ライフサイエンスコーパス: electrophoresis

1 the separation of HMOs by multicapillary gel electrophoresis.

2 ith possible bioactivity, were identified by electrophoresis.

3 ys as a biocompatible detector for capillary electrophoresis.

4 field, can be automated using capillary gel electrophoresis.

5 e with other methods such as LC or capillary electrophoresis.

6 ently labeled primers, followed by capillary electrophoresis.

7 nd DNA fragmentation analyses by agarose gel electrophoresis.

8 e resolution capacity of regular agarose gel electrophoresis.

9 al SDS replacement in SDS-polyacrylamide gel electrophoresis.

10 ling cycle are separated by 4-6% agarose gel electrophoresis.

11 diameter (EMD) can be achieved via gas-phase electrophoresis.

12 stantly detected in gelled milk by capillary electrophoresis.

13 protein changes that were obtained by 2D gel electrophoresis.

14 single-channel electrical recordings and gel electrophoresis.

15 ent reference methods, Kjeldahl and SDS-PAGE electrophoresis.

16 using sodium dodecyl sulfate polyacrylamide electrophoresis.

17 EDA) with various precursor ratios using gel-electrophoresis.

18 gration behavior of protein fragments in gel electrophoresis.

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

20 ce of individual, labelled strands using gel electrophoresis.

21 proteins, confirmed by beta-mannan affinity electrophoresis.

22 rrays as a postcolumn detector for capillary electrophoresis.

23 of proteins, which are carried out after the electrophoresis.

24 ed by FT-IR, SEM, cyclic voltammetry and gel electrophoresis.

25 xtures are demonstrated using capillary zone electrophoresis.

26 sieving compared to free-solution capillary electrophoresis.

27 Proteomics was based on two-dimensional gel electrophoresis (2-DE) along with mass spectrometry iden

28 were investigated using two-dimensional gel electrophoresis (2-DE) followed by mass spectrometry (MS

29 Electrophoresis 2016, 37 (17-18), 2376-2383; Casto et al

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

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

32 uorescence two-dimensional difference in-gel electrophoresis (2D-DIGE)-coupled mass spectrometry scre

33 Two-dimensional electrophoresis (2D-PAGE) for protein fractionation, gra

34 arated by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), and the total mercury concent

35 sociated proteins separated by 2-dimensional electrophoresis (2DE).

36 Size exclusion-HPLC and electrophoresis analysis were used to investigate change

37 device materials commonly used for microchip electrophoresis analysis.

38 esigned/optimized and tested by standard gel electrophoresis analysis.

39 ethod revealed intense RNA bands through gel electrophoresis and a nanodrop spectrophotometer detecte

40 lates were characterized by pulsed-field gel electrophoresis and agr group.

41 PCR coupled with capillary electrophoresis and an array of population genetics tool

42 Proteins were resolved by gel electrophoresis and blotted, and Siglec-8 ligands detect

43 K(a) values have been measured by capillary electrophoresis and calculated at the B3LYP-D3BJ/6-311+G

44 provement in sensitivity over immunofixation electrophoresis and can potentially provide an objective

45 organic acids (AOA) determined by capillary electrophoresis and chemometric analyses.

46 s that the off-line hyphenation of gas-phase electrophoresis and confocal Raman spectroscopy allows d

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

48 Using gel electrophoresis and DNA melting curve analysis, we showe

49 e trapping can occur by linear and nonlinear electrophoresis and electroosmosis reaching an equilibri

50 ed sodium dodecyl sulfate-polyacrylamide gel electrophoresis and high-performance liquid chromatograp

51 n sodium dodecyl sulphate-polyacrylamide gel electrophoresis and high-performance liquid chromatograp

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

53 High-resolution 2-D gel electrophoresis and immunoblot analyses revealed that tr

54 antified with agarose and polyacrylamide gel electrophoresis and immunoblotting.

55 Serum and urine protein electrophoresis and immunofixation, as well as analyses

56 y using circular DNA deep-sequencing, 2D gel electrophoresis and inverse polymerase chain reaction.

57 Capillary zone electrophoresis and ion mobility both coupled to mass sp

58 Using two-dimensional electrophoresis and liquid chromatography-mass spectrome

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

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

61 Two-dimensional differential gel electrophoresis and mass spectrometry were used to ident

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

63 (TPM4) by two-dimensional polyacrylamide gel electrophoresis and mass spectrometry, and its binding t

64 Using capillary electrophoresis and MS-based analyses, we extracted and

65 aracteristics of EAEC using pulsed-field gel electrophoresis and next-generation sequencing.

