ライフサイエンスコーパス: liquid chromatography

1 cetin were the major phenolics identified by liquid chromatography.

2 tified and quantified using high-performance liquid chromatography.

3 s and IPs was determined by high performance liquid chromatography.

4 ability was performed using high-performance liquid chromatography.

5 easured using reverse-phase high-performance liquid chromatography.

6 a smoking machine and analyzed using gas and liquid chromatography.

7 tion and germination, using High Performance Liquid Chromatography.

8 otenoids were determined by high-performance liquid chromatography.

9 ir extracting ability using high performance liquid chromatography.

10 of four intact proteins using reversed-phase liquid chromatography.

11 ADO) from tissues and sorted SIP cells using liquid chromatography.

12 ic acids were quantified by high-performance-liquid-chromatography.

13 two-dimensional chip-based high-performance liquid chromatography (2D chip-HPLC) approach, which ena

14 Recent developments in two-dimensional liquid chromatography (2D-LC) now make separation and an

15 d be operated on a versatile two-dimensional liquid chromatography (2D-LC) setup including several co

16 ic profile was obtained by ultra-performance liquid chromatography, accurate mass spectrometer, and a

17 lycol-labeled liposomes and high performance liquid chromatography analysis revealed accumulation in

18 A ligands were confirmed by high-performance liquid chromatography and liquid chromatography-mass spe

19 val kinetics followed using high-performance liquid chromatography and liquid chromatography-mass spe

20 earrangement, was thoroughly investigated by liquid chromatography and mass and absorption spectrosco

21 Liquid chromatography and Raman spectroscopy (LC-Raman s

22 hinder facile simultaneous quantification by liquid chromatography and tandem mass spectrometry (LC-M

23 soil phases over a period of 112 days using liquid chromatography and tandem mass spectrometry.

24 Advances in Proteomic Technologies such as liquid chromatography coupled tandem mass spectrometry (

25 Integrated 16S ribosomal DNA sequencing and liquid chromatography coupled tandem mass spectrometry (

26 were determined using ultra-high performance liquid chromatography coupled to high resolution mass sp

27 Here we use liquid chromatography coupled to high-resolution and hig

28 cloud point extraction and multidimensional liquid chromatography coupled to high-resolution mass sp

29 imethyl As) was measured by high-performance liquid chromatography coupled to ICP-MS.

30 y enzyme-linked immunosorbent assay (ELISA), liquid chromatography coupled to mass spectrometry (LC-M

31 Liquid chromatography coupled to mass spectrometry (LC-M

32 In the liquid chromatography coupled to mass spectrometry (LC-M

33 rophotometry and the individual compounds by liquid chromatography coupled to mass spectrum, as well

34 ds from mutamba fruit were analysed by using liquid chromatography coupled to tandem mass spectrometr

35 ompatible apricot pistils were created using liquid chromatography coupled to time-of-flight mass spe

36 eight organic acids), Ultra High Performance Liquid Chromatography coupled to triple-quadrupole Mass

37 nalyzed for IPM3 using ultrahigh-performance liquid chromatography coupled with electrospray ionizati

38 The use of liquid chromatography coupled with high-resolution mass

39 Liquid chromatography coupled with high-resolution tande

40 with atom-based heavy isotopes, followed by liquid chromatography coupled with mass spectrometry (LC

41 This observation was confirmed by liquid chromatography coupled with mass spectrometry.

42 nnabinoid concentrations were profiled using liquid chromatography coupled with mass-spectroscopy (UP

43 s were detected using ultra high-performance liquid chromatography coupled with quadruple time-of-fli

44 vent extraction followed by high performance liquid chromatography coupled with quadrupole time of fl

45 NMR and chromatographic techniques (gas and liquid chromatography) coupled to mass spectrometry was

46 s in processed fruit using ultra-performance liquid chromatography, coupled to tandem mass spectromet

