ライフサイエンスコーパス: tryptic digest

1 tect sequences that are not accessible after tryptic digest.

2 opeptides can be isolated selectively from a tryptic digest.

3 entative of the range in peptides found in a tryptic digest.

4 eptides detected from a Shewanellaoneidensis tryptic digest.

5 proximately 700 peptides for a S. oneidensis tryptic digest.

6 ndem mass spectrometry (MS/MS) analysis of a tryptic digest.

7 with both peptide standards and a HeLa cell tryptic digest.

8 ified as serine 461 by HPLC-MS analysis of a tryptic digest.

9 s of angiotensin peptides and a cytochrome c tryptic digest.

10 liquid chromatography-mass spectrometry of a tryptic digest.

11 mino acid sequence by Edman degradation of a tryptic digest.

12 f 6%, from a 62.5 ng load of human cell line tryptic digest.

13 mplarily shown for a pesticide mixture and a tryptic digest.

14 ted form, prepared in a bovine serum albumin tryptic digest.

15 ve to abundant nonphosphorylated peptides in tryptic digests.

16 cities of 130-420 for analytes from proteome tryptic digests.

17 ealed by the appearance of a new fragment in tryptic digests.

18 nalysis of both soluble and membrane protein tryptic digests.

19 by SDS-PAGE and LC-MS/MS analysis of in-gel tryptic digests.

20 pplied for the study of whole-proteome mouse tryptic digests.

21 for CE/MS of peptides, proteins, and protein tryptic digests.

22 -MS) for the high-resolution analysis of mAb tryptic digests.

23 Dissociation (HCD) spectra or spectra of non-tryptic digests.

24 s conducted with peptide solutions mimicking tryptic digests.

25 verified using standard peptides and protein tryptic digests.

26 romatography/tandem mass spectrometry of NFT tryptic digests.

27 tandem mass spectrometry (MS/MS) analysis of tryptic digests.

28 dem mass spectrometry (LC-MS/MS) analyses of tryptic digests.

29 luding neuronal tissue releasate and protein tryptic digests.

30 A dilution series of a HeLa tryptic digest (5-0.05 ng/uL) was used to explore the se

31 a 1% false-discovery rate (FDR) from a yeast tryptic digest (95% confidence, p = 0.019).

32 imeric IGPS from Escherichia coli (HisHF) by tryptic digest and FABMS.

33 or measurements of a complex fungal proteome tryptic digest and provide improved confidence or number

34 ilico identify the peptides from the E. coli tryptic digest and show the increased confidence in pept

35 c acid improved the signal-to-noise ratio of tryptic digests and gave a 3-fold increase in the number

36 ted by partial amino acid microsequencing of tryptic digests and immunologic reactivity.

37 cations were studied by LC-MS/MS analyses of tryptic digests and included DTT-reversible events, e.g.

38 approach to identification of peptides (from tryptic digests) and to separation of charge-state distr

39 was evaluated using a Shewanella oneidensis tryptic digest, and approximately 15-amol detection limi

40 ior to cleanup by immunoaffinity extraction, tryptic digest, and preconcentration by solid-phase extr

41 The photolabeled kinase was subjected to tryptic digest, and the fragments were separated by chro

42 f fluorescein-labeled model peptides and BSA tryptic digest are demonstrated using the microchip HPLC

43 n, some phosphorylated peptides generated by tryptic digest are small and hydrophilic and, thus, are

44 pmol or less of isoaspartate and works with tryptic digests as well as intact proteins.

45 On-chip tryptic digest assays were then performed on the capture

46 pray ionization mass spectrometry mapping of tryptic digests before and after liver transplantation.

