ライフサイエンスコーパス: gel electrophoresis

1 l migration behavior of protein fragments in gel electrophoresis.

2 esence of individual, labelled strands using gel electrophoresis.

3 he PCR amplification of STR loci followed by gel electrophoresis.

4 mplifications with ISSR and SCoT and agarose gel electrophoresis.

5 tion studies by high-resolution clear native gel electrophoresis.

6 which were indistinguishable by pulsed-field gel electrophoresis.

7 target protein with the results read out by gel electrophoresis.

8 spectroscopy, circular dichroism and native gel electrophoresis.

9 flow cytometry, fluorescence microscopy, and gel electrophoresis.

10 rmations of a DNA nanoswitch and decoding by gel electrophoresis.

11 nt extracts and conducted SDS-polyacrylamide gel electrophoresis.

12 mined by infectivity assays and pulsed-field gel electrophoresis.

13 mosomal DNA damage monitored by pulsed-field gel electrophoresis.

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

15 covalently coupled species were confirmed by gel electrophoresis.

16 interacting proteins, readily detectable by gel electrophoresis.

17 ducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

18 lates is easier and faster than pulsed-field gel electrophoresis.

19 n density gradient centrifugation and native gel electrophoresis.

20 of their metabolism in tissue homogenates by gel electrophoresis.

21 alorimetric and spectroscopic methods and by gel electrophoresis.

22 600 to 9,000 nucleotides as seen by alkaline gel electrophoresis.

23 carried out by DNA melting curve analysis or gel electrophoresis.

24 for the separation of HMOs by multicapillary gel electrophoresis.

25 logy field, can be automated using capillary gel electrophoresis.

26 ls and DNA fragmentation analyses by agarose gel electrophoresis.

27 erized by FT-IR, SEM, cyclic voltammetry and gel electrophoresis.

28 d the resolution capacity of regular agarose gel electrophoresis.

29 eneral SDS replacement in SDS-polyacrylamide gel electrophoresis.

30 nnealing cycle are separated by 4-6% agarose gel electrophoresis.

31 of protein changes that were obtained by 2D gel electrophoresis.

32 in single-channel electrical recordings and gel electrophoresis.

33 ne (EDA) with various precursor ratios using gel-electrophoresis.

34 rmined by densitometry analysis on 1D and 2D gels electrophoresis.

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

36 itivity and dynamic range of two-dimensional gel electrophoresis (2-DE) are currently hampering its u

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

38 Using two-dimensional difference gel electrophoresis (2D-DIGE) and label-free quantitativ

39 pproach involving two dimensional difference gel electrophoresis (2D-DIGE) and mass spectrometry (MS)

40 s of TRIM32 using 2D fluorescence difference gel electrophoresis (2D-DIGE) in order to further explor

41 Here, we used two dimensional-differential gel electrophoresis (2D-DIGE) to compare protein express

42 n fluorescence two-dimensional difference in-gel electrophoresis (2D-DIGE)-coupled mass spectrometry

43 technique called two-dimensional difference gel electrophoresis (2D-DIGE).

44 separated by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), and the total mercury con

45 erformed using two-dimensional difference in-gel electrophoresis(2D-DIGE) followed by mass spectromet

46 munofixation and nondenaturing 2-dimensional gel electrophoresis (2DGE).

47 isoelectric point is a critical part of 2-D gel electrophoresis, a key precursor of proteomics, wher

48 amples are resolved by native polyacrylamide gel electrophoresis, after which fluorescence-resonance

49 Two-dimensional gel electrophoresis analysis demonstrates a replication

50 st designed/optimized and tested by standard gel electrophoresis analysis.

51 Cl method revealed intense RNA bands through gel electrophoresis and a nanodrop spectrophotometer det

52 isolates were characterized by pulsed-field gel electrophoresis and agr group.

