ライフサイエンスコーパス: reverse-phase

1 Finally, a separate size-exclusion reversed-phase 2D-LC-CRMS method was developed to captur

2 lycoproteins with integrated, sequential C18 reverse phase and porous graphitized carbon-LC-ESI-QTOF-

3 using orthogonal UPLC separation strategies (reversed phase and HILIC) in both positive and negative

4 gradient or a multifactorial combination in reversed phase and ion exchange chromatography (RPLC and

5 We combined reversed-phase and hydrophilic interaction liquid chroma

6 We report here the important features of reverse phase-based nanoLC-MS/MS analysis of permethylat

7 f peptides fractionated off-line by basic pH reversed-phase (bRP) chromatography.

8 th other mononucleosides were separated by a reverse-phase C(18) column and quantified by mass spectr

9 philic addition reaction after separation by reverse-phase C18 at acidic pH.

10 the sample and purification of oxysterols by reversed phase C18-SPE followed by HPLC-MS/MS analysis.

11 were eluted isocratically within 5 min on a reversed-phase C18 column without interference from endo

12 and 3D LC-MS/MS separation protocols (all of reversed-phase C18 functionality) to a tryptic digest of

13 of the samples with solid-phase extractions: reversed-phase (C18) and strong cation-exchange (SCX).

14 determined by HPLC-PDA-MS (APCI(+)), using a reverse phase C30 column.

15 In this study, we confirmed using C30 reversed-phase (C30RP) ultra-high-performance liquid chr

16 Two-dimensional reversed-phase capillary liquid chromatography (2D RPLC)

17 per demonstrates for the first time that C18 reversed-phase capillary liquid chromatography (Cap-LC)

18 A biocompatible filter, orthogonal reversed-phase/cation-exchange columns (RP/IEX-HPLC), UV

19 differences in selectivity across a range of reversed-phase chemistries, achieving the purification o

20 ow changes in sialic acid composition affect reverse phase chromatographic retention times: sialic ac

21 y identified a candidate sharing the precise reverse-phase chromatographic and MS characteristics of

22 A rapid and economically affordable reverse-phase chromatographic approach based on a core-s

23 The method entails an aqueous extraction and reversed phase chromatographic separation using pentaflu

24 mixture of chemicals in the AF extract with reversed-phase chromatographic fractionation and subsequ

25 er onto n-alkane-modified silica surfaces in reversed-phase chromatographic particles.

26 iopharmaceutical characterization to enhance reversed-phase chromatographic performance of peptide se

27 nto the C(18)-derivatized silica surfaces of reversed-phase chromatographic silica particles.

28 and organization on the internal surfaces of reversed-phase chromatographic silica particles.

29 After a short reversed-phase chromatographic step for desalting the sa

30 sSEC fractions could be further separated by reverse phase chromatography (RPC) coupled online with h

31 C with ion exchange chromatography (IEC) and reverse phase chromatography (RPC) for intact protein se

32 ion as a hybrid form of conventional HIC and reverse phase chromatography.

33 protein extracts obtained were separated by reverse-phase chromatography (RP-HPLC-UV).

34 e (SMRT) dataset, an experimentally acquired reverse-phase chromatography retention time dataset cove

35 ize exclusion chromatography (SEC), ion-pair reversed phase chromatography (IPRP), and hydrophilic in

36 es (aqueous extract) combined with HILIC and reversed phase chromatography and time-of-flight mass sp

37 Ion exchange and high pH reversed phase chromatography are often used for this pu

38 Reversed phase chromatography, electrospray ionization-M

39 e partial separation of oxidation isomers by reversed phase chromatography.

40 in both identity as well as purity, ion-pair reversed-phase chromatography (IP-RP) at high temperatur

41 Using complementary reversed-phase chromatography (RPC) and hydrophilic inte

42 graphy seleno-amino acids were determined by reversed-phase chromatography (RPC) coupled to ICP-MS.

43 rial size exclusion chromatography (sSEC) to reversed-phase chromatography (RPC) expanded coverage of

44 Here, we show that nonaqueous reversed-phase chromatography can be coupled to mass-spe

45 esting times were analyzed using ion-pairing reversed-phase chromatography coupled to an ICPMS/MS det

46 philic interaction liquid chromatography and reversed-phase chromatography enables the investigation

47 tography (HILIC) for the aqueous extract and reversed-phase chromatography for the organic.

48 it is orthogonal to hydrophobicity on which reversed-phase chromatography is based.