47 The liquid chromatography, coupled with tandem mass spectrom

48 27/209 lipids (13.3%) detected by liquid chromatography-coupled mass spectrometry (LC-MS)

49 An ultra-high-performance liquid chromatography-diode array detector-mass spectrom

50 ermination were achieved by high performance liquid chromatography-diode-array detection while confir

51 Using liquid chromatography-drift tube ion mobility-mass spect

52 The model utilizes ultrahigh-performance liquid chromatography electrospray ionization quadrupole

53 10/300 GL size exclusion chromatography, and liquid chromatography-electrospray ionisation tandem mas

54 ass spectrometry (CIMS) and ultraperformance liquid chromatography/electrospray ionization mass spect

55 Non-targeted and suspect analyses with liquid chromatography/electrospray/high-resolution mass

56 of IMS in high-throughput workflows such as liquid chromatography-fluorescence-mass spectrometry (LC

57 nalysed using reverse phase high performance liquid chromatography for esketamine.

58 ve Liquid-Liquid Microextraction, coupled to Liquid Chromatography, for the determination of flavonol

59 -Ab) followed by fast protein size exclusion liquid chromatography (FPLC) purification.

60 Liquid chromatography high resolution mass spectrometry

61 Ultrahigh-performance liquid chromatography high-resolution mass spectrometry

62 tablished a validated ultra-high-performance liquid chromatography high-resolution mass spectrometry

63 nt samples were collected and measured using liquid chromatography high-resolution mass spectrometry

64 at two WWTPs in Switzerland, measured using liquid chromatography high-resolution mass spectrometry,

65 We adopted SAX for liquid chromatography high-resolution MS nontarget scree

66 roasted coffee products by isotope dilution liquid chromatography-high resolution mass spectrometry,

67 ME) chemical biopsy tool in combination with liquid chromatography-high resolution mass spectrometry.

68 sed on mixed-mode solid-phase extraction and liquid chromatography-high resolution mass spectrometry.

69 ing immunoaffinity purification coupled with liquid chromatography-high resolution tandem mass spectr

70 d enabled quantification by high-performance liquid chromatography-high-resolution mass spectrometry

71 ntargeted screening by ultrahigh-performance liquid chromatography-high-resolution mass spectrometry

72 rometry (ICPMS), and hydrophilic interaction liquid chromatography (HILIC) - electrospray-OrbitrapMS.

73 s with different pH, hydrophilic interaction liquid chromatography (HILIC), strong cation and anion e

74 t-cutting IPRP-, AEX-hydrophilic interaction liquid chromatography(HILIC)/MS method for quantificatio

75 Spectroscopy (SPME-GC-MS), High-Performance Liquid Chromatography (HPLC) (for the quantification of

76 2 ng/mL (3.9 to 40.5 nM) by high-performance liquid chromatography (HPLC) (this information was obtai

77 nded isomers by traditional high-performance liquid chromatography (HPLC) and mass spectrometry (MS)

78 rations were analysed using high-performance liquid chromatography (HPLC) and minerals by inductively

79 d using an immobilized IdeS-high-performance liquid chromatography (HPLC) column as a first dimension

80 rtaken to elucidate NMR and high-performance liquid chromatography (HPLC) data for these late-stage d

81 4b, was resolved by chiral high-performance liquid chromatography (HPLC) into its enantiomers, and a

82 These techniques, such as high-performance liquid chromatography (HPLC) or total organic carbon, of

83 uices have been analyzed by high-performance liquid chromatography (HPLC) to measure whole amino acid

84 es using time-resolved NMR, high-performance liquid chromatography (HPLC), and mass spectrometry demo

85 d method and analyzed using high-performance liquid chromatography (HPLC), fourier transform infrared

86 rine-containing analytes by high-performance liquid chromatography (HPLC)-ICPMS/MS but none about uti

87 and the gold standard test, high-performance liquid chromatography (HPLC).

88 HMOs were measured by high performance liquid chromatography (HPLC).

89 tracted and fractionated by high-performance liquid chromatography (HPLC).