53 Proteins were resolved by gel electrophoresis and blotted, and Siglec-8 ligands de

54 Two-dimensional blue native polyacrylamide gel electrophoresis and coimmunoprecipitation showed tha

55 Using gel electrophoresis and DNA melting curve analysis, we s

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

57 of inositol phosphates using polyacrylamide gel electrophoresis and high-performance liquid chromato

58 mbined sodium dodecyl sulfate-polyacrylamide gel electrophoresis and high-performance liquid chromato

59 on on sodium dodecyl sulphate-polyacrylamide gel electrophoresis and high-performance liquid chromato

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

61 High-resolution 2-D gel electrophoresis and immunoblot analyses revealed tha

62 Gel electrophoresis and immunoblot analysis were used to

63 using sodium dodecyl sulfate poly acrylamide gel electrophoresis and immunoblotting showed acid-solub

64 e quantified with agarose and polyacrylamide gel electrophoresis and immunoblotting.

65 y both sodium dodecyl sulfate polyacrylamide gel electrophoresis and immunofluorescence staining to c

66 ology using circular DNA deep-sequencing, 2D gel electrophoresis and inverse polymerase chain reactio

67 assessed by using 2-dimensional differential gel electrophoresis and label-free mass spectrometry in

68 CBG of healthy individuals were monitored by gel electrophoresis and LC-MS/MS to determine the cleava

69 me profiling, a method combining blue-native gel electrophoresis and liquid chromatography tandem mas

70 Two-dimensional gel electrophoresis and mass spectrometry demonstrated t

71 Two-dimensional gel electrophoresis and mass spectrometry revealed signi

72 Native polyacrylamide gel electrophoresis and mass spectrometry revealed that

73 Two-dimensional differential gel electrophoresis and mass spectrometry were used to i

74 omic two-dimensional fluorescence difference gel electrophoresis and mass spectrometry, and further v

75 ain (TPM4) by two-dimensional polyacrylamide gel electrophoresis and mass spectrometry, and its bindi

76 Comparative gel electrophoresis and mass spectrometry-based proteomi

77 This interaction was confirmed using native gel electrophoresis and mass spectrometry.

78 sible transmission routes using pulsed-field gel electrophoresis and multi-locus variable number of t

79 chain reaction-temporal temperature gradient gel electrophoresis and next-generation sequencing.

80 y characteristics of EAEC using pulsed-field gel electrophoresis and next-generation sequencing.

81 We monitored plasmid DNA degradation using gel electrophoresis and qPCR with both short amplicons (

82 o band-based typing techniques (pulsed-field gel electrophoresis and repetitive extragenic palindromi

83 doped silica shell were separated by agarose gel electrophoresis and scanned by a conventional fluore

84 everal applications including polyacrylamide gel electrophoresis and sensing devices.

85 hine by quantifying the images obtained from gel electrophoresis and showed that our system is compar

86 Native polyacrylamide gel electrophoresis and size exclusion chromatography de

87 ilter assay, analytical ultracentrifugation, gel electrophoresis and size-exclusion chromatography),

88 infection by one and two-dimensional agarose gel electrophoresis and Southern hybridization.

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

90 evaluated for relatedness using pulsed-field gel electrophoresis and staphylococcal cassette chromoso

91 ricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis and subsequent image analysis.

92 tive DNA cleavage is confirmed by denaturing gel electrophoresis and surface group pKa measurement.

93 separated by two-dimensional polyacrylamide gel electrophoresis and then identified by electrospray

94 he separation of proteins by one-dimensional gel electrophoresis and trypsin digestion, their identif

95 other Belgian hospitals) using pulsed-field gel electrophoresis and WGS.