47 mics experiments rely on prefractionation of tryptic digests before online liquid chromatography-mass

48 ade in terms of the capability of separating tryptic digests between the mixed-mode phase and C18 rev

49 quantities (100 ng) of a Pyrococcus furiosus tryptic digest, but with mass-limited amounts (5 ng) CE

50 Analysis of tryptic digests by MALDI-TOF MS does not provide enough

51 Employing a Saccharomyces cerevisiae tryptic digest, careful consideration of several perform

52 is by MALDI-FT-ICR-MS, de novo sequencing of tryptic digested CHH by nano-LC/ESI-Q-TOF MS and intact

53 ntiated from nonmodified peptides in complex tryptic digests created upon proteolysis of proteins aft

54 racterization of products from these partial tryptic digests demonstrated that approximately 90% of t

55 ional mapping of phosphopeptides in complete tryptic digests demonstrated that the reduced phosphoryl

56 Mass spectrometry of tryptic digests determined the sole linkage point to be

57 online LC-MS analysis of hemoglobin and its tryptic digests directly from microliters of blood, achi

58 rotein groups using only 100-1000 ng of HeLa tryptic digest (equivalent to ~500-5,000 cells).

59 produce missed cleavage peptides in protein tryptic digests even at prolonged digestion times.

60 lack widow spiders and performed in-solution tryptic digests followed by MS/MS analysis to identify n

61 were determined by mass spectral analyses of tryptic digest fragments of cross-linked hemoglobin, emp

62 Peptide sequence analysis of a tryptic digest from immunoaffinity-purified Pa showed 10

63 tified by mass spectrometric sequencing of a tryptic digest from the protein band on SDS-PAGE associa

64 is further demonstrated for the analysis of tryptic digests from different colorectal cancer cell li

65 The LC-MS chromatographic peak profiles of tryptic digests from OXY, bovine Hb, human Hb, and equin

66 erine-containing peptide was identified from tryptic digests from Sulfolobus solfataricus P1 by liqui

67 Tryptic-digested gelatins were measured using HPLC/MS an

68 For yeast cytosolic tryptic digests > 100,000 polypeptides were detected, an

69 roups were identified from just 1 ng of HeLa tryptic digest hereby increasing detection sensitivity a

70 e separation of nucleic acids, proteins, and tryptic digests in combination with UV absorbance detect

71 Peptide sequences identified in the 70 kDa tryptic digest include iPLA(2)beta residues 7-53, sugges

72 ixtures of BSA and human serum albumin (HSA) tryptic digests indicated that ion series searches with

73 Typically, TTR or its tryptic digest is analyzed by MALDI-TOF MS, liquid chrom

74 targeting cysteine-containing peptides in a tryptic digest is described.

75 ing a 10-1000 fold-excess of enzyme, (v) the tryptic digest is directly transferred to a perfusion di

76 ngly and multiply phosphorylated peptides in tryptic digests is demonstrated at low-nanomolar protein

77 resis-tandem mass spectrometry (CE-MS/MS) of tryptic digests is described.

78 Using peptide mapping of tryptic digests, LC/MS, and amino acid sequence analysis

79 tides as well as biological peptides bearing tryptic digest-like features and peptides with post-tran

80 it-lamp stereophotomicroscopy, western blot, tryptic-digest/mass spectrometry electrospray ionisation

81 s spectrometry (MS/MS) analysis of an in-gel tryptic digest matched the protein sequence of thimet ol

82 kephalin and angiotensin II, spiked in a BSA tryptic digest matrix at different concentrations.

83 e containing 20 fmol of human growth hormone tryptic digest mixed with the bovine serum protein diges

84 ximately 400 for the separation of a complex tryptic digest mixture when the sample preparation inclu

85 ratio of IgG and bovine serum albumin (BSA) tryptic digest mixtures reached to 1:500.

86 With only 100 mug of tryptic digested, nonstimulated HeLa protein and 45 h of

87 Our method used a tryptic digest of 12 purified glycoproteins, glycopeptid

88 okinetic elution and sample stacking using a tryptic digest of 16 proteins to maximize peptide identi

89 ed peptides were purified from an exhaustive tryptic digest of [32P]ANPP-labeled Na+/K(+)-ATPase.