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

67 SDS-PAGE due to their close proximity during electrophoresis and poor sensitivity of commonly used st

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

69 by quantifying the images obtained from gel electrophoresis and showed that our system is comparable

70 independently determined by two-dimensional electrophoresis and showed that the two methods are in g

71 Native polyacrylamide gel electrophoresis and size exclusion chromatography demons

72 In this context, we now compare capillary electrophoresis and spectroscopic characterization of ve

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

74 uated for relatedness using pulsed-field gel electrophoresis and staphylococcal cassette chromosome m

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

76 er Belgian hospitals) using pulsed-field gel electrophoresis and WGS.

77 Pulsed-field gel electrophoresis and whole-genome sequencing were perform

78 phenotype (reference) status (ascertained by electrophoresis) and at least 1 year of follow-up and th

79 ns can be performed both in continuous (zone electrophoresis) and discontinuous (moving boundary) ele

80 d dimer formation as revealed by blue-native electrophoresis; and (ii) simultaneous substitution of e

81 s, we developed an integrated capillary zone electrophoresis apparatus to fractionate bacteria from c

82 y gel-eluted liquid fractionation entrapment electrophoresis are then described.

83 Using ultra-sensitive capillary electrophoresis assays, we quantified nitrites (products

84 Accordingly, barcode PCR-CE (PCR-capillary electrophoresis) assays are described, which do not requ

85 iven by electroosmotic flow exceeded that of electrophoresis at locations radial to the electrode dis

86 gous strains (defined by field-inversion gel electrophoresis banding pattern), emm types, and emm clu

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

88 Capillary electrophoresis-based selection of aptamers for protein

89 e it possible to rationally design capillary electrophoresis-based selection of DNA aptamers for prot

90 d by any laboratory with access to capillary electrophoresis-based sequencing equipment.

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

92 Electrophoresis-based size-selection followed by qRT-PCR

93 rbance spectroscopy; circular dichroism; and electrophoresis-based techniques.

94 We generalize this band-collision gel electrophoresis (BCGE) approach to other reaction types,

95 lating integrated HIV DNA using pulsed-field electrophoresis before performing sequencing.

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

97 t is based on Blue Native Polyacrylamide Gel Electrophoresis (BN-PAGE) and dot immunoblotting for qua

98 Here, we adapt gel electrophoresis by fabricating two or more wells in the

99 zation and have been investigating capillary electrophoresis (CE) and hybrid microchip electrophoresi

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

101 Here, capillary electrophoresis (CE) coupled to electrospray ionization

102 Capillary electrophoresis (CE) coupled to single particle inductiv

103 hly poloymorphic SSR primers and a capillary electrophoresis (CE) detection system.

104 Quantification of sugars by capillary electrophoresis (CE) have been previously reported.

105 exchange chromatography (CEX) and capillary electrophoresis (CE) have recently been coupled to mass

106 recent years, as modern commercial capillary electrophoresis (CE) instrumentation is well equipped to

107 efficiency for protein analysis in capillary electrophoresis (CE) is a challenging topic in which pro

108 Capillary electrophoresis (CE) is a highly efficient separation me

109 extraction (HF-LPME) to commercial capillary electrophoresis (CE) is demonstrated, which enables the

110 ial, most laboratories use PCR and Capillary Electrophoresis (CE) to construct a genetic profile base

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

112 ction on an integrated RT-qPCR-CE (capillary electrophoresis (CE)) microfluidic chip.

113 hange chromatography, microfluidic capillary electrophoresis (CE), and MALDI-MS were adopted to resol

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

115 The capillary electrophoresis (CE)-based hybridization assay proved to

116 LIF) system was demonstrated using capillary electrophoresis (CE)-ESI-MS in the analysis of aminopyre

117 M HClO(4)) have been determined by capillary electrophoresis (CE)-inductively coupled plasma mass spe

118 -art liquid chromatography (LC) or capillary electrophoresis (CE)-MS methods.

119 assays were carried out using the capillary electrophoresis (CE).

120 Continuous-flow electrophoresis (CFE) separates a stream of a multicompo

121 , residual activity, effect of bentonite and electrophoresis characterization of laccase in the prese

122 Using pulse field gel electrophoresis combined with PCR-based copy number anal

123 While protein electrophoresis conducted in capillaries and microchanne

124 PTS) labeling, and multiplexed capillary gel electrophoresis coupled to laser-induced fluorescence de

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

126 Proteome Database generated using capillary electrophoresis coupled to mass spectrometry.

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

128 mino acid standard compounds using capillary electrophoresis coupled with high-resolution mass spectr

129 phase extraction microcartridge in capillary electrophoresis coupled with mass spectrometry.