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

97 Pulsed-field gel electrophoresis and whole-genome sequencing were per

98 The gel-electrophoresis and peptide mass fingerprint analyse

99 In addition, proteins were separated by gel-electrophoresis and selected spots were characterise

100 RS-PCR was performed with conventional gel electrophoresis, and PCR was used for toxin gene ide

101 ed, and/or quantified using ultrafiltration, gel electrophoresis, and RT-qPCR (quantitative reverse t

102 ze-exclusion chromatography, two-dimensional gel electrophoresis, and small angle x-ray scattering an

103 were analysed by two-dimensional difference gel electrophoresis, and the differentially regulated pr

104 rotein degradation with time was assessed by gel-electrophoresis, and mineral products formed were ch

105 ques for observing such DNA knots (primarily gel electrophoresis) are limited to bulk methods and cir

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

107 Using a lab-based gel electrophoresis assay and a rapid, field-ready light

108 signed RNA nanostructure is characterized by gel electrophoresis, atomic force microscopy and cryogen

109 been characterized by native polyacrylamide gel electrophoresis, atomic force microscopy, and cryoge

110 mologous strains (defined by field-inversion gel electrophoresis banding pattern), emm types, and emm

111 A 2-dimensional polyacrylamide gel electrophoresis-based comparative proteomics analysi

112 We generalize this band-collision gel electrophoresis (BCGE) approach to other reaction ty

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

114 that is based on Blue Native Polyacrylamide Gel Electrophoresis (BN-PAGE) and dot immunoblotting for

115 mplex isolated by blue native polyacrylamide gel electrophoresis (BN-PAGE) from digitonin-solubilized

116 PP4 complexes by blue native polyacrylamide gel electrophoresis (BN-PAGE) indicates that PP4 holoenz

117 hromatography and blue native polyacrylamide gel electrophoresis (BN-PAGE) to demonstrate BbHtrA olig

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

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

120 tion of poly-L-lysine oligomers by capillary gel electrophoresis (CGE), molar mass distribution of en

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

122 ues by sodium dodecyl sulfate polyacrylamide gel electrophoresis confirmed that the primary targets o

123 Gel electrophoresis confirmed that the protein distribut

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

125 H-(1)H nuclear magnetic resonance and native gel electrophoresis confirmed the formation of a paralle

126 d (APTS) labeling, and multiplexed capillary gel electrophoresis coupled to laser-induced fluorescenc

127 ntified using two-dimensional polyacrylamide gel electrophoresis coupled with matrix-assisted laser d

128 rmination of malting barley that may replace gel electrophoresis currently used for this purpose.

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

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

131 Gel electrophoresis demonstrated that the heated WPI and

132 different heights using denaturant gradient gel electrophoresis (DGGE) fingerprinting.

133 s proplatelet-producing MKs by 2D difference gel electrophoresis (DIGE) and polysome profiling, respe

134 ed approach of non-denaturing polyacrylamide gel electrophoresis, dynamic light scattering, confocal

135 37, as assessed by pulsed-field and Gardella gel electrophoresis, electron microscopy, and single-mol

136 nd separation resolution provided by thermal gel electrophoresis enabled rapid screening of native pr

137 ison with traditional methodologies based on gel electrophoresis, especially in the case of overlappi

138 nstituents and by complementary quantitative gel electrophoresis experiments.

139 ESBL-associated H30Rx subclone, pulsed-field gel electrophoresis, extended virulence genotyping, and

140 n dynamics simulations, with thermophoresis, gel electrophoresis, fluorescence correlation spectrosco

141 fluorescent staining of DNA and proteins in gel electrophoresis, fluorescence guided surgery, or as

142 vitro techniques (TWJ-screen, polyacrylamide gel electrophoresis, fluorescence resonance energy trans

143 roteomic approach based on a two-dimensional gel electrophoresis followed by liquid chromatography-ta

144 total (32)P-activity) and by polyacrylamide gel electrophoresis followed by phosphorimaging (to dete

145 e analysis was performed using 2D difference gel electrophoresis followed by protein identification v

146 IgE-reactive proteins were identified by 2D gel electrophoresis, followed by Western blot with poole

147 onium sulfate precipitation and subjected to gel electrophoresis for protein separation.

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

149 that migrated more slowly in native agarose gel electrophoresis from A36V mutant than from the wild-

150 fluidic free-standing kinetic polyacrylamide gel electrophoresis (fsKPAGE) assay.

