ライフサイエンスコーパス: polyacrylamide gel electrophoresis

1 chromatography) and 2D-PAGE (two-dimensional polyacrylamide gel electrophoresis).

2 rotein backbones (via sodium dodecyl sulfate-polyacrylamide gel electrophoresis).

3 as a stain for visualizing nucleic acids in polyacrylamide gel electrophoresis.

4 by gel permeation chromatography and native-polyacrylamide gel electrophoresis.

5 on and quantitation of proteins separated by polyacrylamide gel electrophoresis.

6 s were resolved using sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

7 rate as the wild-type AcrB trimer in native polyacrylamide gel electrophoresis.

8 or the 58-kDa size by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

9 ed by one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

10 labeled substrates followed by analysis with polyacrylamide gel electrophoresis.

11 based on non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

12 ails were purified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

13 tor was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis.

14 ell lysates were analyzed by two-dimensional polyacrylamide gel electrophoresis.

15 -Shp and holo-HtsA was examined using native polyacrylamide gel electrophoresis.

16 cts were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

17 , to various dT(n) oligomers was examined by polyacrylamide gel electrophoresis.

18 , and the immunoprecipitates were run on SDS-polyacrylamide gel electrophoresis.

19 o the DAT detected by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

20 raphy and preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

21 eins were resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

22 immunohistochemical analysis and blue native polyacrylamide gel electrophoresis.

23 id chromatography and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

24 motile cells, as assessed by two-dimensional polyacrylamide gel electrophoresis.

25 tion of proteins, followed by sodium dodecyl-polyacrylamide gel electrophoresis.

26 d using different extracts and conducted SDS-polyacrylamide gel electrophoresis.

27 HP genotype was determined by polyacrylamide gel electrophoresis.

28 mately 25 kDa on 12% sodium dodecyl sulphate-polyacrylamide gel electrophoresis.

29 rhoea attributable to rotavirus with EIAs or polyacrylamide gel electrophoresis.

30 torage protein fractions, in one-dimensional polyacrylamide gel electrophoresis (1D-PAGE) and two-dim

31 By revisiting the yeast two-dimensional polyacrylamide gel electrophoresis (2-D PAGE) in similar

32 us labrax) fillets using the two-dimensional polyacrylamide gel electrophoresis (2-DE) technique.

33 Using two-dimensional polyacrylamide gel electrophoresis (2D PAGE), we identif

34 he protein components by two-dimensional SDS-polyacrylamide gel electrophoresis (2D SDS-PAGE).

35 of soybean seed proteins for two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and mass sp

36 atients with de novo AML using 2-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and phospho

37 e max) root hair cells using two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and shotgun

38 In this study, we used two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and tandem

39 Two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) is the comm

40 expression was determined by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) of retinal

41 roteomic analyses, including two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) separation

42 lectrophoresis (1D-PAGE) and two-dimensional polyacrylamide gel electrophoresis (2D-PAGE).

43 fraction yielding on sodium dodecyl sulfate-polyacrylamide gel electrophoresis a single band with an

44 n was carried out by sodium dodecyl sulphate polyacrylamide gel electrophoresis after pre-fractionati

45 The samples are resolved by native polyacrylamide gel electrophoresis, after which fluoresc

46 bikunin GAG mixture obtained by preparative polyacrylamide gel electrophoresis, allowed the determin

47 mensional blue native-sodium dodecyl sulfate-polyacrylamide gel electrophoresis analyses showed that

48 using one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis and identifi

49 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis demonstrated

50 Careful sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of tobacco n

51 Two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis previously i

52 Blue native-polyacrylamide gel electrophoresis analysis showed that

53 hylakoids post cross linking and blue-native polyacrylamide gel electrophoresis analysis shows that T

54 to the synthase using sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis.

55 orption mass spectrometry and by blue native polyacrylamide gel electrophoresis analysis.

