ライフサイエンスコーパス: MALDI-MS

1 MALDI MS detection of secreted peptides was demonstrated

2 MALDI MS imaging and single-cell profiling are important

3 MALDI MS suggests that during ethane (C2) dithiol exchan

4 MALDI MS, HPLC, and LC-MS revealed that the rate of enzy

5 MALDI MS/MS analysis of peptide fragments generated from

6 MALDI-MS analysis of small molecules has historically be

7 MALDI-MS analysis of the water isolates in group 1 match

8 MALDI-MS data corroborate the biochemical studies and su

9 MALDI-MS data revealed several fucosylated tri- and tetr

10 MALDI-MS identified proteolytic fragments from ovalbumin

11 MALDI-MS imaging analysis of hair samples has recently b

12 MALDI-MS showed similar spectra for P and F but not for

13 MALDI-MS signals can be enhanced by 3-5 orders of magnit

14 MALDI-MS takes advantage of the difference in molecular

15 MALDI-MS/MS identified the 90-kDa band as the protein ZA

16 omparison between the two forms eliminates a MALDI-MS low m/z bias commonly associated with this tech

17 ince the information that is obtained from a MALDI-MS measurement depends on the choice of MALDI matr

18 bility separation has been integrated into a MALDI-MS/MS experiment to categorize major, minor, and t

19 investigated by two complementary methods: a MALDI-MS method and a semi-preparative sub-fractionation

20 most commonly used illicit drug worldwide, a MALDI-MS method for the detection and mapping of cannabi

21 ack of a high-resolution, high mass accuracy MALDI-MS/MS platform for proteomics, Fourier transform i

22 After MALDI MS analysis, a majority of the analyte remains for

23 idic chip to a biosensing unit, such as AMS, MALDI-MS or protein microarray-type biochips.

24 combining genomics/proteomics databases and MALDI MS for the rapid characterization of microorganism

25 cobalt-loaded beads, tryptic digestion, and MALDI MS analysis are performed in an array format, with

26 surface was preserved and imaged by SPR and MALDI MS.

27 This was followed by trypsinolysis and MALDI MS analysis, leading to the quantification of a la

28 s triggering the allergy by IACE with UV and MALDI MS detection.

29 , high resolution mass by Q-ToF analysis and MALDI-MS allowed identification of compounds, such as p-

30 nd direct correlation of electrophoretic and MALDI-MS results.

31 tryptic digestion, selective enrichment, and MALDI-MS analysis.

32 Immunoblot and MALDI-MS/MS analyses revealed that IgE from crustaceans

33 entified as DHRS9 by immunoprecipitation and MALDI-MS sequencing.

34 he sample surface with the heating laser and MALDI-MS imaging to map the resulting products.

35 ducts obtained were identified by ESI-MS and MALDI-MS and characterised by ESI-MS(n).

36 ionization-mass spectrometry (MALDI-MS) and MALDI-MS imaging (MSI) of small molecule drugs and endog

37 /ionization mass spectrometry (MALDI-MS) and MALDI-MS/MS provides an alternative approach for in situ

38 ncentrations of avidin to the two probes and MALDI-MS analysis of avidin contained in the solution re

39 esorption/ionization-mass spectrometry (m-AP-MALDI-MS).

40 plications for certain applications, such as MALDI MS imaging where laser beam focusing as fine as po

41 serve dual roles: (1) They can be applied as MALDI-MS target plates for direct and highly sensitive b

42 UV-vis and (1)H NMR profiles as well as MALDI-MS data show a rapid and irreversible loss of the

43 Single SPE bead MALDI MS offers a novel approach to investigate peptide

44 ng generic membrane protein samples for both MALDI-MS studies of membrane-protein complexes and shotg

45 dition of matrix, and subsequent analysis by MALDI MS, resulted in mass spectra dominated by peaks co

46 The oligosaccharides were also analyzed by MALDI MS after releasing the glycans from glycoproteins

47 using solid-phase extraction and analyzed by MALDI MS.

48 protein whose molecular weight (20,497 Da by MALDI MS) agrees well with the molecular weight of the h

49 MALDI MS analysis, CE separation followed by MALDI MS detection consumes nearly 10-fold less sample (

50 ing period, the target slides were imaged by MALDI MS.

51 -casein (S1 and S2 forms, as was revealed by MALDI MS) were found to bind with the extracted IgE Abs,

52 ckroach allergen Bla g 2 was accomplished by MALDI-MS.