130 ied using two-dimensional polyacrylamide gel electrophoresis coupled with matrix-assisted laser desor

131 Herein, we utilize native capillary zone electrophoresis coupled with MS to characterize the prot

132 en bonding, were confirmed by capillary zone electrophoresis (CZE) and molecular docking simulations.

133 Capillary zone electrophoresis (CZE) can produce high-resolution separa

134 can be directly coupled with capillary zone electrophoresis (CZE) for separation.

135 Capillary zone electrophoresis (CZE) is one important alternative becau

136 re separated using sheathless capillary zone electrophoresis (CZE)-MS and reversed-phase liquid chrom

137 mass spectrometry (MS/MS) or capillary zone electrophoresis (CZE)-MS/MS.

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

139 Sodium dodecyl sulfate polyacrylamide gel electrophoresis demonstrated that 60% sorbitol could ret

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

141 for the first time the creation of microchip electrophoresis devices with ~50 mum cross-sectional dim

142 ferent heights using denaturant gradient gel electrophoresis (DGGE) fingerprinting.

143 associated fluorophore associated capillary electrophoresis (DSA-FACE) on a serum sample 1 week afte

144 pproach of non-denaturing polyacrylamide gel electrophoresis, dynamic light scattering, confocal micr

145 enzyme-linked immunosorbent assay, capillary electrophoresis, electrochemical biosensors have been us

146 ion of these glycoproteins using a microchip electrophoresis-electrochemical detection (ME-ED) platfo

147 as assessed by pulsed-field and Gardella gel electrophoresis, electron microscopy, and single-molecul

148 of ASA and its cyclic forms using capillary electrophoresis-electrospray ionization-time-of-flight m

149 Gas-phase electrophoresis employing a nano-electrospray differenti

150 eparation resolution provided by thermal gel electrophoresis enabled rapid screening of native protei

151 alances electrokinetic (EK) motion, that is, electrophoresis (EP) and electro-osmotic flow (EOF).

152 DNA, the mobilities predicted by the Manning electrophoresis equation are reasonably close to the obs

153 tuents and by complementary quantitative gel electrophoresis experiments.

154 rate and collect charged analytes, free-flow electrophoresis (FFE) has become a useful tool for the p

155 namics simulations, with thermophoresis, gel electrophoresis, fluorescence correlation spectroscopy (

156 orescent staining of DNA and proteins in gel electrophoresis, fluorescence guided surgery, or as rati

157 o techniques (TWJ-screen, polyacrylamide gel electrophoresis, fluorescence resonance energy transfer-

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

159 al (32)P-activity) and by polyacrylamide gel electrophoresis followed by phosphorimaging (to detect i

160 resis (sIFE) and urine (uIFE) immunofixation electrophoresis for classification of complete response

161 commend regular monitoring for EBV and serum electrophoresis for MG in MS patients in the first 3 mon

162 lymerase chain reaction monitoring and serum electrophoresis for monoclonal gammopathy (MG or M-prote

163 m sulfate precipitation and subjected to gel electrophoresis for protein separation.

164 we have explored nonaqueous micro free-flow electrophoresis for this purpose and present its suitabi

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

166 proteoliposomes, as shown by blue native gel electrophoresis, gel filtration, and determination of in

167 Here, gradient elution moving boundary electrophoresis (GEMBE), a robust and miniaturized elect

168 The nanogel electrophoresis generates separation efficiencies of 500

169 ary separations based on sieving rather than electrophoresis had similar precision in both area and m

170 High-speed capillary electrophoresis (HSCE) is implemented using a 10 cm tota

171 ry electrophoresis (CE) and hybrid microchip electrophoresis (hybrid-MCE) as alternatives to the typi

172 Gel electrophoresis identified the presence of organic mater

173 Ideal-filter capillary electrophoresis (IFCE) allows selection of protein binde

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

175 Micro-electrophoresis implemented with a diffusion barrier, wh

176 Limits of detection for microchip electrophoresis in 3D printed microfluidic devices were

177 We demonstrated for the first time microchip electrophoresis in a 3D printed device of three PTB biom

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

179 DNA (dsDNA) have been measured by capillary electrophoresis in solutions containing 0.01-1.0 M sodiu

180 However, analysis from affinity capillary electrophoresis indicated an increment in protein volume

181 ion via polymerase chain reaction (PCR), gel electrophoresis indicated that only cereal samples conta

182 bust (with basic PCR methods and agarose gel electrophoresis), informative, and applicable in measuri

