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

1 m the protein and analyzed by flow injection electrospray mass spectrometry.

2 efficiency size-exclusion chromatography and electrospray mass spectrometry.

3 and whole protein masses were measured with electrospray mass spectrometry.

4 to the ring as confirmed by high-resolution electrospray mass spectrometry.

5 the cAPK type IIbeta R-subunit was probed by electrospray mass spectrometry.

6 n and high performance liquid chromatography/electrospray mass spectrometry.

7 lowing more effective subsequent analysis by electrospray mass spectrometry.

8 ring the NEM modification stoichiometries by electrospray mass spectrometry.

9 e mixture were determined by high resolution electrospray mass spectrometry.

10 adout of thin-layer chromatography plates by electrospray mass spectrometry.

11 regarding the use of hydrocarbon solvents in electrospray mass spectrometry.

12 s determined by electrophoretic profiles and electrospray mass spectrometry.

13 and dimeric forms) can be characterized with electrospray mass spectrometry.

14 portant ionization mechanism in negative ion electrospray mass spectrometry.

15 ith laser-induced fluorescence detection and electrospray mass spectrometry.

16 /- 5 Da as measured by liquid chromatography electrospray mass spectrometry.

17 ographic concentration of the fragments, and electrospray mass spectrometry.

18 ity chromatography and liquid chromatography-electrospray mass spectrometry.

19 bioconjugates were characterized by HPLC and electrospray mass spectrometry.

20 trix-assisted laser desorption/ionization or electrospray mass spectrometry.

21 20 s to D(2)O/phosphate buffer (pH 5.7), by electrospray mass spectrometry.

22 ts examined by either (32)P-end-labelling or electrospray mass spectrometry.

23 ER, and B-PER from Pierce Chemical Co. using electrospray mass spectrometry.

24 eta-lactams in an 1:1 ratio as determined by electrospray mass spectrometry.

25 lent flavin is at the FAD level as judged by electrospray mass spectrometry.

26 terised by N-terminal protein sequencing and electrospray mass spectrometry.

27 h a m/z of 572 as determined by negative ion electrospray mass spectrometry.

28 cific mAba, followed by their examination by electrospray mass spectrometry.

29 amoylation of the enzyme, as demonstrated by electrospray mass spectrometry.

30 n of proteins and peptides by capillary HPLC-electrospray mass spectrometry.

31 g electrophoresis, liquid chromatography and electrospray mass spectrometry.

32 wild-type and mutant enzymes and analyzed by electrospray mass spectrometry.

33 were confirmed by fast-atom bombardment and electrospray mass spectrometry.

34 to have the appropriate molecular weight by electrospray mass spectrometry.

35 phosphocellulose paper absorption method or electrospray mass spectrometry.

36 alyzed by liquid chromatography coupled with electrospray mass spectrometry.

37 d Ypt1p was purified by HPLC and analyzed by electrospray mass spectrometry.

38 y a combination of peptide fragmentation and electrospray mass spectrometry.

39 le microdroplet environments using contained-electrospray mass spectrometry.

40 retention time matching and confirmation by electrospray mass spectrometry.

41 tion of p53 family homotetramers by nanoflow electrospray mass spectrometry.

42 profile concurs with that obtained by using electrospray mass spectrometry.

43 B (BoNT/B) present in 0.5 mL of serum using electrospray mass spectrometry.

44 dopsis, are dodecamers as determined by nano-electrospray mass spectrometry.

45 All compounds were also analyzed by NMR and electrospray mass spectrometry.

46 rroborated by positive and negative ion mode electrospray mass spectrometry.

47 Its presence in solution is corroborated by electrospray mass spectrometry.

48 attainable with conventional direct infusion electrospray mass spectrometry.

49 rophoresis and molecular ion at m/z 41886 by electrospray mass spectrometry.

50 ated product was unambiguously identified by electrospray mass spectrometry.

51 rm polymers, as evidenced by high-resolution electrospray mass spectrometry.

52 in human meibomian gland secretions by using electrospray mass spectrometry.

53 on, cross-linked peptides were identified by electrospray mass spectrometry.

54 verse micelles encapsulating myoglobin using electrospray mass spectrometry.

55 ominant component of meibum when examined by electrospray mass spectrometry.

56 They were also characterized in solution by electrospray mass spectrometry.

57 dimension fingerprint), which is measured by electrospray mass spectrometry.

58 lymers and analyzed by liquid chromatography-electrospray mass spectrometry.

59 confirmed using high-resolution positive ion electrospray mass spectrometry.

