ライフサイエンスコーパス: two-dimensional gel electrophoresis

1 flowering in biological quadruplicate using two-dimensional gel electrophoresis.

2 yringae pv tomato DC3000 were analyzed using two-dimensional gel electrophoresis.

3 xpression were observed in each condition by two-dimensional gel electrophoresis.

4 rometry of immunoreactive bands separated by two-dimensional gel electrophoresis.

5 onal MPA-induced proteins were identified by two-dimensional gel electrophoresis.

6 ination between the IM and OM was evident by two-dimensional gel electrophoresis.

7 purified by DNA affinity chromatography and two-dimensional gel electrophoresis.

8 c point values of 0.01, without the need for two-dimensional gel electrophoresis.

9 imension fractions to proteins visualized by two-dimensional gel electrophoresis.

10 ormance liquid chromatography technology and two-dimensional gel electrophoresis.

11 s identified using Western blot analysis and two-dimensional gel electrophoresis.

12 y detected by enhanced chemiluminescence and two-dimensional gel electrophoresis.

13 sphatases, and the proteins were analyzed by two-dimensional gel electrophoresis.

14 abeled on cysteine residues and separated by two-dimensional gel electrophoresis.

15 rx I to a more acidic species as assessed by two-dimensional gel electrophoresis.

16 ge ABCA1 migrated to the alpha position in a two-dimensional gel electrophoresis.

17 Phosphoproteins were analyzed by two-dimensional gel electrophoresis.

18 of the same cell populations was done using two-dimensional gel electrophoresis.

19 on with that of nitrogen-replete cells using two-dimensional gel electrophoresis.

20 te polyacrylamide gel electrophoresis and by two-dimensional gel electrophoresis.

21 ed total proteins of Streptomyces griseus by two-dimensional gel electrophoresis.

22 immunoblot, and Northern blot analyses, and two-dimensional gel electrophoresis.

23 cation intermediates from the chromosome via two-dimensional gel electrophoresis.

24 y used to identify plant proteins arrayed by two-dimensional gel electrophoresis.

25 ensitive restriction enzyme was subjected to two-dimensional gel electrophoresis.

26 llowing separation of tachyzoite antigens by two-dimensional gel electrophoresis.

27 PhoP/PhoQ regulon mutations were compared by two-dimensional gel electrophoresis.

28 maize shoot mitochondria and was resolved by two-dimensional gel electrophoresis.

29 tially upregulated by eIF-4E, as revealed by two-dimensional gel electrophoresis.

30 on of defense genes by H2O2 were analyzed by two-dimensional gel electrophoresis.

31 and the wild-type strain were compared using two-dimensional gel electrophoresis.

32 ous identification of proteins isolated from two-dimensional gel electrophoresis.

33 osition among cellular proteins separated by two-dimensional gel electrophoresis.

34 itherto uncharacterized hnRNP constituent in two-dimensional gel electrophoresis.

35 oration of 32PO4 into proteins detected with two-dimensional gel electrophoresis.

36 ARNT immunoprecipitations were subjected to two-dimensional gel electrophoresis.

37 mutant and wild-type males were assessed by two-dimensional gel electrophoresis.

38 expressed in vitro and analysis by one- and two-dimensional gel electrophoresis.

39 bovis and M. tuberculosis, as determined by two-dimensional gel electrophoresis.

40 eed proteome analyses were also performed by two-dimensional gel electrophoresis.

41 ation of radical cleavage agents followed by two-dimensional gel electrophoresis.

42 -DM protein extracts were separated by using two-dimensional gel electrophoresis.

43 thal variants of PICV, investigated by using two-dimensional gel electrophoresis.

44 the immunoprecipitated protein complexes by two-dimensional gel electrophoresis.

45 Proteins were resolved and quantified by two-dimensional gel electrophoresis.

46 from biofilm grown in vitro and separated by two-dimensional gel electrophoresis.

47 its highly metastatic variant LNCaP-LN3, by two-dimensional gel electrophoresis.

48 and 34 non-AD patients were separated using two-dimensional gel electrophoresis.

49 were analysed using a proteomics technique: two dimensional gel electrophoresis (2-DE).

