ライフサイエンスコーパス: reversed-phase

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

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

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

4 ve validated the credentialing platform with reversed-phase and hydrophilic interaction liquid chroma

5 We combined reversed-phase and hydrophilic interaction liquid chroma

6 upon eluent composition explains the typical reversed-phase behavior (decreasing in retention followi

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

8 romatographic separation was achieved with a reversed phase C18 column.

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

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

11 duced protein digests were separated using a reversed-phase C18 column, partially reduced by post-col

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

15 ne UHPLC separation into 8 fractions using a reversed-phase C4 column led to approximately twice as m

16 arried out by binary gradient technique on a reversed-phase C8 Zorbax column and the detection was ma

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

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

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

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

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

22 tribute to explain the retention behavior of reversed-phase chromatographic columns when used under h

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

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

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

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

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

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

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

30 (ACE) in the first separation dimension and reversed phase chromatography (RP) in the second separat

31 y ionizable or retained analytes amenable to reversed phase chromatography and electrospray ionizatio

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

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

34 HPLC-ICP-MS based on ion-paired reversed phase chromatography for the selenium speciatio

35 extracts of apple peels were fractionated by reversed phase chromatography using gradient elution of

36 Reversed phase chromatography, electrospray ionization-M

37 (salt-free) ion exchange chromatography and reversed phase chromatography-mass spectrometry allowed

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

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

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

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

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

43 Prymnesins were separated by reversed-phase chromatography and detected by positive-m

44 es were isolated using cationic exchange and reversed-phase chromatography and identified by (1)H NMR

45 ample preparation, off-line fractionation by reversed-phase chromatography at pH 10, immobilization o

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

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

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

49 collected, pooled together and subjected to reversed-phase chromatography for further purification.

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

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

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

53 ge of the analysis using subzero temperature reversed-phase chromatography is presented.

54 Reversed-phase chromatography revealed that most SAR11 b

55 techniques and peptide retention modeling in reversed-phase chromatography to generate a data set suf

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

57 Purification was based on miniature reversed-phase chromatography, a procedure suitable for

58 AH was separated using ultra-filtration and reversed-phase chromatography, and assessment of the fra

59 e to separate the isomers, or who were using reversed-phase chromatography, gave rise to multi-modal

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

61 actionated by off-gel isoelectrofocusing and reversed-phase chromatography.

62 tissue patches were directly collected on a reversed phase column and analyzed using an on-column ex

63 se, cellulase), the compounds separated on a reversed phase column by gradient elution and detected b

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

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

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

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

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

69 A C-18 reversed-phase column, acetonitrile-trifluoroacetic acid

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

71 sing high performance liquid chromatography (reversed phase columns, UV-Vis diode array detector) at

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

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

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

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

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

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

78 ing TFA as an acid modifier to a formic acid/reversed phase gradient, providing additional resolving

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

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

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

82 Reversed phase high pressure liquid chromatography (RP-H

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

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

85 planar chromatography, using water-wettable reversed phase high-performance thin-layer chromatograph

86 A rapid reversed-phase high performance liquid chromatographic m

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

88 ere separated and quantified by an isocratic reversed-phase high performance liquid chromatography (H

89 Reversed-phase high performance liquid chromatography (R

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 broadly be categorised into normal phase or reversed-phase high performance liquid chromatography.

95 d against immunoaffinity column (IAC) tandem reversed-phase high pressure liquid chromatography with

96 affinity column (IAC), and identification by reversed-phase high pressure liquid chromatography with

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

98 Both, reversed-phase high-performance liquid chromatography (H

99 tudy, we present the development of coupling reversed-phase high-performance liquid chromatography (H

100 A strategy using reversed-phase high-performance liquid chromatography (H

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

102 rometry (ICPMS), coupled to nano ion pairing reversed-phase high-performance liquid chromatography (n

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

104 iltration, gel filtration chromatography and reversed-phase high-performance liquid chromatography (R

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

106 A reversed-phase high-performance liquid chromatography me

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

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

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

110 y solid-phase peptide synthesis, purified by reversed-phase high-performance liquid chromatography, a

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

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

113 culating phylloquinone was measured by using reversed-phase high-performance liquid chromatography.

