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

4 fluorescence detection or by high efficiency thin layer chromatography.

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

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

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

8 mass spectrometry, infrared spectrometry and thin layer chromatography.

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

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

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

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

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

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

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

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

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

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

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

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

21 of enantioenriched secondary alcohols using thin-layer chromatography.

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

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

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

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

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

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

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

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

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

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

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

33 Thin layer chromatography analysis of the hydrolysis rea

34 Thin layer chromatography analysis reveals that T, dihyd

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

36 Thin-layer chromatography analysis indicated that the in

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

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

39 Thin layer chromatography and gas chromatography mass sp

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

41 Thin layer chromatography and radioimmunoassays indicate

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

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

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

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

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

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

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

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

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

51 Thin-layer chromatography and gas chromatography-mass sp

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

53 Thin-layer chromatography and gas chromatography-mass sp

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

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

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

57 Thin-layer chromatography and HPAEC-PAD revealed glucose

58 Thin-layer chromatography and HPLC analyses showed high

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

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

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

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

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

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

65 Thin-layer chromatography and mass spectroscopy assays d

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

92 Thin-layer chromatography demonstrated an accumulation o

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

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

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

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

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

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

99 Thin-layer chromatography experiments revealed an enrich

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 Two-dimensional thin layer chromatography of nucleotide extracts confirm

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

143 Thin layer chromatography of the nucleotide sugars in th

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

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

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

147 Thin-layer chromatography of whole blood identified a sp

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

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

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

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

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

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

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

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

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

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

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

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

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

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

162 Thin layer chromatography revealed that major outer memb

163 Analysis by thin layer chromatography revealed that reactive chlorin

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

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

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

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

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

169 Analysis by thin-layer chromatography showed rapid transformation of

170 Thin-layer chromatography showed that the product of alp

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

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

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

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

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

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

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

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

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

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

181 Initial thin layer chromatography (TLC) analysis indicated that

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

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

184 Thin layer chromatography (TLC) and phytochemical analys

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

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

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

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

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

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

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

192 Thin layer chromatography (TLC), Fourier transform infra

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

208 Thin-layer chromatography (TLC) using radiolabeled phosp

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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