50 ions in the sensitivity and dynamic range of two-dimensional gel electrophoresis (2-DE) are currently

51 In spite of two-dimensional gel electrophoresis (2-DE) being an effe

52 el) products were compared to raw pork using two-dimensional gel electrophoresis (2-DE) coupled to im

53 e public infrastructure for dissemination of two-dimensional Gel Electrophoresis (2-DE) proteomics da

54 liquid isoelectric focusing prefractionation/two-dimensional gel electrophoresis (2-DE) to identify a

55 nd Burkholderia multivorans were analyzed by two-dimensional gel electrophoresis (2-DE), followed by

56 asic immobilized pH gradient strips prior to two-dimensional gel electrophoresis (2-DE).

57 ax), two complementary proteomic approaches, two-dimensional gel electrophoresis (2-DGE) and semicont

58 d to detection of protein spots separated by two-dimensional gel electrophoresis (2D-GE) and identifi

59 GELBANK is a publicly available database of two-dimensional gel electrophoresis (2DE) gel patterns o

60 st commonly accomplished by a combination of two-dimensional gel electrophoresis (2DE) to separate an

61 II-like epithelial cells by high-resolution two-dimensional gel electrophoresis (2DE).

62 ApoA-1 isoforms were purified by two-dimensional gel electrophoresis (2DGE) and assessmen

63 The methodological advance in two-dimensional gel electrophoresis (2DGE) has been the

64 gy for conducting proteomic studies has been two-dimensional gel electrophoresis (2DGE), but this app

65 ing pH gel electrophoresis (NEPHGE) forms of two-dimensional gel electrophoresis (2DGE), coupled with

66 n analytes, as opposed to techniques such as two-dimensional gel electrophoresis (2DIGE) or mass spec

67 lasmic reticulum that could be identified by two-dimensional gel electrophoresis after cleavage with

68 Two-dimensional gel electrophoresis allowed us to conclu

69 OF4 grown at pH 7.5 and 10.5, as studied by two-dimensional gel electrophoresis analyses, did not ex

70 Two-dimensional gel electrophoresis analysis demonstrate

71 deglutathionylation and confirmed in vivo by two-dimensional gel electrophoresis analysis.

72 RNase Z(L) performed by limited proteolysis, two dimensional gel electrophoresis and mass spectrometr

73 Two dimensional gel electrophoresis and tryptic peptide

74 Using two-dimensional gel electrophoresis and a specific antib

75 Preparative two-dimensional gel electrophoresis and amino acid seque

76 Two-dimensional gel electrophoresis and atomic force mic

77 argets for (14)C-monocrotaline pyrrole using two-dimensional gel electrophoresis and autoradiographic

78 Extracts from PIMT-KO mice were subjected to two-dimensional gel electrophoresis and blotted onto mem

79 C (PIPLC) treatment, and after separation by two-dimensional gel electrophoresis and blotting, a chai

80 Two-dimensional gel electrophoresis and chemical modific

81 eome of vaccine strain Rev 1 was analyzed by two-dimensional gel electrophoresis and compared to that

82 Two-dimensional gel electrophoresis and electron microsc

83 By employing two-dimensional gel electrophoresis and electron microsc

84 By using two-dimensional gel electrophoresis and electrospray ion

85 ual mitochondrial tRNAs were separated using two-dimensional gel electrophoresis and enzymatically se

86 We have used two-dimensional gel electrophoresis and genomic DNA micr

87 cellular cysteine protease were separated by two-dimensional gel electrophoresis and identified by am

88 Isolated proteins were separated by two-dimensional gel electrophoresis and identified by ma

89 iles of the smooth and rugose variants using two-dimensional gel electrophoresis and identified one p

90 Analysis of the secreted apoE by one- and two-dimensional gel electrophoresis and immunoblotting s

91 virion-associated GAPDH and La protein using two-dimensional gel electrophoresis and immunoblotting.

92 s were identified and quantified by one- and two-dimensional gel electrophoresis and immunostaining w

93 ng the entire PKD1 intron 21 was analyzed by two-dimensional gel electrophoresis and it exhibited sha

94 , using an arylomycin derivative, along with two-dimensional gel electrophoresis and liquid chromatog

95 Combining two-dimensional gel electrophoresis and liquid chromatog

96 Here we used two-dimensional gel electrophoresis and mass spectrometr

97 Moreover, by two-dimensional gel electrophoresis and mass spectrometr

98 face-specific labelling with high-resolution two-dimensional gel electrophoresis and mass spectrometr

99 ing the greening process using techniques of two-dimensional gel electrophoresis and mass spectrometr