49 ass of cationic ion-interaction reagents for reversed-phase chromatography is introduced in the prese

50 Reversed-phase chromatography revealed that most SAR11 b

51 hylls and bacteriochlorophylls) was based on reversed-phase chromatography with a methanol-acetone gr

52 oxylic acid cycle (TCA cycle), by mixed-mode reversed-phase chromatography, on a CSH Phenyl-Hexyl col

53 ns, iodate and nitrate, is demonstrated on a reverse phase column by a transient prior injection of h

54 sample to the MS through a UV-flow cell and reverse phase column to separate UV-induced products for

55 separation of eight vitamin K compounds on a reversed phase column in 10 min.

56 ographic separation was achieved using a C18 reversed phase column with gradient elution of basic mob

57 A separation by LC was achieved using a reversed-phase column and a gradient of water/acetonitri

58 A Kinetex C18 reversed-phase column was proposed under gradient elutio

59 d detection of tryptophan are performed on a reversed-phase column with fluorescence detection within

60 cing the retention of organic acids on a C18 reversed-phase column.

61 A high pH, low pH, reversed-phase data independent 2D-LC-MS(E) proteomic pl

62 ses strong cation-exchange (SCX) followed by reversed-phase desalting to remove Ficoll, a synthetic p

63 gradient mode were performed both in common reversed-phase eluents and environmental friendly ethano

64 Purpose To assess the effectiveness of reverse phase encoding in correcting DWI geometric disto

65 Conclusion Reverse phase encoding is a simple-to-implement method f

66 PET/MRI tumor data was improved by using the reverse phase encoding method (0.4%-44%).

67 rials and Methods In this prospective study, reverse phase encoding method was implemented with 3.0-T

68 We found high pH reversed-phase fractionation a useful tool to increase a

69 through solid-phase extraction (SPE) with a reversed phase functionalized polymeric sorbent and spik

70 ance liquid chromatography method with a C18 reverse-phase fused-core column has been developed for t

71 e protein array (RPPA), termed polymer-based reverse phase glycoprotein array (polyGPA), to capture a

72 e generation of droplets is also possible in reversed phase gradient elution mode as demonstrated by

73 A targeted reversed-phase gradient UPLC-MS/MS assay has been develo

74 sed a central composite design to optimise a reverse phase high performance liquid chromatographic me

75 Some phenolic components were analyzed by reverse phase high performance liquid chromatography (RP

76 Plasma samples were analysed using reverse phase high performance liquid chromatography for

77 tate, alpha-tocopherol and gamma-tocopherol, reverse phase high performance liquid chromatography for

78 nt study, a new chromatographic method using reverse-phase high performance liquid chromatography cou

79 rum retinol concentration was measured using reverse-phase high performance liquid chromatography.

80 termined by using analytical method based on reverse-phase high-performance liquid chromatography (RP

81 using the combination of gel filtration and reverse-phase high-performance liquid chromatography (RP

82 On the basis of reverse-phase high-performance liquid chromatography (RP

83 Plasma total CoQ was measured by reverse-phase high-performance liquid chromatography wit

84 rum retinol concentration was measured using reverse-phase high-performance liquid chromatography.

85 embranes, cation exchange chromatography and reversed phase high performance liquid chromatography wa

86 tion with solid phase extraction followed by reversed phase high performance liquid chromatography.

87 gated for their phenolic profile by means of reversed phase high-performance liquid chromatography co

88 A robust analytical method, using reversed phase high-performance liquid chromatography wi

89 cids in sour cassava starch wastewater using reversed-phase high performance liquid chromatography (H

90 ention times of N-glycopeptides separated by reversed-phase high performance liquid chromatography (R

91 ermination of vitamin E, being comparable to reversed-phase high performance liquid chromatography ch

92 pic labeling followed by analysis via online reversed-phase high performance liquid chromatography co

93 Cleavage products were analyzed with reversed-phase high performance liquid chromatography, a

94 A method combining aqueous extraction, reversed-phase high-performance capillary liquid chromat

95 These subunits were separated by ion-pair reversed-phase high-performance liquid chromatography (I

96 rapid determination of phenolic compounds by reversed-phase high-performance liquid chromatography (R

97 se peptide chemistry and characterized using reversed-phase high-performance liquid chromatography an

98 A reversed-phase high-performance liquid chromatography me

99 Quantitation of protein concentrations by reversed-phase high-performance liquid chromatography pr

100 We used C18 reversed-phase high-performance liquid chromatography to

101 A method using reversed-phase high-performance liquid chromatography wi

102 tions of the Osborne fractions determined by reversed-phase high-performance liquid chromatography, s

103 imple method was developed using ion-pairing reversed-phase high-performance liquid chromatography-el

104 ts of crude Ou-gon extract were separated by reversed-phase high-performance liquid chromatography.

