戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                              RP HPLC peaks are represented by bands of different inte
2                                              RP-HPLC and LC-MS/MS profil1 for soybean, flaxseed and o
3                                              RP-HPLC and PAGE analyses of the fully deprotected AUCCG
4                                              RP-HPLC combined with chemometrics is a robust tool for
5                                              RP-HPLC indicated that salt enhanced the macromolecular
6                                              RP-HPLC peptide profiling revealed that the AcPs activit
7                                              RP-HPLC resolves the isoforms of purified apoA-I and apo
8                                              RP-HPLC was similarly able to quantify the main phenolic
9                                              RP-HPLC was used to quantify DHA, MGO and hydroxymethylf
10                                              RP-HPLC, LC-MS, and NMR experiments indicate that the pr
11                                              RP-HPLC-DAD-FLU separation enabled us to identify 20 der
12                                              RP-HPLC-ESI-MS/MS results showed different peptides occu
13 ification of the metabolite collected from a RP HPLC column further separated the radiolabeled materi
14                                            A RP-HPLC method has therefore been developed for their di
15                                            A RP-HPLC method, developed for the separation and quantif
16 e report the development and validation of a RP-HPLC method with fluorometric detection of derivatize
17 he quantification was carried out by using a RP-HPLC method, based on a pre-column derivatization wit
18                                           An RP-HPLC method was developed which permitted the quality
19  colorants were separated and analyzed by an RP-HPLC/DAD system.
20                                We present an RP-HPLC method for the determination of the octanol-wate
21                                We present an RP-HPLC method, for the determination of logPoct values
22 ed penicillins, which were analysed using an RP-HPLC method, validated according to the European Deci
23 and its authenticity was determined using an RP-HPLC method.
24 of this study was to develop and validate an RP-HPLC-DAD method for the simultaneous quantification o
25 of this study was to develop and validate an RP-HPLC-DAD method for the simultaneous quantification o
26 obtained after limited tryptic digestion and RP-HPLC.
27  (PsTx), was purified by cation exchange and RP-HPLC and has a molecular mass of about 24 kDa.
28  combining size-exclusion, ion-exchange, and RP-HPLC chromatographies.
29 omatography, OFFGEL isoelectric focusing and RP-HPLC.
30                                  SE-HPLC and RP-HPLC methods were used to quantification of protein/g
31 estion products were analyzed by RP-HPLC and RP-HPLC-ESI-MS/MS.
32                             With the MIR and RP-HPLC more accurate classifications of samples by regi
33  used a newly developed radioimmunoassay and RP-HPLC to detect mppOFQ/N(160-187) in mouse hypothalami
34 DSC, CD, and NMR) and bioanalytical (SEC and RP-HPLC-MS) methods.
35 using a combination of mass spectrometry and RP-HPLC separation and bioassays.
36 arated into fractions by ultrafiltration and RP-HPLC.
37 d by standard analytical techniques, such as RP-HPLC, ESI-MS, and NMR spectroscopy.
38 haracterized using different methods such as RP-HPLC, GP-HPLC, SDS-PAGE and LC-MS/MS.
39        The combination of techniques such as RP-HPLC-UV, GFAAS and MALDI-TOF-MS allowed the identific
40 essfully proven: NP-HPLC-UV/vis/FLD-bioassay-RP-HPLC-UV/vis-ESI(-)-MS with a valve switch and NP-HPLC
41 5%) and purity of the LPOS were evaluated by RP HPLC and MS-spectroscopy of the released oligonucleot
42  12b were cleaved by acidolysis, purified by RP HPLC, and isolated in high yield and purity, demonstr
43 tion of the epimers has been accomplished by RP-HPLC, allowing full characterization and incorporatio
44 tion of CA down to 0.2%, w/w was achieved by RP-HPLC-DAD using aqueous acetonitrile elution solvent (
45 e fractionated and the fractions analysed by RP-HPLC-ICP-MS coupled with ESI-Q-TOF-MS.
46 igested with MMP-20 and Klk4 and analyzed by RP-HPLC and by mass spectrometry.
