ライフサイエンスコーパス: electrophoresis

1 gration behavior of protein fragments in gel electrophoresis.

2 ctroscopy, circular dichroism and native gel electrophoresis.

3 cytometry, fluorescence microscopy, and gel electrophoresis.

4 se bioseparations, particularly in capillary electrophoresis.

5 d by densitometry analysis on 1D and 2D gels electrophoresis.

6 LC/MS and LC-MS/MS following monodimensional electrophoresis.

7 ions of a DNA nanoswitch and decoding by gel electrophoresis.

8 xtracts and conducted SDS-polyacrylamide gel electrophoresis.

9 14)C-radiolabelling followed by high-voltage electrophoresis.

10 d by infectivity assays and pulsed-field gel electrophoresis.

11 mal DNA damage monitored by pulsed-field gel electrophoresis.

12 ood samples were collected for serum protein electrophoresis.

13 in micro/nanofluidic assays and in capillary electrophoresis.

14 s were also performed by two-dimensional gel electrophoresis.

15 ilk are based on HPLC, mass spectrometry and electrophoresis.

16 migration was realized using electroosmosis/electrophoresis.

17 lently coupled species were confirmed by gel electrophoresis.

18 ic acids by gradient elution moving boundary electrophoresis.

19 eracting proteins, readily detectable by gel electrophoresis.

20 ng sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

21 s is easier and faster than pulsed-field gel electrophoresis.

22 correlation between biosensors and capillary electrophoresis.

23 tal-Phen complexes and analyzed by capillary electrophoresis.

24 ce of individual, labelled strands using gel electrophoresis.

25 proteins, confirmed by beta-mannan affinity electrophoresis.

26 CR amplification of STR loci followed by gel electrophoresis.

27 fications with ISSR and SCoT and agarose gel electrophoresis.

28 es the transition from cell lysis to protein electrophoresis.

29 studies by high-resolution clear native gel electrophoresis.

30 h were indistinguishable by pulsed-field gel electrophoresis.

31 get protein with the results read out by gel electrophoresis.

32 on by co-electro-osmotic flow capillary zone electrophoresis.

33 of two distinct M proteins in immunofixation electrophoresis.

34 Two-dimensional electrophoresis (2-DE) and matrix-assisted laser desorpt

35 ity and dynamic range of two-dimensional gel electrophoresis (2-DE) are currently hampering its utili

36 Using two-dimensional difference gel electrophoresis (2D-DIGE) and label-free quantitative pr

37 ach involving two dimensional difference gel electrophoresis (2D-DIGE) and mass spectrometry (MS).

38 re, we used two dimensional-differential gel electrophoresis (2D-DIGE) to compare protein expression

39 hnique called two-dimensional difference gel electrophoresis (2D-DIGE).

40 rmed using two-dimensional difference in-gel electrophoresis(2D-DIGE) followed by mass spectrometry(L

41 electric point is a critical part of 2-D gel electrophoresis, a key precursor of proteomics, where di

42 The gel supports protein electrophoresis after concurrent in situ chemical lysis

43 es are resolved by native polyacrylamide gel electrophoresis, after which fluorescence-resonance ener

44 Two-dimensional electrophoresis analysis of B. burgdorferi B31A3 and a s

45 Electrophoresis analysis revealed that HHP treatment sig

46 ss two parallel electrodes via sequential DC electrophoresis and AC dielectrophoresis (DEP), and with

47 n and peptide formation were evaluated using electrophoresis and chromatography.

48 c field simulation by COMSOL model suggested electrophoresis and dielectrophoresis as likely mechanis

49 by size-exclusion chromatography, native gel electrophoresis and electron microscopy.

50 to maintain noncovalent interactions during electrophoresis and facilitates method development.

51 inositol phosphates using polyacrylamide gel electrophoresis and high-performance liquid chromatograp

52 is indices were separated by two-dimensional electrophoresis and identified by tandem mass spectromet

53 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and image densitometry were used to dete

54 Gel electrophoresis and immunoblot analysis were used to det

55 g sodium dodecyl sulfate poly acrylamide gel electrophoresis and immunoblotting showed acid-soluble c

56 antified with agarose and polyacrylamide gel electrophoresis and immunoblotting.