105 mass spectrometry (MS), in combination with reversed-phase high-pressure liquid chromatography (HPLC

106 Reversed-phase, high-performance liquid chromatography (

107 Species separation was accomplished with reverse phase-high performance liquid chromatography (HP

108 ng a C18 matrix followed by semi-preparative reverse phase-high performance liquid chromatography (SP

109 The reverse phase-high pressure liquid chromatography chroma

110 protein fractions generated were analyzed by reversed phase-high performance liquid chromatography an

111 ex, and its subsequent detection by Ion-Pair-Reversed Phase-High Performance Liquid Chromatography-Di

112 ased on enzymatic extraction with subsequent reversed-phase-high-pressure liquid chromatography (RP-H

113 ts of samples (10 mug), we developed high-pH reverse phase (Hp-RP) combined with stop-and-go extracti

114 Reverse phase HPLC show higher hydrophobicity of fluorin

115 and FMOC-derivatization preceded analysis by reverse phase HPLC with fluorescence.

116 ct [Ru(phbpy)(phen)(NCMe)]PF(6), followed by reverse phase HPLC, led to the separation and characteri

117 sted backbiting chain end scission, based on reverse-phase HPLC analysis.

118 purified from salivary gland homogenates by reverse-phase HPLC and identified by mass spectrometry a

119 solubility, as measured by UV absorbance and reverse-phase HPLC experiments.

120 ing of a double filtration step coupled with reverse-phase HPLC fractionation of Chlamydia-infected H

121 dases upon cheese proteins were separated by reverse-phase HPLC to give 28 fractions.

122 and the sterols are identified/quantified by reversed phase HPLC coupled to tandem mass spectrometry

123 AGE modification sites in plasma proteins by reversed phase HPLC mass spectrometry in tryptic plasma

124 Reversed phase HPLC provided multiple turnover rates and

125 Also reversed phase HPLC-DAD method was developed and validat

126 Here, employing reversed-phase HPLC coupled with sensitive mass spectrom

127 Reversed-phase HPLC enables the isolation of the all-tra

128 ze exclusion chromatography for homogeneity, reversed-phase HPLC for purity (99%), peptide digest LC-

129 We here present a simple reversed-phase HPLC method for purity control of a serie

130 ans- and cis-beta-Carotenes were analyzed by reversed-phase HPLC method using a mobile phase containi

131 (BioLCCC) describes polypeptide retention in reversed-phase HPLC using the basic principles of statis

132 The derivatives were separated via reversed-phase HPLC with gradient elution.

133 he main aspects of polypeptide separation in reversed-phase HPLC.

134 Reverse phase-HPLC, GC-FID and rapid resolution-LC/tande

135 oked olives were monitored by HPLC/MS-MS and reversed-phase-HPLC methods along different procedures:

136 and wax ester species were separated on the reversed-phase HPTLC plates.

137 onidase (GUS) enzymes cause drug toxicity by reversing Phase II glucuronidation in the gastrointestin

138 We have analyzed GAGs in C. elegans using reversed-phase ion-pairing HPLC, mass spectrometry and i

139 present the development and application of a reversed-phase lauryl methacrylate-based monolith, forme

140 Reverse-phase LC-MS afforded fast separation according t

141 We report the development of a reverse-phase LC-MS/MS method for bacterial phospholipid

142 metabolites can be efficiently separated by reversed phase LC and ionized by electrospray ionization

143 ide molecular weight and retention time on a reversed phase LC column.

144 luate its performance, we analyzed data from reversed phase LC-MS and hydrophilic interaction chromat

145 0 to 100% MeOH and analyzed with untargeted reversed phase LC-MS showed that the highest number of m

146 by the combination of online two-dimensional reversed-phase LC (2D-LC) operated in high and low pH bu

147 ork, we coupled strong cation exchange (SCX)-reversed-phase LC (RPLC) to CZE-MS/MS for large-scale ph

148 romatographic retention on the commonly used reversed-phase LC columns and the resulting severe ioniz

149 ct lists that are generated empirically from reversed-phase LC-MS studies.