53 Analysis by MALDI-MS showed that the level of EPA incorporated into

54 For phosphopeptide analysis by MALDI-MS, a 2,5-dihydroxybenzoic acid matrix containing

55 ass resolution during subsequent analysis by MALDI-MS.

56 ptide-bound nanoparticles can be analyzed by MALDI-MS to provide highly sensitive detection of the ta

57 peptides that can be effectively analyzed by MALDI-MS to those that are hydrophobic and solubility-li

58 ved by trypsin into peptides and analyzed by MALDI-MS using mascot search engine, immunoprecipitation

59 hotorhabdus and Xenorhabdus were analyzed by MALDI-MS(2), and a database comprising MS(2) data from e

60 CKWAKWAK/colloid conjugates were analyzed by MALDI-MS, and the mass spectra show (M + H)(+), (M + Na)

61 wo samples are then combined and analyzed by MALDI-MS.

62 then moved to the spot, which is analyzed by MALDI-MS.

63 oligonucleotides, which are characterized by MALDI-MS.

64 ysis and imaging of various lipid classes by MALDI-MS.

65 nsity of larger protein ions was detected by MALDI-MS following laser ablation.

66 s with their molecular weights determined by MALDI-MS, and (iii) electrophoretic profiles of N-glycan

67 Apolipoproteins profiling is done by MALDI-MS, and lipids are analyzed using gold nanoparticl

68 te knowledge in the analysis of this drug by MALDI-MS.

69 solution, and identification of the dyes by MALDI-MS in a single experimental step for forensic purp

70 The enrichment followed by MALDI-MS analyses is carried out for the identification

71 richment and enzymatic digestion followed by MALDI-MS analysis, can be completed within 10 min.

72 eling with benzoylhistamine (BH) followed by MALDI-MS.

73 on of peptides in collected RPC fractions by MALDI-MS/MS.

74 omatographic fractions and identification by MALDI-MS/MS.

75 platform for other diverse interrogations by MALDI-MS, surface plasmon resonance, and quartz crystal

76 from the NP-surface) monitoring of OxPLs by MALDI-MS (i.e., the Nano-MALDI approach).

77 lar cross-linking evaluation as performed by MALDI-MS and SEC under dissociating conditions revealed

78 of AGE profile for MG and G was performed by MALDI-MS.

79 king the presence of degradation products by MALDI-MS.

80 plex corroborated the conclusions reached by MALDI-MS analyses.

81 cellular metabolites, which was revealed by MALDI-MS.

82 econdary cross-linking site was sequenced by MALDI-MS/MS as linking Gln360 in actin to Lys98 on cofil

83 ral and sialylated glycans simultaneously by MALDI-MS.

84 matrix and analysis of the sample in situ by MALDI-MS.

85 identifiable metabolites has been studied by MALDI-MS and SIMS imaging.

86 n ionization-tandem mass spectrometry (CapLC-MALDI-MS/MS), and ultraperformance liquid chromatography

87 has been visualized, making the off-line CE-MALDI MS a promising strategy for enhanced neuropeptidom

88 A new method for displaying CE-MALDI-MS data for proteolytic digests is described.

89 ., spot-to-spot) of the resulting whole cell MALDI-MS profiles.

90 duction of the geobacillins using whole-cell MALDI-MS and five were shown to produce geobacillin I, b

91 assays, liquid and affinity chromatography, MALDI-MS analysis, and de novo sequencing identified thi

92 Conventional MALDI MS and GALDI MS were compared regarding lipid anal

93 tryptic digest of beta-casein, conventional MALDI MS revealed only one monophosphopeptide, while use

94 de fragments were compared with conventional MALDI MS on a standard MALDI plate.

95 Conventional MALDI-MS analysis showed limited sensitivity for analysi

96 Data were collected from two different MALDI-MS instruments: a time-of-flight and a linear ion

97 Compared with direct MALDI MS analysis, CE separation followed by MALDI MS de

98 of peptide coverage as compared with direct MALDI MS analysis.

99 e lowest detectable concentration for direct MALDI-MS analysis was found to be 10(4)cfu/mL.

100 ce of the positively charged polymers during MALDI-MS analyses enhances peptide ion signals by almost

101 ted the desorption/ionization process during MALDI-MS; however, these fungi may be successfully analy

102 ly, and consumption of the whole spot during MALDI-MS analysis is typically accomplished within few s

103 ing stereoselective analytical methods, i.e. MALDI MS fragmentation analysis and LC-MS/MS.