151 nto proteoliposomes, as shown by blue native gel electrophoresis, gel filtration, and determination o

152 eparations directly in native polyacrylamide gel electrophoresis gels, enabling unprecedented resolut

153 Although PCR and gel electrophoresis have been integrated, replenishing t

154 Although gel electrophoresis identified 11 proteins that were dif

155 Two-dimensional differential in-gel electrophoresis identified abnormal actin-interactin

156 Gel electrophoresis identified the presence of organic m

157 for protein detection in texture analysis of gel electrophoresis images.

158 among NEC, sepsis and control cohorts using gel electrophoresis, immunoblot and mass spectrometry.

159 A reduced size upon native gel electrophoresis indicated an alteration of the struc

160 Gel electrophoresis indicated that increased heat stabil

161 ication via polymerase chain reaction (PCR), gel electrophoresis indicated that only cereal samples c

162 e robust (with basic PCR methods and agarose gel electrophoresis), informative, and applicable in mea

163 Gel electrophoresis is a powerful experimental method to

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

165 dynamic light scattering, and polyacrylamide gel electrophoresis, is reported for the loading and pro

166 sequencing, two-dimensional differential in-gel electrophoresis, macromolecule biosynthesis assays a

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

168 ve (trypomastigote) forms by two-dimensional gel electrophoresis/matrix-assisted laser desorption ion

169 lyses included strain typing by pulsed-field gel electrophoresis, mec and accessory gene regulator gr

170 apid, high-throughput fluorescence capillary gel electrophoresis method as an alternative to traditio

171 , this is the first report of a new diagonal gel electrophoresis method to isolate and identify metal

172 ibe several assays using this core capillary gel electrophoresis methodology to accelerate study of n

173 taminant sweeping-blue native-polyacrylamide gel electrophoresis (MICS-BN-PAGE).

174 counterparts and analyzed by polyacrylamide gel electrophoresis mobility shifts.

175 n hospitals underwent typing by pulsed-field gel electrophoresis, multilocus sequence typing, and WGS

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

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

178 We applied comparative native gel electrophoresis of chloroplast protein complexes fol

179 Similarly, both S1 nuclease and 2D gel electrophoresis of DNA topoisomers did not detect an

180 They used the technique of gel electrophoresis of enzymes and proteins to study var

181 extracted from transformedNicotiana tabacum Gel electrophoresis of leaf extracts revealed a consiste

182 Blue native-polyacrylamide gel electrophoresis of mitochondrial extracts combined w

183 targeted proteomic assay with polyacrylamide gel electrophoresis of single cell lysates followed by a

184 Two-dimensional gel electrophoresis of wheat leaves resolved more than 3

185 ithin the gene were determined by denaturing gel electrophoresis or automated capillary-based cycle s

186 Results were visualized using either gel electrophoresis or nucleic acid lateral flow immunoa

187 using unique pathogens typed by pulsed-field gel electrophoresis, overall success rates at TOC in m-M

188 en to be successful by native polyacrylamide gel electrophoresis (PAGE) and cryogenic electron micros

189 racterized such DNA motifs by polyacrylamide gel electrophoresis (PAGE) and fluorescence spectroscopy

190 Polyacrylamide Gel Electrophoresis (PAGE) and Latex Agglutination Test

191 sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) in a PDMS/glass microfluidic

192 is difficult because routine polyacrylamide gel electrophoresis (PAGE) methods lack the separation r

193 ilities of glycoconjugates on polyacrylamide gel electrophoresis (PAGE), as compared with those of AP

194 c networks and the utility of polyacrylamide gel electrophoresis (PAGE), we develop a technique for f

195 E. coli O157:H7 or E. coli O61 pulsed-field gel electrophoresis pattern combinations, or with a stra

196 E. coli O157:H7 or E. coli O61 pulsed-field gel electrophoresis pattern combinations, or with a stra

197 coli isolates had similar PFGE (pulsed field gel electrophoresis) patterns and the same MLST (multilo

198 ular subtyping methods, such as pulsed-field gel electrophoresis (PFGE) and 7-gene multilocus sequenc

