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1 and whole protein masses were measured with electrospray mass spectrometry.
2 to the ring as confirmed by high-resolution electrospray mass spectrometry.
3 the cAPK type IIbeta R-subunit was probed by electrospray mass spectrometry.
4 n and high performance liquid chromatography/electrospray mass spectrometry.
5 ring the NEM modification stoichiometries by electrospray mass spectrometry.
6 e mixture were determined by high resolution electrospray mass spectrometry.
7 adout of thin-layer chromatography plates by electrospray mass spectrometry.
8 regarding the use of hydrocarbon solvents in electrospray mass spectrometry.
9 s determined by electrophoretic profiles and electrospray mass spectrometry.
10 and dimeric forms) can be characterized with electrospray mass spectrometry.
11 portant ionization mechanism in negative ion electrospray mass spectrometry.
12 ith laser-induced fluorescence detection and electrospray mass spectrometry.
13 /- 5 Da as measured by liquid chromatography electrospray mass spectrometry.
14 ographic concentration of the fragments, and electrospray mass spectrometry.
15 ity chromatography and liquid chromatography-electrospray mass spectrometry.
16 bioconjugates were characterized by HPLC and electrospray mass spectrometry.
17 trix-assisted laser desorption/ionization or electrospray mass spectrometry.
18 20 s to D(2)O/phosphate buffer (pH 5.7), by electrospray mass spectrometry.
19 ts examined by either (32)P-end-labelling or electrospray mass spectrometry.
20 ER, and B-PER from Pierce Chemical Co. using electrospray mass spectrometry.
21 eta-lactams in an 1:1 ratio as determined by electrospray mass spectrometry.
22 lent flavin is at the FAD level as judged by electrospray mass spectrometry.
23 terised by N-terminal protein sequencing and electrospray mass spectrometry.
24 h a m/z of 572 as determined by negative ion electrospray mass spectrometry.
25 cific mAba, followed by their examination by electrospray mass spectrometry.
26 amoylation of the enzyme, as demonstrated by electrospray mass spectrometry.
27 n of proteins and peptides by capillary HPLC-electrospray mass spectrometry.
28 g electrophoresis, liquid chromatography and electrospray mass spectrometry.
29 wild-type and mutant enzymes and analyzed by electrospray mass spectrometry.
30 were confirmed by fast-atom bombardment and electrospray mass spectrometry.
31 to have the appropriate molecular weight by electrospray mass spectrometry.
32 phosphocellulose paper absorption method or electrospray mass spectrometry.
33 alyzed by liquid chromatography coupled with electrospray mass spectrometry.
34 d Ypt1p was purified by HPLC and analyzed by electrospray mass spectrometry.
35 y a combination of peptide fragmentation and electrospray mass spectrometry.
36 retention time matching and confirmation by electrospray mass spectrometry.
37 Its presence in solution is corroborated by electrospray mass spectrometry.
38 tion of p53 family homotetramers by nanoflow electrospray mass spectrometry.
39 profile concurs with that obtained by using electrospray mass spectrometry.
40 B (BoNT/B) present in 0.5 mL of serum using electrospray mass spectrometry.
41 rm polymers, as evidenced by high-resolution electrospray mass spectrometry.
42 dopsis, are dodecamers as determined by nano-electrospray mass spectrometry.
43 dimension fingerprint), which is measured by electrospray mass spectrometry.
44 All compounds were also analyzed by NMR and electrospray mass spectrometry.
45 rroborated by positive and negative ion mode electrospray mass spectrometry.
46 attainable with conventional direct infusion electrospray mass spectrometry.
47 rophoresis and molecular ion at m/z 41886 by electrospray mass spectrometry.
48 ated product was unambiguously identified by electrospray mass spectrometry.
49 in human meibomian gland secretions by using electrospray mass spectrometry.
50 on, cross-linked peptides were identified by electrospray mass spectrometry.
51 verse micelles encapsulating myoglobin using electrospray mass spectrometry.
52 ominant component of meibum when examined by electrospray mass spectrometry.
53 They were also characterized in solution by electrospray mass spectrometry.
54 lymers and analyzed by liquid chromatography-electrospray mass spectrometry.
55 confirmed using high-resolution positive ion electrospray mass spectrometry.