104 In the quest for novel and more efficient MALDI MS matrices, curcumin is revealed to be a versatil

105 improved spot quality enables 2-30x enhanced MALDI-MS signals along with substantial reductions of th

106 -line sample purification technique for EWOD-MALDI-MS will enable development of integrated high-thro

107 te sample to be concentrated on the film for MALDI MS analysis.

108 ice as matrix is of particular interest for MALDI MS profiling and imaging applications since matrix

109 tial application of graphene as a matrix for MALDI MS analysis of practical samples in complex sample

110 AW-based sample-matrix deposition method for MALDI MS was developed and characterized by a strong ins

111 bility in the sample preparation process for MALDI MS is reported.

112 Key challenges for MALDI-MS measurements of bacteria are overcoming the rel

113 fabrication of a titanium bacterial chip for MALDI-MS produced from a simple, cost effective and rapi

114 ng, and matrix/analyte cocrystallization for MALDI-MS analyses.

115 We present an improved method for MALDI-MS analysis of proteins that have been electroblot

116 An in-line sample purification method for MALDI-MS, which relies on the electrowetting-on-dielectr

117 ch low pI peptides from complex mixtures for MALDI-MS detection.

118 f 48 purified, digested samples prepared for MALDI-MS can be generated in 4 h, with only 30 min of op

119 y extract peptides from aqueous solution for MALDI-MS detection.

120 The new ILM is suitable for MALDI-MS analysis of mixtures containing oligosaccharide

121 Untypical for MALDI-MS, high charge states of multiply protonated spec

122 the Clin Pro tool, the obtained results from MALDI-MS data were validated.

123 Furthermore, MALDI-MS analysis of the avidin retained on the two prob

124 ssful interface of optical microscopy-guided MALDI MS and CE-ESI-MS for sequential chemical profiling

125 Optically guided MALDI MS provides a high-throughput assessment of lipid

126 were rapidly analyzed with optically guided MALDI MS to classify each cell into established cell typ

127 Optically guided MALDI MS was used to identify individual pancreatic isle

128 However, MALDI-MS has a reputation of not being suitable for quan

129 hy, 1H NMR, 13C NMR, HMQC, UV-visible, HPLC, MALDI-MS, and electrochemistry.

130 lly normal heterozygote (hexb+/-) by imaging MALDI-MS.

131 erous other lipid subclasses; hence, imaging MALDI-MS could be used for "lipidomic" studies.

132 illustrate the usefulness of tissue-imaging MALDI-MS with matrix deposition by OCN for histologic co

133 We here present an immuno-MALDI-MS approach for the combined quantification of two

134 paraffin wax film (Parafilm M) for improved MALDI MS analysis of low-abundance peptide mixtures, inc

135 Automated analyses in MALDI MS are complicated by the uneven distribution of a

136 aration record was consecutively analyzed in MALDI MS and ICP MS instruments.

137 detected or detected with low sensitivity in MALDI MS because of other dominant phospholipids.

138 n of more informative product ion spectra in MALDI MS/MS profiling and imaging experiments.

139 compared to the current "gold" standards in MALDI MS, and new insights into the mechanisms and proce

140 ignals with a static 6 Da mass difference in MALDI-MS and the change in relative abundance of any gly

141 ye mixture promotes sufficient ionization in MALDI-MS: addition of common MALDI matrices does not imp

142 tetraalkylphosphonium-based ionic liquids in MALDI-MS allowed detection of small molecule dyes withou

143 s of cysteine-containing labeled peptides in MALDI-MS (matrix-assisted laser desorption/ionization ma

144 4-fold increase in signal-to-noise ratio in MALDI-MS analysis for a low abundance protein, hemopexin

145 This study investigated MALDI MS detection and mapping capabilities for a large

146 desorption/ionization mass spectrometry (IR-MALDI-MS), it has not found a wider use due to limitatio

147 ntegrated selective enrichment target (ISET)-MALDI-MS analysis was implemented with ssDNA aptamer fun

148 rating the applicability of the aptamer/ISET-MALDI-MS analysis in clinical samples.

149 was 10 fmol in buffer using the aptamer/ISET-MALDI-MS configuration as confirmed by MS/MS fragmentati

150 The aptamer/ISET-MALDI-MS platform also displayed a limit of detection of

151 dy fragment background reduction in the ISET-MALDI-MS readout is presented.

