ライフサイエンスコーパス: TLC

1 TLC analysis of (14)C-labeled bile acids synthesized in

2 TLC analysis of phospholipid showed altered profiles upo

3 TLC analysis of reaction products revealed the presence

4 TLC and HPLC analysis of the incubation mixture of these

5 TLC and phorbol myristate acetate increased cytosolic pM

6 TLC failed to increase MARCKS phosphorylation in HuH-NTC

7 TLC increased PM-PKC and decreased PM-MRP2 in both HuH-N

8 TLC studies of the extracted polyphenols from kodo mille

9 TLC was used to detect Gb(3) in tissues from a newborn c

10 TLC, BMI, and hemoglobin had a limited predictive value,

11 TLC, but not cAMP, increased MARCKS phosphorylation in H

12 TLC-S induced global calcium oscillations and extended c

13 TLC-S-induced calcium signals were not inhibited by atro

14 TLC/DAPPI-MS was applied for lipids of vernix caseosa, a

15 t lung (RV = 6.6 +/- 2.4, FRC = 6.1 +/- 2.1, TLC = 6.4 +/- 2.6; P = 0.51).

16 VA increased significantly, but only to 20% TLC (p < 0.05).

17 mental results from NMR spectroscopy, GC, 3D-TLC as well as proximate analysis permitted the observed

18 regulatory network are expressed in the A7.6/TLC lineage.

19 alveolar recruitment as VL increased to 80% TLC (p < 0.05).

20 ediate (RV = 8.9 +/- 3.1, FRC = 8.1 +/- 2.9, TLC = 7.4 +/- 3.6; P = 0.26) and dependent lung (RV = 6.

21 A TLC method was developed to allow for rapid and inexpens

22 A TLC-densitometric assay was developed and validated for

23 During a TLC-AMS analysis, the TLC plate was sent to the conveyer

24 ined spot sampling from separated bands on a TLC plate (one or multiple spots), scanning of a complet

25 on of the test analytes was carried out on a TLC plate followed by blotting and the acquisition of di

26 ernal solution) pool of mercury to produce a TLC.

27 antitation of the product L-[14C]Asp using a TLC system.

28 rest were confirmed by eluting zones using a TLC-MS interface.

29 hearing, is also controlled by an additional TLC mechanism.

30 After TLC separation, the plate is rotated 90 degrees and the

31 ng lipids and their oxidation products after TLC separation allowed assignment of the native unsatura

32 he resulting sensor solution onto an alumina TLC plate.

33 etween FEV(1) and FVC (r = 0.81), FEV(1) and TLC (r = 0.61), and FVC and TLC (r = 0.80), and a lack o

34 , FRC (45.4 +/- 18.5 to 62.1 +/- 15.3%), and TLC (84.8 +/- 15.0 to 103.1 +/- 15.3%), whereas patients

35 for automated analysis of lipid extracts and TLC eluates and suggests that indirect high-performace (

36 ight lung during breath-holds at RV, FRC and TLC.

37 as present at residual volume (RV), FRC, and TLC in all subjects.

38 .81), FEV(1) and TLC (r = 0.61), and FVC and TLC (r = 0.80), and a lack of correlation between FEV(1)

39 assaying the crude reaction mixture (GC and TLC) and a procedure for the isolation, purification and

40 y combinations of cation exchange, HPLC, and TLC, and the fractions were assayed for biological activ

41 ivated cell sorting, immunofluorescence, and TLC assays demonstrated that both CD39 protein expressio

42 = 0.68 +/- 0.23 L, FVC = 2.56 +/- 7.3 L, and TLC = 143 +/- 22% predicted).

43 TC and TLC feeding increased proliferation of large cholangiocy

44 We evaluated if TC and TLC induction of ABAT expression was dependent on activa

45 TC and TLC stimulate proliferation of small and large cholangio

46 Antioxidant TLC assay-guided isolation on the methanol extract led t

47 capacity [TLC]; -1.55 g/L per year [0.24] at TLC plus functional residual capacity [FRC]; and -1.60 g

48 [0.27] at TLC; -2.16 g/L per year [0.26] at TLC plus FRC, and -2.05 g/L per year [0.28] at FRC).

49 ed-start group (-2.26 g/L per year [0.27] at TLC; -2.16 g/L per year [0.26] at TLC plus FRC, and -2.0

50 Measurement of lung density with CT at TLC alone provides evidence that purified A1PI augmentat

51 However, at TLC perfusion was significantly lower in non-dependent l

52 tor computed tomography less than -950 HU at TLC.