57 th sodium dodecyl sulfate polyacrylamide gel electrophoresis and immunofluorescence staining to confi

58 ssed by using 2-dimensional differential gel electrophoresis and label-free mass spectrometry in pret

59 of healthy individuals were monitored by gel electrophoresis and LC-MS/MS to determine the cleavage s

60 rofiling, a method combining blue-native gel electrophoresis and liquid chromatography tandem mass sp

61 and pulp juice, resolved by two dimensional electrophoresis and major spots subjected to mass spectr

62 We applied microchip electrophoresis and MALDI-TOF-MS-based glycomic procedur

63 ed mainly of 11S globulin as was observed by electrophoresis and mass spectrometry analysis.

64 Two-dimensional gel electrophoresis and mass spectrometry demonstrated that

65 Two-dimensional gel electrophoresis and mass spectrometry revealed significa

66 Native polyacrylamide gel electrophoresis and mass spectrometry revealed that a tr

67 two-dimensional fluorescence difference gel electrophoresis and mass spectrometry, and further verif

68 Comparative gel electrophoresis and mass spectrometry-based proteomics o

69 s interaction was confirmed using native gel electrophoresis and mass spectrometry.

70 e transmission routes using pulsed-field gel electrophoresis and multi-locus variable number of tande

71 n reaction-temporal temperature gradient gel electrophoresis and next-generation sequencing.

72 s of Joule heating-enhanced diffusion during electrophoresis and observe approximately 50% protein lo

73 f highly polymorphic STRs by using capillary electrophoresis and pedigree-based designs.

74 The gel-electrophoresis and peptide mass fingerprint analyses re

75 next generation sequencing (NGS), capillary electrophoresis and pyrosequencing under the term 'NGS+'

76 monitored plasmid DNA degradation using gel electrophoresis and qPCR with both short amplicons ( app

77 nd-based typing techniques (pulsed-field gel electrophoresis and repetitive extragenic palindromic-PC

78 d silica shell were separated by agarose gel electrophoresis and scanned by a conventional fluorescen

79 In addition, proteins were separated by gel-electrophoresis and selected spots were characterised by

80 Here, we show by blue-native gel electrophoresis and stable isotope labeling in cell cult

81 ne-sodium dodecyl sulfate-polyacrylamide gel electrophoresis and subsequent image analysis.

82 ent study compared the accuracy of an OFFGEL electrophoresis and tandem mass spectrometry-based prote

83 66 isolates was done using pulsed-field gel electrophoresis and whole-genome sequencing (WGS).

84 n, Forster resonance energy transfer, native electrophoresis, and chemical crosslinking suggest that

85 iple-negative charge, separated by microchip electrophoresis, and detected by laser-induced fluoresce

86 ared spectroscopy, x-ray diffraction, native electrophoresis, and electron microscopy techniques.

87 in degradation with time was assessed by gel-electrophoresis, and mineral products formed were charac

88 RS-PCR was performed with conventional gel electrophoresis, and PCR was used for toxin gene identif

89 and/or quantified using ultrafiltration, gel electrophoresis, and RT-qPCR (quantitative reverse trans

90 e analysed by two-dimensional difference gel electrophoresis, and the differentially regulated protei

91 polymerization occurred, as evidenced by the electrophoresis, and the gelation resulted in a well-sta

92 urther protein separation by two-dimensional electrophoresis, and utilizing mass spectrometry, we now

93 m, a sequence alignment viewer and a virtual electrophoresis are displayed as parts of the primer des

94 Here, both ion mobility and capillary electrophoresis are used to follow the folding transitio

95 for observing such DNA knots (primarily gel electrophoresis) are limited to bulk methods and circula

96 ere compared with the results from capillary electrophoresis as a basic standard method.

97 molecular level by native polyacrylamide gel electrophoresis, as well as the network function at the

98 bodies with immunofixation and serum protein electrophoresis assays may lead to underestimation of co

99 A stacking approach in capillary electrophoresis based on the reversal of the analytes' e

100 Through MS and microchip electrophoresis-based glycomic methods, several potentia

101 XPAR combined with high-resolution capillary electrophoresis-based single-strand conformation polymor

102 in almost all studies, with pulse field gel electrophoresis being most commonly used.

103 complexes by blue native polyacrylamide gel electrophoresis (BN-PAGE) indicates that PP4 holoenzyme

104 atography and blue native polyacrylamide gel electrophoresis (BN-PAGE) to demonstrate BbHtrA oligomer

105 ents, and/or micelles during blue native gel electrophoresis (BN-PAGE).

