ライフサイエンスコーパス: thin-layer chromatography

1 onjugates with several amino acids, based on thin layer chromatography.

2 mass spectrometry and gave a single band on thin layer chromatography.

3 fluorescence detection or by high efficiency thin layer chromatography.

4 es, membrane phospholipids were separated by thin layer chromatography.

5 high pressure liquid chromatography, and on thin layer chromatography.

6 oradiography of radiolabeled glucosamine and thin layer chromatography.

7 fatty acids and triacylglycerols (TAG) using thin layer chromatography.

8 h triacylglycerol (TAG) levels determined by thin layer chromatography.

9 mass spectrometry, infrared spectrometry and thin layer chromatography.

10 alyzed the lipid composition of the SC using thin-layer chromatography.

11 ct from excess ATP by organic extraction and thin-layer chromatography.

12 the radiochemical yield according to instant thin-layer chromatography.

13 ied by the diacylglycerol kinase assay using thin-layer chromatography.

14 were all more than 90% according to instant thin-layer chromatography.

15 a membrane component that was identified by thin-layer chromatography.

16 istamine from [3H]histidine was assayed with thin-layer chromatography.

17 sess each tracer metabolism by reverse-phase thin-layer chromatography.

18 extracted and phospholipids were obtained by thin-layer chromatography.

19 ching DTBS reactions at pH 4 and isolated by thin-layer chromatography.

20 g reactions with acridonetagged compounds by thin-layer chromatography.

21 , and radiolabeling was monitored by instant thin-layer chromatography.

22 ples using multi-imaging by high-performance thin-layer chromatography.

23 radiochemical yields were monitored by radio-thin-layer chromatography.

24 ques, mass spectrometry, enzyme kinetics and thin-layer chromatography.

25 tative determination of the fast reaction by thin-layer chromatography.

26 new tracers was determined by reversed-phase thin-layer chromatography.

27 was identified by (1)H NMR spectroscopy and thin-layer chromatography.

28 ated from the interfering compounds by micro-thin-layer chromatography.

29 l organic molecules on fluorescent plates in thin-layer chromatography.

30 of enantioenriched secondary alcohols using thin-layer chromatography.

31 nuclear nuclear magnetic resonance and radio thin-layer chromatography.

32 hromatography, mild alkaline hydrolysis, and thin-layer chromatography.

33 xidized, as shown by ultraviolet spectra and thin-layer chromatography.

34 The application of preparative thin layer chromatography-2,2-diphenyl-1-picrylhydrazyl

35 tern blot, immunofluorescent staining, radio-thin-layer chromatography, a malachite green assay, and

36 ed 95% by strip chromatography using instant thin-layer chromatography/acetone and paper/saline.

37 onversion of uridine to Psi was monitored by thin-layer chromatography after digestion to single nucl

38 The active fraction from thin-layer chromatography also contained an unidentified

39 Two-dimensional thin layer chromatography analyses of lipid extracts fro

40 Thin layer chromatography analysis of the hydrolysis rea

41 Thin layer chromatography analysis reveals that T, dihyd

42 ntly increased LPCAT activity as assessed by thin layer chromatography analysis with substrate prefer

43 Thin-layer chromatography analysis indicated that the in

44 Thin-layer chromatography analysis of BODIPY (4,4-difluo

45 lysis products was almost identical based on thin-layer chromatography analysis.

46 Thin layer chromatography and gas chromatography mass sp

47 Thin layer chromatography and lipidomics demonstrated th

48 and progesterone metabolism was analyzed by thin layer chromatography and liquid chromatography-mass

49 tiple lipid products that were identified by thin layer chromatography and mass spectrometry as diacy

50 human serum at 37 C was analyzed using radio-thin layer chromatography and radio-high-performance liq

51 Thin layer chromatography and radioimmunoassays indicate

52 antitation methods such as end labeling with thin layer chromatography and radiolabeling by glycosyla

53 nces, phenolic profiling by high-performance thin layer chromatography and ultra-high-performance liq

54 lands were determined using high performance thin layer chromatography and were found to be broadly s

55 termined their kinetic parameters using both thin-layer chromatography and a recently developed polym