90 ilar results were obtained when evaluating a tryptic digest of a cellular lysate, representing a more

91 ure phosphoserine-containing peptides from a tryptic digest of a complex peptide mixture in which its

92 Analysis of a tryptic digest of a covalently modified IGF-1R kinase fr

93 strated by fractionating the separation of a tryptic digest of a known protein mixture onto the micro

94 r isoelectric focusing (IEF) of a methylated tryptic digest of a mixture of alpha-S-casein and beta-c

95 ability to separate peptide mixtures, e.g., tryptic digest of a protein, is illustrated and compared

96 electrospray interface for the analysis of a tryptic digest of a sample of intermediate protein compl

97 of identified peptides from an analysis of a tryptic digest of a yeast whole cell lysate.

98 Mass spectrometry analysis of a tryptic digest of acetylated AcsA (AcsA(Ac)) identified

99 strated for a mock mixture of peptides and a tryptic digest of alphaS1-casein.

100 differentially labeled proteomic sample of a tryptic digest of an E. coli lysate.

101 In addition, the analysis of a tryptic digest of apomyoglobin by nanoLC-dual ESI-FT-ICR

102 For the Glu-C/tryptic digest of apomyoglobin, approximately 66% of the

103 The intact and the tryptic digest of AuNCs@ew were characterized by mass sp

104 a carboxyl-terminal fragments from a partial tryptic digest of beta while DAP-Q labels only the carbo

105 In the case of analyzing a tryptic digest of beta-casein, conventional MALDI MS rev

106 as performed in the presence of a background tryptic digest of bovine albumin.

107 Application of the method to a tryptic digest of bovine coagulation factor V resulted i

108 yses of complex biological samples such as a tryptic digest of bovine serum albumin and a carnitine s

109 peptides from injection of only 1 pmol of a tryptic digest of bovine serum albumin using an eluent f

110 illary LC for the analysis of substance P, a tryptic digest of bovine serum albumin, and a phosphopep

111 was initially evaluated in the analysis of a tryptic digest of bovine serum albumin.

112 t was added as a trace marker component to a tryptic digest of bovine serum proteins or to a human gr

113 LC-MS/MS analysis of a tryptic digest of BSA demonstrated that these cleavages

114 In addition, a tryptic digest of BSA demonstrates baseline resolution o

115 A Chromeo P503 labeled tryptic digest of BSA was used as a complex mixture to a

116 Peptide sequences of four peptides from a tryptic digest of cytochrome c (approximately 1 pmol dep

117 The approach is illustrated by examining a tryptic digest of cytochrome c and by identifying a pept

118 (reference standard), the accurate mass of a tryptic digest of cytochrome c was measured.

119 bilities of 2D FT-ICR MS are explored with a tryptic digest of cytochrome c with both ECD and IRMPD a

120 For a tryptic digest of cytochrome c, approximately 78% of the

121 ion trap mass spectrometry and compared to a tryptic digest of Deinococcus radiodurans.

122 ber of peptides and proteins identified in a tryptic digest of E. coli cell lysate increased by 13% a

123 the enzyme transglutaminase 2) or the peptic-tryptic digest of gliadin (in native and deamidated form

124 e peptide-specific hybridomas responded to a tryptic digest of HEL or to naturally processed HEL pept

125 ously uncharacterized phosphopeptides from a tryptic digest of human beta 4 integrin, isolated from c

126 igh performance liquid chromatography of the tryptic digest of inactivated enzyme yields a single rad

127 o distinguish the cross-linked peptides in a tryptic digest of IRCX-cross-linked ubiquitin.

128 wing fast protein liquid chromatography of a tryptic digest of MAP2, suggesting that multiple modific

129 o acid sequence coverage was attained from a tryptic digest of myoglobin in < 5 min from an 80% aceto

130 ety of multiply charged model peptides and a tryptic digest of myoglobin.