150 For a reversed-phase LC-MS/MS analysis of nine algal strains,

151 We use a reversed-phase LC/DTIM-MS workflow able to profile and q

152 h-resolution accurate mass spectrometry with reverse phase liquid chromatography fractionation and ma

153 used method for peptide mapping is based on reverse phase liquid chromatography with mass spectromet

154 d microbial swab samples were analyzed using reverse phase liquid chromatography with tandem mass spe

155 However, their reverse-phase liquid chromatograph mass spectrometry pep

156 up, cation exchange chromatography (CEX) and reverse-phase liquid chromatography (RPLC) were used as

157 abeling with amino acids in cell culture and reverse-phase liquid chromatography mass spectrometry, w

158 ent digestion using trypsin were analyzed by reverse-phase liquid chromatography-mass spectrometry.

159 modifiers for the online coupling of high pH reversed phase liquid chromatography (HPH-RPLC) in the f

160 he first dimension ((1)D) followed by low pH reversed phase liquid chromatography (LPH-RPLC) in the s

161 alternative to HIC is reported here: native reversed phase liquid chromatography (nRPLC).

162 Complementary reversed phase liquid chromatography (RPLC) and hydrophi

163 Then, following an online reversed phase liquid chromatography (RPLC) column reduc

164 Reversed phase liquid chromatography (RPLC) is a widely

165 ed batch experiments with size-exclusion and reversed phase liquid chromatography and in situ infrare

166 Reversed phase liquid chromatography coupled with MS-MS

167 are compared to those derived by denaturing reversed phase liquid chromatography using an oa-ToF MS

168 Reversed phase liquid chromatography with mass spectrome

169 up level of analysis, its complementarity to reversed phase liquid chromatography, and its hyphenatio

170 utilizing differential isotope labeling and reversed phase liquid chromatography-tandem mass spectro

171 The following isocratic high-performance reversed-phase liquid chromatographic conditions were so

172 Both hydrophilic interaction and reversed-phase liquid chromatographic separation along w

173 profile is commonly performed by ion-pairing reversed-phase liquid chromatography (IPRP) with a mobil

174 italizes on multidimensional high-resolution reversed-phase liquid chromatography (LC) separation for

175 s indicated that incorporation of m-NBA into reversed-phase liquid chromatography (LC) solvents impro

176 The platform combines reversed-phase liquid chromatography (LC) with online fl

177 capillary zone electrophoresis (CZE)-MS and reversed-phase liquid chromatography (LC)-MS, and then f

178 ne method combining size-exclusion (SEC) and reversed-phase liquid chromatography (RP-HPLC) using a n

179 ophilic interaction chromatography (HILIC) x reversed-phase liquid chromatography (RP-LC) separation

180 ated the utility of SERS in conjunction with reversed-phase liquid chromatography (RP-LC), for the de

181 erformed using various custom-made prototype reversed-phase liquid chromatography (RPLC) columns rang

182 adequate removal of the stationary phase of reversed-phase liquid chromatography (RPLC) columns.

183 Currently, peptide mapping with reversed-phase liquid chromatography (RPLC) coupled to m

184 ds mostly rely on gas chromatography (GC) or reversed-phase liquid chromatography (RPLC) coupled with

185 The fractions were separated further by reversed-phase liquid chromatography (RPLC) coupled with

186 ne digestion, followed by a ((2)D) on-column reversed-phase liquid chromatography (RPLC) for reductio

187 Most analytical methods rely on reversed-phase liquid chromatography (RPLC), which is qu

188 Despite recent technological advances in reversed-phase liquid chromatography (RPLC)-mass spectro

189 f ECM proteins, and rapid digestion prior to reversed-phase liquid chromatography (RPLC)-MS analysis.

190 th high confidence and high throughput using reversed-phase liquid chromatography (RPLC)-tandem mass

191 nteraction liquid chromatography (HILIC) and reversed-phase liquid chromatography (RPLC)] together wi

192 pipeline that combines superficially porous reversed-phase liquid chromatography (SPLC), Fourier tra

193 rs Nochowski from 2012 and 2013 season using reversed-phase liquid chromatography combined with negat

194 This platform combines reversed-phase liquid chromatography in parallel with bi

195 -cut multidimensional strong-cation-exchange-reversed-phase liquid chromatography proteomics analysis

196 ple cleanup in a 96-well-plate format before reversed-phase liquid chromatography tandem mass spectro

197 lkaline hydrolysis (1 h at 37 degrees C) and reversed-phase liquid chromatography with negative elect

198 ituted in 25muL acetonitrile and analyzed by reversed-phase liquid chromatography with tandem mass sp

199 When compared to reversed-phase liquid chromatography, the MMLC protocol

200 protein groups were identified in single-run reversed-phase liquid chromatography-electrospray ioniza

201 Here, we present a targeted reversed-phase liquid chromatography-high-resolution mas

202 ILIC-MS/MS) for polar pesticides, and; (iii) reversed-phase liquid chromatography-tandem mass spectro

203 ics and amine metabolomics analyses via nano reversed-phase liquid chromatography-tandem mass spectro

204 rate a mixture of four intact proteins using reversed-phase liquid chromatography.