106 que capability to resolve isomers, microchip electrophoresis can yield complementary analytical infor

107 e separated by surfactant-mediated capillary electrophoresis (CE) and quantitated by integrating fluo

108 automated with the use of standard capillary electrophoresis (CE) based equipment employing fluoresce

109 th a conventional low-conductivity capillary electrophoresis (CE) buffer.

110 Capillary electrophoresis (CE) coupled to single particle inductiv

111 ation of some of the features of a capillary electrophoresis (CE) instrument to speed up the process.

112 Capillary electrophoresis (CE) is a complementary solution-phase t

113 A microchip capillary electrophoresis (CE) separation with mini-CIT detection

114 ion of stacking techniques used in capillary electrophoresis (CE) to microchip CE (MCE) in order to i

115 e mobility of system eigenpeaks in capillary electrophoresis (CE) was experimentally found to decreas

116 oped and applied a stacking chiral capillary electrophoresis (CE) with laser-induced fluorescence det

117 we describe the first coupling of capillary electrophoresis (CE) with muFFE to perform 2D CE x muFFE

118 ography-mass spectrometry (LC-MS), capillary electrophoresis (CE), or gas chromatography (GC).

119 Its determination by capillary electrophoresis (CE), using a routine method, is intrins

120 their use in applications such as capillary electrophoresis (CE), where their compact footprint and

121 (DEN)-gas combined with sheathless capillary electrophoresis (CE)-ESI-MS was evaluated for glycopepti

122 -ROESY), completed with studies by capillary electrophoresis (CE).

123 -visible (UV-VIS) spectroscopy and capillary electrophoresis (CE).

124 further enhance multiplexing capability, the electrophoresis channel dimensions were optimized for re

125 While protein electrophoresis conducted in capillaries and microchanne

126 by sodium dodecyl sulfate polyacrylamide gel electrophoresis confirmed that the primary targets of th

127 The presence of a band at 407bp on gel electrophoresis confirmed the amplified product.

128 e mono-, di- and tri-phosphates by capillary electrophoresis coupled to mass spectrometry (CE-MS).

129 e urinary proteome was analysed by capillary electrophoresis coupled to mass spectrometry.

130 t different surface coatings using capillary electrophoresis coupled to single particle inductively c

131 ation of malting barley that may replace gel electrophoresis currently used for this purpose.

132 ative time-resolved emission two-dimensional electrophoresis (CuTEDGE) technology facilitates in-dept

133 Here, we report on capillary zone electrophoresis (CZE) coupled via a commercial CESI shea

134 o coat capillaries for use in capillary zone electrophoresis (CZE).

135 r characterized using double one-dimensional electrophoresis (D1-DE).

136 labeled according to their pulsed-field gel electrophoresis data for strain differentiation.

137 Gel electrophoresis demonstrated that the heated WPI and WPI

138 hannel detection for capillary and microchip electrophoresis detection.

139 itional chromatographic approaches, a hybrid electrophoresis device with electrochemical preprocessin

140 sorption/ionization (MALDI) MS and capillary electrophoresis electrospray ionization (CE-ESI)-MS are

141 roscale metabolite extraction, and capillary electrophoresis electrospray ionization mass spectrometr

142 Capillary zone electrophoresis-electrospray ionization-tandem mass spec

143 with traditional methodologies based on gel electrophoresis, especially in the case of overlapping p

144 MR, EPR, resonance Raman and UV-vis spectra, electrophoresis, etc.

145 tuents and by complementary quantitative gel electrophoresis experiments.

146 he hyphenation of production-scale free-flow electrophoresis (FFE) and sheathless electrospray ioniza

147 We used free-flow electrophoresis (FFE) to isolate monoclonal antibody cha

148 omic approach based on a two-dimensional gel electrophoresis followed by liquid chromatography-tandem

149 -reactive proteins were identified by 2D gel electrophoresis, followed by Western blot with pooled or

150 ydrogels facilitate gel-pore expansion after electrophoresis for efficient and uniform immunoprobing.

151 xchanger based on the principle of free-flow electrophoresis for miscible organic/aqueous fluids.

152 than RS-PCR performed with conventional gel electrophoresis for typing of S. aureus isolates of bovi

153 t migrated more slowly in native agarose gel electrophoresis from A36V mutant than from the wild-type

154 dic free-standing kinetic polyacrylamide gel electrophoresis (fsKPAGE) assay.