56 itionally, as determined by high-performance thin-layer chromatography and autoradiography, RDEC-1 ad

57 Identities were confirmed by thin-layer chromatography and by derivatization with p-d

58 t of the SerA alpha KG reductase reaction by thin-layer chromatography and by enzyme assays showing t

59 and DRMs were separated by two-dimensional, thin-layer chromatography and converted to methyl esters

60 in-l-sulfoxide were also identified by using thin-layer chromatography and derivatization with p-dime

61 ction of cyclic di-GMP using two-dimensional thin-layer chromatography and found that strains carryin

62 Thin-layer chromatography and gas chromatography-mass sp

63 ant glycopeptidolipids were characterized by thin-layer chromatography and gas chromatography-mass sp

64 Thin-layer chromatography and gas chromatography-mass sp

65 rols and bile acids were further analyzed by thin-layer chromatography and gas-liquid chromatography.

66 The assay is far more rapid than thin-layer chromatography and high-performance liquid ch

67 It was analyzed after 5 min by instant thin-layer chromatography and high-performance liquid ch

68 Thin-layer chromatography and HPAEC-PAD revealed glucose

69 Thin-layer chromatography and HPLC analyses showed high

70 Proteinuric urine was fractionated by thin-layer chromatography and HPLC, and the effects of t

71 desaturation or elongation were monitored by thin-layer chromatography and HPLC.

72 eport for the first time the coupling of the thin-layer chromatography and IMS.

73 omatography and preparative high-performance thin-layer chromatography and its structure unambiguousl

74 eling efficiency was determined with instant thin-layer chromatography and magnetic separation.

75 Using thin-layer chromatography and mass spectrometry, we firs

76 Thin-layer chromatography and mass spectroscopy assays d

77 ized by colony morphology, lipid profile via thin-layer chromatography and matrix-assisted laser deso

78 radiochemical purity, as determined by radio-thin-layer chromatography and radio-high-performance liq

79 f parent (134)Ce-was confirmed through radio-thin-layer chromatography and reverse-phase high-perform

80 Ceramide species were quantified by thin-layer chromatography and scintillography.

81 tions as the test system for the coupling of thin-layer chromatography and SERS (TLC-SERS), which has

82 ys were further purified by high-performance thin-layer chromatography and shown to comigrate with co

83 CAT assays were performed by both thin-layer chromatography and the fluor diffusion method

84 Using both thin-layer chromatography and the periodate-thiobarbitur

85 eparated from other potential metabolites by thin-layer chromatography and visualized under UV light.

86 , and androgen metabolites were separated by thin-layer chromatography and were quantified using a ra

87 Prior separation of gangliosides by thin-layer chromatography and/or high-performance liquid

88 ude reaction mixture (gas chromatography and thin layer chromatography) and a procedure for the isola

89 ecovered by organic extraction, displayed by thin layer chromatography, and quantified by liquid scin

90 atom bombardment-negative ion spectrometry, thin-layer chromatography, and (1)H and (13)C NMR spectr

91 LC high-resolution tandem mass spectrometry, thin-layer chromatography, and gas chromatography-flame

92 l tests, a siderophore utilization bioassay, thin-layer chromatography, and mass spectroscopy indicat

93 d by high-performance liquid chromatography, thin-layer chromatography, and microbiological assays.

94 Quantum-mechanical calculations, thin-layer chromatography, and nuclear magnetic resonanc

95 of Mycobacterium species, analyzed them with thin-layer chromatography, and tested them in a murine f

96 Released BCG lipids were resolved by thin-layer chromatography, and they migrated similarly t

97 nds, termed lipid-1 and lipid-2, migrated on thin-layer chromatography as a doublet.