205 a combination of hydrophilic interaction and reversed-phase liquid chromatography.

206 A reversed-phase liquid chromatography/mass spectrometry (

207 separation of longer peptides, combined with reversed phase-liquid chromatography (RP-LC) using colum

208 any previous SPE of phenolic compounds using reversed-phase materials.

209 uch as they differ from the well-studied C18 reversed phase media.

210 lid-phase extraction columns consisting of a reversed phase, mixed-mode anion exchange, and mixed-mod

211 -EtOAc-MeOH-H2O mixtures in normal-phase and reverse phase mode, respectively.

212 rmal-phase chromatography and carotenoids by reverse-phase mode.

213 ethod for predicting UPLC retention times in reversed phase mode.

214 methanol-water (6:5:6:5 v/v) was used in the reversed phase mode.

215 -affinity flow configuration hyphenated with reversed phase nanoflow chromatography and coupled with

216 olumn in the first dimension for enrichment, reversed phase nanoLC column in the second dimension for

217 ndem C18/C30 column system under non-aqueous reversed phase (NARP) chromatography conditions.

218 iter scale, by using a single octanol-filled reversed-phase, octadecylsilane-modified (C18-silica) ch

219 these linear tetraphosphates are purified by reverse phase or anion exchange HPLC, yielding triethyla

220 d into their corresponding enantiomers under reversed-phase, polar organic and normal-phase condition

221 ystals demonstrating negative refraction and reversed phase propagation.

222 ression and cisplatin treatment we performed Reverse Phase Protein Analysis (RPPA).

223 for protein expression using immunoblot and reverse phase protein array (RPPA) and then subjected to

224 from 11 tumor types using the antibody based reverse phase protein array (RPPA) technology.

225 in expression after radiation, we utilized a reverse phase protein array (RPPA) to identify significa

226 Reverse phase protein array (RPPA) was performed on 205

227 Here, we report a novel functionalized reverse phase protein array (RPPA), termed polymer-based

228 Reverse phase protein array analysis suggested additiona

229 Through reverse phase protein array analysis, we demonstrate tha

230 eveal the dynamic regulations by integrating reverse phase protein array data and the stiffness assoc

231 Reverse phase protein array further demonstrated activat

232 eceptor sequencing, immunohistochemistry and reverse phase protein array profiling (RPPA) on OS speci

233 -TRAP1 transgenic mice by RNA sequencing and reverse phase protein array reveals modulation of oncoge

234 We also used Reverse Phase Protein Array screening to identify differ

235 Unbiased reverse phase protein array studies and subsequent valid

236 Reverse phase protein array suggested that high expressi

237 ons and did protein profiling analysis using reverse phase protein array; ii) computationally develop

238 In this study, Reverse Phase Protein Arrays (RPPA) and targeted mass sp

239 proteomic platforms (planar and bead array, reverse phase protein microarray, phosphoflow, AQUA and

240 eptor (EGFR) phosphorylation, as assessed by reverse-phase protein analysis.

241 High-throughput reverse-phase protein array (RPPA) technology allows for

242 Reverse-phase protein array (RPPA) technology uses panel

243 er OGT inhibition or knock-down, employing a reverse-phase protein array (RPPA).

244 ice were identified using RNA sequencing and reverse-phase protein array analyses.

