affinity RNA pull-down followed by mass spectrometry analysis, we found two RNA-binding pro

286 matrix-assisted laser desorption ionization mass spectrometry analysis, we here identify a key compo

287 Here, using mass spectrometry analysis, we identified components fro

288 Using mass spectrometry analysis, we identified three serine r

289 Using affinity purification and mass spectrometry analysis, we identify differential bin

290 Using quantitative mass spectrometry analysis, we observed a MELK-mediated

291 (15)N2 tracer experiments and isotope ratio mass spectrometry analysis, we observed that seep N2 fix

292 ered lacticin 481 biosynthetic machinery and mass spectrometry analysis, we show here that the LctA l

293 ng an FGFR1c-specific antibody together with mass spectrometry analysis, we show that RPTECs express

294 oupled with nanoliquid chromatography-tandem mass spectrometry analysis, we show that the in planta m

295 Using pulldown assays combined with mass spectrometry analysis, we show that the Itch PRR pr

296 Peptide fragments for mass spectrometry analysis were obtained directly on gan

297 ciated peptides during liquid chromatography-mass spectrometry analysis, which can easily be misident

298 sotope-dilution liquid chromatography-tandem mass spectrometry analysis, which can serve as a general

299 By combining mass spectrometry analysis with small interfering RNA sc

300 An autonomous metabolomic workflow combining mass spectrometry analysis with tandem mass spectrometry