183 ed proteins, peptide separation by capillary electrophoresis, ionization by an ultrasensitive electro

184 Free-flow electrophoresis is a tool for the continuous fractionati

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

186 uencing, two-dimensional differential in-gel electrophoresis, macromolecule biosynthesis assays and f

187 The combination of inductive nESI and micro-electrophoresis makes it possible to perform efficient i

188 2D electrophoresis maps of exposed cells were compared to n

189 Capillary electrophoresis mass spectrometry (CE-MS) is an establis

190 With surface sampling capillary electrophoresis mass spectrometry (SS-CE-MS), endogenous

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

192 Capillary zone electrophoresis-mass spectrometry (CE-MS) is a mature an

193 titative metabolomics assays using capillary electrophoresis-mass spectrometry (CE-MS) on brain sampl

194 Capillary electrophoresis-mass spectrometry (CE-MS), matrix-assist

195 mass) when multisegment injection-capillary electrophoresis-mass spectrometry (MSI-CE-MS) and CE wit

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

197 multisegment injection-nonaqueous-capillary electrophoresis-mass spectrometry (MSI-NACE-MS) as a mul

198 Capillary electrophoresis-mass spectrometry is a powerful techniqu

199 Electrochemistry-capillary electrophoresis-mass spectrometry measurements revealed

200 er affinity solid-phase extraction capillary electrophoresis-mass spectrometry method is described fo

201 sent a versatile and flexible capillary zone electrophoresis-mass spectrometry screening method for H

202 theoretical plates achieved in the capillary electrophoresis-mass spectrometry setup were 80%-95% of

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

204 Microchip electrophoresis (ME) is ideally suited for this task.

205 Capillary zone electrophoresis method has been developed and parameters

206 A capillary electrophoresis method is reported that integrates a uni

207 is is the first report of a new diagonal gel electrophoresis method to isolate and identify metallopr

208 of this work was the use of a capillary zone electrophoresis method with UV-vis detection in associat

209 nant sweeping-blue native-polyacrylamide gel electrophoresis (MICS-BN-PAGE).

210 capacity for binding SF1, as measured by the electrophoresis mobility shift assay.

211 uous separation mechanism of micro free-flow electrophoresis (muFFE) is a straightforward, suitable t

212 spitals underwent typing by pulsed-field gel electrophoresis, multilocus sequence typing, and WGS.

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

214 Pulsed-field gel electrophoresis of 174 of 179 NTHi isolates from 18- to

215 We applied comparative native gel electrophoresis of chloroplast protein complexes followe

216 Two-dimensional gel electrophoresis of wheat leaves resolved more than 300 p

217 Results were visualized using either gel electrophoresis or nucleic acid lateral flow immunoassay

218 the basis of on-line connection of capillary electrophoresis over a short separation path with contin

219 g unique pathogens typed by pulsed-field gel electrophoresis, overall success rates at TOC in m-MITT

220 erized such DNA motifs by polyacrylamide gel electrophoresis (PAGE) and fluorescence spectroscopy and

221 Polyacrylamide Gel Electrophoresis (PAGE) and Latex Agglutination Test (LAT

222 difficult because routine polyacrylamide gel electrophoresis (PAGE) methods lack the separation resol

223 ies of glycoconjugates on polyacrylamide gel electrophoresis (PAGE), as compared with those of APTS.

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

225 coli O157:H7 or E. coli O61 pulsed-field gel electrophoresis pattern combinations, or with a strain S

226 coli O157:H7 or E. coli O61 pulsed-field gel electrophoresis pattern combinations, or with a strain S

227 no acid composition, secondary structure and electrophoresis pattern) and techno-functional propertie

228 subtyping methods, such as pulsed-field gel electrophoresis (PFGE) and 7-gene multilocus sequence ty

229 using PCR detection of GES, pulse-field gel electrophoresis (PFGE) and WGS for the second cluster.

230 Pulsed-field gel electrophoresis (PFGE) was applied as a first-line appro

231 Pulsed-field gel electrophoresis (PFGE) was performed on isolates from ca

232 ion (PCR) detection of GES, pulsed-field gel electrophoresis (PFGE), and WGS for the second cluster.

233 triction digest technology (pulsed-field gel electrophoresis [PFGE]) to shotgun sequencing of the ent

234 er means (traditional MLST, pulsed-field gel electrophoresis [PFGE], and single-nucleotide variant [S

235 hese limitations, a microfluidic thermal gel electrophoresis platform was developed to provide high-s

236 e control raw samples, while the protein gel electrophoresis profile remained unaffected.