152 g a thrombin specific aptamer linked to ISET-MALDI-MS detection, a proof of concept of antibody fragm

153 and Omnitrope) were compared using the iTRAQ/MALDI-MS method to determine the similarity between thei

154 ting (or not submitting) samples to the K200 MALDI MS analysis kit containing N-succinimidyl iodo-ace

155 LC MALDI MS and isobaric tag for relative and absolute quan

156 in case of simple peptide mixtures or by LC-MALDI MS for complex substrate mixtures and used for the

157 The multiplexed LC-MALDI MS provides a high-throughput platform to utilize

158 ingly, we extended a strategy for offline LC-MALDI MS/MS analysis using a precursor ion exclusion lis

159 n individual neuronal processes for off-line MALDI MS analyses.

160 rom complex samples followed by the off-line MALDI-MS analysis.

161 idity of analysis hold the promise of making MALDI MS an essential tool for the physicochemical chara

162 ly (mass error </= 0.1%) such that high-mass MALDI-MS was able to identify the site for N-linked glyc

163 eluate in the microchannel, IEF-micropillar-MALDI-MS is demonstrated to be a suitable platform for d

164 rix-assisted laser desorption/ionization MS (MALDI-MS).

165 peptides that are undetectable during normal MALDI-MS analysis are selectively detected.

166 Here, obscured MALDI-MS signals of a synthetic small molecule pharmaceu

167 showed a 5-15-fold increase in intensity of MALDI MS signal in the positive ion mode, relative to th

168 The use of MALDI MS opens new opportunities for characterization an

169 Application of MALDI-MS, ESI-MS, and IM-MS to the polymer-peptide bioma

170 oughput proteomics and other applications of MALDI-MS.

171 tion, peptide desalting, and, in the case of MALDI-MS, matrix and analyte cocrystallization on target

172 ere used for the study of reproducibility of MALDI-MS measurements.

173 3-5-fold) improvement in the sensitivity of MALDI-MS detection compared to unwashed sample spots.

174 cule quantification are compared to those of MALDI-MS.

175 The model was based on MALDI MS signal intensity (MALDI score) from bronchial t

176 The merits of ES MS/MS or MALDI MS/MS for protein identification in a results-driv

177 andem MS spectra of native tryptic peptides, MALDI MS/MS analysis of a sulfonated tryptic peptide con

178 using computer simulation and by performing MALDI-MS analysis directly from the open microchannel.

179 By using the multiple-place MALDI MS targets, we estimate that 100 assays could be r

180 a novel MALDI sample target for quantitative MALDI-MS applications, which addresses the limitations m

181 ESI-MS and recently MALDI-MS methodologies are important strategies for inve

182 Other biomedical applications of SAW-MALDI MS are currently being developed, aiming at fast p

183 arison between different samples in a single MALDI-MS analysis.

184 mass assignments were confirmed with in situ MALDI MS/MS and capillary electrophoresis-electrospray i

185 orption/ionization tandem mass spectrometry (MALDI MS(n), n = 2, 3, and 4).

186 aser desorption ionzation mass spectrometry (MALDI MS) analysis.

187 ser desorption/ionization mass spectrometry (MALDI MS) and liquid chromatography tandem mass spectrom

188 ser desorption/ionization mass spectrometry (MALDI MS) experiment is strongly influenced by the bindi

189 ser desorption/ionization mass spectrometry (MALDI MS) for the analysis of PEDOT directly on sDSCs.

190 ser Desorption Ionisation Mass Spectrometry (MALDI MS) in laboratory settings, research is still need

191 ser desorption/ionization mass spectrometry (MALDI MS) is presented.

192 ser desorption ionization mass spectrometry (MALDI MS) mass-to-charge ratio features to build a predi

193 ser desorption ionization mass spectrometry (MALDI MS) matrix candidate.

194 ser desorption ionization mass spectrometry (MALDI MS) peptide and protein profiling of Islets of Lan

195 ser desorption/ionization mass spectrometry (MALDI MS), for quantitative analysis of sulfated oligosa

196 ser desorption ionization mass spectrometry (MALDI MS).

197 ser desorption/ionization mass spectrometry (MALDI MS).

198 ser desorption/ionization mass spectrometry (MALDI MS).