100 By using a combination of two-dimensional gel electrophoresis and mass spectrometr

101 We used a proteomic approach involving two-dimensional gel electrophoresis and mass spectrometr

102 Two-dimensional gel electrophoresis and mass spectrometr

103 f human and microbial cells, improvements in two-dimensional gel electrophoresis and mass spectrometr

104 steine protease cathepsin B, as indicated by two-dimensional gel electrophoresis and mass spectrometr

105 The present study used two-dimensional gel electrophoresis and mass spectrometr

106 red cells of Arabidopsis in conjunction with two-dimensional gel electrophoresis and mass spectrometr

107 d from rat primary hepatocyte cultures using two-dimensional gel electrophoresis and mass spectrometr

108 Two-dimensional gel electrophoresis and mass spectrometr

109 Using two-dimensional gel electrophoresis and mass spectrometr

110 A proteomic technique combining two-dimensional gel electrophoresis and mass spectrometr

111 Two-dimensional gel electrophoresis and mass spectrometr

112 spinach (Spinacia oleracea) was analyzed by two-dimensional gel electrophoresis and mass spectrometr

113 se large B cell lymphoma to conduct unbiased two-dimensional gel electrophoresis and mass spectrometr

114 Analysis of phosphorylated peptides by two-dimensional gel electrophoresis and mass spectrometr

115 Two-dimensional gel electrophoresis and mass spectrometr

116 In addition, two-dimensional gel electrophoresis and mass spectrometr

117 By using a combination of two-dimensional gel electrophoresis and mass spectrometr

118 Proteomic analysis combining two-dimensional gel electrophoresis and mass spectrometr

119 , 3, 4, 5, and 6 weeks after flowering using two-dimensional gel electrophoresis and matrix-assisted

120 own in a liquid medium was analyzed by using two-dimensional gel electrophoresis and matrix-assisted

121 lterations in protein expression detected by two-dimensional gel electrophoresis and matrix-assisted

122 he theoretical proteome experimentally using two-dimensional gel electrophoresis and matrix-assisted

123 Following two-dimensional gel electrophoresis and matrix-assisted

124 ere compared upon 9-day drought stress using two-dimensional gel electrophoresis and nano-scale liqui

125 lecular mass >90 kDa) as individual spots by two-dimensional gel electrophoresis and next analyze com

126 Two-dimensional gel electrophoresis and phosphatase trea

127 Using two-dimensional gel electrophoresis and PowerBlot (antib

128 I, outer membrane proteins were separated by two-dimensional gel electrophoresis and probed using poo

129 brane fraction of bacteria were separated by two-dimensional gel electrophoresis and subjected to Wes

130 sing of Lhca3 is documented independently by two-dimensional gel electrophoresis and tandem mass spec

131 n NOD/LtJ and CD1 mice were identified using two-dimensional gel electrophoresis and tandem mass spec

132 ted p95 from NCI-H1688 cells was isolated by two-dimensional gel electrophoresis and then digested wi

133 reatment of intact cells and was purified by two-dimensional gel electrophoresis and then sequenced b

134 ollowing heat shock of wheat seedlings using two-dimensional gel electrophoresis and Western analysis

135 covalent GALT heterogeneity using denaturing two-dimensional gel electrophoresis and Western blot ana

136 We used one- and two-dimensional gel electrophoresis and Western blot ana

137 ding microarray, quantitative real-time PCR, two-dimensional gel electrophoresis and Western blot ana

138 alpha6 NC1 domains and then characterized by two-dimensional gel electrophoresis and Western blotting

139 Two-dimensional gel electrophoresis and western blotting

140 Proteins were separated by two-dimensional gel electrophoresis, and 125 protein spo

141 Protein samples were separated by two-dimensional gel electrophoresis, and antigens expres

142 tion, by a mobility shift change detected by two-dimensional gel electrophoresis, and by immunoblotti

143 This immunoprecipitate was subjected to two-dimensional gel electrophoresis, and coimmunoprecipi

144 After two-dimensional gel electrophoresis, and immunoaffinity

145 SDS-PAGE, two-dimensional gel electrophoresis, and immunoblot anal

146 dimensional gel electrophoresis, immunoblot, two-dimensional gel electrophoresis, and layered express