47      The digestion products were analyzed by RP-HPLC and RP-HPLC-ESI-MS/MS.
48 eptides (WSP) were extracted and analyzed by RP-HPLC.
49 e complex peptide mixture can be analyzed by RP-HPLC; however, only the level of total clipping is id
50 xy-2'-deoxyguanosine (8-OHdG) as assessed by RP-HPLC (MS).
51          All cultivars were characterized by RP-HPLC, gel permeation HPLC and R5 and G12 ELISA.
52 r disease versus physiological conditions by RP-HPLC chromatography, ProteinChip technology, and QSta
53      N-acetylserotonin (NAS) was detected by RP-HPLC in human skin extracts.
54 netic variants were successfully detected by RP-HPLC.
55  vitamin B12 concentration was determined by RP-HPLC with UV detection, after prior matrix isolation
56 of 1.551-196.89 mg/g of PRF as determined by RP-HPLC.
57 roteins behaved differently when examined by RP-HPLC chromatography and surface-enhanced laser desorp
58 otential furfural compounds were examined by RP-HPLC-DAD in 20 commercial milk-based powdered infant
59 were further chromatographed and examined by RP-HPLC-ESI-MS.
60 tion of the disulfide-linked DM1 followed by RP-HPLC allowed estimation of purity of MAb-linked DM1 a
61     We found limited proteolysis followed by RP-HPLC-MS to be less time-consuming for sample preparat
62 y potential, FIV and FV were fractionated by RP-HPLC and then analyzed by LC-MS/MS to identify peptid
63  The active fraction was purified further by RP-HPLC, the chemoattractant protein appearing as a sing
64 roducts of AANAT activity were identified by RP-HPLC with fluorimetric detection in human skin and in
65 15-kDa C-terminal fragment was identified by RP-HPLC, which bound to CaM-agarose in the presence but
66  gallic and ellagic acids were identified by RP-HPLC-DAD, also coupled to off-line matrix assisted la
67 T was realized within 35 min as indicated by RP-HPLC and verified later by thermodynamically driven r
68 embly by method (A), the linkers isolated by RP-HPLC at pH approximately 2.2 were added to D at neutr
69                  A byproduct was isolated by RP-HPLC from the resin-cleaved crude product of each ben
70              The [(11)C]ERGO was isolated by RP-HPLC with a molar activity of 690 TBq/mmol.
71 thionine, can be identified at ppb levels by RP-HPLC-ICPMS, since standards are readily available.
72 rating these highly hydrophilic molecules by RP-HPLC as these compounds are eluted closely after the
73 e mitochondrial ribosomal proteins (MRPs) by RP-HPLC is described.
74 lected bioactive compounds were performed by RP-HPLC.
75 PST-2), subsequent separation of products by RP-HPLC, and mass spectrometry analysis.
76 oba L. and pharmaceutical ginkgo products by RP-HPLC, based on the theory of terpene trilactones ioni
77 ever, the separation selectivity provided by RP-HPLC has been limited to the hydrophobicity-based res
78 id phase peptide methodology and purified by RP-HPLC.
79  and the peptides were partially purified by RP-HPLC.
80 sing standard Fmoc chemistry and purified by RP-HPLC; all intermediate and final products were verifi
81 r 1Dx5 and 1Dy10 (L8) and were quantified by RP-HPLC and GP-HPLC.
82  [3H]CM-DTT separated from excess reagent by RP-HPLC.
83 cts of activated platelets were separated by RP-HPLC demonstrating the coelution of 12(S)-HETE with f
84                        Proteins separated by RP-HPLC have potential inhibitory and antioxidant activi
85 ed from each synthesis and were separated by RP-HPLC to yield enantiomerically pure 6-9.
86 ioxidant activities of proteins separated by RP-HPLC were observed in glutein-2 and albumin, respecti
87  with [3H]CM-DTT, peptides were separated by RP-HPLC, and aliquots of each fraction were counted for
88 ere purified from bovine liver, separated by RP-HPLC, and identified by 2D PAGE techniques and immuno
89 reomers of compounds 24a-f were separated by RP-HPLC.