53 ragm length, we measured diaphragm length at TLC, using plain chest roentgenograms (CXRs), in 25 pati

54 ver, the annual rate of lung density loss at TLC alone was significantly less in patients in the A1PI

55 The annual rate of lung density loss at TLC and FRC combined did not differ between groups (A1PI

56 ry (HPTLC-ESI-MS) via the elution-head-based TLC-MS Interface.

57 s combined, proton signal difference between TLC total lung capacity and RV residual volume correlate

58 BMI, TLC, and hemoglobin were each associated with but poorly

59 Further analysis by TLC, MS, and NMR verified the active HPLC fraction as al

60 in N18 and C6 control cells when analyzed by TLC.

61 activity in parental and resistant cells by TLC.

62 Gb(3) was detected by TLC in kidney and brain, but not in the gastrointestinal

63 high-temperature annealing is determined by TLC.

64 validated by TR4 binding assays followed by TLC and nuclear magnetic resonance.

65 arated by methanol precipitation followed by TLC.

66 the YopT cleavage products of Rho GTPases by TLC and determined their chemical structure by MS.

67 ed PKC-mediated phosphorylation of MARCKS by TLC.

68 The levels of free polyamines obtained by TLC were higher in organic vegetables.

69 nes contents compared with those obtained by TLC.

70 as identified as phosphatidylcholine (PC) by TLC using alkali treatment, molybdenum blue staining, an

71 Assessment of purified preparations by TLC reveal that UCP1 retains tightly bound cardiolipin,

72 Global calcium signals, produced by TLC-S application, displayed vectorial apical-to-basal p

73 y and scanning densitometry, and resolved by TLC and HPLC with subpicomole detection.

74 vent extracted for metabolites, separated by TLC and quantified using radioisotope scanning.

75 t approach for detecting lipids separated by TLC.

76 ce and absence of photooxidizer was shown by TLC to proceed as follows: SQ-->SQ-[OOH]+SQ epoxide.

77 ucts (1a,b) matched the natural substance by TLC or (1)H NMR spectroscopic analysis, suggesting one o

78 nance spectroscopic analyses supplemented by TLC-MS analyses of derived neoglycolipids.

79 calcium signals could still be triggered by TLC-S in a calcium-free external solution.

80 ple development lanes on a reversed-phase C8 TLC plate and by imaging inked lettering on a paper surf

81 reasing residual volume/total lung capacity (TLC) (P = 0.02) and % predicted residual volume/TLC (P =

82 were CT lung density at total lung capacity (TLC) and functional residual capacity (FRC) combined, an

83 sidual volume (RV), and total lung capacity (TLC) were determined at baseline and at 6 months.

84 ital capacity (FVC) and total lung capacity (TLC) were measured.

85 n the dependent 4 cm at total lung capacity (TLC), affects the dependent 11 cm at functional residual

86 o, residual volume (RV)/total lung capacity (TLC), AHR, and Scond values significantly improved.

87 transplant FEV(1), FVC, total lung capacity (TLC), diffusing capacity of carbon monoxide (DL(CO)), an

88 espite a well-preserved total lung capacity (TLC).

89 C+1 L 1 L above FRC ], total lung capacity [ TLC total lung capacity ]) with breath holds of 10-11 se

90 capacity and -950 HU at total lung capacity [TLC]).

91 L per year [SE 0.25] at total lung capacity [TLC]; -1.55 g/L per year [0.24] at TLC plus functional r

92 and amperometry at a custom thin-layer cell (TLC) detector.

93 nanometer-sized cylindrical thin layer cell (TLC) formed by etching the surface of a disk-type platin

94 ells, the precursors of trunk lateral cells (TLC), one of the three types of migratory mesenchymal ce

95 ime were determined by hydrolysis and chiral TLC separations, allowing for the clear conclusion that

96 II) have been determined by chromatographic (TLC, GLC, and HPLC) and spectral (UV, MS, and 1H NMR) me

97 lysis of saffron thin layer chromatographic (TLC) patterns was introduced.

98 Initial thin layer chromatography (TLC) analysis indicated that phosphatidylethanolamine (P

99 eaction mixtures (thin layer chromatography (TLC) and gas chromatography (GC)) and procedures for the

100 of polyamines by thin layer chromatography (TLC) and gas chromatography (GC), nitrate and response t

101 e identified with thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC),

102 then analyzed by thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC).