147 Using a combination of RT-PCR, two-dimensional gel electrophoresis, and MALDI-TOF-based

148 ets, we used a combination of photolabeling, two-dimensional gel electrophoresis, and mass spectromet

149 hese were characterized by protein analysis, two-dimensional gel electrophoresis, and mass spectromet

150 Proteins were separated by two-dimensional gel electrophoresis, and phosphoproteins

151 Purified PFs were analyzed by two-dimensional gel electrophoresis, and several protein

152 Size-exclusion chromatography, two-dimensional gel electrophoresis, and small angle x-r

153 r human colon cancer, using high-resolution, two-dimensional gel electrophoresis, and thereby identif

154 from S. pyogenes cultures by high-resolution two-dimensional gel electrophoresis, and used immunoblot

155 obtained from computational genome analysis, two-dimensional gel electrophoresis, and whole-genome tr

156 phase isoelectrophoresis and high resolution two-dimensional gel electrophoresis, apolipoprotein L wa

157 of proteins separated by one-dimensional or two-dimensional gel electrophoresis, as it can be easily

158 rial proteins were isolated and separated by two-dimensional gel electrophoresis based on their charg

159 roughput profiling technologies that current two-dimensional gel electrophoresis cannot achieve.

160 Notably, two-dimensional gel electrophoresis combined with protei

161 nting the complete L. pneumophila genome and two-dimensional gel electrophoresis combined with Wester

162 Two-dimensional gel electrophoresis confirmed binding of

163 he locus encoding the 16-kDa gamma-zein, and two-dimensional gel electrophoresis confirmed the 16-kDa

164 sought in CSF but no previous study has used two-dimensional gel electrophoresis coupled with mass sp

165 A functional proteomics approach utilizing two-dimensional gel electrophoresis coupled with mass sp

166 a set of complementary approaches, including two-dimensional gel electrophoresis coupled with matrix-

167 Protein expression profiling employed two-dimensional gel electrophoresis coupled with tandem

168 matured to a technology platform way beyond two-dimensional gel electrophoresis, delivering on its p

169 Western blotting and two-dimensional gel electrophoresis demonstrated a signi

170 Cl-solubilized HIP preparations separated by two-dimensional gel electrophoresis demonstrated direct

171 Proteomic analysis by two-dimensional gel electrophoresis demonstrated downreg

172 Mass spectroscopy and two-dimensional gel electrophoresis demonstrated phospho

173 Nonetheless, two-dimensional gel electrophoresis demonstrated that fe

174 ns by fast protein liquid chromatography and two-dimensional gel electrophoresis demonstrated the pre

175 land stages, MSP2 did not appear to vary, by two-dimensional gel electrophoresis, during continuous p

176 Biochemical analyses included one- and two-dimensional gel electrophoresis, electrospray mass s

177 We monitor the course of extrusion by two-dimensional gel electrophoresis experiments as a fun

178 comparison of predictions with results from two-dimensional gel electrophoresis experiments.

179 biotin, treated with PI-PLC, and analyzed by two-dimensional gel electrophoresis followed by avidin b

180 Comparative proteomics using two-dimensional gel electrophoresis followed by computer

181 th CpB, then subjected membrane fractions to two-dimensional gel electrophoresis followed by ligand b

182 analyzed by a proteomic approach based on a two-dimensional gel electrophoresis followed by liquid c

183 lly expressed proteins were identified after two-dimensional gel electrophoresis followed by liquid c

184 By use of two-dimensional gel electrophoresis followed by liquid c

185 Using two-dimensional gel electrophoresis followed by MALDI-TO

186 Using two-dimensional gel electrophoresis followed by mass spe

187 Two-dimensional gel electrophoresis followed by mass spe

188 harvest, Yorrel, Tanjil and Coromup, through two-dimensional gel electrophoresis followed by mass spe

189 Purified samples were subjected to two-dimensional gel electrophoresis followed by mass spe

190 released upon hydration was performed using two-dimensional gel electrophoresis followed by mass spe

191 Two-dimensional gel electrophoresis followed by phosphor

192 Isotope-coded affinity tag analysis and two-dimensional gel electrophoresis followed by tandem m

193 d tissue using two independent technologies, two-dimensional gel electrophoresis followed by tandem m

194 Two-dimensional gel electrophoresis followed by Western

195 xists in at least four species detectable by two-dimensional gel electrophoresis followed by Western

196 commonly accomplished by the combination of two-dimensional gel electrophoresis for protein separati