90 eadily accessible for complete separation by RP-HPLC and detailed characterization by in-line MS anal
91 ut quantitative analysis of gliadin types by RP-HPLC to verify its correlation with the amount of tox
92 s(1)-Cys(7) disulfide, which was verified by RP-HPLC and MALDI-ToF-MS.
93 stion products by LC-MSMS, SDS-PAGE, and C18 RP-HPLC monitored with fluorescence and UV detectors.
94                                   First a C4 RP-HPLC column was used, then a C18 RP Microbore column
95 hase high-performance liquid chromatography (RP HPLC).
96 sequentially fractionated by chromatography (RP-HPLC) and each fraction was tested for antimutagenic
97 hase high-performance liquid chromatography (RP-HPLC) analysis of mAb A samples showed three distinct
98 hase high-performance liquid chromatography (RP-HPLC) analysis, accumulation of terephthalic acid (Ta
99 hase high-performance liquid chromatography (RP-HPLC) and its applications are described.
100 d phase high pressure liquid chromatography (RP-HPLC) and mass spectrometry (MS) were used for identi
101 hase-high performance liquid chromatography (RP-HPLC) and matrix assisted laser desorption ionisation
102 hase high-performance liquid chromatography (RP-HPLC) and matrix-assisted laser desorption/ionization
103 hase-high performance liquid chromatography (RP-HPLC) and quantified in a primer extension assay from
104 hase high-performance liquid chromatography (RP-HPLC) and separated by capillary zone electrophoresis
105 hase-high performance liquid chromatography (RP-HPLC) and then subjected to chemometric evaluation.
106 hase high-performance liquid chromatography (RP-HPLC) and tracking the presence of degradation produc
107 hase high-performance liquid chromatography (RP-HPLC) assays developed in our laboratory.
108 hase high performance liquid chromatography (RP-HPLC) combined with chemometrics.
109 hase high performance liquid chromatography (RP-HPLC) coupled off-line with CS-MAS for the identifica
110 hase high-performance liquid chromatography (RP-HPLC) coupled with electrospray ionization mass spect
111 hase-high-performance liquid chromatography (RP-HPLC) demonstrated robust lung, liver, and spleen BMM
112 hase high-performance liquid chromatography (RP-HPLC) eluent fractions, either before or after lyophi
113 hase high-performance liquid chromatography (RP-HPLC) equipped with UV-visible detection.
114 hase High-Performance Liquid Chromatography (RP-HPLC) for MFE standardization.
115 hase high-performance liquid chromatography (RP-HPLC) led to the production of several peptide fracti
116 hase high-performance liquid chromatography (RP-HPLC) method was developed for detection and quantifi
117 hase high-performance liquid chromatography (RP-HPLC) purification handle, allowing the separation of
118 d-phase-high-pressure liquid chromatography (RP-HPLC) separation and parallel ICPMS and electrospray
119 hase high performance liquid chromatography (RP-HPLC) to determine honeys' phenolic profiles.
120 C) and reversed-phase liquid chromatography (RP-HPLC) using a new spiked gradient profile is presente
121 hase high-performance liquid chromatography (RP-HPLC) was developed and performed for verification of
122 hase high-performance liquid chromatography (RP-HPLC) was utilized to distinguish between durum and c
123 hase high-performance liquid chromatography (RP-HPLC) were found to be complementary in the study of
124 hase high-performance liquid chromatography (RP-HPLC) with absorption (UV) detection and quantitative
125 hase high performance liquid chromatography (RP-HPLC) with photodiode array (PDA) detector was used t
126 hase high-performance liquid chromatography (RP-HPLC), and electrospray ionization mass spectrometry
127 d-phase high-pressure liquid chromatography (RP-HPLC), differential scanning calorimetry (DSC), and d
128 hase high performance liquid chromatography (RP-HPLC), followed by post-column addition of lithium sa
129 d-phase high-pressure liquid chromatography (RP-HPLC), gel electrophoresis (SDS-PAGE), or strong cati
130 hase high-performance liquid chromatography (RP-HPLC), is active in a bioassay using A. brasiliana; i
131 hase high-performance liquid chromatography (RP-HPLC), using a new column of faster resolution was va
132 hase high-performance liquid chromatography (RP-HPLC).
