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1 Reversed-phase, high-performance liquid chromatography (
2 d (size-exclusion chromatography followed by reversed phase high performance liquid chromatography).
3 Edman sequencing and radioanalysis using C18 reverse phase high performance liquid chromatography.
4 resolved the protein into three peaks using reverse phase high performance liquid chromatography.
5 purification of the resultant peptides using reverse phase high performance liquid chromatography.
6 ) mouse tissues following gel filtration and reverse phase high performance liquid chromatography.
7 nheim was fractionated into several peaks by reverse phase high performance liquid chromatography.
8 concentrations were analyzed with the aid of reverse phase high performance liquid chromatography.
9 ating column chromatography followed by C-18 reverse phase high performance liquid chromatography.
10 g, polymer-based C18-like, and analytical C4 reverse phase high performance liquid chromatography.
11 NA following their separation using ion pair reverse phase high-performance liquid chromatography.
12 thionylation of each protein were assayed by reverse phase-high performance liquid chromatography.
13 e, and two radiolabeled peptides isolated by reverse phase-high performance liquid chromatography.
14 and purifying the N-terminal 1-55 peptide by reverse-phase high performance liquid chromatography.
15 mouse small intestine by gel filtration and reverse-phase high performance liquid chromatography.
16 e isolated from reduced and alkylated EC3 by reverse-phase high performance liquid chromatography.
17 and the resulting peptides were separated by reverse-phase high performance liquid chromatography.
18 ge chromatography, isoelectric focusing, and reverse-phase high performance liquid chromatography.
19 8 protease and the peptides were resolved by reverse-phase high performance liquid chromatography.
20 by their differences in hydrophobicity using reverse-phase high performance liquid chromatography.
21 rum retinol concentration was measured using reverse-phase high performance liquid chromatography.
22 solid-phase extraction on silica gel and by reverse-phase high-performance liquid chromatography.
23 e-2,3-dialdehyde (NDA) and quantification by reverse-phase high-performance liquid chromatography.
24 ected by changes in their elution pattern on reverse-phase high-performance liquid chromatography.
25 lecules were acid eluted and fractionated by reverse-phase high-performance liquid chromatography.
26 nd the peptide was purified in good yield by reverse-phase high-performance liquid chromatography.
27 eles albimanus through molecular sieving and reverse-phase high-performance liquid chromatography.
28 rum retinol concentration was measured using reverse-phase high-performance liquid chromatography.
29 ted to the methyl ester, and fractionated by reverse-phase high-performance liquid chromatography.
30 The purity of proteins was demonstrated by reverse-phase high-performance liquid chromatography.
31 a product that co-elutes with anandamide on reverse-phase high-performance liquid chromatography.
32 harose column chromatography, Mono-S, and C4 reverse-phase high-performance liquid chromatography.
33 through radio-thin-layer chromatography and reverse-phase high-performance liquid chromatography.
34 l filtration chromatography and two steps of reverse-phase high-performance liquid chromatography.
35 n gingival crevicular fluid was estimated by reverse-phase high-performance liquid chromatography.
36 ival crevicular fluid (GCF) was estimated by reverse-phase high-performance liquid chromatography.
37 ts of MIANS-labeled protein were analyzed by reversed phase high performance liquid chromatography.
38 tion with solid phase extraction followed by reversed phase high performance liquid chromatography.
39 The new BBN constructs were purified by reversed phase high-performance liquid chromatography.
40 mensional method: size exclusion followed by reversed-phase high performance liquid chromatography.
41 te-polyacrylamide gel electrophoresis and/or reversed-phase high performance liquid chromatography.
42 te-polyacrylamide gel electrophoresis and/or reversed-phase high performance liquid chromatography.
43 tographic methods to obtain a single peak by reversed-phase high performance liquid chromatography.
44 broadly be categorised into normal phase or reversed-phase high performance liquid chromatography.
45 te-polyacrylamide gel electrophoresis and/or reversed-phase high-performance liquid chromatography.