56 Blue Native polyacrylamide gel electrophoresis, analytical ultracent

57 ions were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and 3-dimensional flu

58 Further, using native polyacrylamide gel electrophoresis and a yeast two-hybri

59 Small angle X-ray scattering, native polyacrylamide gel electrophoresis and activity assays w

60 Native polyacrylamide gel electrophoresis and analytical gel fi

61 sly unidentified A-minor junctions by native polyacrylamide gel electrophoresis and atomic force micr

62 Co-affinity purification, non-denaturing polyacrylamide gel electrophoresis and bis(maleimido)hex

63 atic protein-SDS complexes formed during SDS polyacrylamide gel electrophoresis and brings a new tool

64 Results from blue native polyacrylamide gel electrophoresis and chemical cross-li

65 Two-dimensional blue native polyacrylamide gel electrophoresis and coimmunoprecipita

66 which is evaluated by sodium dodecyl sulfate polyacrylamide gel electrophoresis and corresponding Wes

67 tion were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and dot blot, using b

68 imer was observed under native conditions by polyacrylamide gel electrophoresis and fast protein liqu

69 or the presence of inositol phosphates using polyacrylamide gel electrophoresis and high-performance

70 rized these protein complexes by blue native polyacrylamide gel electrophoresis and identified approx

71 eins were isolated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and identified by mas

72 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and image densitometr

73 Two-dimensional SDS-polyacrylamide gel electrophoresis and immunoblotting wi

74 n fragments were quantified with agarose and polyacrylamide gel electrophoresis and immunoblotting.

75 and analyzed by both sodium dodecyl sulfate polyacrylamide gel electrophoresis and immunofluorescenc

76 -L1; L4-S1) were retrieved and 2-dimensional polyacrylamide gel electrophoresis and immunohistocytoch

77 either separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and in-gel digestion

78 ied as calmodulins by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and liquid chromatogr

79 women (18-39 years old) by combining native-polyacrylamide gel electrophoresis and liquid chromatogr

80 on on two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and mass spectrometri

81 LOS by silver-stained sodium dodecyl sulfate-polyacrylamide gel electrophoresis and mass spectrometri

82 Native polyacrylamide gel electrophoresis and mass spectrometry

83 ns were identified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and mass spectrometry

84 e gel electrophoresis/sodium dodecyl sulfate-polyacrylamide gel electrophoresis and mass spectrometry

85 Next, we used two-dimensional polyacrylamide gel electrophoresis and mass spectrometry

86 gle band at 42 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and molecular ion at

87 ns by two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis and peptide mass fing

88 tions are usually separated using denaturing polyacrylamide gel electrophoresis and quantified using

89 ion are then determined by primer extension, polyacrylamide gel electrophoresis and quantitative anal

90 s are used in several applications including polyacrylamide gel electrophoresis and sensing devices.

91 d chimeric ORF50 proteins, using Blue Native polyacrylamide gel electrophoresis and size exclusion ch

92 ot analysis, immunohistochemistry, acid urea-polyacrylamide gel electrophoresis and sodium dodecyl su

93 unreacted enzyme and oligonucleotide by SDS-polyacrylamide gel electrophoresis and subjected to in-g

94 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and subsequent elutio

95 by performing tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis and subsequent image

96 bility as a trimer on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and the capacity to p

97 ents were first separated by two-dimensional polyacrylamide gel electrophoresis and then identified b

98 ducts are size-fractionated using denaturing polyacrylamide gel electrophoresis and visualized by flu

99 31.7 and 26.1 kDa) in sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blot anal

100 otein migration using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blotting

101 nventional methods of sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blotting

102 peptide fragments over time were assessed by polyacrylamide gel electrophoresis and Western blotting.