90 ial can be determined using high performance liquid chromatography (HPLC).

91 tives to the typically used high-performance liquid chromatography (HPLC).

92 neuroblastoma cell lines by high performance liquid chromatography (HPLC).

93 of OTA was established by a high-performance liquid chromatography (HPLC-FD) with a limit of detectio

94 r carnosine quantification (high-performance liquid chromatography - HPLC).

95 lution fractionation (CEF), high temperature liquid chromatography (HTLC), and thermal gradient inter

96 Seleno-amino acids were determined by liquid chromatography-ICP MS.

97 i-residual extraction that uses QuEChERS and liquid chromatography in tandem with triple quadrupole m

98 cobalt in kefir samples by high performance liquid chromatography-inductively coupled plasma-optical

99 that on a low dispersion ultrahigh-pressure liquid chromatography instrument, columns between 10 and

100 his study, we demonstrate the use of coupled liquid chromatography, ion mobility spectrometry, and ma

101 only performed by ion-pairing reversed-phase liquid chromatography (IPRP) with a mobile phase contain

102 ed and acid hydrolyzed before analysis using liquid chromatography-isotope ratio mass spectrometry (L

103 analysis of six cyclosporin analogues using liquid chromatography (LC) and differential mobility spe

104 We applied advanced liquid chromatography (LC) and mass spectrometry (MS) te

105 es is the drift in analyte retention time as liquid chromatography (LC) columns wear, forcing targete

106 We employed liquid chromatography (LC) coupled to high-resolution ma

107 lls to perform solid phase extraction (SPE), liquid chromatography (LC) fraction collection, LC-NMR-m

108 s have shown that ESI-FT-ICR hyphenated with liquid chromatography (LC) is a promising approach to al

109 provement compared with the state-of-the-art liquid chromatography (LC) or capillary electrophoresis

110 -resolution MS (HRMS) approach that employed liquid chromatography (LC)-amenable thin-film microextra

111 Suspect and nontarget screening with liquid chromatography (LC)-high-resolution tandem mass s

112 This can be performed within one liquid chromatography (LC)-MS(2) experiment or at the re

113 electrophoresis (CZE)-MS and reversed-phase liquid chromatography (LC)-MS, and then fragmented using

114 e quantitative data, instead of conventional liquid chromatography (LC)-MS, the use of a guard column

115 ed using both gas chromatography (GC)-MS and liquid chromatography (LC)-MS.

116 action between fullerenes and saccharides in liquid chromatography (LC).

117 of metabolites from tumor lysates following liquid chromatography (LC).

118 plex TMT method coupled with two-dimensional liquid chromatography (LC/LC) for extensive peptide frac

119 ing gas chromatography mass spectrometry and liquid chromatography mass spectrometry for metabolite p

120 -based instruments, and (iii) high flow rate liquid chromatography mass spectrometry platforms.

121 Aqueous seed extracts were found by liquid chromatography mass spectrometry to contain selen

122 We employed liquid chromatography mass spectrometry to search for th

123 riety of analytical tools, including gas and liquid chromatography, mass spectrometry (MS), and nucle

124 Liquid chromatography-mass spectrometry (LC-MS) affords

125 tion, often however incompatible with direct liquid chromatography-mass spectrometry (LC-MS) analysis

126 ified the levels of each ABX in the brain by liquid chromatography-mass spectrometry (LC-MS) at PND 2

127 ak detection and the peak integration in raw liquid chromatography-mass spectrometry (LC-MS) data.