131 HPLC/MS analysis of a tryptic digest of NPR-ECD identified five glycosylated p

132 ctural analysis of the peptides of the total tryptic digest of oat phyA, we found that the photorecep

133 system was used to identify a peptide from a tryptic digest of ovalbumin using standard addition and

134 ution chromatogram of a fluorescently tagged tryptic digest of ovalbumin.

135 -containing peptides was demonstrated with a tryptic digest of ribonuclease A.

136 IMS-MS analysis was assessed using a complex tryptic digest of S. cerevisiae proteins.

137 The approach was tested on tryptic digest of Saccharomyces cerevisiae histones.

138 When applied to a global tryptic digest of Shewanella oneidensis proteins, an ord

139 selective enrichment of phosphopeptides from tryptic digest of standard protein (alpha-casein, beta-c

140 Mass spectrometric analysis of a tryptic digest of Stt3p showed that the peptide containi

141 LC/MS/MS analysis of a tryptic digest of the 51 kDa subunit from GS-NDH reveale

142 LC/MS/MS analysis of a tryptic digest of the 51-kDa polypeptide revealed that c

143 A tryptic digest of the bovine alpha-crystallin A chain yi

144 A tryptic digest of the ClAc-DMDDF-inactivated enzyme yiel

145 pparatus for complex mixtures, 5 microg of a tryptic digest of the cytosolic proteins of yeast was an

146 mance liquid chromatographic analysis of the tryptic digest of the HOCl-treated proteinase demonstrat

147 On the basis of complete mapping of total tryptic digest of the iodoacetamide-modified oat phytoch

148 HPLC, MS. and MSMS, and identified it in the tryptic digest of the ISC beta-actin.

149 -glycosylated peptide from an unfractionated tryptic digest of the lectin of the coral tree, Erythrin

150 Analysis of a tryptic digest of the main reversed phase-high pressure

151 strated using consecutive analyses of global tryptic digest of the microbe Shewanella oneidensis.

152 quencing of peptides obtained from an in-gel tryptic digest of the monomer and tetramer by tandem mas

153 Tryptic digest of the protein extracted from a sodium do

154 liquid chromatography/ESIMS analysis of the tryptic digest of the protein followed by subsequent mat

155 The MALDI MS analysis of a tryptic digest of the protein showed a number of potenti

156 demonstrated by applying 50 and 38 fmol of a tryptic digest of the proteins beta-lactoglobulin and bo

157 An in-gel tryptic digest of the purified protease was analyzed by

158 Mass spectrometry analysis of the tryptic digest of the reaction product indicated that so

159 Tandem mass spectroscopy of a tryptic digest of this 12.5 kDa protein identified it as

160 D LC-MS/MS) approach was used to analyze the tryptic digest of toxoid as a whole.

161 eparations of a model mixture of peptides, a tryptic digest of trypsinogen, and < 0.05% of an individ

162 version in TPI, which could be detected in a tryptic digest of tumor-derived TPI by mass spectrometry

163 We also subjected a tryptic digest of VV ATI to liquid chromatography electr

164 ll of reversed-phase C18 functionality) to a tryptic digest of whole Jurkat cell lysate to estimate t

165 protein digests of known concentrations, and tryptic digests of 2-DGE-separated proteins.

166 omparison of two-dimensional peptide maps of tryptic digests of 32P-labeled recombinant cPLA2 and hum

167 by high performance liquid chromatography of tryptic digests of 32P-labeled recombinant cPLA2 showed

168 Tryptic digests of 32P-phosphorylated and -immunoprecipi

169 Tryptic digests of [32P]PPK contain a predominant 32P-la

170 Tryptic digests of A1 and A2 subtypes of BoNT were analy

171 resent in the Gly(136)-Arg(147) peptide from tryptic digests of AGT reacted with DBE.

