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

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

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

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

4 en bromide cleavage to facilitate subsequent mass spectrometry analysis.

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

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

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

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

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

10 complex in planta by immunoprecipitation and mass spectrometry analysis.

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

12 leasing from glycoproteins/glycopeptides for mass spectrometry analysis.

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

14 1 using chemical cross-linking combined with mass spectrometry analysis.

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

16 ve fluorophotometry, electron microscopy and mass spectrometry analysis.

17 wise gradient elution and electrosprayed for mass spectrometry analysis.

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

19 l sugar analogs in plasma cells coupled with mass spectrometry analysis.

20 ance peptides usually not observed by direct mass spectrometry analysis.

21 cts with NM II by co-immunoprecipitation and mass spectrometry analysis.

22 d by two-dimensional gel electrophoresis and mass spectrometry analysis.

23 e an electrospray from the capillary tip for mass spectrometry analysis.

24 e iminium using liquid chromatography-tandem mass spectrometry analysis.

25 igh-performance liquid chromatography-tandem mass spectrometry analysis.

26 ed by redox two-dimensional PAGE followed by mass spectrometry analysis.

27 ues were determined by liquid chromatography/mass spectrometry analysis.

28 ther methods for desalting proteins prior to mass spectrometry analysis.

29 the substrate, and the formation of ions for mass spectrometry analysis.

30 was analyzed by liquid chromatography-tandem mass spectrometry analysis.

31 ein (PML) as a Fas-interacting protein using mass spectrometry analysis.

32 sphorylation sites were identified by tandem mass spectrometry analysis.

33 TAP) based on its biochemical properties and mass spectrometry analysis.

34 hromatography and identified as nucleolin by mass spectrometry analysis.

35 digestion model combined to high resolution mass spectrometry analysis.

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

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

38 uctural information available through native mass spectrometry analysis.

39 ed by affinity purification and quantitative mass spectrometry analysis.

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

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

42 nsuming using traditional gas chromatography mass spectrometry analysis.

43 and liquid chromatography coupled to tandem mass spectrometry analysis.

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

45 In mass spectrometry analysis, 12 new acetylated lysine sit

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

47 Mass spectrometry analysis also enabled the identificati

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

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

50 Mass spectrometry analysis and coimmunoprecipitation (co

51 By using mass spectrometry analysis and coimmunoprecipitation ass

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

53 46 in human IRF5 isoform 1), as evidenced by mass spectrometry analysis and detection with a phosphos

54 Mass spectrometry analysis and four further crystal stru

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

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

57 Mass spectrometry analysis and in vitro validation revea

58 tional techniques such as gas chromatography-mass spectrometry analysis and TBARS values.

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

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

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

62 Analysis of lignin structure demands mass spectrometry analysis, and identification of oligom

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

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

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

66 Using mass spectrometry analysis based on capturing endophilin

67 in good agreement with field ionization (FI) mass spectrometry analysis, but performed at atmospheric

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

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

70 In conclusion, mass spectrometry analysis combined with site-directed m

71 Triple quadrupole mass spectrometry analysis conducted during the reaction

72 Mass spectrometry analysis confirmed that all Arg residu

73 Further mass spectrometry analysis confirmed that the isolated F

74 Mass spectrometry analysis demonstrated cell-cell commun

75 Mass spectrometry analysis demonstrated that cytoplasmic

76 Mass spectrometry analysis demonstrated that only one Ga

77 Mass spectrometry analysis detected a 4.6-fold increase

78 Using tandem mass spectrometry analysis followed by immunoblotting, w

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

80 somers, we report the preparation and tandem mass spectrometry analysis for multiple sulfated or acet

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

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

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

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

85 Mass spectrometry analysis has determined its formula to

86 Our mass spectrometry analysis has independently identified

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

88 ent study using liquid chromatography/tandem mass spectrometry analysis have elucidated signaling net

89 After mass spectrometry analysis, higher amounts of low molecu

90 croextraction followed by gas chromatography-mass spectrometry analysis (HS-SPME-GC-MS), were carried