98 lergic patient sera (n = 39) was assessed by thin-layer chromatography as well as by direct and inhib

99 esterone, as measured by using a radiometric thin-layer chromatography assay, while 5beta-DHP reducti

100 used to study the expression of FAAH, and a thin-layer chromatography-based approach was used to mea

101 Second, we designed a thin-layer chromatography-based assay in which the mobil

102 Active fractions were detected by the thin-layer chromatography-bioautography method and chara

103 m membranes and separated by two-dimensional thin layer chromatography bound human SP-D with high aff

104 Alternative assays have employed thin-layer chromatography, but this procedure is time-co

105 Further analysis of these two species by thin layer chromatography confirmed their identification

106 Thin-layer chromatography confirmed that a dynamic and/o

107 Phosphoamino acid analysis by thin-layer chromatography confirmed that Pkn1 and PknD a

108 This biological analogue of thin layer chromatography consists of arrays of asymmetr

109 Thin-layer chromatography demonstrated an accumulation o

110 Using thin layer chromatography, DETA-NO (100 microM) suppress

111 In contrast to previous published studies, thin-layer chromatography did not support the hypothesis

112 y high-performance liquid chromatography and thin-layer chromatography, disclosed that some of these

113 compounds was performed by high-performance thin-layer chromatography-electrospray ionization mass s

114 analyzed by flow cytometry, high-performance thin-layer chromatography, enzymatic degradation, and MA

115 by CD34(+) cells was not detected by either thin-layer chromatography, enzyme immunoassay, or differ

116 Thin-layer chromatography experiments revealed an enrich

117 lustering approach based on high-performance thin-layer chromatography fingerprints and UHPLC-HRMS da

118 a phospholipid VLSFA levels were measured by thin-layer chromatography followed by gas chromatography

119 hase extraction and centrifugal acceleration thin-layer chromatography, followed by red-green-blue (R

120 separation by normal-phase high-performance thin-layer chromatography, followed by spray detection w

121 ocedure consists of detergent separation via thin-layer chromatography, followed by visualization wit

122 ne (PCOOH) as substrate and high performance thin layer chromatography for quantitative peroxide anal

123 phy steps and, in some cases, time-consuming thin-layer chromatography for purification.

124 GM1 was quantified with thin-layer chromatography for total cellular GM1 and flo

125 Bioassay-guided fractionation paired with thin-layer chromatography, GC-MS, and LC-MS analyses sug

126 thin-layer chromatography, high performance thin-layer chromatography, high performance liquid chrom

127 cts was carried out by paper chromatography, thin-layer chromatography, high performance thin-layer c

128 SMase activity was assessed by quantitative thin-layer chromatography, high-performance liquid chrom

129 s N-(butanoyl)-L-homoserine lactone (BHL) by thin-layer chromatography, high-pressure liquid chromato

130 Using thin-layer chromatography, high-pressure liquid chromato

131 Lipids were identified by high performance thin layer chromatography (HP-TLC) and tandem mass spect

132 f dairy cream, supported by high-performance thin-layer chromatography (HP-TLC) and time-domain nucle

133 al methods or physico-chemical methods (e.g. thin-layer chromatography, HPLC, LC-MS/MS).

134 A high performance thin layer chromatography (HPTLC) method was developed f

135 ingolipids were analyzed by high-performance thin layer chromatography (HPTLC), gas chromatography (G

136 macrocarpon) extracts using high performance thin layer chromatography (HPTLC)-densitometry is presen

137 ter-wettable reversed phase high-performance thin-layer chromatography (HPTLC RP18 W) plates, with de

138 were performed in situ the high-performance thin-layer chromatography (HPTLC) adsorbent.

139 type had an R(f) of 0.62 on high-performance thin-layer chromatography (HPTLC) and a characteristic v

140 In this context, high-performance thin-layer chromatography (HPTLC) coupled with bioassays

141 The procedure comprises high-performance thin-layer chromatography (HPTLC) coupled with six bacte

142 activity were detected via high-performance thin-layer chromatography (HPTLC) in a planar yeast estr

143 samples were analyzed using high-performance thin-layer chromatography (HPTLC) in direct combination

144 High-performance thin-layer chromatography (HPTLC) is an advantageous ana

145 elets by flow cytometry and high-performance thin-layer chromatography (HPTLC) of isolated platelet g

146 rayed onto the surface of a high-performance thin-layer chromatography (HPTLC) plate.