128 Liquid chromatography-mass spectrometry (LC-MS) delivers

129 Peptide mapping coupled with liquid chromatography-mass spectrometry (LC-MS) has beco

130 Liquid chromatography-mass spectrometry (LC-MS) has been

131 igosaccharides are characterized by advanced liquid chromatography-mass spectrometry (LC-MS) methods

132 er dissociation (ETD) on each precursor on a liquid chromatography-mass spectrometry (LC-MS) timescal

133 The results were validated by liquid chromatography-mass spectrometry (LC-MS), exhibit

134 hromatography-mass spectrometry (GC-MS), and liquid chromatography-mass spectrometry (LC-MS), which d

135 is a commonly used mobile phase additive in liquid chromatography-mass spectrometry (LC-MS)-based bi

136 ative and absolute quantitation (iTRAQ) with Liquid chromatography-mass spectrometry (LC-MS/MS) prote

137 oups were analyzed and PyCs quantified using liquid chromatography-mass spectrometry (LC-MS/MS).

138 Conventional chiral liquid chromatography-mass spectrometry (LC/MS) HTE meth

139 the glycolipids is performed using nanoflow liquid chromatography-mass spectrometry (nanoLC-MS).

140 ght scattering (DLS) and ultra high pressure liquid chromatography-mass spectrometry (UHPLC-MS), we s

141 r standard methods such as Ultra Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS) and En

142 Liquid chromatography-mass spectrometry analyses identif

143 Using high-performance liquid chromatography-mass spectrometry analysis, we det

144 The controlled liquid chromatography-mass spectrometry and (18)O-labell

145 les were determined by spectrophotometry and liquid chromatography-mass spectrometry and compared wit

146 Hepatic metabolites were measured by liquid chromatography-mass spectrometry and correlated w

147 We also measured total S1P by liquid chromatography-mass spectrometry and isolated HDL

148 Liquid chromatography-mass spectrometry and microarray c

149 Liquid chromatography-mass spectrometry experiments reve

150 s fractionated and analyzed by high-pressure liquid chromatography-mass spectrometry in order to inve

151 Untargeted liquid chromatography-mass spectrometry metabolomics was

152 in fatty acids (SCFAs) were measured using a liquid chromatography-mass spectrometry platform.

153 g high-performance liquid chromatography and liquid chromatography-mass spectrometry showed that capt

154 We used liquid chromatography-mass spectrometry to analyze plasm

155 We also used liquid chromatography-mass spectrometry to characterize

156 roliquid extraction for surface analysis and liquid chromatography-mass spectrometry to locate sterol

157 analyzed using gradient ultracentrifugation, liquid chromatography-mass spectrometry, and shotgun lip

158 Using two-dimensional electrophoresis and liquid chromatography-mass spectrometry, we studied APOE

159 Using aptamer-based proteomics and liquid chromatography-mass spectrometry-based (LC-MS-bas

160 (GlycoStore), exoglycosidase digestions, and liquid chromatography-mass spectrometry.

161 spray mass spectrometry and high-performance liquid chromatography-mass spectrometry.

162 ts, real-time polymerase chain reaction, and liquid chromatography-mass spectrometry.

163 or quantification of TFV-DP and 3TC-TP using liquid chromatography-mass spectrometry.

164 ites were analyzed by gas chromatography and liquid chromatography-mass spectrometry.

165 using trypsin were analyzed by reverse-phase liquid chromatography-mass spectrometry.

166 y high-performance liquid chromatography and liquid chromatography-mass spectrometry.

167 n peptide profiles were assessed using novel liquid chromatography-mass spectrometry/mass spectroscop

168 an online three-dimensional high-performance liquid chromatography/mass spectrometry (3D-HPLC/MS) app

169 For this purpose, a four-dimensional-liquid chromatography/mass spectrometry (4D-LC/MS) metho

170 lipofuscin fluorophore A2E in the RPE using liquid chromatography/mass spectrometry (LC/MS) showing

171 within a biological system, most commonly by liquid chromatography/mass spectrometry (LC/MS).

172 24 adults were analyzed by ultra-performance liquid chromatography/mass spectrometry (UPLC-MS).

173 ecular formulas of unknown compounds in both liquid chromatography/mass spectrometry and mass spectro

174 A liquid chromatography method coupling diode-array and fl

175 on to those obtained by the High-performance liquid chromatography method.