133 hase high-performance liquid chromatography (RP-HPLC).
134 hase high performance liquid chromatography (RP-HPLC).
135 hase-high performance liquid chromatography (RP-HPLC).
136 e phase high pressure liquid chromatography (RP-HPLC).
137 hase high performance liquid chromatography (RP-HPLC).
138 e separated by reverse-phase chromatography (RP-HPLC-UV).
139                                  We combined RP-HPLC and mass spectrometry to identify secreted or sh
140 cted to a much higher precision than current RP-HPLC models.
141 P-HPTLC(fix)-UV/Vis/FLD-pYAVAS-FLD-heart cut-RP-HPLC-DAD-HRMS/MS.
142 matography coupled to diode array detection (RP-HPLC/DAD) was developed using a fused core pentafluor
143               Overall, the current developed RP-HPLC method could detect both green coloured syntheti
144 dic) compounds has been studied on different RP-HPLC columns in buffers of varying ionic strength.
145 eled and labeled counterparts coelute during RP-HPLC separation but exhibit a sufficient mass differe
146  the tumor-specific CTLs, an aliquot of each RP-HPLC fraction was added to the autologous, B-lymphobl
147  a combination of capillary electrophoresis, RP-HPLC, and NMR spectroscopy, we show that WbpB and Wbp
148                                     Finally, RP-HPLC based fractionation of POCIS extracts and testin
149 ar weight (M(r)) in fractions collected from RP-HPLC.
150 PEG and PEGylated compounds were eluted from RP-HPLC, and the HPLC stream was mixed with diethylmethy
151              To this aim a previous gradient RP-HPLC method with DAD detection was modified and valid
152                    In comparison to gradient RP-HPLC, the resolving power of the described CEC method
153 is study as a marker in reverse-phased HPLC (RP-HPLC) analyses of adenovirus for the quantitation of
154 ization to rapidly analyze 19 amino acids in RP-HPLC/DAD with pre-column derivatization using o-phtha
155                         No peaks appeared in RP-HPLC chromatograms of globulin for either species.
156 ter soluble extracts (WSEs) were employed in RP-HPLC to differentiate between various peptide fractio
157 t for all molecular interactions involved in RP-HPLC.
158                                           IP RP HPLC is also suitable for the separation and purifica
159                                           IP RP HPLC provides a fast and reliable alternative to clas
160                           RNA purified by IP RP HPLC exhibits improved stability.
161 e high performance liquid chromatography (IP RP HPLC) is presented as a new, superior method for the
162                        The versatility of IP RP HPLC for RNA analysis is demonstrated.
163                                           IP-RP HPLC, MALDI-TOF MS, exonuclease digests, and a simple
164 mer pairs were separated and collected by IP-RP HPLC.
165 e high-performance liquid chromatography (IP-RP HPLC) techniques were combined to determine the seque
166          Partial sequence information for IP-RP HPLC fractions was obtained from analyzing exonucleas
167                      Clearly, QRT-PCR and IP-RP-HPLC are powerful and versatile tools for the detecti
168 e high-performance liquid chromatography (IP-RP-HPLC) and detected by UV spectroscopy as well as Orbi
169 e high-performance liquid chromatography (IP-RP-HPLC) procedure has been developed for nonisotopic de
170 uid Chromatography-Diode Array Detection (IP-RP-HPLC-DAD).
171 re than one splice variant was expressed, IP-RP-HPLC identified the specific homoduplex products, as
172 h-performance liquid chromatography (nano-IP-RP-HPLC).
173                                       The IP-RP-HPLC procedure specifically detects and quantifies S-
174                            The protein-level RP-HPLC and the high-pH RP-HPLC peptide-level separation
175 /CIS-MS and APCI-MS procedures after on-line RP-HPLC separation.