199 Pulsed-field gel electrophoresis (PFGE) and multi-locus sequence typi

200 tion using PCR detection of GES, pulse-field gel electrophoresis (PFGE) and WGS for the second cluste

201 d of SmaI restriction digestion pulsed-field gel electrophoresis (PFGE) for typing S. aureus Forty-tw

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

203 he United States and to compare pulsed-field gel electrophoresis (PFGE) to the combination of ribosom

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

205 Pulsed-field gel electrophoresis (PFGE) was performed on isolates fro

206 Pulsed-field gel electrophoresis (PFGE) was performed to test genetic

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

208 eaction (PCR) detection of GES, pulsed-field gel electrophoresis (PFGE), and WGS for the second clust

209 included Western blot analysis, pulsed-field gel electrophoresis (PFGE), polymerase chain reaction, a

210 ular subtyping methods, such as pulsed-field gel electrophoresis (PFGE), were critical in detecting o

211 olution, especially compared to pulsed-field gel electrophoresis (PFGE).

212 typing (CRISPR-MVLST), and (iv) pulsed-field gel electrophoresis (PFGE).

213 macrorestriction patterns after pulsed-field gel electrophoresis (PFGE).

214 the interpretation of data from pulsed-field gel electrophoresis (PFGE).

215 r length-based methods, such as pulsed-field gel electrophoresis (PFGE); however, conventional multil

216 ermining bacterial relatedness (pulsed-field gel electrophoresis [PFGE]) remains essentially unchange

217 restriction digest technology (pulsed-field gel electrophoresis [PFGE]) to shotgun sequencing of the

218 other means (traditional MLST, pulsed-field gel electrophoresis [PFGE], and single-nucleotide varian

219 me these limitations, a microfluidic thermal gel electrophoresis platform was developed to provide hi

220 o the control raw samples, while the protein gel electrophoresis profile remained unaffected.

221 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of transglutaminase-treated

222 rmal annealing, their characterization using gel electrophoresis, purification, and direct visualizat

223 lexes using spectroscopy, pull-downs, native gel electrophoresis, quantitative mass spectrometry and

224 wide range of molecular interactions using a gel electrophoresis readout.

225 until 120min of hydrolysis were evaluated by gel electrophoresis, relative fluorescence intensity, em

226 Gel electrophoresis results confirmed that DNA cleavage

227 Gel electrophoresis results indicated that plasmid linea

228 Based on native MS and polyacrylamide gel electrophoresis results, the abundances of hairpin a

229 Native gel electrophoresis revealed a rapidly-modulated recipro

230 Gel electrophoresis revealed substantial digestion of mi

231 arker validation by PCR and low-cost agarose gel electrophoresis revealed that 92.5% were polymorphic

232 s, coimmunoprecipitation and two-dimensional gel electrophoresis revealed that CAR can form a homodim

233 The results of 2-D fluorescence difference gel electrophoresis revealed that DLA prevented the decr

234 2-D gel electrophoresis revealed that protein profiles of in

235 Blue-native gel electrophoresis revealed that TbTim62 is present pri

236 Secondary gel electrophoresis run performed on the bands extracted

237 zed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis SDS-PAGE-immunoblotting with patient

238 realized by sodium dodecyl sulfate capillary gel electrophoresis (SDS CGE) with head-column field-amp

239 studied in sodium dodecyl sulfate capillary gel electrophoresis (SDS-CGE) in the interval from 15 to

240 scles using sodium dodecyl sulphate glycerol gel electrophoresis (SDS-GGE).

241 The sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis of the OM reveal

242 Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) analysis revealed the loc

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

244 rane designed to allow proteins separated by gel electrophoresis (SDS-PAGE) to be detected as peptide

245 Denaturing polyacrylamide gel electrophoresis (SDS-PAGE) was used to separate prot

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

247 ) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).

248 d by sodium dodecyl sulphate-polyaccrylamide gel electrophoresis (SDS-PAGE).

249 using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

250 ed by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE).