60 to bind a stoichiometric amount of Neu5Ac by electrospray mass spectrometry.

61 ble copper center were established using +ve electrospray mass spectrometry.

62 sence of NAD(+), was studied by HPLC-coupled electrospray mass spectrometry.

63 ar magnetic resonance (NMR) and positive-ion electrospray mass spectrometry.

64 , and the haloacetic acids are detected with electrospray-mass spectrometry.

65 r level by microextraction with detection by electrospray-mass spectrometry.

66 urier transform infrared, and flow injection electrospray-mass spectrometry.

67 omplexes were unambiguously identified using electrospray mass spectrometry, (1)H NMR spectroscopy, a

68 seudotetramers were analyzed by native-state electrospray mass spectrometry, a significant shift in t

69 isolated, purified, and characterized using electrospray mass spectrometry, absorption spectroscopy,

70 new application of affinity capture-elution electrospray mass spectrometry (ACESI-MS) to assay the e

71 Km, Vmax and Ki (for thyroxine), obtained by electrospray mass spectrometry agreed with those obtaine

72 Electrospray mass spectrometry allows direct identificat

73 itrile/water mobile phase system and on-line electrospray mass spectrometry analysis in the positive

74 ys in conjunction with liquid chromatography-electrospray mass spectrometry analysis indicate that th

75 Electrospray mass spectrometry analysis of the peptides

76 t properties for the separation and on-line, electrospray, mass spectrometry analysis of peptides and

77 Electrospray mass spectrometry and 1H NMR spectroscopy w

78 ic extracts of the chips were analysed using electrospray mass spectrometry and 28 phenolic and furan

79 of the amino acids was determined by online electrospray mass spectrometry and calculated by newly d

80 , ring-opened products were characterized by electrospray mass spectrometry and collision induced dis

81 MR and electronic absorption spectroscopies, electrospray mass spectrometry and DFT computations.

82 mitochondrial cytochrome c (cyt c) by using electrospray mass spectrometry and electron spin resonan

83 ) was released with thrombin and analyzed by electrospray mass spectrometry and found to yield the M(

84 oligosaccharide fractions and established by electrospray mass spectrometry and high performance liqu

85 ere readily identified using direct infusion electrospray mass spectrometry and high-performance liqu

86 reased C16 and C24 ceramide as determined by electrospray mass spectrometry and induced apoptosis in

87 ificant consequences for systems that employ electrospray mass spectrometry and ion-mobility spectrom

88 hods are combined with liquid chromatography-electrospray mass spectrometry and nanoelectrospray MS/M

89 mation of this material was characterized by electrospray mass spectrometry and two-dimensional 1H-NM

90 halic acids was studied by using competitive electrospray mass spectrometry and UV-Visible spectrosco

91 iques resulted in lower detection limits for electrospray mass-spectrometry and revealed eighty-five

92 cifically coordinated K(+) (as determined by electrospray mass spectrometry) and, hence, presumably o

93 s characterized by chemical degradations, by electrospray mass spectrometry, and by several nuclear m

94 d proteolysis with N-terminal sequencing and electrospray mass spectrometry, and deletion analysis to

95 uch as amino acid analysis, peptide mapping, electrospray mass spectrometry, and Edman protein sequen

96 rminal microsequencing, cross-link analysis, electrospray mass spectrometry, and immunoassay.

97 ups, have been synthesized, identified using electrospray mass spectrometry, and isolated using an ap

98 ne- and two-dimensional gel electrophoresis, electrospray mass spectrometry, and N-terminal amino aci

99 on of analytical ultracentrifugation, native electrospray mass spectrometry, and negative stain and c

100 tigated by paramagnetic 1H NMR spectroscopy, electrospray mass spectrometry, and peptide sequence ana

101 by gamma-rays, the products were analyzed by electrospray mass spectrometry, and rate constants of mo

102 cular weight of the mutant was determined by electrospray mass spectrometry, and the presence of the

103 identified by N-terminal microsequencing and electrospray mass spectrometry, and then mapped onto the

104 ques, with a mass of 50,825 +/-10 daltons by electrospray mass spectrometry, and with a pI of 5.0.

105 ong as shown by proton NMR characterization, electrospray mass spectrometry, and X-ray analysis.