46 ty by semipreparative cation exchange and/or reversed-phase high-performance liquid chromatography.
47 supernatants were purified to homogeneity by reversed-phase high-performance liquid chromatography.
48 , and their sterol profiles were analyzed by reversed-phase high-performance liquid chromatography.
49 e, and a 3H-labeled fragment was purified by reversed-phase high-performance liquid chromatography.
50 etic acid, derivatized, and analyzed by C-18 reversed-phase high-performance liquid chromatography.
51 lated rabbit platelets by gel filtration and reversed-phase high-performance liquid chromatography.
52 was isolated and purified to homogeneity by reversed-phase high-performance liquid chromatography.
53 Serum samples were analyzed via reversed-phase high-performance liquid chromatography.
54 culating phylloquinone was measured by using reversed-phase high-performance liquid chromatography.
55 ially available labeling kit and isolated by reversed-phase high-performance liquid chromatography.
56 The labeled product was purified by reversed-phase high-performance liquid chromatography.
57 (18)F-FB-IL2 was purified by reversed-phase high-performance liquid chromatography.
58 a commercially available kit and isolated by reversed-phase high-performance liquid chromatography.
59 ts of crude Ou-gon extract were separated by reversed-phase high-performance liquid chromatography.
60 , was purified by strong cation exchange and reverse-phase high performance liquid chromatographies.
61 t from DNA with the synthetic standards in a reversed-phased high-performance liquid chromatography.
62 Using reverse-phase high-performance liquid chromatography, (1
63 Epitope mapping using limited proteolysis, reversed phase high-performance liquid chromatography, a
64 ng peptide fragments were fractionated using reversed phase high-performance liquid chromatography, a
65 was purified to homogeneity by conventional reversed-phase high performance liquid chromatography, a
66 bunit by electrophoresis, mass spectrometry, reversed-phase high performance liquid chromatography, a
67 Cleavage products were analyzed with reversed-phase high performance liquid chromatography, a
68 chloroacetaldehyde, separated by ion-paired reversed-phase high-performance liquid chromatography, a
69 y solid-phase peptide synthesis, purified by reversed-phase high-performance liquid chromatography, a
70 sulfate polyacrylamide gel electrophoresis, reversed-phase high-performance liquid chromatography, a
71 hanol and steroids were further separated by reverse-phase high-performance liquid chromatography, al
72 n was chemically synthesized and analyzed by reverse-phase high performance liquid chromatography, am
73 Product analysis by reversed phase high performance liquid chromatography an
74 protein fractions generated were analyzed by reversed phase-high performance liquid chromatography an
75 Reversed-phase high performance liquid chromatography an
76 ing a combination of affinity chromatography/reversed-phase high performance liquid chromatography an
77 Using this assay, which involves reversed-phase high-performance liquid chromatography an
78 phy, enzymatically digested, and analyzed by reversed-phase high-performance liquid chromatography an
79 se peptide chemistry and characterized using reversed-phase high-performance liquid chromatography an
80 Reversed-phase high-performance liquid chromatography an
81 We report the use of peptide map analysis by reversed-phase high-performance liquid chromatography an
82 The reaction products were isolated by reverse phase high performance liquid chromatography, an
83 lowed by separation and quantification using reverse phase high performance liquid chromatography, an
84 Peptide fragments were fractionated by reverse-phase high-performance liquid chromatography, an
85 The digest was fractionated by reverse-phase high-performance liquid chromatography, an
86 Fatty acid profiles were assessed by reverse-phase high-performance liquid chromatography, an
87 modification as evident by both SDS-PAGE and reverse phase-high performance liquid chromatography ana
88 Reverse-phase high-performance liquid chromatography ana
89 ltered muropeptide profile, as determined by reverse-phase high-performance liquid chromatography ana
90 Reverse-phase high-performance liquid chromatography ana
91 Reverse-phase high-performance liquid chromatography ana
92 yields two fragments of VEGF as indicated by reverse phase high performance liquid chromatography and