91 Tandem mass spectrometry analysis identified a novel phosphoryl

92 two-dimensional liquid chromatography tandem mass spectrometry analysis identified a total of 1291 di

93 Mass spectrometry analysis identified BRI1 phosphorylati

94 Mass spectrometry analysis identified five phosphosites,

95 eted liquid chromatography-multistage tandem mass spectrometry analysis identified foliar PAs up to d

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

97 Our mass spectrometry analysis identified INSL6 as a novel C

98 CIEF immunoassay and immunoprecipitation mass spectrometry analysis identified peptides starting

99 Mass spectrometry analysis identified specific lysine re

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

101 Mass spectrometry analysis identified the pol II subunit

102 Mass spectrometry analysis identified this protein as th

103 Mass spectrometry analysis identified threonine 32 as a

104 Mass spectrometry analysis identified two asparagine res

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

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

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

108 Exome sequencing and mass spectrometry analysis in paired brain-blood samples

109 fluorescence and inductively coupled plasma mass spectrometry analysis indicate that copper in the A

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

111 Mass spectrometry analysis indicated that the complex co

112 We report mass spectrometry analysis indicating that peroxynitrite

113 Proteomic mass spectrometry analysis is becoming routine in clinic

114 al of the entrapped proteolytic products for mass spectrometry analysis is described.

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

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

117 d it could significantly simplify the tandem mass spectrometry analysis method and procedure with an

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

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

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

121 Liquid chromatography/tandem mass spectrometry analysis of a PAP-enriched sample reve

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

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

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

125 oad-spectrum, conserved-site PCR paired with mass spectrometry analysis of amplicons (PCR/electrospra

126 Mass spectrometry analysis of anti-CD36 immuno-precipita

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 Mass spectrometry analysis of BON1 further suggests that

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

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

132 Using mass spectrometry analysis of complex HLA-bound peptide

133 Mass spectrometry analysis of conditioned medium derived

134 Mass spectrometry analysis of CSB identified lysine (K)

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

136 Mass spectrometry analysis of ESV proteins found no matc

137 ng laser-ablation inductively coupled plasma mass spectrometry analysis of experimentally induced dif

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

141 Mass spectrometry analysis of FliI immunoprecipitates sh

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

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

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

145 Mass spectrometry analysis of histone modifications reve

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

147 Mass spectrometry analysis of immunocaptured CI identifi

148 Liquid chromatography - tandem mass spectrometry analysis of immunoprecipitates by mono

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

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

151 Comparative mass spectrometry analysis of immunopurified FBXW11 prot

152 Mass spectrometry analysis of immunopurified rat brain e

153 Mass spectrometry analysis of isolated proteolytic fragm

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

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

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

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

158 Mass spectrometry analysis of many phospholipids is pref

159 Mass spectrometry analysis of membrane proteins that wer

160 Mass spectrometry analysis of microglia culture media id

161 In contrast, mass spectrometry analysis of monoubiquitinated poliota

162 stematic affinity purification combined with mass spectrometry analysis of N- and C-tagged cytoplasmi

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

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

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

169 Mass spectrometry analysis of phosphospecific immunoprec

170 Mass spectrometry analysis of plasma and brain samples i

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

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

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

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

175 on the basis of bioinformatics and top-down mass spectrometry analysis of protein modifications in p

176 Through mass spectrometry analysis of proteins co-immunoprecipit

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

178 Mass spectrometry analysis of proteins that co-immunopre

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

180 Liquid chromatography-tandem mass spectrometry analysis of proteolytic digests of ina

181 Mass spectrometry analysis of purified KIF3A showed that

182 Mass spectrometry analysis of purified mutant LPS was us

183 Mass spectrometry analysis of purified p120 identified c

184 Mass spectrometry analysis of Rab1 purified from a yeast

185 Mass spectrometry analysis of recombinant STAT3 protein

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

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

188 Immunoprecipitation and subsequent mass spectrometry analysis of the cellular proteins from

189 g ((15)N) of E. coli RNA in conjunction with mass spectrometry analysis of the combined heavy- and li

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 Mass spectrometry analysis of the in vitro methyltransfe