103 irect coupling of thin-layer chromatography (TLC) and mass spectrometry (MS).

104 ol describes both thin-layer chromatography (TLC) and microtiter plate assays, which use bioluminesce

105 Thin layer chromatography (TLC) and phytochemical analysis were used to compare the

106 ly substituted by thin layer chromatography (TLC) grade silica.

107 tering (SERS) and thin-layer chromatography (TLC) is presented that employs silver-polymer nanocompos

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

109 GAT activity is a thin layer chromatography (TLC) method, which is not amenable to screening a large

110 bsequent multiple thin-layer chromatography (TLC) overlay detection of individual GSLs with a mixture

111 of cholera, to a thin layer chromatography (TLC) plate containing mouse intestinal extracts, we foun

112 ate, sprayed onto thin layer chromatography (TLC) plates (alox, silica gel, reversed phase silica gel

113 ponents of LDL by thin layer chromatography (TLC) revealed that the bioactive component of LDL comigr

114 Thin-layer chromatography (TLC) showed that rGidA contains an FAD cofactor.

115 Interfacing thin layer chromatography (TLC) with ambient mass spectrometry (AMS) has been an im

116 a means to couple thin-layer chromatography (TLC) with mass spectrometry.

117 ine on silica gel thin-layer chromatography (TLC) with the specified buffer system.

118 beled strands via thin-layer chromatography (TLC), and in the solid state by X-ray crystallographic a

119 Thin layer chromatography (TLC), Fourier transform infrared (FTIR) analysis, and me

120 matography [GC]), thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC), Wes

121 atography (HPLC), thin layer chromatography (TLC), mass spectrometry (MS), nuclear magnetic resonance

122 and identified by thin layer chromatography (TLC), this method was used to confirm the composition of

123 metal clusters by thin-layer chromatography (TLC), which is simple yet surprisingly efficient.

124 Thin-layer chromatography (TLC), which is widely used for separation of glycolipids

125 development of a thin-layer chromatography (TLC)-based quality control system.

126 irect sampling by thin-layer chromatography (TLC)-ESI-MS provides a powerful approach to elucidate de

127 ation by indirect thin layer chromatography (TLC)-MALDI-time-of-flight (TOF)-MS against an internal b

128 A549 separated by thin-layer chromatography (TLC).

129 se extraction and thin-layer chromatography (TLC).

130 and is similar to thin-layer chromatography (TLC; for solution-phase chemistry) in its potential for

131 r or high-performance liquid chromatography (TLC or HPLC) analysis and specific in vitro phosphorylat

132 PPEC retains the advantages of classical TLC but has the ability to separate a substantially high

133 PPEC is more efficient than classical TLC.

134 alkaloid analysis employed silica gel-coated TLC plates, mobile phase composed of chloroform:methanol

135 Commercial TLC plates were used and no post-separation processing o

136 s insignificant and trap-limited conduction (TLC) dominates.

137 nations called targeted layered containment (TLC) of influenza antiviral treatment and prophylaxis an

138 ation by PPEC is faster than by conventional TLC, and an example is presented of a 24-fold enhancemen

139 the values determined with the conventional TLC assay.

140 8) adjusting for age, Total Leukocyte count (TLC) and pretreatment levels of ALT, irrespective of liv

141 type 1 (HIV-1) load, total lymphocyte count (TLC), body mass index (BMI), and hemoglobin measured at

142 marked lymphopenia (total lymphocyte count [TLC] </=1200 cells/muL).

143 This transgranular liquation cracking (TLC) occurs at very low contact stresses (between 1.1 an

144 e x wavenumber x intensity three-dimensional TLC-SERS plots.

145 rmation was detected by gel electrophoresis, TLC analysis, and mass spectrometry.

146 All of the mAbs were useful for ELISA, TLC immunooverlay, and immunocytochemistry.

147 ied using a phosphor-imager system following TLC separation.

148 ycosphingolipid was readily demonstrated for TLC/ESI-MS and 20 pmol for TLC/ESI-MS/MS production scan

149 demonstrated for TLC/ESI-MS and 20 pmol for TLC/ESI-MS/MS production scanning to derive the sacchari

150 ce, fragile glycolipids can be desorbed from TLC plates without fragmentation, even to the point that

151 nment of structures to lipids extracted from TLC plates because of artifactual oxidation after the pl

152 , cholesteryl esters, and hydrocarbons, from TLC and high-performance thin-layer chromatography (HPTL

153 rmal blotting, analytes are transferred from TLC plates to nanocomposite films before being imaged vi

154 When fabricated within silica gel TLC plate, the fluo-spot sensor features high sensitivit

155 hnique is comparable with that of silica gel TLC.