93 ree adducts were isolated by semipreparative reverse phase high-performance liquid chromatography and
94 defensins, RTD-2 and RTD-3, were purified by reverse-phase high performance liquid chromatography and
95 S) in 634 patients with documented CAD using reverse-phase high-performance liquid chromatography and
96 s (GSTs) of the alpha, mu, and pi classes by reverse-phase high-performance liquid chromatography and
97 Two complementary approaches utilizing reverse-phase high-performance liquid chromatography and
98 Peptides were separated by reverse-phase high-performance liquid chromatography and
99 xtracts of SEB-1 sebocytes were separated by reverse-phase high-performance liquid chromatography and
100 active CoA metabolites are then separated by reverse-phase high-performance liquid chromatography and
101 of [14C]AA to [14C]PGE2, quantitated through reverse-phase-high-performance liquid chromatography and
102 etected and identified on straight-phase and reverse-phase high-performance liquid chromatography as
103 es of eight alkyl, aromatic, and fluorinated reversed-phase high-performance liquid chromatography bo
104 ermination of vitamin E, being comparable to reversed-phase high performance liquid chromatography ch
105 rhAT was analyzed and compared with phAT by reverse phase high-performance liquid chromatography, ci
106 Reversed phase high performance liquid chromatography co
107 conjugates behaved similarly under identical reversed phase high-performance liquid chromatography co
108 gated for their phenolic profile by means of reversed phase high-performance liquid chromatography co
109 ed to identify and quantify the saponins and reversed phase-high performance liquid chromatography co
110 pic labeling followed by analysis via online reversed-phase high performance liquid chromatography co
111 omatographic separations were carried out by reversed-phase high-performance liquid chromatography co
112 reactions, analysis of benzamide produced by reverse-phase high-performance liquid chromatography com
113 lysis of the immature and mature seed oil by reverse-phase high-performance liquid chromatography con
114 nt study, a new chromatographic method using reverse-phase high performance liquid chromatography cou
115 glutathione S-transferase (GST) resolved by reversed-phase high performance liquid chromatography cr
116 Reverse-phase high-performance liquid chromatography dem
117 ex, and its subsequent detection by Ion-Pair-Reversed Phase-High Performance Liquid Chromatography-Di
118 The application of in-line reversed-phase high-performance liquid chromatography-el
119 imple method was developed using ion-pairing reversed-phase high-performance liquid chromatography-el
120 ere also studied by temperature profiling in reversed-phase high performance liquid chromatography, f
121 Plasma samples were analysed using reverse phase high performance liquid chromatography for
122 tate, alpha-tocopherol and gamma-tocopherol, reverse phase high performance liquid chromatography for
123 Samples were analyzed by reverse-phase high-performance liquid chromatography for
124 achidonyl glyceride (2-AG), as identified by reverse phase high-performance liquid chromatography, ga
125 We show using analytical reverse phase, high performance liquid chromatography (H
126 n phenols isolated from lake sediments using reversed phase high performance liquid chromatography (H
127 were exposed to 430-nm light and examined by reversed-phase high performance liquid chromatography (H
128 cids in sour cassava starch wastewater using reversed-phase high performance liquid chromatography (H
129 ere separated and quantified by an isocratic reversed-phase high performance liquid chromatography (H
130 the degrading microspheres was monitored by reversed-phase high performance liquid chromatography (H
131 olution was analyzed in a masked fashion, by reversed-phase high-performance liquid chromatography (H
132 Currently, reversed-phase high-performance liquid chromatography (H
133 A reversed-phase high-performance liquid chromatography (H
134 A reversed-phase high-performance liquid chromatography (H
135 Reversed-phase high-performance liquid chromatography (H
136 h ethyl acetate and subsequent separation by reversed-phase high-performance liquid chromatography (H
137 ng conditions, and peptides were isolated by reversed-phase high-performance liquid chromatography (H