176 gh performance liquid chromatography method (RP-HPLC) was established to quantify the peptides.
177 romatography in line with time-of-flight MS (RP-HPLC-TOF/MS) revealed adducts of +162 and +324 Da to
178 ance liquid chromatography coupling with MS (RP-HPLC-MS).
179 erythroleukemia cell line lysate, the IEF-NP RP HPLC produced improved resolution of low mass and bas
180               It is demonstrated that IEF-NP RP HPLC provides a viable alternative to the 2-D gel sep
181 d-phase HPLC in the second dimension (IEF-NP RP HPLC).
182                                 Using IEF-NP RP HPLC, approximately 700 bands were resolved in a pI r
183     In this work, it is demonstrated that NP RP HPLC with MALDI-TOFMS detection may serve as a rapid
184                              Nonporous (NPS) RP-HPLC has been used to rapidly separate proteins from
185                              With the aid of RP-HPLC and chiral SFC separation techniques, the new di
186 ed out in two peptide fractions (A and B) of RP-HPLC collected at retention time (RT) 24 and 28min re
187                                        CA of RP-HPLC results of the matured cheeses revealed the pres
188                          This combination of RP-HPLC and CZE was able to uniquely resolve all of the
189 ography (HPLC) and an on-line combination of RP-HPLC and electrospray ionization mass spectrometry.
190 ulation method applied to the integration of RP-HPLC chromatograms allowed for the generation of a pe
191 , glutenins) has been determined by means of RP-HPLC, to assess the inter- and intra-batch variabilit
192                                  By means of RP-HPLC-ICPMS/ESMS, we investigated Capelin oil ( Mallot
193                     After the third round of RP-HPLC, mass spectrometry was used to sequence individu
194 uilt-in peristaltic pump, enabled the use of RP-HPLC with gradient elution and up to 100% organic com
195  report details and experience of our use of RP-HPLC-CLND-MS to characterize and quantify small amoun
196 metabolite that migrated at 17.5-18.5 min on RP-HPLC.
197 le, and eluted as a single symmetric peak on RP-HPLC.
198 ter eluting [(99m)TcO]depreotide products on RP-HPLC were confirmed to be the anti and syn diastereom
199                The digests were separated on RP-HPLC and analyzed by MS/MS on Q-Tof Global mass spect
200               This paper presents a study on RP-HPLC determination of the content of indole compounds
201 ysed for nitrate and nitrite by an optimised RP-HPLC technique with isocratic elution using n-octylam
202 sis of bovine acid whey, by 1D- and 2D-PAGE, RP-HPLC and intact-mass mass spectrometry showed that th
203 sis of bovine acid whey, by 1D- and 2D-PAGE, RP-HPLC and intact-mass mass spectrometry showed that th
204 eate <=3 kDa were characterized by SDS-page, RP-HPLC and MALDI-TOF-MS.
205 -48 digestion fragments in bulk by SDS-PAGE, RP-HPLC, and MALDI-TOF proves that the previous pepsin e
206                            Thus, an ion-pair RP-HPLC method for the simultaneous determination of lac
207 by the determination of furosine by ion-pair RP-HPLC-UV.
208 bsequent MALDI-TOF analysis of the partially RP-HPLC purified peptides yielded a fraction containing
209 that underlie the development of all peptide RP-HPLC applications: (i) a larger surface area leads to
210 ing the basic principles of gradient peptide RP-HPLC and solidify our collective efforts in acquiring
211    The protein-level RP-HPLC and the high-pH RP-HPLC peptide-level separations performed the best, id
212  diastereomers were separated by preparative RP-HPLC in 13% yield from D-Val.
213       I and Id were separated by preparative RP-HPLC.
214 pplications, we developed a simple and rapid RP-HPLC method based on isosbestic point detection.
215  peptides incidentally collected in the same RP-HPLC fraction were well resolved from the glycopeptid
216 ize the potential of underexplored selective RP-HPLC for quantifying ligands on NMs, which does not r
217 ification was carried out by semipreparative RP HPLC followed by lyophilization and yielded a compoun
218                                   Sequential RP-HPLC fractionation of the active extracts produced bo
219  formic acid), even with highly inert silica RP-HPLC columns of normal dimensions.