156 itioning control software package (HandsFree TLC/MS) were used to enable the automated sampling and i

157 ncept and the associated software (HandsFree TLC/MS) were developed to control the surface sampling p

158 However, TLC can be coupled to an external ion source MALDI-Fouri

159 d suggests that indirect high-performace (HP)TLC-MALDI-TOF-MS with automated data acquisition is a vi

160 gh performance thin layer chromatography (HP-TLC) and tandem mass spectrometry (MS/MS) analysis, with

161 The method makes use of a hybrid TLC-MALDI plate in which a silica layer and a MALDI laye

162 or suspected liver disease, particularly if TLC is <1200 cells/muL.

163 Importantly, TLC even enabled the challenging separation of a multico

164 lted in statistically significant changes in TLC.

165 ed with significant and similar decreases in TLC and residual volume (RV).

166 ough this may result in a minor reduction in TLC resolution.

167 ed directly with postoperative reductions in TLC and RV, and also with increases in transdiaphragmati

168 eline variables predictive of death included TLC, fibrosis, skewness, and kurtosis.

169 ith relative quantities obtained by indirect TLC-MALDI-TOF-MS.

170 ion of analytes in bands separated on intact TLC plates (up to 10 cmx10 cm).

171 sis that TLC-induced MRP2 retrieval involves TLC-mediated activation of PKC followed by MARCKS phosph

172 ion, and air trapping (FEV1, 0.73 +/- 0.2 L; TLC, 7.3 +/- 1.6 L; residual volume [RV], 4.8 +/- 1.4 L)

173 tive in ATP synthesis as shown by dual-label TLC and bioluminescence assays.

174 gh-performance liquid (HPLC) and thin-layer (TLC) chromatographic methods for the detection and quant

175 bility with purification methods such as LC, TLC and HPLC; (ii) for the rapid identification and quan

176 the limits of scan speed, detection levels, TLC phase, and eluting solvents were investigated and di

177 r fluorescence and can be stored for on-line TLC/ESI-MS analysis at a later stage without reduction i

178 ected with phosphorylation-deficient MARCKS, TLC failed to increase MARCKS phosphorylation or decreas

179 The main advantages of the new micro-TLC assay are (i) low cost, (ii) multiple measurements,

180 OPLC instrumentation include use of narrower TLC plate dimensions and refined design of the eluate ex

181 lation pressure-volume (PV) curves from near TLC to FRC in 49 healthy, sedated, spontaneously breathi

182 A new TLC-MALDI direct coupling method which recovers approxim

183 standards separated using normal-phase (NP)-TLC and NP-HPTLC were established.

184 ory airflow at 80% of TLC, and 55% at 70% of TLC.

185 tion in maximal expiratory airflow at 80% of TLC, and 55% at 70% of TLC.

186 nly partially protects against the action of TLC when added at the same time, but it too is able to p

187 rt an additive effect in the amelioration of TLC-induced cholestasis in isolated rat hepatocyte coupl

188 Finally, combined application of TLC-S and the inflammatory mediator bradykinin caused mo

189 The median number of treatment cycles of TLC D-99 was three (range, one to 10 cycles), and the me

190 The poor limit of detection of TLC is overcome by coupling with SERS, and dyes which co

191 (P = .007) and the total cumulative dose of TLC D-99 (P = .032).

192 es), and the median total cumulative dose of TLC D-99 was 405 mg/m2 (range, 135 to 1,065 mg/m2).

193 In women, EELV (% of TLC) also increased with aging, the senior and elderly s

194 The effect of TLC may be mediated via protein kinase C (PKC).

195 herapeutic benefit to the dose escalation of TLC D-99 in this study.

196 examined by comparing the spatial extent of TLC-spotted Rh6G via fluorescence and then the SERS-base

197 Initial preconditioning of TLC plates is necessary to achieve high sensitivity dete

198 bly attributable to the dose and schedule of TLC D-99 used in this trial, as well as the patient's li

199 ate was sent to the conveyer from a stack of TLC plates placed in the storage box.