138 First, we established a separation in reversed-phase high-performance liquid chromatography (H
139 Both, reversed-phase high-performance liquid chromatography (H
140 tudy, we present the development of coupling reversed-phase high-performance liquid chromatography (H
141 A strategy using reversed-phase high-performance liquid chromatography (H
142 Here we describe a facile, reversed-phase high-performance liquid chromatography (H
143 g the O- or N-sulfate groups and purified by reversed-phase high-performance liquid chromatography (H
144 The method uses C18 reversed-phase high-performance liquid chromatography (H
145 xtracted by perchloric acid and separated by reversed-phase high-performance liquid chromatography (H
146 Catechin fractions were identified using reverse phase high performance liquid chromatography (HP
147 HLA-A2.1(+) breast adenocarcinoma and loaded reverse phase high-performance liquid chromatography (HP
148 Species separation was accomplished with reverse phase-high performance liquid chromatography (HP
149 placenta using concanavalin A-Sepharose and reverse-phase high performance liquid chromatography (HP
150 Reverse-phase high performance liquid chromatography (HP
151 iphosphate (ATP) as the phosphate source and reverse-phase high-performance liquid chromatography (HP
152 blished to purify nicotinamide cofactors via reverse-phase high-performance liquid chromatography (HP
153 the fluorescent substrate BODIPY C12-SPM and reverse-phase high-performance liquid chromatography (HP
154 ialdehyde (OPA) precolumn derivatization and reverse-phase high-performance liquid chromatography (HP
155 molecular species of PC were quantified with reverse-phase high-performance liquid chromatography (HP
156 PZA concentration in plasma was measured by reverse-phase high-performance liquid chromatography (HP
157 action in organic solvents and separation by reverse-phase high-performance liquid chromatography (HP
158 ted animals was determined and quantified by reverse-phase high-performance liquid chromatography (HP
159 mbardment mass spectrometry and two types of reverse-phase high-performance liquid chromatography (HP
160 12B cultures is achieved in 7 to 21 days by reverse-phase high-performance liquid chromatography (HP
161 ectric focusing for identifying deamidation, reverse-phase high-performance liquid chromatography (HP
162 can be resolved and purified using ion-pair, reverse-phase high-performance liquid chromatography (HP
163 Ion-pair, reverse-phase high-performance liquid chromatography (HP
164 w concentrations of organic Fe ligands using reverse-phase high-performance liquid chromatography (HP
165 studies, then identified and quantified with reverse-phase high-performance liquid chromatography (HP
166 can be separated completely or partially by reverse-phase high-performance liquid chromatography (HP
167 Ion-pair reversed-phase high performance liquid chromatography (I
168 These subunits were separated by ion-pair reversed-phase high-performance liquid chromatography (I
169 uch as capillary electrophoresis or ion-pair reversed-phase high-performance liquid chromatography (I
170 A rapid and accurate ion-pairing reversed-phase high-performance liquid chromatography (I
171 d were studied by using electron microscopy, reversed-phase high-performance liquid chromatography, i
172 Analyzing the enriched samples by reversed phase high-performance liquid chromatography in
173 hydrolyzates were subsequently separated by reversed-phase high-performance liquid chromatography in
174 Results from reversed-phase high-performance liquid chromatography in
175 ass spectrometry (MALDI-TOF MS) and ion-pair-reverse-phase high-performance liquid chromatography (IP
176 Reversed-phase high-performance liquid chromatography is
177 A specialized form of ion-pair reversed-phase high-performance liquid chromatography is
178 e preparation, several approaches, including reversed-phase high-performance liquid chromatography, l
179 consistent with those determined by various reversed-phase, high-performance liquid chromatography m
180 Lys-C digests were mass analyzed by on-line reversed-phase-high-performance liquid chromatography ma
181 s, anion-exchange chromatography, normal and reverse-phase high-performance liquid chromatography, ma
182 Our reversed-phase high-performance liquid chromatography-ma
183 Using a newly developed nonradioactive reverse-phase high-performance liquid chromatography/mas
184 A reversed-phase high-performance liquid chromatography me