155 An investigation by capillary electrophoresis fully confirmed these results.

156 ations directly in native polyacrylamide gel electrophoresis gels, enabling unprecedented resolution

157 Novel high-resolution melting and capillary electrophoresis genotyping techniques were designed and

158 Capillary electrophoresis greatly improved glycoform separation fo

159 tern blot based on microfluidic or capillary electrophoresis have been developed that enable higher-t

160 onstrated for ion chromatography x capillary electrophoresis (ICxCE) separation of low-molecular-mass

161 Although gel electrophoresis identified 11 proteins that were differe

162 Two-dimensional differential in-gel electrophoresis identified abnormal actin-interacting pr

163 protein detection in texture analysis of gel electrophoresis images.

164 rial synthasomes were investigated by native electrophoresis, immunoprecipitation, and sucrose densit

165 vering the nuclease target site by capillary electrophoresis in a sequenator.

166 Despite the ever growing use of capillary electrophoresis in biomedical research and the biopharma

167 oposes the improvement of an agarose gel DNA electrophoresis in order to allow for a quantitative est

168 erved, only aggregation, as indicated by the electrophoresis in polyacrylamide/agarose gel profile.

169 Gel electrophoresis indicated that increased heat stability

170 of apoptotic melanoma cells, and single-cell electrophoresis indicated that mensacarcin causes geneti

171 limitations of either conventional capillary electrophoresis instruments as well as electrophoretic l

172 Free-solution capillary electrophoresis is a robust technique for the separation

173 Nanogel electrophoresis is an inexpensive, rapid, and simple alt

174 Visualizing nucleic acids by gel electrophoresis is one of the most common techniques in

175 all peptides to large proteins, in capillary electrophoresis is used as examples in this study.

176 elivering a drug without the solvent through electrophoresis, is developed.

177 mic light scattering, and polyacrylamide gel electrophoresis, is reported for the loading and protect

178 During electrophoresis, Joule (or resistive) heating degrades s

179 Methods of kinetic capillary electrophoresis (KCE) may facilitate highly efficient ho

180 Kinetic capillary electrophoresis (KCE) methods are useful in the study of

181 Here, we present a novel capillary electrophoresis-laser-induced fluorescence detection (CE

182 mization (AAR) in conjunction with capillary electrophoresis mass spectrometry was applied to 13 Buyi

183 and a number of empty BMC variants by 2D-gel electrophoresis, mass spectrometry, transmission electro

184 rm based on multisegment injection-capillary electrophoresis-mass spectrometry (MSI-CE-MS) was develo

185 es based on multisegment injection-capillary electrophoresis-mass spectrometry (MSI-CE-MS).

186 The adoption of capillary electrophoresis-mass spectrometry methods (CE-MS) for gl

187 nization by NHERF1, a combined 2-dimensional electrophoresis-matrix-assisted laser desorption/ionizat

188 A home-made microchip electrophoresis (MCE) device was used to quantitate two

189 are quantification using microchip capillary electrophoresis (MCE), the chip-to-chip variabilities in

190 ne, high-throughput, microdialysis-capillary electrophoresis (MD-CE) assay for measuring the in vivo

191 ed a high-throughput microdialysis-capillary electrophoresis (MD-CE) assay for monitoring branched ch

192 asily positioned in the capillary to support electrophoresis mediated microanalysis using neuraminida

193 ine, solid phase extraction, capillary zone, electrophoresis method combined with diode-array detecto

194 chemical techniques, such as a new capillary electrophoresis method, nuclear magnetic resonance, and

195 several assays using this core capillary gel electrophoresis methodology to accelerate study of nucle

196 This article describes two capillary electrophoresis methods capable of resolving 17 amino ac

197 nterparts and analyzed by polyacrylamide gel electrophoresis mobility shifts.

198 tion signal of chip moving reaction boundary electrophoresis (MRBE).