220 le (ACN) SPE fraction and the most active SP RP-HPLC peptide fraction (SP RP-HPLC 25_F28), respective
221 e-high performance liquid chromatography (SP RP-HPLC).
222  most active SP RP-HPLC peptide fraction (SP RP-HPLC 25_F28), respectively.
223 fied following UPLC-ESI MS/MS analysis of SP RP-HPLC 25_F28.
224 nce liquid chromatography mass spectrometry (RP-HPLC/MS).
225 UV-Vis spectroscopy, B(11)-NMR spectroscopy, RP-HPLC, microscale thermophoresis, and X-ray photoelect
226                  These results indicate that RP-HPLC separates effectively various wheat samples into
227                                          The RP-HPLC fraction with highest antioxidant activity conta
228  their preparation and purification, and the RP-HPLC recovery of the chain ligation intermediates.
229 s the main component, was carried out by the RP-HPLC method.
230 hemokine was demonstrated by identifying the RP-HPLC separated tryptic and endoprotease Glu-C peptide
231          The heterogeneities observed in the RP-HPLC have been determined to arise from unpaired cyst
232   Two predominant peaks were observed in the RP-HPLC profiles of all protein fractions.
233 the DPPH assay as well as injection into the RP-HPLC system containing a PFP (pentafluorophenyl) colu
234                                   One of the RP-HPLC fractions (B) showed the presence of 14 amino ac
235 dentical mass spectra, a comparison of their RP-HPLC chromatograms suggested that the two forms were
236                                 According to RP-HPLC experiments, the highest concentration of phenol
237  investigations indicate that in addition to RP-HPLC-ICPMS/ESI-MS a range of different derivatization
238  separation selectivity highly orthogonal to RP-HPLC.
239                                   Similar to RP-HPLC prediction studies, we anticipate future develop
240                                  Traditional RP-HPLC with approximately 3-mum particles has shown gen
241  (KTI) and Bowman-Birk inhibitor (BBI) using RP-HPLC was achieved, and its consistency with a traditi
242      This hydrolysate was separated by using RP-HPLC and three fractions with high antioxidant activi
243  Cu-Chl in foodstuffs and beverages by using RP-HPLC with UV-vis detector.
244             Bottom-up characterization using RP-HPLC/MS peptide mapping and accurate mass measurement
245  domesticus) fit for human consumption using RP-HPLC with UV detection.
246 rol, 6-shogaol, and 8-ginerol contents using RP-HPLC-DAD.
247  for sustained release, was determined using RP-HPLC at neutral pH yielding analogues with shorter as
248 and fraction 7 (F7) acquired from dPEP using RP-HPLC exhibited the strongest growth and metabolism pr
249 e resulting peptides were fractionated using RP-HPLC and analyzed by CE-MS yielding a total of 28538
250 igosaccharides from salts and proteins using RP-HPLC with a formic acid/acetonitrile/water mobile pha
251 balt-containing peptides were purified using RP-HPLC.
252       The beta-carotene was quantified using RP-HPLC at bimonthly intervals for a period of six month
253  arachidonic acid (AA) were quantified using RP-HPLC with charged aerosol detection in a range of com
254 tereomeric peptides could be separated using RP-HPLC in most cases.
255                 Further characterization via RP-HPLC-ESI-MS identified the main phenolics as hydroxyc
256 es of four Egyptian cultivars of linseed via RP-HPLC-DAD-QTOF-MS and MS/MS.
257 ypsin, individual peptides were obtained via RP-HPLC and were assayed for monosaccharides by strong a
258 r analyzed by beta-ionone quantification via RP-HPLC.
259 oride groups were synthesized, purified with RP HPLC, and characterized with MALDI-TOF MS and enzyme
260 dification was synthesized and purified with RP HPLC.
261                                Compared with RP-HPLC MS analysis of the same mixture in terms of spee

 
Page Top