185 developed a stability-indicating, ion-pair, reversed-phase high-performance liquid chromatography me
186 Here we present a reversed-phase high-performance liquid-chromatography me
187 peptides was verified by LC-ESI-MS/MS and a reverse phase high performance liquid chromatography met
188 Reverse phase-high performance liquid chromatography, mi
189 dged by mass spectrometry, retention time in reverse-phase high performance liquid chromatography, mi
190 omplex intact LPS mixtures by using nanoflow reversed-phase high-performance liquid chromatography (n
191 rometry (ICPMS), coupled to nano ion pairing reversed-phase high-performance liquid chromatography (n
192 lamide gel electrophoresis Western blotting, reverse phase-high performance liquid chromatography, N-
193 lotriacetic acid resin and by microcapillary reverse-phase high-performance liquid chromatography nan
194 Using microcapillary reverse-phase high-performance liquid chromatography-nan
195 conversion extracellularly (as determined by reverse phase high performance liquid chromatography of
196 Three 32P-labeled peptides were isolated by reverse-phase high performance liquid chromatography of
197 release the peptides with sample cleanup by reversed-phase high-performance liquid chromatography on
198 ased on our intriguing findings, we compared reversed-phase high-performance liquid chromatography pe
199 d to screen peptides isolated from CT26, one reverse-phase high performance liquid chromatography pep
200 Quantitation of protein concentrations by reversed-phase high-performance liquid chromatography pr
201 n the seeds of 141 samples was determined by reversed phase high-performance liquid chromatography (R
202 d subjected to three rounds of separation by reversed phase-high performance liquid chromatography (R
203 pounds of non-V. vinifera grapes, using both reversed phase-high performance liquid chromatography (R
204 h flow injection analysis (FIA) and gradient reversed-phase high performance liquid chromatography (R
205 ested with CNBr and re-Hsts were purified by reversed-phase high performance liquid chromatography (R
206 Reversed-phase high performance liquid chromatography (R
207 ention times of N-glycopeptides separated by reversed-phase high performance liquid chromatography (R
208 fic detector following species separation by reversed-phase high-performance liquid chromatography (R
209 A reversed-phase high-performance liquid chromatography (R
210 rapid determination of phenolic compounds by reversed-phase high-performance liquid chromatography (R
211 Reversed-phase high-performance liquid chromatography (R
212 spectrometry (TOFMS) following separation by reversed-phase high-performance liquid chromatography (R
213 containing glycopeptides are collected from reversed-phase high-performance liquid chromatography (R
214 amidase activity in rat brain microsomes by reversed-phase high-performance liquid chromatography (R
215 ng, simple photometry, and citrate-selective reversed-phase high-performance liquid chromatography (R
216 Reversed-phase high-performance liquid chromatography (R
217 The (Bn6)A(m) moiety was shown to act as a reversed-phase high-performance liquid chromatography (R
218 iltration, gel filtration chromatography and reversed-phase high-performance liquid chromatography (R
219 The reversed-phase high-performance liquid chromatography (R
220 d from the excess nonradiolabeled peptide by reversed-phase high-performance liquid chromatography (R
221 A secondary screen using reversed-phase high-performance liquid chromatography (R
222 ve analysis of the phosphorylation states by reversed-phase high-performance liquid chromatography re
223 onic acid > EETs > HETEs > DHETs) paralleled reversed-phase high-performance liquid chromatography re
224 Testing of AGPs separated by reverse-phase high-performance liquid chromatography rev
225 d (NIR), mid infrared (MIR) spectroscopy and reverse phase high performance liquid chromatography (RP
226 Some phenolic components were analyzed by reverse phase high performance liquid chromatography (RP
227 Reverse phase high performance liquid chromatography (RP
228 ts were performed on solutions obtained from reverse phase high-performance liquid chromatography (RP
229 llocatechin gallate (EGCG), were analyzed by Reverse Phase High-Performance Liquid Chromatography (RP
230 detect host-origin compound reserpine using Reverse Phase High-Performance Liquid Chromatography (RP