106 heric pressure thermal desorption-extractive electrospray-mass spectrometry (AP/TD-EESI-MS) for the d

107 In this study, we have used a time-resolved electrospray mass spectrometry approach to probe the kin

108 obore liquid chromatography and positive ion electrospray mass spectrometry are applied to the determ

109 olyhedral capsules, characterized by NMR and electrospray mass spectrometry, are around 5 nanometres

110 lyzed for monomeric Abeta using positive ion electrospray mass spectrometry based on the abundance th

111 nate in Chlorella vulgaris culture medium by electrospray mass spectrometry, based on selenium's know

112 Electrospray mass spectrometry carried out on solutions

113 mple treatment and capillary electrophoresis-electrospray mass spectrometry (CE-ESI-MS) for separatio

114 ut microfabricated capillary electrophoresis/electrospray mass spectrometry (CE/ ESI-MS) with automat

115 antibodies, PAGE fractionation patterns and electrospray mass spectrometry comparative analysis have

116 s of the large ribosomal subunit proteins by electrospray mass spectrometry confirmed that the substr

117 Electrospray mass spectrometry confirmed the expected 1:

118 um have been extensively characterized using electrospray mass spectrometry coupled with a fast react

119 Nano electrospray mass spectrometry coupled with traveling wa

120 ss spectrometric technique, charge reduction electrospray mass spectrometry (CREMS), allowing the ana

121 gand-centered events by variable temperature electrospray mass spectrometry, cyclic voltammetry, and

122 Electrospray mass spectrometry demonstrated that casein

123 Furthermore, tandem electrospray mass spectrometry demonstrates that BsIDH,

124 evaluate the monolithic columns by employing electrospray mass spectrometry detection.

125 high-performance liquid chromatography with electrospray mass spectrometry detection.

126 entified in complex mixtures by HPLC-coupled electrospray mass spectrometry due to the partial loss o

127 Electrospray-mass spectrometry elucidated that the lipid

128 As determined by electrospray mass spectrometry, EMF10 is composed of two

129 ple matrix elimination combined on-line with electrospray mass spectrometry (EMPM/ES-MS) for the enha

130 es were characterized by the combined use of electrospray mass spectrometry (ES-MS) and NMR spectrosc

131 that demonstrate the attributes of this EMLC/electrospray mass spectrometry (ES-MS) coupling.

132 ot appear in high abundance in negative mode electrospray mass spectrometry (ES-MS) due to lack of ac

133 ctrophoresis (CZE) coupled with negative ion electrospray mass spectrometry (ES-MS) is used for the d

134 Negative-ion electrospray mass spectrometry (ES-MS) with collision-in

135 ES-DMA is similar to electrospray-mass spectrometry (ES-MS), but measures the

136 peptide, alpha-syn(1-19), was confirmed with electrospray-mass spectrometry (ES-MS).

137 nge of Hammett parameters utilizing positive electrospray mass spectrometry (ESI+ -MS) as the sole qu

138 le compound is determined by high resolution electrospray mass spectrometry (ESI-MS) and confirmed by

139 analytical fragmnent is highly sensitized to electrospray mass spectrometry (ESI-MS) and is easily id

140 cyclic voltammetry, magnetic susceptibility, electrospray mass spectrometry (ESI-MS) and single-cryst

141 Negative-ion electrospray mass spectrometry (ESI-MS) and tandem mass

142 r the coupling of microfabricated devices to electrospray mass spectrometry (ESI-MS) have been develo

143 X-ray crystallography and electrospray mass spectrometry (ESI-MS) show this to be

144 ere further analyzed by ultrahigh resolution electrospray mass spectrometry (ESI-MS), and 8a, togethe

145 e of most of the impurities was confirmed by electrospray mass spectrometry (ESI-MS), and thus, the c

146 Using rapid chemical quench, time-resolved electrospray mass spectrometry (ESI-MS), and Western blo

147 biological samples prior to directly coupled electrospray mass spectrometry (ESI-MS).

148 sive in the presence of HYP, as monitored by electrospray mass spectrometry (ESI-MS).

149 ere characterized by gel electrophoresis and electrospray mass spectrometry (ESI-MS).

150 dducts in the gas-phase, as determined using electrospray mass spectrometry (ESI-MS).

151 of capillary electrochromatography (CEC) to electrospray mass spectrometry (ESI-MS).

152 f-flight mass spectrometry (MALDI-TOF/MS) or electrospray mass spectrometry (ESI/MS) depending on sam

153 Quantification of DAGs by electrospray mass spectrometry (ESI/MS), however, is cha

154 liquid extraction followed by flow injection electrospray mass spectrometry (ESI/MS).

155 Here, we demonstrate that FAIMS (coupled to electrospray/mass spectrometry (ESI/MS)) can broadly bas

156 Electrospray mass spectrometry (ESMS) and nuclear magnet

157 Electrospray mass spectrometry (ESMS) exhibits high-thro

158 real-time mass monitoring by direct-infusion electrospray mass spectrometry (ESMS).