147 hydrocarbons, from TLC and high-performance thin-layer chromatography (HPTLC) plates in MS and MS(2)

148 iance Approach (NMR-HetCA), high-performance thin-layer chromatography (HPTLC), and chemometric techn

149 isolated and identified by high-performance thin-layer chromatography (HPTLC), HPTLC immunostaining,

150 tal samples fractionated by high-performance thin-layer chromatography (HPTLC).

151 these cells was analyzed by high-performance thin-layer chromatography (HPTLC).

152 omplex samples separated by high-performance thin-layer chromatography (HPTLC).

153 ger-containing products via high-performance thin-layer chromatography (HPTLC-UV/Vis/FLD-bioassay).

154 e-transfected CHOP2/1 cells was confirmed by thin-layer chromatography immunostaining using antibodie

155 chromatography, or resorcinol-HC1 spray, but thin-layer chromatography immunostaining with monoclonal

156 By using thin-layer chromatography in conjunction with high-perfo

157 oducts from the cellulose hydrolysis through thin-layer chromatography indicated its endoglucanase ac

158 sis of the products from xylan hydrolysis by thin-layer chromatography indicated its endoxylanase act

159 Thin-layer chromatography is relatively lower cost and p

160 incorporation and purity assays with instant thin-layer chromatography (ITLC) and high-performance li

161 r mobile phases were also applied on instant thin-layer chromatography (ITLC) silica gel plates.

162 rile filtration and quality control (instant thin-layer chromatography (iTLC), HPLC and pH), the radi

163 The carotenoid moiety was identified by thin layer chromatography, light absorption spectroscopy

164 The CAMAG thin-layer chromatography mass spectrometer (TLC-MS) int

165 Thin-layer chromatography, mass spectrometry, and flow c

166 wly developed and validated high performance thin layer chromatography method.

167 and oxidize (14C1)-ascorbate by radiometric thin-layer chromatography method.

168 sh a fast, sensitive HPTLC (high-performance thin-layer chromatography) method that would allow the d

169 we have designated as multi-one-dimensional thin-layer chromatography (MOD-TLC).

170 Using thin-layer chromatography, MS, NMR, and complementation

171 profiling was developed by high-performance thin-layer chromatography multi-imaging (HPTLC-FLD/Vis).

172 terface (after normal-phase high-performance thin-layer chromatography-multi-imaging-bioassay, NP-HPT

173 y taken up was identified as 3H-histamine by thin layer chromatography; no metabolites were detected,

174 Detailed analyses by thin-layer chromatography, nuclear magnetic resonance (N

175 Previous studies using thin layer chromatography of (32)P-postlabeled DNA diges

176 Two-dimensional thin layer chromatography of nucleotide extracts confirm

177 These layers were used for two-dimensional thin layer chromatography of peptides.

178 Thin layer chromatography of the nucleotide sugars in th

179 Two-dimensional thin-layer chromatography of alkaline-hydrolyzed E-32P s

180 s confirmed by hydroxylamine cleavage and by thin-layer chromatography of the liberated fatty acid.

181 Thin-layer chromatography of the methanol-extracted C. g

182 Thin-layer chromatography of whole blood identified a sp

183 in either cell line by glycolipid isolation, thin-layer chromatography, or resorcinol-HC1 spray, but

184 bands recognized by 987P fimbrial probes in thin-layer chromatography overlay assays were further pu

185 electin binding under static conditions with thin-layer chromatography overlay technique employing 32

186 tting the solution onto a C18 reversed-phase thin-layer chromatography plate.

187 I-HIS and PCG with PVA hydrogel films and on thin layer chromatography plates demonstrated the practi

188 h the treatment of wettable high-performance thin layer chromatography plates, post-plate development

189 tion of aniline on precoated aluminum-backed thin-layer chromatography plates and Whatman filter pape

190 y emitter was used for the direct readout of thin-layer chromatography plates by electrospray mass sp

191 al tissues as determined using toxin overlay thin-layer chromatography plates was below the limit of

192 nalytes directly from developed normal-phase thin-layer chromatography plates.

193 sing an Objet Eden 260VS 3D printer, polymer thin layer chromatography platforms were directly fabric

194 A picoliter thin-layer chromatography (pTLC) platform was developed

195 , required time-consuming derivatization and thin-layer chromatography purification.