56 to bind a stoichiometric amount of Neu5Ac by electrospray mass spectrometry.
57 ble copper center were established using +ve electrospray mass spectrometry.
58 lowing more effective subsequent analysis by electrospray mass spectrometry.
59 sence of NAD(+), was studied by HPLC-coupled electrospray mass spectrometry.
60 ar magnetic resonance (NMR) and positive-ion electrospray mass spectrometry.
61 m the protein and analyzed by flow injection electrospray mass spectrometry.
62 efficiency size-exclusion chromatography and electrospray mass spectrometry.
63 , and the haloacetic acids are detected with electrospray-mass spectrometry.
64 r level by microextraction with detection by electrospray-mass spectrometry.
65 urier transform infrared, and flow injection electrospray-mass spectrometry.
66 omplexes were unambiguously identified using electrospray mass spectrometry, (1)H NMR spectroscopy, a
67 seudotetramers were analyzed by native-state electrospray mass spectrometry, a significant shift in t
68 new application of affinity capture-elution electrospray mass spectrometry (ACESI-MS) to assay the e
69 Km, Vmax and Ki (for thyroxine), obtained by electrospray mass spectrometry agreed with those obtaine
71 itrile/water mobile phase system and on-line electrospray mass spectrometry analysis in the positive
72 ys in conjunction with liquid chromatography-electrospray mass spectrometry analysis indicate that th
74 t properties for the separation and on-line, electrospray, mass spectrometry analysis of peptides and
76 ic extracts of the chips were analysed using electrospray mass spectrometry and 28 phenolic and furan
77 of the amino acids was determined by online electrospray mass spectrometry and calculated by newly d
78 , ring-opened products were characterized by electrospray mass spectrometry and collision induced dis
79 MR and electronic absorption spectroscopies, electrospray mass spectrometry and DFT computations.
80 mitochondrial cytochrome c (cyt c) by using electrospray mass spectrometry and electron spin resonan
81 ) was released with thrombin and analyzed by electrospray mass spectrometry and found to yield the M(
82 oligosaccharide fractions and established by electrospray mass spectrometry and high performance liqu
83 reased C16 and C24 ceramide as determined by electrospray mass spectrometry and induced apoptosis in
84 hods are combined with liquid chromatography-electrospray mass spectrometry and nanoelectrospray MS/M
85 mation of this material was characterized by electrospray mass spectrometry and two-dimensional 1H-NM
86 halic acids was studied by using competitive electrospray mass spectrometry and UV-Visible spectrosco
87 iques resulted in lower detection limits for electrospray mass-spectrometry and revealed eighty-five
88 cifically coordinated K(+) (as determined by electrospray mass spectrometry) and, hence, presumably o
89 s characterized by chemical degradations, by electrospray mass spectrometry, and by several nuclear m
90 d proteolysis with N-terminal sequencing and electrospray mass spectrometry, and deletion analysis to
91 uch as amino acid analysis, peptide mapping, electrospray mass spectrometry, and Edman protein sequen
93 ups, have been synthesized, identified using electrospray mass spectrometry, and isolated using an ap
94 ne- and two-dimensional gel electrophoresis, electrospray mass spectrometry, and N-terminal amino aci
95 on of analytical ultracentrifugation, native electrospray mass spectrometry, and negative stain and c
96 tigated by paramagnetic 1H NMR spectroscopy, electrospray mass spectrometry, and peptide sequence ana
97 by gamma-rays, the products were analyzed by electrospray mass spectrometry, and rate constants of mo
98 cular weight of the mutant was determined by electrospray mass spectrometry, and the presence of the
99 identified by N-terminal microsequencing and electrospray mass spectrometry, and then mapped onto the
100 ques, with a mass of 50,825 +/-10 daltons by electrospray mass spectrometry, and with a pI of 5.0.
101 ong as shown by proton NMR characterization, electrospray mass spectrometry, and X-ray analysis.