103 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and western-blot anal

104 gel-based separation (sodium dodecyl sulfate-polyacrylamide gel electrophoresis) and analysis by liqu

105 d by circular dichroism spectroscopy, native polyacrylamide gel electrophoresis, and enzyme-linked im

106 acterized concerning size by gel filtration, polyacrylamide gel electrophoresis, and mass spectrometr

107 ate targets were resolved by two-dimensional polyacrylamide gel electrophoresis, and phosphorylated g

108 c and quasi-elastic light scattering, native polyacrylamide gel electrophoresis, and ultracentrifugat

109 ichroism spectroscopy, native and denaturing polyacrylamide gel electrophoresis, and UV-visible-near-

110 hosphoprotein staining after two-dimensional polyacrylamide gel electrophoresis, as well as column-ba

111 at protein as seen by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, as well as the great

112 rchitecture at the molecular level by native polyacrylamide gel electrophoresis, as well as the netwo

113 The results of a native polyacrylamide gel electrophoresis assay using JR-FL tri

114 d disrupted NPM oligomer formation by native polyacrylamide gel electrophoresis assay.

115 gh its application in sodium dodecyl sulfate-polyacrylamide gel electrophoresis assays as well as sol

116 y gel mobility shift, beta-galactosidase and polyacrylamide gel electrophoresis assays identified a n

117 KCNQ4 subunits, as reported by nondenaturing polyacrylamide gel electrophoresis, at C643 at the end o

118 structures have been characterized by native polyacrylamide gel electrophoresis, atomic force microsc

119 no acids in cell culture to acetic acid-urea polyacrylamide gel electrophoresis (AU-PAGE) and matrix-

120 A 2-dimensional polyacrylamide gel electrophoresis-based comparative pro

121 In this study, we have developed a polyacrylamide gel electrophoresis-based screening metho

122 lly achieved by a combination of blue-native polyacrylamide gel electrophoresis (BN-PAGE) for separat

123 I-LHCII supercomplex isolated by blue native polyacrylamide gel electrophoresis (BN-PAGE) from digito

124 sis of PP2A and PP4 complexes by blue native polyacrylamide gel electrophoresis (BN-PAGE) indicates t

125 Blue native polyacrylamide gel electrophoresis (BN-PAGE) is a powerf

126 ize exclusion chromatography and blue native polyacrylamide gel electrophoresis (BN-PAGE) to demonstr

127 tion and one- or two-dimensional blue native polyacrylamide gel electrophoresis (BN-PAGE).

128 r mitochondria were subjected to blue native polyacrylamide gel electrophoresis (BNGE) to separate OX

129 of Ebola virus NP by sodium dodecyl sulfate-polyacrylamide gel electrophoresis by 5 and 15 kDa, resp

130 achieved within 6h using continuous elution polyacrylamide gel electrophoresis (CE-PAGE) on commerci

131 idence for this hypothesis has come from SDS-polyacrylamide gel electrophoresis, coimmunoprecipitatio

132 ntain intact immune complexes, nondenaturing polyacrylamide gel electrophoresis conditions were inves

133 man plaque tissues by sodium dodecyl sulfate polyacrylamide gel electrophoresis confirmed that the pr

134 lipopolysaccharide by sodium dodecyl sulfate-polyacrylamide gel electrophoresis confirmed the absence

135 ar mass of 180 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresis consistent with the c

136 sized using cetyl trimethylammonium bromide polyacrylamide gel electrophoresis (CTAB-PAGE), for subs

137 From temperature analysis of polyacrylamide gel electrophoresis data for rigid-rod DN

138 tracentrifugation and sodium dodecyl sulfate polyacrylamide gel electrophoresis demonstrated that in

139 Polyacrylamide gel electrophoresis demonstrated that the

140 The application of polyacrylamide gel electrophoresis demonstrated the gene

141 NA treated with 4 was analyzed by denaturing polyacrylamide gel electrophoresis (DPAGE), a technique

142 3 bp DNA fragment, as observed by denaturing polyacrylamide gel electrophoresis (dPAGE).

