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