176 with a shorter UHPLC (ultra-high performance liquid chromatography) method was developed for simultan

177 tographic behavior and a 14-fold increase in liquid chromatography MS (LCMS) sensitivity compared to

178 y using immunoblotting and ultra-performance liquid chromatography MS/MS to analyze the hearts of fas

179 ial to fill in the gap in metabolomics where liquid chromatography-MS-based analyses cannot be applie

180 aphy-tandem mass spectrometry (LC-MS/MS) and liquid chromatography-multiple reaction monitoring (LC-M

181 Liquid chromatography/negative electrospray ionization m

182 g of the mobile phase as in high-performance liquid chromatography nor for generating a vacuum system

183 ydrophilic interaction-ultrahigh-performance liquid chromatography of the fluorescently labeled libra

184 High-performance liquid chromatography or gas chromatography coupled with

185 -of-flight mass spectrometry (GC-TOF MS) and liquid chromatography Orbitrap mass spectrometry (LC-Orb

186 dissipation studies were carried out using a liquid chromatography-Orbitrap mass spectrometry (UHPLC-

187 determination by HPLC-PAD (High performance liquid chromatography - photodiode-array detector) is pr

188 Here, we combine picoliter-scale liquid chromatography (picoLC) with mass spectrometry (M

189 ics therefore typically necessitates offline liquid chromatography prefractionation, a time-consuming

190 In comparison to liquid chromatography prefractionation, FAIMS experiment

191 sional strong-cation-exchange-reversed-phase liquid chromatography proteomics analysis workflow coupl

192 mic analyses using an ultra-high-performance liquid chromatography quadruple time-of-flight mass spec

193 aq)(-) reactions with 15 PFASs identified by liquid chromatography quadrupole time-of-flight mass spe

194 lts were compared with obtained results from liquid chromatography quadrupole time-of-flight mass spe

195 Using liquid chromatography-quadrupole time-of-flight tandem m

196 iltration and reverse-phase high-performance liquid chromatography (RP-HPLC).

197 Complementary reversed phase liquid chromatography (RPLC) and hydrophilic interaction

198 ons were separated further by reversed-phase liquid chromatography (RPLC) coupled with MS for protein

199 ollowed by a ((2)D) on-column reversed-phase liquid chromatography (RPLC) for reduction and fragments

200 and rapid digestion prior to reversed-phase liquid chromatography (RPLC)-MS analysis.

201 n 200 peptides to be monitored over a 30 min liquid chromatography separation.

202 hich the same sample is run by LC-MS in both liquid chromatography solvent with (14)NH(3)-acetate buf

203 Consequently, the potential of high-pressure liquid chromatography tandem mass spectrometry (HPLC-MS/

204 ofiling of male mice liver with quantitative liquid chromatography tandem mass spectrometry (LC-MS/MS

205 ite tend to have low abundances, which makes liquid chromatography tandem mass spectrometry (LC-MS/MS

206 Nano-flow liquid chromatography tandem mass spectrometry (nano-flo

207 For that purpose, a new liquid chromatography tandem mass spectrometry method fo

208 A fast high performance liquid chromatography tandem mass spectrometry multi-met

209 gene sequencing), cytokine, and metabolome (liquid chromatography tandem mass spectrometry) data col

210 Liquid chromatography tandem mass spectrometry-based lip

211 in of 15 kDa, designated as Ppal15kDa, using liquid chromatography tandem mass spectrometry.