143 racterized by multiple techniques, including polyacrylamide gel electrophoresis, dynamic light scatte

144 Circular products have been identified by polyacrylamide gel electrophoresis, enzymatic digestion

145 Native polyacrylamide gel electrophoresis experiments showed th

146 e after separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresis followed by detection

147 e protein mixtures by sodium dodecyl sulfate-polyacrylamide gel electrophoresis followed by in-gel di

148 Quantitative RT-PCR and 2-dimensional polyacrylamide gel electrophoresis followed by MALDI/TOF

149 One-dimensional polyacrylamide gel electrophoresis followed by nanocapil

150 ion and separation by sodium dodecyl sulfate polyacrylamide gel electrophoresis, followed by autoradi

151 Immunoprecipitation and blue native polyacrylamide gel electrophoresis, followed by immunobl

152 s were resolved using sodium dodecyl sulfate-polyacrylamide gel electrophoresis, followed by staining

153 bent assay (ELISA) and two-dimensional (2-D) polyacrylamide gel electrophoresis, followed by Western

154 Using high-resolution polyacrylamide gel electrophoresis for analysis of wall

155 d to second-dimension sodium dodecyl sulfate-polyacrylamide gel electrophoresis for identification of

156 es biphasic ion-exchange chromatography with polyacrylamide gel electrophoresis for protein separatio

157 thetase isoforms, separated by nondenaturing polyacrylamide gel electrophoresis from crude maize extr

158 shift in mobility on sodium dodecyl sulfate-polyacrylamide gel electrophoresis, from a subunit of 37

159 troduce a microfluidic free-standing kinetic polyacrylamide gel electrophoresis (fsKPAGE) assay.

160 s were separated on a sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel after tandem affi

161 tein extracted from a sodium dodecyl sulfate-polyacrylamide gel electrophoresis gel and subjected to

162 Blue native polyacrylamide gel electrophoresis, gel filtration, and

163 chagasic sera and on sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels stained with sil

164 of gH, gB, and gD in sodium dodecyl sulfate-polyacrylamide gel electrophoresis gels was altered by d

165 of thylakoid preparations directly in native polyacrylamide gel electrophoresis gels, enabling unprec

166 re subsequently excised from two-dimensional polyacrylamide gel electrophoresis gels, trypsin digeste

167 RNA polyacrylamide gel electrophoresis identified 94 (50%) s

168 Blue native polyacrylamide gel electrophoresis identified PCFT dimer

169 , followed by two-dimensional sodium dodecyl polyacrylamide gel electrophoresis identified several ca

170 isoelectric focusing sodium dodecyl sulfate polyacrylamide gel electrophoresis (IEF/SDS-PAGE) and fl

171 using two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis, immunoblotting, and

172 tection of simian picobirnaviruses (PBVs) by polyacrylamide gel electrophoresis in fecal specimens of

173 ces cerevisiae subjected to colorless native polyacrylamide gel electrophoresis in the presence of 0.

174 ng, spectroscopy, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis indicated that the ph

175 Native polyacrylamide gel electrophoresis is a powerful approac

176 on microscopy, dynamic light scattering, and polyacrylamide gel electrophoresis, is reported for the

177 Therefore, we introduce a kinetic polyacrylamide gel electrophoresis (KPAGE) microfluidic

178 ologic binding assay, sodium dodecyl sulfate polyacrylamide gel electrophoresis, mass spectrometry, a

179 ntify the modified proteins (two-dimensional polyacrylamide gel electrophoresis; mass spectrometry).

180 gonal two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis method to probe biolo

181 s of tau with altered sodium dodecyl sulfate-polyacrylamide gel electrophoresis migration have a grea

182 ining components with sodium dodecyl sulfate-polyacrylamide gel electrophoresis mobilities that resem

183 ins exhibited similar sodium dodecyl sulfate-polyacrylamide gel electrophoresis mobilities, indicatin

184 ionation coupled with sodium dodecyl sulfate polyacrylamide gel electrophoresis mobility assays enabl

185 s with reactive counterparts and analyzed by polyacrylamide gel electrophoresis mobility shifts.