172 Comparison of tryptic digests of an HIV-1 IN derivative competent for

173 The method was applied to tryptic digests of beta-casein and alpha-casein.

174 Fluorescently labeled products from tryptic digests of beta-casein were analyzed in 13 min w

175 When analyzing tryptic digests of beta-casein, the Fe(III)-NTA-PHEMA br

176 I)-IMAC and ZrO2, was also carried out using tryptic digests of both simple and moderately complex pr

177 the abundances of phosphorylated peptides in tryptic digests of bovine beta-casein and protein kinase

178 Tryptic digests of bovine cytochrome c and beta-lactoglo

179 Analyses of tryptic digests of bovine serum albumin (BSA) by LC-MS-M

180 s pump to perform nanoflow HPLC separations; tryptic digests of bovine serum albumin (BSA), transferr

181 e signature 2-oxo-acid N-terminal peptide in tryptic digests of bronchoalveolar lavage fluid from pat

182 major phosphorylation peaks were detected in tryptic digests of cdb3 separated by reverse phase HPLC.

183 y 90% of tandem mass spectra identified from tryptic digests of complex protein mixtures.

184 In-solution tryptic digests of cooked meats were deposited onto a po

185 In CE separations performed on tryptic digests of dogfish myelin basic protein (MBP) wh

186 Tryptic digests of each band were analyzed by mass spect

187 Tryptic digests of fibrin that underwent differential cr

188 electivity of the approach are presented for tryptic digests of FP-biotinylated trypsin and FP-biotin

189 annosylated peptides from complex samples of tryptic digests of HEK293 and MCF10A whole cell extracts

190 s spectrometry, a peptide (obtained from the tryptic digests of HOCl-treated cyt c) corresponding to

191 sites are enriched by the modified tips from tryptic digests of horse radish peroxidase, chicken avid

192 ionization mass spectrometry (ESI-LC/MS) of tryptic digests of human alphaB-crystallin in the presen

193 standard addition and to distinguish between tryptic digests of human and bovine hemoglobin.

194 Tryptic digests of human serum albumin and human lung ep

195 The SLAC strategy was applied to tryptic digests of human serum, and it was found that mo

196 uantitating, and annotating Cys34 adducts in tryptic digests of human serum/plasma.

197 ies or post-translational modifications from tryptic digests of individual proteins as well as whole

198 n sites after ablation of CypD, we subjected tryptic digests of isolated cardiac mitochondria from wi

199 Phosphopeptide analysis of tryptic digests of Lck from CD45- YAC-1 cells revealed t

200 e phosphorylation sites were detected in the tryptic digests of middle and C-terminal regions of IRS-

201 Alpha-ZrPN were applied for the analysis of tryptic digests of mouse liver and leukemia cell phospho

202 y nor two-dimensional phosphopeptide maps of tryptic digests of NHE3V.

203 e appearance of a phosphopeptide not seen in tryptic digests of p53 from untreated cells.

204 MALDI-TOF mass spectrometric analyses of tryptic digests of platelet-derived FV peptides detected

205 Tryptic digests of polyubiquitinated species contain mod

206 s was demonstrated with several peptides and tryptic digests of protein mixtures by LC-MS/MS experime

207 O2 in the enrichment of phosphopeptides from tryptic digests of protein mixtures.

208 f LC-MALDI-TOF-MS and LC-ESI-TOF-MS data for tryptic digests of protein mixtures.

209 t and detection by LC-MS of pHis peptides in tryptic digests of protein mixtures.

210 Most peptides that are observed from tryptic digests of proteins such as cytochrome c and myo

211 The yielded tryptic digests of proteins were analysed by CZE in four

212 s of peptide mixtures such as those found in tryptic digests of proteins.

213 The device has been evaluated with the tryptic digests of proteins.

214 esorption ionization (MALDI) for analysis of tryptic digests of proteins.