231 DO cheeses were analysed using Urea-PAGE and reverse phase-high performance liquid chromatography (RP
232 This paper also reports the use of reverse-phase high performance liquid chromatography (RP
233 using the combination of gel filtration and reverse-phase high-performance liquid chromatography (RP
234 The reaction progress was followed by reverse-phase high-performance liquid chromatography (RP
235 n, expressed in insect cells and purified by reverse-phase high-performance liquid chromatography (RP
236 On the basis of reverse-phase high-performance liquid chromatography (RP
237 f anandamide congeners was studied using two reverse-phase high-performance liquid chromatography (RP
238 CE and reverse-phase high-performance liquid chromatography (RP
239 cemization and peptide bond hydrolysis using reverse-phase high-performance liquid chromatography (RP
240 termined by using analytical method based on reverse-phase high-performance liquid chromatography (RP
241 nally, acyclovir phosphates were detected by reverse-phase-high performance liquid chromatography (RP
242 emission computed tomography, histology, and reverse-phase-high-performance liquid chromatography (RP
243 mple cleanup strategy and a rapid resolution reverse-phase high-performance liquid chromatography (RR
244 tions of the Osborne fractions determined by reversed-phase high-performance liquid chromatography, s
245 saliva, which was analyzed directly or after reversed phase high-performance liquid chromatography se
246 mples is based on Bligh and Dyer extraction, reverse-phase high-performance liquid chromatography sep
247 ry analysis of all SKP1 peptides resolved by reversed phase-high performance liquid chromatography sh
248 ng a C18 matrix followed by semi-preparative reverse phase-high performance liquid chromatography (SP
249 of chromatographic retention to compare five reversed-phase high-performance liquid chromatography st
250 ry sensitive technology based on an ion-pair reverse-phase high-performance liquid chromatography sys
251 eled smooth muscle cells was performed using reversed-phase high performance liquid chromatography, t
252 urification processes, using methods such as reversed-phase high-performance liquid chromatography, t
253 Using proteolysis, reverse phase high-performance liquid chromatography, ta
254 Using a reverse-phase high performance liquid chromatography tan
255 The CIA was brought to near-homogeneity by reverse-phase high-performance liquid chromatography, te
256 After trypsin digestion and reverse phase high performance liquid chromatography, th
257 abeled peptide from the unlabeled peptide by reverse phase high-performance liquid chromatography, th
260 sequential size exclusion chromatography and reverse-phase high-performance liquid chromatography to
261 a protein separation by monolithic capillary reversed-phase high-performance liquid chromatography to
262 We used C18 reversed-phase high-performance liquid chromatography to
263 pithelium (RPE) and choroid and subjected to reversed-phase high-performance liquid chromatography to
264 of ultracentrifugation, size-exclusion, and reverse-phase high performance liquid chromatography, tr
265 and serum carotenoid content (n = 280, using reversed phase high-performance liquid chromatography) w
266 Using reversed phase high performance liquid chromatography, w
267 ated species, separated and collected during reversed phase high-performance liquid chromatography, w
268 embranes, cation exchange chromatography and reversed phase high performance liquid chromatography wa
269 Reverse-phase high-performance liquid chromatography was
270 Two-dimensional gels, mass spectrometry, and reversed-phase high-performance liquid chromatography we
271 Chromatogram peaks obtained from reverse-phase high performance liquid chromatography wer
272 A robust analytical method, using reversed phase high-performance liquid chromatography wi
273 y elution from the bioautogram to orthogonal reversed-phase high performance liquid chromatography wi
274 n estuarine water and sediment samples using reversed-phase high-performance liquid chromatography wi
275 A method using reversed-phase high-performance liquid chromatography wi
276 Plasma total CoQ was measured by reverse-phase high-performance liquid chromatography wit
277 ansmembrane domains were then purified using reverse-phase high-performance liquid chromatography wit
278 Plasma amino acids were measured using reverse-phase high-performance liquid chromatography wit