200 culture supernatants are chromatographed on TLC plates, which are dried and overlaid with the AHQ bi

201 g and imaging of rhodamine dyes separated on TLC plates were used to illustrate some of the practical

202 series of image pre-processing techniques on TLC images such as compression, inversion, elimination o

203 re were no significant differences in FRC or TLC at baseline.

204 direct linking of a commercial overpressure TLC instrument, OPLC 50, and a Q-TOF mass spectrometer.

205 ow rate (Vmax) depends on preoperative Gu, P TLC, Ptm', and on changes (delta) in these parameters af

206 omatography and preparative high performance TLC and were shown to include at least 5 species.

207 oblastomas were analyzed by high-performance TLC.

208 In cleavage arrested embryos, HNK-1 positive TLC were present on the lateral margins of the neural pl

209 (r = -0.65, P <.001), and percent predicted TLC (r = 0.34, P <.04).

210 ied by liquid chromatography and preparative TLC.

211 ms-PI(3,5)P2 products were detected by radio-TLC analysis.

212 direct comparison with synthetic 2 by radio-TLC-phosphorimaging and LC-ESI(+)-MS-MS.

213 For radio-TLC quality control, various mobile phases were analyzed

214 The new radio-TLC method allows quality control in a short time using

215 ynthetic 3a and 3b by a combination of radio-TLC-phosphorimaging and LC-ESI(-)-MS-MS, as well as chir

216 P cells, dominant-negative (DN) PKC reversed TLC-induced decreases in PM-MRP2 without affecting cAMP-

217 reverse-phase thin layer chromatography (RP-TLC) coupled with phosphorimaging quantified the reactio

218 g function testing (FEV1, FVC, FEV1/FVC, RV, TLC, DLCO, and KCO) and measurement of exhaled nitric ox

219 residual volume to total lung capacity (RV/ TLC) (r = 0.66, p < 0.05) and exhaled CO (r = 0.65, p <

220 noxide (DLCO) (r = -0.47; p = 0.008), and RV/TLC (r = 0.41; p = 0.02).

221 RV and RV/TLC improved at 6 months.

222 The slope between quantitative CT and RV/TLC% was significantly (P =.044) more negative in patien

223 eated patients and correlates with CO and RV/TLC; therefore, it may be a useful noninvasive marker of

224 f residual volume to total lung capacity (RV/TLC%) (r = -0.65, P <.001), and percent predicted TLC (r

225 er a residual volume/total lung capacity (RV/TLC) above the upper limit of normal (RV-HI) or a functi

226 Residual volume/total lung capacity (RV/TLC) ratio decreased at 6 months and remained unchanged

227 However, RV/TLC was not predictive of the increase in FEV(1) among t

228 )/FVC in patients with a low preoperative RV/TLC often increased despite little change in FVC.

229 monocytes predicted residual volume (RV), RV/TLC ratio, and FRC, after adjusting for HDL, but not aft

230 rd preoperative pulmonary function tests, RV/TLC again was found to correlate with the increase in FV

231 The model suggests that RV/TLC is an important predictor of improvement in FVC and

232 Using stepwise regression, we found that RV/TLC was the only preoperative independent predictor of t

233 del of emphysema, the ratio of RV to TLC (RV/TLC) reflects the size mismatch between the hyperinflate

234 e as a proportion of total lung capacity (RV:TLC) did not change in either group.

235 obtain the chemical fingerprints of saffron TLC images.

236 fect, as a cultivation parameter, on saffron TLC patterns.

237 individual neutral GSLs in one and the same TLC run and their structural characterization in crude l

238 Finally, the separated TLC spots were chemically identified using high-performa

239 pling of thin-layer chromatography and SERS (TLC-SERS), which has been used in the current research t

240 cation of different amines on regular silica TLC plates via color changes, analyzed by a statistical

241 Pseudomonas sp. TLC 6-6.5-4 is a free-living multiple-metal-resistant pl

242 thin-layer chromatography mass spectrometer (TLC-MS) interface has been assessed as a tool for the di

243 paration and electrospray mass spectrometry (TLC/ESI-MS) has been accomplished by direct linking of a

244 nchymal transition, using mass spectrometry, TLC immunostaining, and cell staining.