199 We have fabricated a micro free-flow electrophoresis (muFFE) device using a low-cost, consume

200 Continuous micro free flow electrophoresis (muFFE) separations eliminate under samp

201 Nonaqueous capillary electrophoresis (NACE) is very well suited for online co

202 of 50 to 60 kDa that were visualized by gel electrophoresis, nanoparticle tracking analysis and elec

203 o liquid chromatography with micro free flow electrophoresis (nLC x muFFE) to produce high peak capac

204 ce demonstrates the power of micro-free-flow electrophoresis not only as a powerful technique for sep

205 as free light chain, if available, and urine electrophoresis of a sample from a 24-hour urine collect

206 Similarly, both S1 nuclease and 2D gel electrophoresis of DNA topoisomers did not detect any su

207 They used the technique of gel electrophoresis of enzymes and proteins to study variati

208 Nonequilibrium capillary electrophoresis of equilibrium mixtures (NECEEM) is an e

209 ion methods such as nonequilibrium capillary electrophoresis of equilibrium mixtures (NECEEM).

210 racted from transformedNicotiana tabacum Gel electrophoresis of leaf extracts revealed a consistent p

211 Free-flow zonal electrophoresis of microalgal membranes coupled to liqui

212 Blue native-polyacrylamide gel electrophoresis of mitochondrial extracts combined with

213 OFFGEL electrophoresis of the small peptides of both hydrolysat

214 labs) at 37 degrees C for 12 h, separated by electrophoresis on 2 % agarose gels, and visualized with

215 In one approach, proteins are separated by electrophoresis on a microchip that is dragged along a p

216 oth PCR and real-time PCR assays followed by electrophoresis or melting temperature analysis, respect

217 tworks and the utility of polyacrylamide gel electrophoresis (PAGE), we develop a technique for fabri

218 isolates had similar PFGE (pulsed field gel electrophoresis) patterns and the same MLST (multilocus

219 hieve this aim, we performed a PCR-capillary electrophoresis (PCR-CE) approach on olive oil: seed oil

220 Pulsed-field gel electrophoresis (PFGE) and multi-locus sequence typing (

221 SmaI restriction digestion pulsed-field gel electrophoresis (PFGE) for typing S. aureus Forty-two S.

222 despite having the outbreak pulsed-field gel electrophoresis (PFGE) pulsotype.

223 nited States and to compare pulsed-field gel electrophoresis (PFGE) to the combination of ribosomal s

224 Whole-genome-sequencing, pulsed-field gel electrophoresis (PFGE), and a mouse infection model were

225 uded Western blot analysis, pulsed-field gel electrophoresis (PFGE), polymerase chain reaction, and p

226 subtyping methods, such as pulsed-field gel electrophoresis (PFGE), were critical in detecting outbr

227 ion, especially compared to pulsed-field gel electrophoresis (PFGE).

228 ngth-based methods, such as pulsed-field gel electrophoresis (PFGE); however, conventional multilocus

229 implemented, namely, standard capillary zone electrophoresis, pressure assisted zone electrophoresis,

230 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of transglutaminase-treated low

231 Capillary electrophoresis proved to be a sensitive method for eval

232 l 120min of hydrolysis were evaluated by gel electrophoresis, relative fluorescence intensity, emulsi

233 Gel electrophoresis results confirmed that DNA cleavage was

234 Gel electrophoresis revealed substantial digestion of milk p

235 oimmunoprecipitation and two-dimensional gel electrophoresis revealed that CAR can form a homodimer i

236 by sodium dodecyl sulfate-polyacrylamide gel electrophoresis SDS-PAGE-immunoblotting with patient ser

237 ized by sodium dodecyl sulfate capillary gel electrophoresis (SDS CGE) with head-column field-amplifi

238 Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) analysis revealed the localiz

239 in sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), which was eliminated by phos

240 d sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).

241 sodium dodecyl sulphate-polyaccrylamide gel electrophoresis (SDS-PAGE).

242 ration of myofibrillar proteins using OFFGEL electrophoresis, SDS-PAGE and protein identification by

243 ese particles by a combination of native gel electrophoresis, sedimentation velocity, electron micros

244 parallel high-resolution single-cell protein electrophoresis separations for targets accross a wide m

245 Using our Pulse Field Gel Electrophoresis-shift approach, we determined resection

246 Electrophoresis showed that beta-lactoglobulin and low m

247 In addition, protein gel electrophoresis showed that there was only one enriched

248 Capillary electrophoresis shows that this PME is non-processive, h

249 ight scattering, controlled proteolysis, gel electrophoresis, site-directed mutagenesis and microseco

250 This process could be verified by gel electrophoresis, spectroscopically and in vitro confocal

251 we report a strategy that combines microchip electrophoresis, standard addition, enzymatic digestion,

252 n coupled to automated single-cell capillary electrophoresis, statistically significant numbers of pr

253 trafiltration and isoelectric focusing (IEF) electrophoresis steps.