196 ors by flow cytometry, Western blotting, and thin layer chromatography relative to donor age, sex, A1

197 as determined by absorbance at 265 nm and by thin-layer chromatography, respectively.

198 iatal DAT phosphopeptides by two-dimensional thin layer chromatography revealed basal and PKC-stimula

199 Thin layer chromatography revealed that major outer memb

200 Analysis by thin layer chromatography revealed that reactive chlorin

201 is of erythrocyte phospholipid metabolism by thin-layer chromatography revealed significant hydrolysi

202 e chemical form of the stably bound (32)P by thin-layer chromatography revealed that it was all (32)P

203 Furthermore, thin-layer chromatography revealed that McaP cleaves bot

204 In all cases, reverse-phase thin layer chromatography (RP-TLC) coupled with phosphor

205 surface (all-in-one), their high-performance thin-layer chromatography separation and detection via s

206 High performance thin-layer chromatography showed numerous changes in gan

207 Analysis by thin-layer chromatography showed rapid transformation of

208 Thin-layer chromatography showed that the product of alp

209 ls similar to untreated neurons, even though thin layer chromatography shows a greater than 90% inhib

210 ic reaction products of SAT-3 and SAT-4 with thin-layer chromatography, sialidase treatment, and bind

211 he need for analysis of the lipid product by thin-layer chromatography since ceramide-1-phosphate is

212 nding by lectin staining on high-performance thin layer chromatography (solid-phase binding assay).

213 Data obtained using thin-layer chromatography, spectrophotometry, mass spect

214 analysed by RPLC-GC, avoiding the laborious thin layer chromatography step used in the Official Euro

215 he coupling of a rotation planar preparative thin-layer chromatography system on-line with mass spect

216 Using polyethyleneimine-cellulose thin layer chromatography, the guanine nucleotides that

217 Following purification by anion exchange and thin layer chromatography, the major component was shown

218 After the separation of phospholipids by thin-layer chromatography, the 3H activity was determine

219 Initial thin layer chromatography (TLC) analysis indicated that

220 ds for assaying the crude reaction mixtures (thin layer chromatography (TLC) and gas chromatography (

221 s between endogenous levels of polyamines by thin layer chromatography (TLC) and gas chromatography (

222 Thin layer chromatography (TLC) and phytochemical analys

223 material and were efficiently substituted by thin layer chromatography (TLC) grade silica.

224 This study explores the effectiveness of thin layer chromatography (TLC) in combination with bioa

225 Analysis of saponins by thin layer chromatography (TLC) is reported.

226 ional assay for measuring DGAT activity is a thin layer chromatography (TLC) method, which is not ame

227 olerae, the causative agent of cholera, to a thin layer chromatography (TLC) plate containing mouse i

228 SPOT colorimetric or fluorometric assay on a thin layer chromatography (TLC) plate.

229 as well as in the solid state, sprayed onto thin layer chromatography (TLC) plates (alox, silica gel

230 Fractionation of lipid components of LDL by thin layer chromatography (TLC) revealed that the bioact

231 The method combines thin layer chromatography (TLC) to solid surface room-te

232 Interfacing thin layer chromatography (TLC) with ambient mass spectr

233 Thin layer chromatography (TLC), Fourier transform infra

234 gh-performance liquid chromatography (HPLC), thin layer chromatography (TLC), mass spectrometry (MS),

235 soft drinks using C18 SPE and identified by thin layer chromatography (TLC), this method was used to

236 enables relative quantification by indirect thin layer chromatography (TLC)-MALDI-time-of-flight (TO

237 nion exchange chromatography and preparative thin layer chromatography (TLC).

238 Thin-Layer Chromatography (TLC) analysis showed adultera

239 adduct, GS-TFB-F, is separated from PFB-F by thin-layer chromatography (TLC) and can be quantitated b

240 from the mutant strain were identified with thin-layer chromatography (TLC) and high-performance liq

241 drolyzed urine samples were then analyzed by thin-layer chromatography (TLC) and high-performance liq

242 ppropriate method for the direct coupling of thin-layer chromatography (TLC) and mass spectrometry (M

243 The protocol describes both thin-layer chromatography (TLC) and microtiter plate ass

244 In addition, thin-layer chromatography (TLC) can be used to identify

245 Thin-layer chromatography (TLC) hyphenated to bioassays

246 p to 48 reactions has been developed using a thin-layer chromatography (TLC) imaging method.