114 ially available labeling kit and isolated by reversed-phase high-performance liquid chromatography.

115 The labeled product was purified by reversed-phase high-performance liquid chromatography.

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

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

118 Reversed-phase, high-performance liquid chromatography (

119 pounds of non-V. vinifera grapes, using both reversed phase-high performance liquid chromatography (R

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

121 ed to identify and quantify the saponins and reversed phase-high performance liquid chromatography co

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

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

124 monosulfate products that were identified by reversed phase HPLC and by LC-MS/MS.

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

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

127 Reversed phase HPLC provided multiple turnover rates and

128 s) in plant extracts was developed, based on reversed phase HPLC separation of extract components, fo

129 ylcobalamin (OH-Cbl), were well separated by reversed phase HPLC with a C8-HPLC column as the station

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

131 Several conditions of ion-paired reversed phase HPLC-ICP-MS, such as pH of the mobile pha

132 med based on the retention times obtained by reversed phase HPLC.

133 nal NMR spectroscopy, mass spectrometry, and reversed-phase HPLC (log k(w)) and in one case by X-ray

134 s with mAb MF6 and subsequent analysis by C8 reversed-phase HPLC and MS/MS spectrometry and (ii) anal

135 The treated samples were characterized using reversed-phase HPLC and size-exclusion HPLC with absorpt

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

137 Here we used a reversed-phase HPLC coupled with tandem mass spectrometr

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

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

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

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

142 We report here a 35-min reversed-phase HPLC method using a single C30 column kep

143 purification by HPLC, enzymatic hydrolysis, reversed-phase HPLC resolution of the ribonucleosides, a

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

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

146 lmethoxycarbonyl chemistry, characterized by reversed-phase HPLC, and matrix-assisted laser desorptio

147 hioarsenolipids showed much sharper peaks on reversed-phase HPLC, which facilitated their resolution

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

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

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

151 igosaccharides, separated by size exclusion, reversed phase ion-pairing chromatography, and chip-base

152 We present a reversed phase ion-pairing HPLC-ICP-MS method for the se

153 Here we describe and apply a novel reversed-phase ion-pair liquid chromatography purificati

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

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

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

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

158 e the elution strength of aqueous eluents in reversed phase LC is the application of high temperature

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

160 0 to 100% MeOH and analyzed with untargeted reversed phase LC-MS showed that the highest number of m

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

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

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

164 poor chromatographic retention properties in reversed-phase LC, the complex biological matrices, and

165 tes amino acid analysis by standard nanoflow reversed-phase LC-MS setups used for proteomics.

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

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

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

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

170 5 kDa proteolytic fragments were analyzed by reversed phase liquid chromatography (LC) coupled online

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

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

173 Complementary reversed phase liquid chromatography (RPLC) and hydrophi

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

175 Reversed phase liquid chromatography (RPLC) is a widely

176 hic separation techniques, such as nanoscale reversed phase liquid chromatography and capillary elect

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

178 nitines was assessed by off-line coupling to reversed phase liquid chromatography coupled to time-of-

179 Reversed phase liquid chromatography coupled with MS-MS

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

181 rvone, is performed by using on-line coupled reversed phase liquid chromatography with gas chromatogr

182 Reversed phase liquid chromatography with mass spectrome

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

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

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

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

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

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

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

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

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

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

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

194 hilic interaction chromatography (HILIC) and reversed-phase liquid chromatography (RP-LC) were employ

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

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

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

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

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

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

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

202 Reversed-phase liquid chromatography (RPLC) is a widely

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

204 Reversed-phase liquid chromatography (RPLC), which uses

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

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

207 analysis has so far fallen far below that of reversed-phase liquid chromatography (RPLC)-MS/MS.