215 Tryptic digests of purified recombinant mouse AChE (mACh

216 Therefore, tryptic digests of regular and hay milk were analyzed by

217 Tryptic digests of riPLA(2)beta (83 kDa) in the presence

218 The standard peptide mixtures and tryptic digests of samples of different origins were sep

219 with stable isotope coding of peptides from tryptic digests of serum.

220 f flight mass spectrometry was used to study tryptic digests of SHV-1 and S130Gbeta-lactamases (+/- i

221 Tryptic digests of the 150- and 135-kDa proteins yielded

222 LC/MS/MS analysis of tryptic digests of the 51 kDa and 75 kDa polypeptides fr

223 Mass spectrometric analysis of tryptic digests of the gamma-globins verified the amino

224 Peptide mapping of tryptic digests of the inactivated CYP2B6 using electros

225 ity and selectivity is demonstrated with the tryptic digests of the naturally phosphorylated proteins

226 et-Tyr-Trp cross-link (as probed by LC/MS on tryptic digests of the protein), exhibited any correlati

227 S) cross-linked precursors, derived from the tryptic digests of three model proteins (Human Serum Alb

228 od is demonstrated on a model peptide and on tryptic digests of three proteins.

229 echniques was applied to the analysis of the tryptic digests of three well-characterized protein mixt

230 tted the identification of 111 proteins from tryptic digests of total hair from AKR/J-hid/hid mice, w

231 k areas of the two transition fragments from tryptic digests of whey proteins in stored milk protein

232 deglycosylated and intact glycopeptides from tryptic digests of whole influenza virus, we determined

233 furosine results indicated that MRM based on tryptic digests of whole products was a feasible method

234 The method was evaluated using tryptic digests of yeast enolase and alcohol dehydrogena

235 r the gradient separation of peptides from a tryptic digest on a 27-cm-long capillary packed with 1.0

236 B was fully characterized using 100 fmol of tryptic digest on a three-dimensional ion trap mass spec

237 rithm to interpret sequence information of a tryptic digest on alpha-casein s1.

238 xtended now for the direct derivatization of tryptic digests originating from 1-5 microg of proteins

239 48 h in the presence or absence of a peptic-tryptic digest (P-T digest) of gliadin.

240 The comparison of tryptic digest patterns of free and vesicle-bound wild t

241 A 5-kDa tryptic digest peptide fragment containing six acidic re

242 to measure collision cross sections for 968 tryptic digest peptide ions obtained from digestion of c

243 illary columns for the LC-ESI-MS analysis of tryptic digest peptide mixtures.

244 ch is demonstrated by examining a mixture of tryptic digest peptides of ubiquitin.

245 was illustrated by analysis of a mixture of tryptic digest peptides using high- and low-resolution i

246 sing a mixture of cytochrome c and myoglobin tryptic digest peptides.

247 tified and quantified the abundance of 1,056 tryptic-digested peptides, representing 163 proteins in

248 Analysis of tryptic digests prepared from phosphorylated beta2-adren

249 muFFE analysis of a Chromeo P503-labeled BSA tryptic digest produced a 2D separation that made effect

250 mensional separation of bovine serum albumin tryptic digest produced a peak capacity of 4200 (110 in

251 rified using a set of commercially available tryptic digest protein standards analyzed using an ABI 4

252 In the initial stage, markers from tryptic digested protein of chilled, boiled and autoclav

253 d chromatography (LC)/mass spectrometry on a tryptic-digested protein sample.

254 o provide a simple extension of the existing tryptic digest protocols to include carbohydrate analysi

255 Peptide profiles of tryptic-digested recombinant protein and the purified ra

256 dataset, and up to 77% more spectra from non-tryptic digests, relative to a fully supervised approach

257 ing these recommendations on 0.2 ng/muL HeLa tryptic digest results in a 10-fold increase in terms of

258 A partial tryptic digest revealed that, in the presence of agonist

259 ization-mass spectrometry analyses of SERCA1 tryptic digests revealed ca. 66% coverage of the protein

260 Mass spectrometric analysis of CPT-IL tryptic digests revealed the presence of three phosphope

261 MS/IMS/TOF performance for a protein mixture tryptic digest reveals high orthogonality between FAIMS

262 proteins were identified from a 50 ng in-gel tryptic digest sample combining five cuts in a single LC

263 nct S. oneidensis proteins from a 2.5-microg tryptic digest sample in a single 10-h analysis.