247 surface enhanced Raman scattering (SERS) and thin-layer chromatography (TLC) is presented that employ

248 Thin-layer chromatography (TLC) is widely used for food

249 Thin-layer chromatography (TLC) of lipids extracted from

250 ith phospholipase C, (3) subsequent multiple thin-layer chromatography (TLC) overlay detection of ind

251 e 3H labeled and overlaid on two-dimensional thin-layer chromatography (TLC) plates containing either

252 rmore, receptor 1-based low-cost fluorescent thin-layer chromatography (TLC) plates were developed fo

253 lipid classes were separated by a multistep thin-layer chromatography (TLC) procedure in different s

254 Thin-layer chromatography (TLC) showed that rGidA contai

255 The thin-layer chromatography (TLC) strip sensor of Q5 was a

256 Thin-layer chromatography (TLC) using radiolabeled phosp

257 elopment of an analytical platform utilizing thin-layer chromatography (TLC) with colorimetric read-o

258 (DESI) was demonstrated as a means to couple thin-layer chromatography (TLC) with mass spectrometry.

259 ion of arginine and citrulline on silica gel thin-layer chromatography (TLC) with the specified buffe

260 ving the analysis of dye-labeled strands via thin-layer chromatography (TLC), and in the solid state

261 xchange column were further characterized by thin-layer chromatography (TLC), glycosidase digestions,

262 hromatography [LC] gas chromatography [GC]), thin-layer chromatography (TLC), high-performance liquid

263 re the first separation of metal clusters by thin-layer chromatography (TLC), which is simple yet sur

264 Thin-layer chromatography (TLC), which is widely used fo

265 ng of (68)Ga as well as the development of a thin-layer chromatography (TLC)-based quality control sy

266 Direct sampling by thin-layer chromatography (TLC)-ESI-MS provides a powerf

267 iquid (IL)-stabilized, nanomatrix-decorated, thin-layer chromatography (TLC)-MALDI MS method for simu

268 ial cells of the cell line A549 separated by thin-layer chromatography (TLC).

269 e purification by solid-phase extraction and thin-layer chromatography (TLC).

270 le, rapid, and inexpensive and is similar to thin-layer chromatography (TLC; for solution-phase chemi

271 benzylguanine derivative in conjunction with thin layer chromatography to eliminate the use of radioa

272 We used two-dimensional thin-layer chromatography to measure the relative concen

273 s of Cx50 phosphorylation by two-dimensional thin layer chromatography tryptic phosphopeptide profile

274 ensional double-development high-performance thin-layer chromatography (UDDD-HPTLC) method was develo

275 rformed on polyacrylonitrile nanofiber ultra-thin-layer chromatography (UTLC) plates in 1-2 min using

276 Thin-layer chromatography was performed on 89I LA produc

277 In vitro, thin-layer chromatography was performed to evaluate the

278 Thin-layer chromatography was used to detect (p)ppGpp ex

279 esolution cation-exchange chromatography and thin layer chromatography, we demonstrate that neither l

280 Using thin-layer chromatography, we found that MbtK, a conserv

281 on, reversed-phase C(18) chromatography, and thin-layer chromatography, we have purified an extracell

282 ipids, individually isolated and purified by thin-layer chromatography, were elucidated and quantifie

283 In contrast to two-dimensional thin-layer chromatography, which allows for good resolut

284 hOX) by means of silica gel high-performance thin layer chromatography with phosphorimaging detection

285 for these signals that couples separation by thin-layer chromatography with detection using Agrobacte

286 l medium was investigated by immunoblotting, thin-layer chromatography with immunostaining and ELISA,

287 er extract was detected by immunostaining of thin-layer chromatography with monoclonal antibody 5F5,

288 spectively) at 37 degrees C was monitored by thin-layer chromatography with phosphorimaging radiodete

289 thesis that the coupling of high-performance thin-layer chromatography with the yeast estrogen screen