ライフサイエンスコーパス: gel electrophoresis

1 confirmation, SCCmec typing and pulsed-field gel electrophoresis).

2 covalently coupled species were confirmed by gel electrophoresis.

3 interacting proteins, readily detectable by gel electrophoresis.

4 ducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

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

6 n density gradient centrifugation and native gel electrophoresis.

7 of their metabolism in tissue homogenates by gel electrophoresis.

8 alorimetric and spectroscopic methods and by gel electrophoresis.

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

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

11 were extracted and resolved using denaturing gel electrophoresis.

12 ical analysis and blue native polyacrylamide gel electrophoresis.

13 tes can be directly detected with AzBOCEt in gel electrophoresis.

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

15 (approximately 3 MDa) complex in blue-native gel electrophoresis.

16 or genospecies and genotyped by pulsed-field gel electrophoresis.

17 to different xylans was analyzed by affinity gel electrophoresis.

18 mplifications with ISSR and SCoT and agarose gel electrophoresis.

19 r electrical currents during horizontal slab gel electrophoresis.

20 hy and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

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

22 s assessed by two-dimensional polyacrylamide gel electrophoresis.

23 DNA duplex intercalated ethidium bromide and gel electrophoresis.

24 which were indistinguishable by pulsed-field gel electrophoresis.

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

26 l migration behavior of protein fragments in gel electrophoresis.

27 spectroscopy, circular dichroism and native gel electrophoresis.

28 flow cytometry, fluorescence microscopy, and gel electrophoresis.

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

30 nt extracts and conducted SDS-polyacrylamide gel electrophoresis.

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

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

33 esence of individual, labelled strands using gel electrophoresis.

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

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

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

37 e compared to raw pork using two-dimensional gel electrophoresis (2-DE) coupled to image analysis and

38 ets using the two-dimensional polyacrylamide gel electrophoresis (2-DE) technique.

39 Using 2-dimensional differential gel electrophoresis (2D DiGE), 4 of the most significant

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

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

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

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

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

45 aeruginosa using two-dimensional difference gel electrophoresis (2D-DiGE).

46 e the development of 2D intact mtDNA agarose gel electrophoresis (2D-IMAGE) for the separation and de

47 es, including two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) separation and matrix-assi

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

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

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

51 ut by sodium dodecyl sulphate polyacrylamide gel electrophoresis after pre-fractionating with asymmet

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

53 Gel electrophoresis analysis confirms that at least thre

54 Two-dimensional gel electrophoresis analysis demonstrates a replication

55 Pulsed-field gel electrophoresis analysis suggested that 1 pulsotype

56 ectrometry and by blue native polyacrylamide gel electrophoresis analysis.

57 microbiota profiling by denaturing gradient gel electrophoresis and 454/FLX-based 16S rRNA gene ampl

58 ngle X-ray scattering, native polyacrylamide gel electrophoresis and activity assays were used to com

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

60 Proteins were separated by gel electrophoresis and compared to load-matched standar

61 ctures have been thoroughly characterized by gel electrophoresis and cryogenic electron microscopy.

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

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

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

65 Gel electrophoresis and immunoblot analysis were used to

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

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

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

69 hod generally involves laborious radioactive gel electrophoresis and is not conducive to high-through

70 omics approaches, saturation differential in-gel electrophoresis and isotope-coded affinity tagging.

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

72 ring post mortem ageing were investigated by gel electrophoresis and LC-MS/MS analysis.

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

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

75 Two-dimensional gel electrophoresis and mass spectrometry demonstrated t

76 Two-dimensional gel electrophoresis and mass spectrometry revealed signi

77 Native polyacrylamide gel electrophoresis and mass spectrometry revealed that

78 Analysis by gel electrophoresis and mass spectrometry revealed trans

79 Moreover, by two-dimensional gel electrophoresis and mass spectrometry we discovered

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

81 Comparative gel electrophoresis and mass spectrometry-based proteomi

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

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

84 onmental and clinical ESBLEC by pulsed-field gel electrophoresis and multilocus sequence typing and i

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

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

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

88 led with off-chip polymerase chain reaction, gel electrophoresis and Sanger sequencing, a panel of ge

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

90 everal applications including polyacrylamide gel electrophoresis and sensing devices.