102 heric pressure thermal desorption-extractive electrospray-mass spectrometry (AP/TD-EESI-MS) for the d
103 In this study, we have used a time-resolved electrospray mass spectrometry approach to probe the kin
104 obore liquid chromatography and positive ion electrospray mass spectrometry are applied to the determ
105 olyhedral capsules, characterized by NMR and electrospray mass spectrometry, are around 5 nanometres
106 lyzed for monomeric Abeta using positive ion electrospray mass spectrometry based on the abundance th
107 nate in Chlorella vulgaris culture medium by electrospray mass spectrometry, based on selenium's know
109 mple treatment and capillary electrophoresis-electrospray mass spectrometry (CE-ESI-MS) for separatio
110 ut microfabricated capillary electrophoresis/electrospray mass spectrometry (CE/ ESI-MS) with automat
111 antibodies, PAGE fractionation patterns and electrospray mass spectrometry comparative analysis have
112 s of the large ribosomal subunit proteins by electrospray mass spectrometry confirmed that the substr
114 um have been extensively characterized using electrospray mass spectrometry coupled with a fast react
116 ss spectrometric technique, charge reduction electrospray mass spectrometry (CREMS), allowing the ana
117 gand-centered events by variable temperature electrospray mass spectrometry, cyclic voltammetry, and
122 entified in complex mixtures by HPLC-coupled electrospray mass spectrometry due to the partial loss o
125 ple matrix elimination combined on-line with electrospray mass spectrometry (EMPM/ES-MS) for the enha
126 es were characterized by the combined use of electrospray mass spectrometry (ES-MS) and NMR spectrosc
128 ot appear in high abundance in negative mode electrospray mass spectrometry (ES-MS) due to lack of ac
129 ctrophoresis (CZE) coupled with negative ion electrospray mass spectrometry (ES-MS) is used for the d
133 nge of Hammett parameters utilizing positive electrospray mass spectrometry (ESI+ -MS) as the sole qu
134 le compound is determined by high resolution electrospray mass spectrometry (ESI-MS) and confirmed by
135 analytical fragmnent is highly sensitized to electrospray mass spectrometry (ESI-MS) and is easily id
136 cyclic voltammetry, magnetic susceptibility, electrospray mass spectrometry (ESI-MS) and single-cryst
138 r the coupling of microfabricated devices to electrospray mass spectrometry (ESI-MS) have been develo
140 ere further analyzed by ultrahigh resolution electrospray mass spectrometry (ESI-MS), and 8a, togethe
141 e of most of the impurities was confirmed by electrospray mass spectrometry (ESI-MS), and thus, the c
142 Using rapid chemical quench, time-resolved electrospray mass spectrometry (ESI-MS), and Western blo
148 f-flight mass spectrometry (MALDI-TOF/MS) or electrospray mass spectrometry (ESI/MS) depending on sam
151 Here, we demonstrate that FAIMS (coupled to electrospray/mass spectrometry (ESI/MS)) can broadly bas
154 ionization mass spectrometry (ESMS), tandem electrospray mass spectrometry (ESMS-MS, collision-induc
155 y ((1)H, variable-temperature, and DOSY) and electrospray mass spectrometry establish that 20 undergo
161 uor extracts were analyzed by flow-injection electrospray-mass spectrometry (FIE-MS), a novel method
162 ues were identified by Edman degradation and electrospray mass spectrometry following proteolysis and
163 umn without pretreatment and was analyzed by electrospray mass spectrometry following the column swit
164 ona discharge is applied to charge reduction electrospray mass spectrometry for the analysis of compl
167 bohydrate staining and liquid chromatography electrospray mass spectrometry glycopeptide analysis.
169 raphy coupled with diode array detection and electrospray-mass spectrometry (HPLC/DAD/ESI-MS); ninete
171 Tryptic digestion and liquid chromatography electrospray mass spectrometry identified Cys-99 and Cys
173 h determination of dissociation constants by electrospray mass spectrometry in a multiplexed format.
174 enzymatic digestion with exonuclease VII and electrospray mass spectrometry in negative ion mode.
176 ere the increasing importance of the role of electrospray mass spectrometry in the analysis of such p
178 sis products were primarily characterized by electrospray mass spectrometry including tandem mass spe
179 he radiolysis products were characterized by electrospray mass spectrometry including tandem mass spe
181 ar electrokinetic chromatography (MEKC) with electrospray mass spectrometry initiates the development
182 as the front end for a liquid chromatography-electrospray mass spectrometry instrument, is described.