264 Shewanella oneidensis proteins from a 300-ng tryptic digest sample in a single 4-h LC-MS/MS analysis.

265 f the platform was evaluated using an in-gel tryptic digest sample of a gel fraction (15-40 kDa) of a

266 Mass analysis of in-gel tryptic digest samples provided 73% total sequence cover

267 en demonstrated using a bovine serum albumin tryptic digest separated by capillary LC where multiple

268 l 60 F(254S) plate and peptides from protein tryptic digests separated on a ProteoChrom HPTLC Silica

269 Mass spectrometry analysis of tryptic digests showed that Thr(1037) located within the

270 Isolation of the labeled peptide from the tryptic digest shows that Tyr(79) is the only enzymic am

271 The strategy includes periodate oxidation of tryptic digests, solid-phase enrichment of glycopeptides

272 omole amounts of crudely purified samples of tryptic digest solutions of horse cytochrome c and bovin

273 f small molecules and a bovine serum albumin tryptic digest, TASF improved the peak shape and resolut

274 Applied to a Saccharomyces cerevisiae tryptic digest, the approach provided 3 132 confident pe

275 e photolabeled PKCdelta C1B was subjected to tryptic digest, the fragments were separated by online c

276 For these two tryptic digests, the alpha-ZrPN approach is able to capt

277 When used with a tryptic digest, this gave unique information on only hal

278 anoLC-FAIMS-MS/MS of an unfractionated yeast tryptic digest using the modified FAIMS device identifie

279 xoid has been established by analysis of its tryptic digest using two-dimensional liquid chromatograp

280 Peptides were identified from tryptic digests using microsequencing by tandem mass spe

281 Immunoblotting analysis of Pgp tryptic digests using Pgp-specific NH(2)11, C219, and C4

282 A bovine serum albumin tryptic digest was also analyzed, and a sensitivity incr

283 glycosylated via an MS/MS experiment, so the tryptic digest was deglycosylated to confirm the presenc

284 e peptide 66LVNEVTEFAK75, also formed in the tryptic digest, was used as the native reference peptide

285 column that, on aminoterminal sequencing of tryptic digests, was identified as cytokeratin 1.

286 tein groups from as little as 250 pg of HeLa tryptic digest, we demonstrate outstanding sensitivity w

287 eline resolved, and peptides from an albumin tryptic digest were much better resolved than with exist

288 h-efficiency, two-dimensional separations of tryptic digests were achieved using glass microfluidic d

289 The tryptic digests were analyzed by LC-MS/MS, and tryptic p

290 9 and 12 amino acids that represent typical tryptic digests were designed, synthesized, and analyzed

291 ides from human serum immunoglobulin G (IgG) tryptic digests were obviously observed with greatly imp

292 The tryptic digests were passed over an immunoadsorbent spec

293 Tryptic digests were prepared in 50 mM formic acid and l

294 Meat tryptic digests were subjected to peptidomics analysis b

295 with trypsin in protonated solution, and the tryptic digests were then analyzed via liquid chromatogr

296 m fetuin, glycophorin A, ovalbumin and gp120 tryptic digests were used to build a spectral database o

297 t of casein phosphopeptides from a simulated tryptic digest with bovine serum albumin (BSA:casein, 10

298 ocol is based on glycopeptide selection from tryptic digests with serial lectin affinity chromatograp

299 Proteomic experiments performed on HeLa tryptic digests with the modified mass spectrometer impr

300 e liquid chromatography (HPLC) analysis of a tryptic digest yielded an octapeptide within the insert