245 With increasing strain, TLC continues to refine the size of the microstructure u

246 n contrast, taurolithocholic acid 3-sulfate (TLC-S), known to induce Ca(2+) oscillations in acinar ce

247 bile acid, taurolithocholic acid 3-sulfate (TLC-S), on calcium signalling in pancreatic acinar cells

248 Taurolithocholate (TLC) acutely inhibits the biliary excretion of multidrug

249 he monohydroxy bile acid, taurolithocholate (TLC), causes cholestasis in vivo and in isolated perfuse

250 sm, taurocholate (TC) and taurolithocholate (TLC) increase cholangiocyte proliferation.

251 cholangiocytes from rats fed for 1 week TC, TLC, or BA control diet and determined PCNA and ABAT exp

252 rosis in both stellate and acinar cells than TLC-S alone.

253 illations (but at higher concentrations than TLC-S).

254 resent study was to test the hypothesis that TLC-induced MRP2 retrieval involves PKC-mediated MARCKS

255 r, these results support the hypothesis that TLC-induced MRP2 retrieval involves TLC-mediated activat

256 The TLC determinations were similarly made using Merck NH2 F

257 The TLC plate delivery system consists of a storage box, pla

258 During a TLC-AMS analysis, the TLC plate was sent to the conveyer from a stack of TLC p

259 a special solvent tank was designed and the TLC strip was mounted horizontally where the solvent wou

260 As the TLC plate passed through the ELDI source, the chemical c

261 ry DESI emitter charged droplet plume at the TLC plate surface.

262 A very small funnel right below the TLC tip collected the solvent and transferred it to a ne

263 ing blocks to deal, deliver, and collect the TLC plate through an electrospray-assisted laser desorpt

264 t, the use of building blocks to develop the TLC-AMS interface is undoubtedly a green methodology.

265 within 5 min, in contrast to 20 min for the TLC system.

266 d that included direct electrospray from the TLC strip tip, indirect electrospray from a needle conne

267 The number of redox molecules in the TLC could be varied between one and a few hundred by cha

268 dentification of one of the alkaloids in the TLC literature.

269 Development lanes were scanned by moving the TLC plate under computer control while directing the sta

270 e quantitated by radiometric scanning of the TLC plate or by counting in a scintillation counter.

271 method, particularly the substitution of the TLC step common to other methods with HPLC, results in a

272 al resolution due to the irregularity of the TLC surface.

273 was designed to host the pieces cut off the TLC.

274 ccessfully used to identify each spot on the TLC by IMS in a few seconds.

275 alysis of immunostained GSLs directly on the TLC plate using infrared matrix-assisted laser desorptio

276 Detection of saponins on the TLC plates after development and air-drying was done by

277 ent development, separated components on the TLC plates can be detected in the conventional way by no

278 of building blocks to construct and test the TLC-MS interfacing system.

279 ssessment, it has been demonstrated that the TLC-MS interface has the potential to be an effective to

280 in gangliosides are separated using TLC; the TLC plates are attached directly to the MALDI target, wh

281 electrospray from a needle connected to the TLC strip, introducing the moving solvent into the injec

282 Using the TLC-ESI-IMS technique, acceptable separations were achie

283 HPTLC-MS of selected zones, eluted via the TLC-MS Interface into MS, confirmed the identity of coum

284 alyzed to demonstrate the capability of this TLC-ELDI/MS system for high-throughput analysis.

285 ate and determine product quantities through TLC analysis.

286 s study, we have developed a high-throughput TLC-AMS system using building blocks to deal, deliver, a

287 f added after the cells have been exposed to TLC.

288 tical model of emphysema, the ratio of RV to TLC (RV/TLC) reflects the size mismatch between the hype

289 t time and require less solvent than typical TLC methods.

290 Using TLC and liquid chromatography-UV-tandem mass spectrometr

291 on limits for GSH and for GST activity using TLC were found to be as low as 10 pmol/microl and 1 ng/m

292 ol/vol)] were subjected to analyses by using TLC, analytical HPLC, and MS.

293 e reaction products were characterized using TLC, mass spectrometry, and NMR spectroscopy.

294 ature of the enzyme was also confirmed using TLC and a specific substrate.

295 whole brain gangliosides are separated using TLC; the TLC plates are attached directly to the MALDI t

296 ) (P = 0.02) and % predicted residual volume/TLC (P = 0.05).

297 When TLC quality control was performed on silica gel 60 plate

298 AdPLA, we employed radiochemical assays with TLC analysis of the enzyme activity of lysates from COS-

299 -6.40) among the subset of participants with TLC </=1200 cells/muL.

300 PPEC was also performed with TLC plates in a back-to-back configuration, and this dou