251 e these particles by a combination of native gel electrophoresis, sedimentation velocity, electron mi

252 uniquely) K1 capsule and fimH64 Pulsed-field gel electrophoresis separated ST1193-H64 isolates from o

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

254 Using our Pulse Field Gel Electrophoresis-shift approach, we determined resect

255 Gel electrophoresis showed loss in myosin heavy chain (M

256 SDS-gel electrophoresis showed that the distribution pattern

257 In addition, protein gel electrophoresis showed that there was only one enric

258 lated from the gel and reanalyzed by agarose-gel electrophoresis, single-nanoparticle-upconversion mi

259 ic light scattering, controlled proteolysis, gel electrophoresis, site-directed mutagenesis and micro

260 perimental validation from chemical mapping, gel electrophoresis, solution X-ray scattering and cryst

261 This process could be verified by gel electrophoresis, spectroscopically and in vitro conf

262 Gel electrophoresis studies demonstrate the formation of

263 By using blue native/Deriphat-polyacrylamide gel electrophoresis, sucrose density gradients, and isol

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

265 Dynamic Light Scattering and Polyacrylamide Gel Electrophoresis techniques were used to characterize

266 onding plasma fraction were studied using 2D gel electrophoresis techniques.

267 sed on protein separation by two-dimensional gel electrophoresis, the identification of calcium ions

268 Validated by UV-VIS analysis and gel electrophoresis, the single polymerase created a dua

269 a broad selection of techniques from routine gel electrophoresis to advanced single-molecule imaging.

270 ere, we used two-dimensional differential in-gel electrophoresis to analyze hepatic cells in early re

271 an alternative to traditional polyacrylamide gel electrophoresis to characterize nucleic acid metabol

272 and high resolution two-dimensional agarose gel electrophoresis to examine the torsional tension of

273 omposition, we used GC-MS and polyacrylamide gel electrophoresis to measure cell-wall fucose and boro

274 ve exploited the separation power of agarose-gel electrophoresis to purify milligram amounts of homog

275 temperature for each operation and standard gel electrophoresis to read the data.

276 tic mobility shift assays are widely used in gel electrophoresis to study binding interactions betwee

277 The samples were analyzed by gel electrophoresis to visualize a 4.5 kbp band represen

278 fully-denaturing formaldehyde polyacrylamide gel electrophoresis) to prevent annealing of sRNAs to th

279 The North American pulsed-field gel electrophoresis type 1 (NAP1) strain was more preval

280 chromosomal deletions, multiple pulsed-field gel electrophoresis types were identified, one of which

281 f Pa isolates were derived from pulsed-field gel electrophoresis typing.

282 oxidation observed via 2D redox differential gel electrophoresis upon IL-4 treatment suggests more th

283 Pulsed-field gel electrophoresis was conducted to strain type the iso

284 onomeric genomes as assessed by pulsed-field gel electrophoresis was greatly diminished, and DNA-cont

285 Gel electrophoresis was performed to fractionate the com

286 Agarose gel electrophoresis was subsequently used to separate an

287 ic analysis by 2-dimensional differential in-gel electrophoresis was used to determine the reversibil

288 Using gene expression analysis and native gel electrophoresis we characterize the expression and a

289 ion chromatography and native polyacrylamide gel electrophoresis we demonstrated that CCN6 is present

290 By using improved polyacrylamide gel electrophoresis we were able to visualize polyP extr

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

292 By 2D gel electrophoresis, we detect two different kinds of st

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

294 essed protein spots from the two-dimensional gel electrophoresis were analyzed using mass spectrometr

295 magnetic resonance, and denaturing gradient gel electrophoresis were used in these analyzes.

296 es on sodium dodecyl sulphate polyacrylamide gel electrophoresis with a molecular weight of ~7 kDa (7

297 Capillary gel electrophoresis with laser-induced fluorescence dete

298 Two-dimensional difference in-gel electrophoresis with matrix assisted laser desorptio

299 d Abeta aggregation was investigated through gel electrophoresis with Western blotting, transmission

300 otein detection using the minimal difference gel electrophoresis workflow showed improvements in lowe