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, BMI, and hemoglobin had a limited predictive value,

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

11 TLC-S induced global calcium oscillations and extended c

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

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

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

15 % CI: 31.53-38.92), considering 4, 55 and 18 TLC, ELISA and HPLC-based studies (including 354, 9224 a

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

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

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

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

20 A TLC-densitometric assay was developed and validated for

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

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

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

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

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

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

27 btained at total lung capacity (TLC); actual TLC %of predicted and flow; and static transpulmonary pr

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

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

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

31 he resulting sensor solution onto an alumina TLC plate.

32 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

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

34 ination of anion exchange chromatography and TLC, is a very polar and weakly fluorescent compound, wh

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

38 The ratio of post-bronchodilator FVC and TLC(CT) from chest CT (FVC/TLC(CT)) among current and fo

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

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

41 TC and TLC feeding increased proliferation of large cholangiocy

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

43 TC and TLC stimulate proliferation of small and large cholangio

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

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

46 [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).

47 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

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

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

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

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

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

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

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

55 Celltrion, Singapore Biotech, Vor Biopharma, TLC Biopharmaceuticals and Benevolent AI, has consulted

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

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

58 y pure indophenine materials as confirmed by TLC and (1)H NMR analysis.

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

60 high-temperature annealing is determined by TLC.

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

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

63 ed PKC-mediated phosphorylation of MARCKS by TLC.

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

65 nes contents compared with those obtained by TLC.

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

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

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

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

70 raction in the crude extract was revealed by TLC-bioautography at R(f) = 0.78 with molecular weight b

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

72 t approach for detecting lipids separated by TLC.

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

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

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

76 n of glycan samples, glycan visualization by TLC and tandem MS, our integrated platform, allowed the

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

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

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

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

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

82 t, residual volume (RV)/total lung capacity (TLC)% predicted was reduced compared to baseline (p < 0.

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

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

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

86 y pressures obtained at total lung capacity (TLC); actual TLC %of predicted and flow; and static tran

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

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

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

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

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

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

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

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

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

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

97 Thin-Layer Chromatography (TLC) analysis showed adulteration with magenta- and pink

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

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

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

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

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

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

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

105 developed using a thin-layer chromatography (TLC) imaging method.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

125 matrix-decorated, thin-layer chromatography (TLC)-MALDI MS method for simultaneous and rapid separati

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

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

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

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

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

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

132 PPEC is more efficient than classical TLC.

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

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

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

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

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

138 the values determined with the conventional TLC assay.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 We examined the associations between FVC/TLC(CT) quartiles and (1) baseline characteristics, (2)

154 hodilator FVC and TLC(CT) from chest CT (FVC/TLC(CT)) among current and former smokers with PRISm (FE

155 Mortality was lower in the very high FVC/TLC(CT) quartile relative to the other quartiles combine

156 Sm at baseline (n = 1,131), the very low FVC/TLC(CT) quartile was associated with increased gas trapp

157 The very low FVC/TLC(CT) quartile was associated with increased total (IR

158 We examined the utility of FVC/TLC in identifying features of obstructive lung disease.

159 Reduced FVC/TLC(CT) ratio in PRISm is associated with increased symp

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

161 hnique is comparable with that of silica gel TLC.

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

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

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

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

166 The first method is HP- TLC method.

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

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

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

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

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

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

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

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

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

176 .63) | lactate production: 0.005 mmol/min/ L(TLC) (95%CI: 0.004 to 0.007)).

177 ring ILP (Glucose consumption: 1.86 mg/min/L(TLC) (95%CI: -2.09 to -1.63) | lactate production: 0.005

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

203 oblastomas were analyzed by high-performance TLC.

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

205 ), greater lung volumes (mean % of predicted TLC 134.8% vs 109.6%; P < .05) and lower airway resistan

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

207 ied by liquid chromatography and preparative TLC.

208 epimerized to arborisidine upon preparative TLC purification (eluent: MeOH/CHCl(3) saturated with NH

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

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

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

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

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

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

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

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

217 RV and RV/TLC improved at 6 months.

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

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

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

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

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

223 with residual volume/total lung capacity (RV/TLC).

224 at screening that associated with higher RV/TLC% predicted values.

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

226 Short-term ICS/LABA treatment improves RV/TLC% predicted in severe COPD.

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

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

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

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

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

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

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

234 obtain the chemical fingerprints of saffron TLC images.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

254 The TLC determinations were similarly made using Merck NH2 F

255 The TLC elutions were imaged using a cell phone and a LEGO b

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

257 Although the TLC was not able to separate isomeric glycans, the DHB@M

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 al resolution due to the irregularity of the TLC surface.

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

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

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

274 zed magnetic nanoparticles (DHB@MNPs) on the TLC plate with spot homogeneity, which contributed to th

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

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

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

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

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

280 sfer of the samples from a well-plate to the TLC plate.

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

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

289 , (b) biological evaluation using tyrosinase TLC bioautography, (c) inhibitor identification via mass

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

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

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

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

294 drum's acid derivative (1) in parallel using TLC.

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