159 ionization mass spectrometry (ESMS), tandem electrospray mass spectrometry (ESMS-MS, collision-induc

160 y ((1)H, variable-temperature, and DOSY) and electrospray mass spectrometry establish that 20 undergo

161 can be identified only in the vapor phase by electrospray mass spectrometry experiments.

162 Specific and sensitive electrospray mass spectrometry failed to detect even tra

163 Metabolome analysis by flow injection electrospray mass spectrometry (FIE-MS) fingerprinting g

164 Flow injection electrospray mass spectrometry (FIE-MS) metabolite finge

165 Flow injection electrospray-mass spectrometry (FIE-MS) is finding utili

166 uor extracts were analyzed by flow-injection electrospray-mass spectrometry (FIE-MS), a novel method

167 ues were identified by Edman degradation and electrospray mass spectrometry following proteolysis and

168 umn without pretreatment and was analyzed by electrospray mass spectrometry following the column swit

169 ona discharge is applied to charge reduction electrospray mass spectrometry for the analysis of compl

170 n selected cases, peptides were sequenced by electrospray-mass spectrometry fragmentation.

171 Nano-electrospray mass spectrometry gives insight into the st

172 bohydrate staining and liquid chromatography electrospray mass spectrometry glycopeptide analysis.

173 Nanoflow electrospray mass spectrometry has been applied previous

174 raphy coupled with diode array detection and electrospray-mass spectrometry (HPLC/DAD/ESI-MS); ninete

175 ss spectrometry (ICP-MS) and high resolution electrospray mass spectrometry (HR-ESI-MS) allowed the i

176 The negative ion mode, high-resolution electrospray mass spectrometry (HR-ESI-MS) data produced

177 Tryptic digestion and liquid chromatography electrospray mass spectrometry identified Cys-99 and Cys

178 Desorption electrospray mass spectrometry imaging (DESI-MSI) genera

179 Nanospray desorption electrospray mass spectrometry imaging (nano-DESI MSI) e

180 h determination of dissociation constants by electrospray mass spectrometry in a multiplexed format.

181 enzymatic digestion with exonuclease VII and electrospray mass spectrometry in negative ion mode.

182 mass spectrometry and liquid-chromatography electrospray mass spectrometry in real time.

183 ere the increasing importance of the role of electrospray mass spectrometry in the analysis of such p

184 Developments in high-performance electrospray mass spectrometry include sample introducti

185 he radiolysis products were characterized by electrospray mass spectrometry including tandem mass spe

186 sis products were primarily characterized by electrospray mass spectrometry including tandem mass spe

187 Electrospray mass spectrometry indicated that a peptide,

188 ar electrokinetic chromatography (MEKC) with electrospray mass spectrometry initiates the development

189 as the front end for a liquid chromatography-electrospray mass spectrometry instrument, is described.

190 is often used to test the specifications of electrospray mass spectrometry instrumentation.

191 donor-acceptor oligorotaxane foldamer using electrospray mass spectrometry interfaced with ion mobil

192 uster is markedly metal-dependent, extensive electrospray mass spectrometry investigations show that

193 by multinuclear NMR, elemental analysis, and electrospray mass spectrometry is also reported.

194 Electrospray mass spectrometry is used at pH 8.0 in comb

195 -line high-performance liquid chromatography-electrospray mass spectrometry (LC-ESMS) analysis and su

196 the intact proteins by liquid chromatography-electrospray mass spectrometry (LC-ESMS) revealed the ma

197 e high-performance liquid chromatography and electrospray mass spectrometry (LC-ESMS) shows that the

198 been carried out using liquid chromatography-electrospray mass spectrometry (LC-ESMS).

199 igh-performance liquid chromatography (HPLC)-electrospray mass spectrometry (LC-MS) was used to analy

200 xtraction coupled with liquid chromatography/electrospray mass spectrometry (LC/ESI-MS) is described

201 Additionally, liquid chromatography electrospray mass spectrometry (LCMS) revealed that PlcH

202 hrome c, and lysozyme is presented for laser electrospray mass spectrometry (LEMS) and electrospray i

203 Laser electrospray mass spectrometry (LEMS) coupled with offli

204 , 800-nm Ti:sapphire-based femtosecond laser electrospray mass spectrometry (LEMS) experiments, sugge

205 Laser electrospray mass spectrometry (LEMS) is demonstrated fo

206 e, and tetrabutylammonium iodide using laser electrospray mass spectrometry (LEMS) reveal monotonic s

207 s of ammunition, is demonstrated using laser electrospray mass spectrometry (LEMS).