237 ega, RG) were estimated from two-dimensional electrophoresis profiles of meat samples of longissimus

238 annealing, their characterization using gel electrophoresis, purification, and direct visualization

239 Gel electrophoresis results indicated that plasmid lineariza

240 Based on native MS and polyacrylamide gel electrophoresis results, the abundances of hairpin and d

241 r validation by PCR and low-cost agarose gel electrophoresis revealed that 92.5% were polymorphic, sh

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

243 Secondary gel electrophoresis run performed on the bands extracted fro

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

245 died in sodium dodecyl sulfate capillary gel electrophoresis (SDS-CGE) in the interval from 15 to 60

246 s using sodium dodecyl sulphate glycerol gel electrophoresis (SDS-GGE).

247 he sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis of the OM revealed a

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

249 by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and matrix-assisted laser des

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

251 uely) K1 capsule and fimH64 Pulsed-field gel electrophoresis separated ST1193-H64 isolates from other

252 200 nL/min and did not perturb the capillary electrophoresis separation electroosmotic flow as eviden

253 is used for the first time for capillary gel electrophoresis separations of proteins.

254 Gel electrophoresis showed loss in myosin heavy chain (MHC),

255 SDS-gel electrophoresis showed that the distribution patterns of

256 Electrophoresis showed the presence of two AChE bands th

257 negative status on both serum immunofixation electrophoresis (sIFE) and urine (uIFE) immunofixation e

258 d from the gel and reanalyzed by agarose-gel electrophoresis, single-nanoparticle-upconversion micros

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

260 mental validation from chemical mapping, gel electrophoresis, solution X-ray scattering and crystallo

261 Current automated electrophoresis systems for DNA- and RNA-sample quality

262 and simple workflow based on capillary zone electrophoresis-tandem mass spectrometry (CE-MS/MS), in

263 when using multisegment injection-capillary electrophoresis-tandem mass spectrometry (MSI-CE-MS/MS).

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

265 Validated by UV-VIS analysis and gel electrophoresis, the single polymerase created a dual am

266 Electrophoresis throughput is > 2.5 cells/s (70x faster

267 inductive nESI and field amplification micro-electrophoresis to achieve a "dip-and-go" sample loading

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

269 Here, we introduce projection electrophoresis to augment the heavily genomic and trans

270 in miniaturizing analytical methods based on electrophoresis to improve sensitivity and to reduce sam

271 e primary interface used to couple capillary electrophoresis to mass analyzers; however, improved des

272 sition, we used GC-MS and polyacrylamide gel electrophoresis to measure cell-wall fucose and boron (B

273 xploited the separation power of agarose-gel electrophoresis to purify milligram amounts of homogeneo

274 mobility shift assays are widely used in gel electrophoresis to study binding interactions between di

275 The samples were analyzed by gel electrophoresis to visualize a 4.5 kbp band representati

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

277 mosomal deletions, multiple pulsed-field gel electrophoresis types were identified, one of which appe

278 isolates were derived from pulsed-field gel electrophoresis typing.

279 y, we developed a rapid and simple capillary electrophoresis-ultraviolet absorption diode array detec

280 ion conditions in electrochemistry-capillary electrophoresis-ultraviolet-visible spectroscopy measure

281 ge chromatography and microfluidic capillary electrophoresis using the ZipChip platform for comparati

282 nucleotides are used to develop a capillary electrophoresis UV detection method, enabling nucleotide

283 of that observed with a commercial capillary electrophoresis-UV absorbance detection system.

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

285 Gel electrophoresis was performed to fractionate the complex

286 chromatography and native polyacrylamide gel electrophoresis we demonstrated that CCN6 is present as

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

288 Entrapment in the electrophoresis well and low susceptibility to exonuclea

289 The effects of temperature on thermal gel electrophoresis were also characterized.

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

291 netic resonance, and denaturing gradient gel electrophoresis were used in these analyzes.

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

293 n sodium dodecyl sulphate polyacrylamide gel electrophoresis with a molecular weight of ~7 kDa (7kDa-

294 jected to an automated analysis by capillary electrophoresis with capacitively coupled contactless co

295 ate and sulfite in seafood by capillary zone electrophoresis with indirect UV-Vis detection.

296 Capillary gel electrophoresis with laser-induced fluorescence detectio

297 l method to couple microchip-based free-flow electrophoresis with mass spectrometry.

298 nd honey using on-line coupling of capillary electrophoresis with microdialysis.

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

300 rifugation and enriched further by free-flow electrophoresis, yielded >200 proteins known to function