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

209 a combination of single-molecule imaging and reversed-phase liquid chromatography (RPLC).

210 tides were separated into 25 fractions using reversed-phase liquid chromatography (RPLC).

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

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

213 d/l-peptide epimers were separated by online reversed-phase liquid chromatography and fragmented by c

214 ties increased by up to 100-fold compared to reversed-phase liquid chromatography and hydrophilic int

215 The FAIMS approach is compared with reversed-phase liquid chromatography and strong cation e

216 r multilinear double pH/solvent-gradients in reversed-phase liquid chromatography are developed by di

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

218 een light/heavy pairs under various gradient reversed-phase liquid chromatography conditions, major c

219 pe stripping of human skin, were analyzed by reversed-phase liquid chromatography coupled to high-res

220 Reversed-phase liquid chromatography coupled to negative

221 Reversed-phase liquid chromatography has become the pref

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

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

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

225 latform encompassing separation via ion-pair reversed-phase liquid chromatography using monolithic st

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

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

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

229 nd development of these materials for use in reversed-phase liquid chromatography, wide adoption cont

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

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

232 vity in the separation of intact proteins by reversed-phase liquid chromatography-mass spectrometry (

233 olecule is not attainable using conventional reversed-phase liquid chromatography-mass spectrometry m

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

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

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

237 parison to over 600 other materials used for reversed-phase liquid chromatography.

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

239 A reversed-phase liquid chromatography/mass spectrometry (

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

241 flight MS, and hydrophilic interaction- and reversed phase-liquid chromatography-quadrupole time-of-

242 pillary column packed with Waters YMC ODS-AQ reversed phase materials.

243 selectivity compared to conventional bonded reversed-phase materials, along with good peak shape and

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

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

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

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

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

249 Despite the use of reversed phase modes in both dimensions, a satisfactory

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

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

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

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

254 00 cm columns fabricated with 5 mum diameter reversed phase particles and integrated electrospray emi

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

256 ystals demonstrating negative refraction and reversed phase propagation.

257 mode column that has both anion-exchange and reversed-phase properties was used in the first dimensio

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

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

260 he trapping of proteolytic peptides onto the reversed phase resin.

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

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

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

264 Furthermore, polymeric reversed phase (RP) is created by octadecyl amine (ODA)

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

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

267 ssed three liquid chromatographic platforms: reversed phase (RP), aqueous normal phase (ANP), and hyd

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

269 ter-soluble metabolites depending on whether reversed-phase (RP) or hydrophilic interaction liquid ch

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

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

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

273 hilic interaction chromatography (HILIC) and reversed-phase (RPLC) chromatography within one analytic

274 ration with 2 retention time segments, while reversed-phase separation was accomplished within 5.5 mi

275 Reversed-phase separations of nucleosides, nucleotides,

276 romatography (TLC) plates (alox, silica gel, reversed phase silica gel).

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

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

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

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

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

282 from analyzed samples by means of polymeric reversed phase Strata X solid phase extraction (SPE) car

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

284 extracted sample was chromatographed using a reversed phase system involving an Atlantis T3-C18 colum

285 lated peptides are more strongly retained by reversed phase than nonfarnesylated peptides.

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

287 Antibodies were immobilized onto reversed-phase tips, which allows easy and flexible samp

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

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

290 PE) step, and the analytes were separated by reversed-phase ultra high performance liquid chromatogra

291 analysis (EDA) was carried out by combining reversed-phase ultra performance liquid chromatography f

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

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

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

295 these less commonly described conjugates by reversed-phase ultrahigh performance liquid chromatograp

296 re trapped online and then analyzed using an reversed-phase ultrahigh-performance liquid chromatograp

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

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

299 r PA composition using normal-phase HPLC and reversed-phase UPLC-TQD-MS.

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