197 Two-dimensional gel electrophoresis for protein separati

198 ltered polypeptide profile (as determined by two-dimensional gel electrophoresis): formate production

199 c patterns can be reproducibly identified by two-dimensional gel electrophoresis from limited numbers

200 ting of proteins subsequent to separation by two-dimensional gel electrophoresis has identified this

201 Two-dimensional gel electrophoresis identified one compl

202 By using a combination of two-dimensional gel electrophoresis, immunoblot analysis

203 unized animals to brain proteins by one- and two-dimensional gel electrophoresis, immunoblotting, and

204 idation of proteins in AD brain, we utilized two-dimensional gel electrophoresis, immunochemical dete

205 ould be detected in fresh and cultured TM by two-dimensional gel electrophoresis in conjunction with

206 Two-dimensional gel electrophoresis, in vitro activity t

207 Furthermore, analysis by two-dimensional gel electrophoresis indicates that repli

208 Two-dimensional gel electrophoresis is a powerful tool f

209 on, sucrose gradient fractionation, one- and two-dimensional gel electrophoresis, liquid chromatograp

210 e of individuals without the mutation, using two-dimensional gel electrophoresis, mass spectrometry,

211 immunoisolated protein, one-dimensional and two-dimensional gel electrophoresis, matrix-assisted las

212 ote) and infective (trypomastigote) forms by two-dimensional gel electrophoresis/matrix-assisted lase

213 We have developed a two-dimensional gel electrophoresis method to investigat

214 Furthermore, using a two-dimensional gel electrophoresis method, we demonstra

215 alpha-Actinin resolved by two-dimensional gel electrophoresis of activated platele

216 asic isoelectric point shift was detected by two-dimensional gel electrophoresis of AhRY9F.

217 Two-dimensional gel electrophoresis of ARNT coimmunoprec

218 d the hydrodynamic volume of the enzyme, and two-dimensional gel electrophoresis of chymotrypsin-dige

219 Two-dimensional gel electrophoresis of gamma-PAK followe

220 Here we use genetic approaches and two-dimensional gel electrophoresis of genomic DNA to sh

221 increase in H2B acetylation was observed by two-dimensional gel electrophoresis of histones of the h

222 In this study, two-dimensional gel electrophoresis of human lung cancer

223 Two-dimensional gel electrophoresis of isolated membrane

224 Two-dimensional gel electrophoresis of plasma 5 min afte

225 Following one- and two-dimensional gel electrophoresis of purified organell

226 Two-dimensional gel electrophoresis of replication inter

227 mmunoreactive bands were separated, by using two-dimensional gel electrophoresis of the bovine retina

228 Two-dimensional gel electrophoresis of the duplex M13mp2

229 Neutral/neutral two-dimensional gel electrophoresis of the in vitro prod

230 though minor differences were observed after two-dimensional gel electrophoresis of total proteins fr

231 ctrometric analysis of proteins separated by two-dimensional gel electrophoresis of uninfected and in

232 Studies using two-dimensional gel electrophoresis of various brain reg

233 Far-Western blotting of EBP50 isolated by two-dimensional gel electrophoresis or immunoprecipitati

234 the effects of these inhibitors, we compared two-dimensional gel electrophoresis patterns from lysate

235 re identified within the 12-kb region, where two-dimensional gel electrophoresis previously detected

236 peptidase B with a proteomics approach using two-dimensional gel electrophoresis, radioligand blottin

237 iously separated by one-dimensional (1-D) or two-dimensional gel electrophoresis requires significant

238 Two-dimensional gel electrophoresis resolved E1 into the

239 Two-dimensional gel electrophoresis resolved more than 1

240 Two-dimensional gel electrophoresis resolved the 53-kDa

241 us polyacrylamide gel electrophoresis and by two-dimensional gel electrophoresis revealed a continuum

242 Two-dimensional gel electrophoresis revealed an increase

243 Two-dimensional gel electrophoresis revealed pH-dependen

244 Two-dimensional gel electrophoresis revealed that ADF an

245 and mouse livers, coimmunoprecipitation and two-dimensional gel electrophoresis revealed that CAR ca

246 Analyses of the CspI protein on two-dimensional gel electrophoresis revealed that CspI p

247 Analysis by two-dimensional gel electrophoresis revealed that Mycoba

248 Rigorous analysis using two-dimensional gel electrophoresis revealed that the an

249 of vitreous and plasma proteins separated by two-dimensional gel electrophoresis revealed that the IG