245 Reverse-phase protein array analysis of phospho-proteomi

246 Reverse-phase protein array analysis of PKCiota wild-typ

247 Phosphoproteomic profiles from reverse-phase protein array analysis supported by mRNA p

248 one H3 modification, microRNA expression and reverse-phase protein array data for 1,072 cell lines fr

249 Analysis of reverse-phase protein array data indicated that increase

250 ant NRAS melanoma, we used a high-throughput reverse-phase protein array platform to identify signali

251 A reverse-phase protein array revealed that HuR-mediated r

252 ti-E2 antibody-mediated viral suppression, a reverse-phase protein array was used to broadly survey c

253 Our screening, using a reverse-phase protein array, revealed distinct mechanism

254 Of the proteins screened in the reverse-phase protein array, we found that insulin recep

255 A discovery mass spectrometry and reverse-phase protein array-based proteomics dual approa

256 Reverse-phase protein arrays (RPPA) represent a powerful

257 We first identified, by reverse-phase protein arrays, the lymphocyte cell-specif

258 Using reverse-phase protein arrays, we measured expression lev

259 , apoptosis, wound healing assay, as well as reverse-phase protein arrays, western blot and immunoflu

260 les in response to ~170 drug compounds using reverse-phase protein arrays.

261 Downstream events, measured by time-series reverse-phase protein microarrays, high-content imaging,

262 rotein-level alterations, typically by using reversed-phase protein arrays or mass spectrometry, has

263 ry using the omics platforms: microarray and Reverse Phase Proteomic Array.

264 , miR-222-3p, miR-24-1-5p, and miR-31) using reverse-phase proteomic arrays.

265 Results of Reversed Phase Proteomic Array analysis (RPPA) suggests

266 ing a simple, automated strategy utilizing a reverse-phase resin tip-based format and "on-tip" digest

267 developed a novel workflow consisting of one Reverse Phase (RP) C18 column linked in tandem with a Co

268 using an orthogonal strategy in which both a reversed phase (RP) C18 column and a zwitterionic hydrop

269 h is better in HILIC mode than in C5 and C18 reversed phase (RP) chromatography.

270 Nine state-of-the-art reversed phase (RP) columns for ultra-high performance l

271 syl labeled metabolites can be captured on a reversed phase (RP) trap column for large volume injecti

272 tion step by strong cation exchange (SCX) or reversed phase (RP), and LC-MS analysis.

273 We combined NMR spectroscopy, preparative reversed-phase (RP) chromatography, atomic force microsc

274 nteraction liquid chromatography (HILIC) and reversed-phase (RP) separation allows a target analysis

275 tide separation modes applied in proteomics: reversed-phase (RP) separations with different pH, hydro

276 ides and components via cation-exchange (CX) reversed-phase (RP) SPE with strategically regulated pH

277 Reversed-phase separations of nucleosides, nucleotides,

278 ion of the size-variant impurity resolved by reversed-phase size-exclusion 2D-LC.

279 nalytes are preconcentrated onto a dedicated reversed-phase solid-phase extraction (Oasis PRIME-HLB)

280 s, samples (20 mL) were concentrated using a reversed-phase solid-phase extraction (SPE) cartridge, f

281 cross-links as nucleosides, enrichment by a reversed-phase solid-phase extraction column, and nanoLC

282 imization of elution solvent composition for reversed phase SPE of a model system.

283 hanol/water 80:20 (v/v), and cleaned up by a reversed phase/strong cation exchange solid phase extrac

284 njection to assess each tracer metabolism by reverse-phase thin-layer chromatography.

285 icity of these new tracers was determined by reversed-phase thin-layer chromatography.

286 eous HCl solution; unlike current processes, reverse phase transfer is achieved simply using water.

287 g power (0.375nm) was further purified using reversed-phase UFLC and subjected to matrix assisted las

288 In the present study reverse-phase UHPLC-PDA technique was developed at 60 de

289 lyzed applying complementary HILIC and C(18) reversed-phase UHPLC-MS untargeted metabolomic assays.

290 In this study, a reverse-phase ultra-high performance liquid chromatograp

291 Reverse-phase ultra-high-pressure liquid chromatography

292 es were measured with the use of untargeted, reverse-phase ultra-performance liquid chromatography-ta

293 Additionally, reversed-phase ultra-high performance liquid chromatogra

294 of biliverdin were subsequently annotated by reversed-phase ultra-high performance liquid chromatogra

295 ethanesulfonate, (3) sequential ion-exchange/reversed-phase (ultra) high-performance liquid chromatog

296 A fast reversed-phase UPLC method was developed for squalene de

297 approach was based on scaling a conventional reversed-phase UPLC-MS method for urinary profiling from

298 Pressure Liquid Chromatography (MPLC) on the reverse phase using 5L of grape juice.

299 trimodal phase incorporating polar embedded reversed phase, weak anion exchange, and strong cation e

300 ell fisheye lens has a point symmetry with a reverse phase, which makes it possible to realize passiv