212 entrations were analysed by the confirmatory liquid chromatography tandem-mass spectrometry (LC-MS/MS

213 By applying high-performance liquid chromatography tandem-mass spectrometry, we ident

214 main objective of this study was to apply a liquid chromatography-tandem mass spectrometric method t

215 roach enables the end-to-end one-dimensional liquid chromatography-tandem mass spectrometry (1D LC-MS

216 Plasma metabolites were measured using liquid chromatography-tandem mass spectrometry (21 phosp

217 neric reagent, ultratargeted two-dimensional liquid chromatography-tandem mass spectrometry (2D-LC-MS

218 he ng/mL range using hydrophilic interaction liquid chromatography-tandem mass spectrometry (HILIC-MS

219 cated disulfide linkages and free thiols via liquid chromatography-tandem mass spectrometry (LC-MS(2)

220 f traditional ligand-binding assay (LBA) and liquid chromatography-tandem mass spectrometry (LC-MS/MS

221 We thus performed liquid chromatography-tandem mass spectrometry (LC-MS/MS

222 Although liquid chromatography-tandem mass spectrometry (LC-MS/MS

223 Liquid chromatography-tandem mass spectrometry (LC-MS/MS

224 um samples were collected and analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS

225 analysis methods in this assay are based on liquid chromatography-tandem mass spectrometry (LC-MS/MS

226 ts were extracted, digested, and analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS

227 on solid-phase extraction (SPE) followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS

228 This work reports a liquid chromatography-tandem mass spectrometry (LC-MS/MS

229 on of the structural diversity of glycans by liquid chromatography-tandem mass spectrometry (LC-MS/MS

230 Bioanalysis of polar analytes using liquid chromatography-tandem mass spectrometry (LC-MS/MS

231 ed in the laboratory from Mona Lake water by liquid chromatography-tandem mass spectrometry (LC-MS/MS

232 y quantification of enzymatic products using liquid chromatography-tandem mass spectrometry (LC-MS/MS

233 showed that CobB(L) was acetylated by YiaC; liquid chromatography-tandem mass spectrometry (LC-MS/MS

234 We aimed to develop and validate a liquid chromatography-tandem mass spectrometry (LC-MS/MS

235 ent and sensitive analytical method based on liquid chromatography-tandem mass spectrometry (LC-MS/MS

236 Liquid chromatography-tandem mass spectrometry (LC-MS/MS

237 lts to those from the reference method using liquid chromatography-tandem mass spectrometry (LC-MS/MS

238 Liquid chromatography-tandem mass spectrometry (LC-MS/MS

239 The complex mixture was resolved by liquid chromatography-tandem mass spectrometry (LC-MS/MS

240 e data for JWH-018, obtained via a validated liquid chromatography-tandem mass spectrometry (LC-MS/MS

241 specific lipid classes were identified using liquid chromatography-tandem mass spectrometry (LC-MS/MS

242 in-fixed paraffin-embedded (FFPE) tissues by liquid chromatography-tandem mass spectrometry (LC-MS/MS

243 E) method followed by ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS

244 d naturally contaminated maize samples using liquid chromatography-tandem mass spectrometry (UPLC-MS/

245 bolomics was conducted via ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/

246 secretory solutes in plasma and urine using liquid chromatography-tandem mass spectrometry and measu

247 Weekly DBS TFV-DP was measured by validated liquid chromatography-tandem mass spectrometry assay.

248 High performance liquid chromatography-tandem mass spectrometry coupling

249 eactive donors were tested under blind using liquid chromatography-tandem mass spectrometry for ART.

250 The method uses liquid chromatography-tandem mass spectrometry for measu

251 and proinflammatory eicosanoid levels using liquid chromatography-tandem mass spectrometry in 29 mor

252 The tryptophan metabolome was determined by liquid chromatography-tandem mass spectrometry in milk a

253 Using an optimized targeted liquid chromatography-tandem mass spectrometry measureme

254 Now, a group-specific liquid chromatography-tandem mass spectrometry method wa

255 ladioli and multiplexed into a single, rapid liquid chromatography-tandem mass spectrometry multiple

256 finity selection can be interfaced with nano-liquid chromatography-tandem mass spectrometry peptide s

257 We recently performed urine liquid chromatography-tandem mass spectrometry proteomic

258 Ceramide accumulation determined by liquid chromatography-tandem mass spectrometry was demon

259 od allows for sensitive quantification using liquid chromatography-tandem mass spectrometry with de n

260 spectrometry methods (ultrahigh performance liquid chromatography-tandem mass spectrometry) with bro

261 on, immunoblotting, quantitative RT-PCR, and liquid chromatography-tandem mass spectrometry, we studi

262 arried out by quantitative, online capillary liquid chromatography-tandem mass spectrometry.