91 Gel electrophoresis and single-molecule fluorescence res

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

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

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

95 Gel electrophoresis and steady state and time-resolved f

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

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

98 n proteins were submitted to high-resolution gel electrophoresis and tested for IgE reactivity by usi

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

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

101 emistry laboratory equipment for cell lysis, gel electrophoresis and western blotting.

102 We combined 2D gel electrophoresis and whole genome approaches to map g

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

104 The gel-electrophoresis and peptide mass fingerprint analyse

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

106 crobial susceptibility testing, pulsed-field gel electrophoresis, and multiplex PCR for phylotyping t

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

108 were detected by two-dimensional difference gel electrophoresis, and proteins were identified by tan

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

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

111 crRNA-containing complex detected by native gel electrophoresis, and the conserved 5' repeat sequenc

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

113 Proteins were resolved by one-dimensional gel electrophoresis, and tryptic peptides were extracted

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

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

116 (PCR) are exploited using on-column agarose gel electrophoresis as separation and inductively couple

117 taining after two-dimensional polyacrylamide gel electrophoresis, as well as column-based phosphoprot

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

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

120 ion in sodium dodecyl sulfate-polyacrylamide gel electrophoresis assays as well as solution-based kin

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

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

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

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

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

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

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

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

129 r two-dimensional blue native polyacrylamide gel electrophoresis (BN-PAGE).

130 d multilocus sequence typing or pulsed-field gel electrophoresis, but high-resolution examinations of

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

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

133 Gel electrophoresis confirmed that the protein distribut

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

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

136 luorescence-based two-dimensional difference gel electrophoresis, coupled with mass spectrometry, ide

137 ctures have been thoroughly characterized by gel electrophoresis, cryogenic electron microscopy imagi

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

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

140 Gel electrophoresis demonstrated that the heated WPI and

141 ligand binding by ITC and global folding by gel electrophoresis demonstrates the importance of the k

142 Denaturing Gradient Gel Electrophoresis (DGGE) analysis confirmed the above

143 Denaturing gradient gel electrophoresis (DGGE), which compared the overall m

144 y polymerase chain reaction and pulsed-field gel electrophoresis differed from that of B. burgdorferi

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

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

147 nstituents and by complementary quantitative gel electrophoresis experiments.

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

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

150 Using two-dimensional gel electrophoresis followed by MALDI-TOF mass spectrome

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

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

153 method combines the high separation power of gel electrophoresis for protein separation with the high

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

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

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

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

158 Pulsed-field gel electrophoresis genotyping indicated that the outbre

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

160 Although gel electrophoresis identified 11 proteins that were dif

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

162 cusing sodium dodecyl sulfate polyacrylamide gel electrophoresis (IEF/SDS-PAGE) and fluorescence meas

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

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

165 egular clusters of illness, and pulsed-field gel electrophoresis in conjunction with whole-genome seq

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

167 Gel electrophoresis indicated that increased heat stabil

168 Gel electrophoresis is a powerful experimental method to

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

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

171 efore, we introduce a kinetic polyacrylamide gel electrophoresis (KPAGE) microfluidic assay that dire

172 ro using a low-temperature EDTA-free agarose gel electrophoresis (LTEAGE) procedure.

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

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

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

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

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

178 counterparts and analyzed by polyacrylamide gel electrophoresis mobility shifts.

179 Forty CR-Kp were genotyped by pulsed field gel electrophoresis, multilocus sequence typing (MLST),

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

181 plicability of the method, 10 gel bands from gel electrophoresis of an albumin-depleted human plasma

182 Agarose gel electrophoresis of DNA and RNA is routinely performe

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

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

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

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

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

188 Moreover, polyacrylamide gel electrophoresis of the enriched extract revealed the

189 Studies using two-dimensional gel electrophoresis of various brain regions combined wi

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

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

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

193 sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) method for measuring the amou

194 chemical lysis and subsequent polyacrylamide gel electrophoresis (PAGE) of the single-cell lysate.