184 uster is markedly metal-dependent, extensive electrospray mass spectrometry investigations show that
187 -line high-performance liquid chromatography-electrospray mass spectrometry (LC-ESMS) analysis and su
188 the intact proteins by liquid chromatography-electrospray mass spectrometry (LC-ESMS) revealed the ma
189 e high-performance liquid chromatography and electrospray mass spectrometry (LC-ESMS) shows that the
191 igh-performance liquid chromatography (HPLC)-electrospray mass spectrometry (LC-MS) was used to analy
192 xtraction coupled with liquid chromatography/electrospray mass spectrometry (LC/ESI-MS) is described
194 hrome c, and lysozyme is presented for laser electrospray mass spectrometry (LEMS) and electrospray i
196 , 800-nm Ti:sapphire-based femtosecond laser electrospray mass spectrometry (LEMS) experiments, sugge
198 e, and tetrabutylammonium iodide using laser electrospray mass spectrometry (LEMS) reveal monotonic s
201 r mass of 25440.6 Da, which was confirmed by electrospray mass spectrometry (Mexpt = 25439.9 +/- 1.4
203 etermination of molecular weight (MW), using electrospray mass spectrometry (MS), of the polymerase c
204 diameter of the spray tip employed for nano-electrospray mass spectrometry (nano-ES-MS) upon mass sp
205 erto unidentified species is investigated by electrospray mass spectrometry of aqueous AH(2) droplets
206 onable agreement with 47, 173 Da obtained by electrospray mass spectrometry of the purified enzyme.
207 e flavin to the polypeptide has permitted LC-electrospray mass spectrometry of the reaction product t
208 nalysis of products by liquid chromatography-electrospray-mass spectrometry on the basis of fragments
209 The method is also compatible with online electrospray mass spectrometry, permitting the identific
210 inding assay based on pulsed ultrafiltration/electrospray mass spectrometry (PUF/ESMS) to tentatively
212 SDS-polyacrylamide gel electrophoresis and electrospray mass spectrometry revealed the 32-kDa speci
213 bstrate kinetic studies, and high-resolution electrospray mass spectrometry, revised steady-state kin
214 ersed-phase liquid chromatography coupled to electrospray mass spectrometry (RP-LC/ESI-MS) was used t
215 osphopeptide mapping, Edman degradation, and electrospray mass spectrometry, serine residues 283, 300
217 in the presence of H(2)(18)O and analyzed by electrospray mass spectrometry showed that the ADPRase-c
218 y immunoblotting, N-terminal sequencing, and electrospray mass spectrometry showed that trypsin cleav
219 CTLA-4 and CD80 using carbohydrate analysis, electrospray mass spectrometry, size exclusion chromatog
223 rption, electron paramagnetic resonance, and electrospray mass spectrometry suggest the redox cofacto
226 eans to facilitate the resolution of ions in electrospray mass spectrometry that differ in mass and c
228 ne thin-layer chromatographic separation and electrospray mass spectrometry (TLC/ESI-MS) has been acc
229 wed by rapid chemical quench, using HPLC and electrospray mass spectrometry to analyze the 5'-dA form
230 rix-assisted laser desorption ionization and electrospray mass spectrometry to analyze the entire pro
232 tides of the 29-kDa band were analyzed using electrospray mass spectrometry to identify the protein.
233 the latter has been used in conjunction with electrospray mass spectrometry to probe the formation of
234 nts offer further evidence of the ability of electrospray mass spectrometry to provide binding inform
236 educed and reduced proteins were analyzed by electrospray-mass spectrometry to establish the compleme
237 1)H NMR, diffusion-ordered spectroscopy NMR, electrospray mass spectrometry, transmission electron mi
238 s supported by resonance Raman spectroscopy, electrospray mass spectrometry using isotopically enrich
239 choice to study brevetoxins in negative mode electrospray mass spectrometry using the anion attachmen
245 encing of the oligosaccharide products using electrospray mass spectrometry with collision-induced di
246 f monoclonal antibodies, 1H-NMR, FAB-MS, and electrospray mass spectrometry with collision-induced di
248 ied using liquid chromatography-negative ion electrospray mass spectrometry with the trapping cartrid
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