263 c analysis using nano ultra-high performance liquid chromatography-tandem mass spectrometry.

264 ecretory solutes at baseline, using targeted liquid chromatography-tandem mass spectrometry.

265 ysis and product formation were monitored by liquid chromatography-tandem mass spectrometry.

266 Here, we performed ultrahigh performance liquid chromatography-tandem mass spectroscopy (UPLC-MS/

267 -labeling sample handling and digestion, the liquid chromatography-tandem MS analysis of the digested

268 e results were validated by high performance liquid chromatography technique.

269 lyzed by C-13 nuclear magnetic resonance and liquid chromatography time-of-flight mass spectrometry.

270 ma samples were analyzed by high-performance liquid chromatography to detect intact tracer and radioa

271 ofluorescence, immunoblots, high-performance liquid chromatography (to measure creatine levels), qRT-

272 s were measured using ultra-high performance liquid chromatography - triple quadrupole tandem mass sp

273 uent analysis by ultrahigh-performance micro-liquid chromatography-triple quadrupole time-of-flight t

274 this method in a fast ultra-high performance liquid chromatography (UHPLC) analysis to integrate wide

275 eversed-phase (C30RP) ultra-high-performance liquid chromatography (UHPLC) coupled to high resolution

276 rrent state-of-the-art in ultrahigh-pressure liquid chromatography (UHPLC) instrumentation.

277 tudy, a reverse-phase ultra-high performance liquid chromatography (UHPLC) method with fluorescence a

278 ation conditions with ultra-high-performance liquid chromatography (UHPLC) method.

279 tides were analyzed by ultrahigh-performance liquid chromatography (UHPLC) multiple-reaction monitori

280 time to extract whereas Ultra High pressure liquid chromatography (UHPLC-DAD) was used to quantify T

281 ive, rugged and safe) extraction step, and a liquid chromatography-ultra violet-fluorescence (HPLC-UV

282 d on SS-MSPME coupling with high-performance liquid chromatography-ultraviolet (HPLC-UV).

283 n denaturing size-exclusion ultraperformance liquid chromatography (UPLC) coupled with intact protein

284 itation of N-glycome using ultra-performance liquid chromatography (UPLC), weak anion exchange-UPLC,

285 ng was measured by affinity high-performance liquid chromatography, whereas the lipophilicity of each

286 amins were determined using high-performance liquid chromatography with a diode array detection.

287 nephrines (R(2) > 0.99) and high-performance liquid chromatography with an electrochemical detection

288 High-performance liquid chromatography with diode array (HPLC-DAD) and li

289 thomyl before analysis by a high-performance liquid chromatography with diode array detection.

290 d side and end products) by high-performance liquid chromatography with diode array detector (HPLC-DA

291 roterenol at each increment were measured by liquid chromatography with electrochemical detection and

292 tured epithelia using ultra-high-performance liquid chromatography with high-resolution mass spectrom

293 st analyses of bispecific antibodies rely on liquid chromatography with mass spectrometry (LC-MS), wh

294 ative status using official methods, gas and liquid chromatography with mass spectrometry and nuclear

295 posure, were measured using high-performance liquid chromatography with mass spectrometry detection f

296 nal methods for urinary HP analysis based on liquid chromatography with native fluorescence detection

297 Liquid chromatography with tandem mass spectrometry was

298 ab samples were analyzed using reverse phase liquid chromatography with tandem mass spectrometry.

299 imultaneously determined by high performance liquid chromatography with ultraviolet detection (HPLC-U

300 This method was integrated into a liquid chromatography workflow and used to evaluate prof