199 ch incorporates MALDI-ToF mass spectrometry (MALDI-MS) analysis as a means of determining the mutatio

200 ser desorption/ionization-mass spectrometry (MALDI-MS) analysis of lipid extracts, which promotes hom

201 ser desorption/ionization mass spectrometry (MALDI-MS) analysis offers a route to rapid and sensitive

202 ser desorption ionization mass spectrometry (MALDI-MS) and electrospray-MS methods in order to quanti

203 ser desorption ionization-mass spectrometry (MALDI-MS) and MALDI-MS imaging (MSI) of small molecule d

204 ser desorption/ionization mass spectrometry (MALDI-MS) and MALDI-MS/MS provides an alternative approa

205 ser desorption/ionization-mass spectrometry (MALDI-MS) and the results can be used to distinguish bet

206 ser desorption/ionization mass spectrometry (MALDI-MS) depends on the effectiveness of the matrix dep

207 ser desorption ionization-mass spectrometry (MALDI-MS) detection of these peptides in the presence of

208 ser desorption ionization-mass spectrometry (MALDI-MS) except the phospholipids where laser desorptio

209 ser desorption/ionization mass spectrometry (MALDI-MS) for imaging latent human fingerprints, which h

210 ser desorption/ionization mass spectrometry (MALDI-MS) for the analysis of high-mass proteins require

211 ser desorption/ionization mass spectrometry (MALDI-MS) for the analysis of low molecular weight compo

212 ser desorption/ionization mass spectrometry (MALDI-MS) has been used for lipid analysis; however, one

213 ser desorption/ionization mass spectrometry (MALDI-MS) has proved useful for the characterization of

214 ser desorption/ionization-mass spectrometry (MALDI-MS) imaging.

215 ser desorption/ionization mass spectrometry (MALDI-MS) is a fast analysis tool employed for the detec

216 ser desorption/ionization mass spectrometry (MALDI-MS) is a well-established analytical technique for

217 ser desorption/ionization mass spectrometry (MALDI-MS) is an important technological aspect of tissue

218 ser desorption ionization mass spectrometry (MALDI-MS) is frequently compromised by the heterogeneous

219 ser desorption/ionization mass spectrometry (MALDI-MS) is reported.

220 ser desorption ionization mass spectrometry (MALDI-MS) profiling and imaging for the detection and ma

221 ser desorption/ionization-mass spectrometry (MALDI-MS) represent a challenge in some proteomic analys

222 ionization-time-of-flight mass spectrometry (MALDI-MS) to confirm the presence of all sequences and y

223 ser desorption/ionization mass spectrometry (MALDI-MS) to directly analyze protein profiles in mouse

224 ser desorption ionization mass spectrometry (MALDI-MS) was used for peptide identification.

225 ser desorption ionization mass spectrometry (MALDI-MS) was used to analyze phospholipids and proteins

226 ser desorption/ionization-mass spectrometry (MALDI-MS) was used to analyze the whole cells of both re

227 ser desorption ionization mass spectrometry (MALDI-MS) were used in combination to obtain quantitativ

228 ser desorption/ionization-mass spectrometry (MALDI-MS) with a single stage of MS have been used to im

229 ser desorption/ionization-mass spectrometry (MALDI-MS), a common technique used for characterizing sy

230 ser desorption/ionization mass spectrometry (MALDI-MS).

231 ser desorption/ionization mass spectrometry (MALDI-MS).

232 ser desorption/ionization mass spectrometry (MALDI-MS).

233 ser desorption ionization mass spectrometry (MALDI-MS).

234 ser desorption/ionization-mass spectrometry (MALDI-MS).

235 ser desorption/ionization mass spectrometry (MALDI-MS).

236 ser desorption/ionization mass spectrometry (MALDI-MS).

237 ser desorption/ionization-mass spectrometry (MALDI-MS).

238 ser desorption/ionization mass spectrometry (MALDI-MS).

239 ser desorption/ionization mass spectrometry (MALDI-MS).

240 ser desorption/ionization mass spectrometry (MALDI-MS).

241 ser desorption ionization mass spectrometry (MALDI-MS).

242 ser desorption ionization mass spectrometry (MALDI-MS).

243 ser desorption/ionization mass spectrometry (MALDI-MS).

244 ser desorption ionization mass spectrometry (MALDI-MS); sample preparation and data collection mode d

245 orption/ionization tandem mass spectrometry (MALDI-MS/MS) and by comparing results with information c

246 orption/ionization-tandem mass spectrometry (MALDI-MS/MS), nanoelectrospray-MS/MS (NanoES-MS/MS) or l

247 orption ionization tandem mass spectrometry (MALDI-MS/MS).

248 ser desorption ionization mass spectroscopy (MALDI-MS).