195 MALDI-TOF mass spectrometry analysis of the MCV synthesized using

196 Mass spectrometry analysis of the native protein confirm

197 Mass spectrometry analysis of the oocyte recording mediu

198 MALDI-TOF mass spectrometry analysis of the reaction mixture furth

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

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

201 Mass spectrometry analysis of these polypeptides resulte

202 tion, nanospray liquid chromatography tandem mass spectrometry analysis of tryptic peptides, followed

203 Through mass spectrometry analysis of ubiquitinated RelA, we ide

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

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

206 lditol acetates, the peptidoglycan by GC/MS (mass spectrometry) analysis of the unique amino acid dia

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

208 e 3, one of the PAD targets we identified by mass-spectrometry analysis of spinal cord deiminated pro

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

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

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

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

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

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

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

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

217 hromatography-electrospray ionization-tandem mass spectrometry analysis revealed a distinct interacti

218 Mass spectrometry analysis revealed a reducing terminal

219 Coimmunoprecipitation and mass spectrometry analysis revealed an interaction betwe

220 Mass spectrometry analysis revealed eight sites of O-Glc

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

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

223 Mass spectrometry analysis revealed that DPP4 (dipeptidy

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

225 Mass spectrometry analysis revealed that in vivo the occ

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

227 Mass spectrometry analysis revealed that NaxD is essenti

228 Mass spectrometry analysis revealed that non-muscle myos

229 Mass spectrometry analysis revealed that residues Lys(19

230 Mass spectrometry analysis revealed that Scabin labels t

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

232 Mass spectrometry analysis revealed that the VIB-1 prote

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 specific Cdc7-dependent phosphorylation, and mass spectrometry analysis reveals a dynamic and complex

238 Mass spectrometry analysis reveals that NAD simultaneous

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

240 0 kDa on SDS-PAGE and did not contain Gbeta5 Mass spectrometry analysis showed no other proteins to b

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

242 Immunoprecipitation and mass spectrometry analysis showed that Mon1a associates

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

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

245 Mass spectrometry analysis showed that the wild type gly

246 Mass spectrometry analysis showed that these peptides ar

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

248 uman enzyme, while rapid dilution assays and mass spectrometry analysis suggest that the compound is

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

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

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

252 We first reveal by mass spectrometry analysis that Ser890 of the Kv11.1 ion

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

254 ition to global liquid chromatography-tandem mass spectrometry analysis, the targeted approach of mul

255 Using mass spectrometry analysis, the threonine residue at pos

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

257 ducted a global liquid chromatography/tandem mass spectrometry analysis to compare metastatic and non

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

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

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

261 ic focusing and liquid chromatography-tandem mass spectrometry analysis to generate proteomic profile

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

263 We employed tandem mass spectrometry analysis to identify sites of ADP-ribo

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

265 These salts need to be removed prior to mass spectrometry analysis to reduce ion suppression; so

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

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

268 ic samples, we have developed the Metabolite Mass Spectrometry Analysis Tool (MMSAT).

269 Temperature programmed desorption with mass spectrometry analysis (TPD-MS) and X-ray photoelect

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

271 iochemical assays, in silico prediction, and mass spectrometry analysis using the multidimensional pr

272 Liquid chromatography-tandem mass spectrometry analysis using triple quadruple analys

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

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

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

276 A purification, limited Lys-C digestion, and mass spectrometry analysis was used in the study to quan

277 Time-of-flight secondary-ion mass spectrometry analysis was used to determine the dep

278 Immunoprecipitation-mass spectrometry analysis was used to identify interact

279 Liquid chromatography-tandem mass spectrometry analysis was used to identify proteins

280 Mass spectrometry analysis was used to identify the solu

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

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

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

284 Using coaffinity purification coupled to mass spectrometry analysis, we examined protein associat

285 Using mass spectrometry analysis, we found that VLVs contained

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

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

288 Using mass spectrometry analysis, we identified three serine r

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

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

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

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

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

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

295 sites of ubiquitin attachment identified by mass spectrometry analysis were lysine residues at amino

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

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

298 Mass spectrometry analysis with high mass resolution (>2

299 By combining mass spectrometry analysis with small interfering RNA sc

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