254 Gel electrophoresis studies demonstrate the formation of non

255 sing blue native/Deriphat-polyacrylamide gel electrophoresis, sucrose density gradients, and isolated

256 A simple capillary electrophoresis system was built with LED induced fluore

257 that are analyzed by a three-dimensional gel electrophoresis system.

258 h readily supports high-throughput capillary electrophoresis systems by significantly speeding up the

259 online sample preparation and capillary zone electrophoresis-tandem mass spectrometry (CZE-MS/MS) bot

260 lteration with soybean and corn by capillary electrophoresis-tandem mass spectrometry was accomplishe

261 l data found in the literature (pulsed field electrophoresis technique).

262 ng plasma fraction were studied using 2D gel electrophoresis techniques.

263 of cations and anions by dual-capillary zone electrophoresis, the separation of cationic amino acids

264 zone electrophoresis, pressure assisted zone electrophoresis, the simultaneous separation of cations

265 only five peaks are observed using capillary electrophoresis, these peaks can be modeled as sums of t

266 oad selection of techniques from routine gel electrophoresis to advanced single-molecule imaging.

267 we used two-dimensional differential in-gel electrophoresis to analyze hepatic cells in early respon

268 This study used capillary zone electrophoresis to measure rates of heterodimerization a

269 urrent study, we report the use of capillary electrophoresis to rapidly generate mismatch fidelity pr

270 perature for each operation and standard gel electrophoresis to read the data.

271 ss estimated, using SDS-PAGE and native-PAGE electrophoresis, to be 86kDa.

272 ed sample storage compartment of a capillary electrophoresis unit and the separation capillary was al

273 in (>/=200 mg per 24 hours) in urine protein electrophoresis (UPEP).

274 PCR-capillary electrophoresis using nine microsatellites demonstrates

275 BSI was interfaced to a capillary electrophoresis-UV instrument using a polyimide coated f

276 weight estimated by NATIVE-PAGE and SDS-PAGE electrophoresis was approximately 60 kDa.

277 Pulsed-field gel electrophoresis was conducted to strain type the isolate

278 eric genomes as assessed by pulsed-field gel electrophoresis was greatly diminished, and DNA-containi

279 Temperature gradient capillary electrophoresis was introduced to enhance separation sel

280 Hemoglobin electrophoresis was used to detect structural hemoglobin

281 sing gene expression analysis and native gel electrophoresis we characterize the expression and assem

282 By using improved polyacrylamide gel electrophoresis we were able to visualize polyP extracte

283 Using synthetic peptides and native gel electrophoresis, we coarsely mapped the CaM-binding doma

284 By 2D gel electrophoresis, we detect two different kinds of struct

285 microfluidic device adapted for single-cell electrophoresis, we perform 100s to 1000s of simultaneou

286 d protein spots from the two-dimensional gel electrophoresis were analyzed using mass spectrometry.

287 ral very diverse configurations and modes of electrophoresis were successfully implemented, namely, s

288 imate composition, amino acids, minerals and electrophoresis] were determined.

289 ies pairing peptide reporters with capillary electrophoresis will provide valuable data regarding abe

290 Good quality capillary electrophoresis with capacitively coupled contactless co

291 Capillary electrophoresis with laser-induced fluorescent detection

292 Capillary zone electrophoresis with mass spectrometry (CZE-MS) has grea

293 Capillary zone electrophoresis with mass spectrometry (CZE-MS) is an or

294 ere is a method using microfluidic capillary electrophoresis with mass spectrometry detection (CE-MS)

295 Two-dimensional difference in-gel electrophoresis with matrix assisted laser desorption io

296 membrane (FLM) were determined by capillary electrophoresis with ultraviolet detection (CE-UV).

297 Simple and inexpensive capillary electrophoresis with UV-detection method (CE-UV) was opt

298 curve analysis based on temperature-gradient electrophoresis within 3h, which is at least 3-fold decr

299 ction sensitivity relative to capillary zone electrophoresis, without impacting separation resolution

300 n detection using the minimal difference gel electrophoresis workflow showed improvements in lowest l