249 e.g., fluorescence correlation spectroscopy, MALDI-MS, and fluorescence microscopy).

250 Standard MALDI-MS reagents, analytes, concentrations, and recipes

251 Such MALDI-MS methods require mass measurement at ultrahigh r

252 It was found that MALDI MS images could be used to visualize regions sampl

253 These results demonstrate that MALDI-MS analysis can rapidly and accurately classify sp

254 We demonstrate that MALDI-MS can detect peptide concentrations as low as 500

255 b Callinectes sapidus were detected from the MALDI MS imaging traces, enabling a 4- to 6-fold increas

256 ls of a specific phenotype obtained from the MALDI MS imaging-based molecular classification using hi

257 Our results show that the MALDI MS/MS analysis of sulfonated tryptic peptides can

258 In group 2, the MALDI-MS-based determination confirmed the identity of 1

259 Additionally, the MALDI-MS approach was successfully used on tumor tissue

260 demonstrated substantial improvements in the MALDI-MS analysis of the particulate methane monooxygena

261 we observe an unexpected enhancement in the MALDI-MS signal for extracted peptides ionized in the pr

262 provides at least a 10-fold increase of the MALDI-MS-signal.

263 ons of the typical lateral variations of the MALDI-MS.

264 on using ImageJ software to substantiate the MALDI-MS results.

265 d labeled lipids, which agreed well with the MALDI-MS imaging results.

266 Three MALDI-MS sample/matrix preparation approaches were evalu

267 olecular weights have been confirmed through MALDI-MS measurements of samples purified by HPLC.

268 mined, and the potential for high-throughput MALDI-MS/MS quantification is demonstrated.

269 highly sensitive and specific alternative to MALDI MS for imaging of TAGs from tissue sections.

270 tochastic neighbor embedding were applied to MALDI MS images acquired from tissue which had been samp

271 ene) monolithic column, have been coupled to MALDI MS and MS/MS through an off-line continuous deposi

272 e coupling of high-resolution separations to MALDI MS without degradation in separation efficiency, t

273 EASI-MS data was also compared to MALDI-MS, and found to display richer compositional info

274 By applying the DWT to MALDI-MS spectra, the spectra were simultaneously smooth

275 the primary enveloped virion preparation to MALDI-MS/MS (matrix-assisted laser desorption ionization

276 ymatic digestion and sample cleanup prior to MALDI-MS analysis.

277 means of directly interfacing separations to MALDI-MS, reducing the amount of time required for tradi

278 can be further exploited for ultrasensitive MALDI-MS analyses of peptides and peptide mixtures.

279 range (at least 2 orders of magnitude) using MALDI MS in case of simple peptide mixtures or by LC-MAL

280 x 10(7) to 1.28 x 10(2) were analyzed using MALDI-MS to obtain the threshold detection sensitivity.

281 mitation, current proteomic approaches using MALDI-MS/MS involve high-energy collision-induced dissoc

282 le of a two-linear-mass-analyzer array using MALDI-MS for mixtures of commercially available proteins

283 rect analysis of the captured bacteria using MALDI-MS.

284 ractions were subsequently analyzed by using MALDI-MS and electrospray ionization (ESI)-MS to identif

285 e experiments and measured the results using MALDI-MS: (i) insulin disulfide reductions in dithiothre

286 ied in 1 muL drop on the leaf surfaces using MALDI-MS.

287 e found to be generally below 15% when using MALDI-MS.

288 desorption ionization-mass spectrometry (UV-MALDI-MS).

289 The present IACE-UV/MALDI MS method required only 2 muL of blood serum and a

290 While MALDI-MS of Escherichia coli cells desorbed from a stand

291 mammalian cells in a manner compatible with MALDI MS measurements.

292 The sequence of the core is identified with MALDI MS/MS and its structure is probed with 2D IR spect

293 When interfaced with MALDI MS, the SAW atomizer constitutes a valuable tool f

294 of the experimental factors associated with MALDI-MS studies of microorganisms.

295 nd peptide immunoprecipitation combined with MALDI-MS detection.

296 y, binding efficiency and compatibility with MALDI-MS analysis.

297 We also demonstrated the compatibility with MALDI-MS of a new dye, MemCode, which is specifically de

298 tantly, endo-beta-galactosidase coupled with MALDI-MS allowed these two epitopes, for the first time,

299 e and dried under vacuum before imaging with MALDI-MS.

300 ty of combining a metabolomics workflow with MALDI-MS to identify the biomarkers that may regulate th