195 Using polyacrylamide gel electrophoresis (PAGE) to separate monomeric from di

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

197 s spectrometry (LC-MS/MS) and polyacrylamide gel electrophoresis (PAGE).

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

199 ere compared using phylotyping, pulsed-field gel electrophoresis (PFGE) analysis, sequence typing, an

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

201 same period were compared using pulsed-field gel electrophoresis (PFGE) and multilocus sequence typin

202 Pulsed-field gel electrophoresis (PFGE) and multilocus variable numbe

203 uating the genotypic diversity, pulsed-field gel electrophoresis (PFGE) and/or enterobacterial repeti

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

205 Pulsed-field gel electrophoresis (PFGE) has been the gold standard ap

206 Pulsed-field gel electrophoresis (PFGE) is a common method used to ty

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

208 omosome mec (SCCmec) typing and pulsed-field gel electrophoresis (PFGE) subtyping.

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

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

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

212 tilocus sequence typing (MLST), pulsed-field gel electrophoresis (PFGE), and array-based comparative

213 Susceptibility testing, pulsed-field gel electrophoresis (PFGE), and multilocus sequence typi

214 olates were determined by using pulsed-field gel electrophoresis (PFGE), multilocus sequence typing (

215 The typing methods included pulsed-field gel electrophoresis (PFGE), multilocus variable number t

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

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

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

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

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

221 gold standard subtyping method, pulsed-field gel electrophoresis (PFGE).

222 atia isolates was determined by pulsed-field gel electrophoresis (PFGE).

223 Isolates were typed by pulsed-field gel electrophoresis (PFGE).

224 ntimicrobial susceptibility and pulsed-field gel electrophoresis (PFGE).

225 relatedness was evaluated with pulsed-field gel electrophoresis (PFGE).

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

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

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

229 single cells into microwells, lysis in situ, gel electrophoresis, photoinitiated blotting to immobili

230 Pulsed-field gel electrophoresis profiles of a sample of isolates wer

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

232 al component analysis of denaturing gradient gel electrophoresis profiles was evident in adult mice.

233 patterns and indistinguishable pulsed-field gel electrophoresis profiles.

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

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

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

237 Gel electrophoresis results confirmed that DNA cleavage

238 Native gel electrophoresis revealed a rapidly-modulated recipro

239 Gel electrophoresis revealed substantial digestion of mi

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

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

242 2-D gel electrophoresis revealed that protein profiles of in

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

244 Analysis of interacting proteins by gel electrophoresis revealed the endogenous ribonuclease

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

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

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

248 ising sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) combined with principal c

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

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

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

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

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

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

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

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

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

258 ined cells and DNA fragmentation assay using gel electrophoresis showed clear fragmentation in the ch

259 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showed modification with 1-3 PEG cha

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

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

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

263 ST-1 (which corresponds to pulsed-field gel electrophoresis strain type NAP1/ribotype 027) was t

264 Gel electrophoresis studies demonstrate the formation of

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

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

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

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

269 Single cell gel electrophoresis (the comet assay), continues to gain

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

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

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

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

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

275 Indeed, by only using gel electrophoresis to grossly enrich GSK-3beta from who

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

277 We apply agarose gel electrophoresis to sensitively evaluate protein bind

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

279 nolone-resistant North American pulsed-field gel electrophoresis type 1 (NAP1) strain in Clostridium

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

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

282 mplex protein mixtures, two-dimensional (2D) gel electrophoresis was combined with in-gel MAAH, affin

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 Agarose gel electrophoresis was subsequently used to separate an

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

287 Blue native polyacrylamide gel electrophoresis was used to isolate and characterize

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

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

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

291 on chromatography, and native polyacrylamide gel electrophoresis, we demonstrate that Nrdp1 self-asso

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

293 Last, using polyacrylamide gel electrophoresis, we showed that added GIPCs facilita

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

295 peared to be clonal by standard pulsed-field gel electrophoresis, whole-genome sequencing revealed su

296 lococcal surface proteins by two-dimensional gel electrophoresis with a ligand overlay assay with hTS

297 tection approach with the CGE-LIF (capillary gel electrophoresis with laser-induced fluorescence) tec

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