208 In this study a direct electrospray mass spectrometry method is described for t

209 r mass of 25440.6 Da, which was confirmed by electrospray mass spectrometry (Mexpt = 25439.9 +/- 1.4

210 Electrospray mass spectrometry, molecular modeling, X-ra

211 etermination of molecular weight (MW), using electrospray mass spectrometry (MS), of the polymerase c

212 diameter of the spray tip employed for nano-electrospray mass spectrometry (nano-ES-MS) upon mass sp

213 erto unidentified species is investigated by electrospray mass spectrometry of aqueous AH(2) droplets

214 onable agreement with 47, 173 Da obtained by electrospray mass spectrometry of the purified enzyme.

215 e flavin to the polypeptide has permitted LC-electrospray mass spectrometry of the reaction product t

216 nalysis of products by liquid chromatography-electrospray-mass spectrometry on the basis of fragments

217 The method is also compatible with online electrospray mass spectrometry, permitting the identific

218 inding assay based on pulsed ultrafiltration/electrospray mass spectrometry (PUF/ESMS) to tentatively

219 Kinetic measurements and electrospray mass spectrometry revealed that the first a

220 SDS-polyacrylamide gel electrophoresis and electrospray mass spectrometry revealed the 32-kDa speci

221 bstrate kinetic studies, and high-resolution electrospray mass spectrometry, revised steady-state kin

222 ersed-phase liquid chromatography coupled to electrospray mass spectrometry (RP-LC/ESI-MS) was used t

223 osphopeptide mapping, Edman degradation, and electrospray mass spectrometry, serine residues 283, 300

224 Electrospray mass spectrometry showed covalent linkage o

225 in the presence of H(2)(18)O and analyzed by electrospray mass spectrometry showed that the ADPRase-c

226 y immunoblotting, N-terminal sequencing, and electrospray mass spectrometry showed that trypsin cleav

227 CTLA-4 and CD80 using carbohydrate analysis, electrospray mass spectrometry, size exclusion chromatog

228 chromatographic effluent online prior to the electrospray mass spectrometry source.

229 We present detailed electrospray mass spectrometry studies of binding specif

230 Typical solvents used for electrospray mass spectrometry such as methanol and mixt

231 rption, electron paramagnetic resonance, and electrospray mass spectrometry suggest the redox cofacto

232 Nondissociating nanoflow-electrospray mass spectrometry suggests that the tetrame

233 A multidimensional electrospray mass spectrometry technique was used to map

234 eans to facilitate the resolution of ions in electrospray mass spectrometry that differ in mass and c

235 Using electrospray mass spectrometry, the PB and BM plasma of

236 ne thin-layer chromatographic separation and electrospray mass spectrometry (TLC/ESI-MS) has been acc

237 wed by rapid chemical quench, using HPLC and electrospray mass spectrometry to analyze the 5'-dA form

238 rix-assisted laser desorption ionization and electrospray mass spectrometry to analyze the entire pro

239 We have used high resolution electrospray mass spectrometry to determine that this ga

240 tides of the 29-kDa band were analyzed using electrospray mass spectrometry to identify the protein.

241 the latter has been used in conjunction with electrospray mass spectrometry to probe the formation of

242 nts offer further evidence of the ability of electrospray mass spectrometry to provide binding inform

243 In this article, we report the use of electrospray mass spectrometry to study the self-associa

244 educed and reduced proteins were analyzed by electrospray-mass spectrometry to establish the compleme

245 1)H NMR, diffusion-ordered spectroscopy NMR, electrospray mass spectrometry, transmission electron mi

246 s supported by resonance Raman spectroscopy, electrospray mass spectrometry using isotopically enrich

247 choice to study brevetoxins in negative mode electrospray mass spectrometry using the anion attachmen

248 Electrospray mass spectrometry was used to characterize

249 Electrospray mass spectrometry was used to determine the

250 Using electrospray mass spectrometry, we demonstrate here that

251 Using liquid chromatography/electrospray mass spectrometry, we found that the reacti

252 Inhibition ELISA, immunoblotting, and electrospray-mass spectrometry were used to confirm that

253 encing of the oligosaccharide products using electrospray mass spectrometry with collision-induced di

254 f monoclonal antibodies, 1H-NMR, FAB-MS, and electrospray mass spectrometry with collision-induced di

255 Negative ion electrospray mass spectrometry with selected ion monitor

256 ied using liquid chromatography-negative ion electrospray mass spectrometry with the trapping cartrid