250 Furthermore, two-dimensional gel electrophoresis revealed that the ol

251 Two-dimensional gel electrophoresis revealed the absence

252 pectrometry analysis of proteins resolved by two-dimensional gel electrophoresis revealed the presenc

253 Analysis of protein synthesis by two-dimensional gel electrophoresis reveals a class of g

254 The method employs two-dimensional gel electrophoresis, separating genomic

255 A 38-kDa protein was resolved by two-dimensional gel electrophoresis, sequenced, and iden

256 One- and two-dimensional gel electrophoresis showed a decrease in

257 Two-dimensional gel electrophoresis showed a prominent s

258 Two-dimensional gel electrophoresis showed increased amo

259 proteins from wild type and a nat4 mutant by two-dimensional gel electrophoresis showed no evidence t

260 Analysis with two-dimensional gel electrophoresis showed stretch-depen

261 Analysis of replication intermediates using two-dimensional gel electrophoresis showed that adozeles

262 Analysis of replication fork movement using two-dimensional gel electrophoresis showed that the dele

263 Electron microscopy and two-dimensional gel electrophoresis showed that the heli

264 Analysis of Elk-1 using two-dimensional gel electrophoresis shows that following

265 Two-dimensional gel electrophoresis studies with isoelec

266 cted ribosomal proteins detected by previous two-dimensional gel electrophoresis studies.

267 ution using only micro-amounts of protein, a two-dimensional gel electrophoresis system was employed.

268 Maize RPS6 was analyzed by the use of two-dimensional gel electrophoresis systems, in vivo lab

269 ve Y' telomeres of yeast were analyzed using two-dimensional gel electrophoresis techniques.

270 Here, we show by two-dimensional gel electrophoresis that Abf2p promotes

271 iction Landmark Genomic Scanning (RLGS) is a two-dimensional gel electrophoresis that assesses the me

272 protein synthesis in V. cholerae and show by two-dimensional gel electrophoresis that the stress resp

273 In two-dimensional gel electrophoresis, the 50-kDa human am

274 (Bos indicus) based on protein separation by two-dimensional gel electrophoresis, the identification

275 tion to examine 24 human meningiomas and did two-dimensional gel electrophoresis to determine protein

276 We used two-dimensional gel electrophoresis to examine both stea

277 ovel nonreceptor substrates of GRK2, we used two-dimensional gel electrophoresis to find cellular pro

278 Samples were analyzed using high-resolution two-dimensional gel electrophoresis to identify differen

279 We used two-dimensional gel electrophoresis to identify proteins

280 dified osmotic shock periplasmic extract and two-dimensional gel electrophoresis to identify substrat

281 By two-dimensional gel electrophoresis, total protein synth

282 ll extracts derived from E-FABP null mice by two-dimensional gel electrophoresis using anti-4-HNE ant

283 specific role of SUB in parasite physiology, two-dimensional gel electrophoresis was carried out on S

284 ination of in situ 32P labeling and one- and two-dimensional gel electrophoresis was used to acquire

285 tand the role of SrhSR, differential display two-dimensional gel electrophoresis was used to analyze

286 The method of two-dimensional gel electrophoresis was used to detect t

287 entify additional genes in the OxyR regulon, two-dimensional gel electrophoresis was used to isolate

288 Two-dimensional gel electrophoresis was used to resolve

289 Two-dimensional gel electrophoresis was used to study re

290 By using two-dimensional gel electrophoresis, we demonstrate that

291 Using two-dimensional gel electrophoresis, we find that loss o

292 In the current studies, utilizing giant two-dimensional gel electrophoresis, we find that orbita

293 Combining subcellular fractionation with two-dimensional gel electrophoresis, we found that a set

294 Using two-dimensional gel electrophoresis, we identified multi

295 Using two-dimensional gel electrophoresis, we identified varia

296 Using two-dimensional gel electrophoresis, we obtained evidenc

297 Using two-dimensional gel electrophoresis, we show for the fir

298 ferentially expressed protein spots from the two-dimensional gel electrophoresis were analyzed using

299 spots were selected from separations made by two-dimensional gel electrophoresis, which were analyzed

300 ration of staphylococcal surface proteins by two-dimensional gel electrophoresis with a ligand overla