186 Upon native polyacrylamide gel electrophoresis, moreover, oligomeriz

187 Today, 2-dimensional polyacrylamide gel electrophoresis, multidimensional liq

188 was determined using sodium dodecyl sulfate-polyacrylamide gel electrophoresis/N-terminal sequencing

189 were synthesized and shown by nondenaturing polyacrylamide gel electrophoresis (native PAGE) to have

190 possessed an M(r) on sodium dodecyl sulfate-polyacrylamide gel electrophoresis of 38,500.

191 cells using specific enzymatic assays, urea-polyacrylamide gel electrophoresis of cell extracts, and

192 Two-dimensional polyacrylamide gel electrophoresis of CSF from normal su

193 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of cytosol and membra

194 kDa, and analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis of LF under reducing

195 Blue native-polyacrylamide gel electrophoresis of mitochondrial extr

196 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of proteins associate

197 a single-cell targeted proteomic assay with polyacrylamide gel electrophoresis of single cell lysate

198 Moreover, polyacrylamide gel electrophoresis of the enriched extra

199 ding to FGF.FGFR complexes were subjected to polyacrylamide gel electrophoresis (PAGE) analysis and d

200 y has been proven to be successful by native polyacrylamide gel electrophoresis (PAGE) and cryogenic

201 rus core protein (HBcAg) was separated using polyacrylamide gel electrophoresis (PAGE) and electro-bl

202 s and the methods of mass spectrometry (MS), polyacrylamide gel electrophoresis (PAGE) and nuclear ma

203 Both native polyacrylamide gel electrophoresis (PAGE) and pore-limit

204 The method uses polyacrylamide gel electrophoresis (PAGE) followed by qu

205 Native polyacrylamide gel electrophoresis (PAGE) gel shifts as

206 using (TGF) and sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) in a PDMS/glas

207 and label-free sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) method for mea

208 SDS-polyacrylamide gel electrophoresis (PAGE) of fAbeta samp

209 Urea-polyacrylamide gel electrophoresis (PAGE) of partially d

210 cally optimize chemical lysis and subsequent polyacrylamide gel electrophoresis (PAGE) of the single-

211 separation matrix pore-size at the head of a polyacrylamide gel electrophoresis (PAGE) separation cha

212 Using polyacrylamide gel electrophoresis (PAGE) to separate mo

213 Native polyacrylamide gel electrophoresis (PAGE) was integrated

214 al microfluidic architecture that integrates polyacrylamide gel electrophoresis (PAGE) with immunoblo

215 PCR products were analyzed by polyacrylamide gel electrophoresis (PAGE), confirmed via

216 pendent data were obtained by SDS and native polyacrylamide gel electrophoresis (PAGE), differential

217 of microfluidic networks and the utility of polyacrylamide gel electrophoresis (PAGE), we develop a

218 glutathiolate in water and then separated by polyacrylamide gel electrophoresis (PAGE).

219 action time points and then fractionating by polyacrylamide gel electrophoresis (PAGE).

220 cificity and frequency of dX using two-phase polyacrylamide gel electrophoresis (PAGE).

221 aphy-tandem mass spectrometry (LC-MS/MS) and polyacrylamide gel electrophoresis (PAGE).

222 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of transglut

223 thin strips from the print are subjected to polyacrylamide gel electrophoresis, providing a straight

224 vine serum; SDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel electrophoresis; RANKL, receptor acti

225 ize-exclusion chromatography and blue native polyacrylamide gel electrophoresis revealed a modular Ba

226 ltatatC and parent strain by two-dimensional polyacrylamide gel electrophoresis revealed an alteratio

227 sion profiles obtained using two-dimensional polyacrylamide gel electrophoresis revealed complex chan

228 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis revealed that in the

229 data, two-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis revealed that incorpo

230 Analysis by denaturing polyacrylamide gel electrophoresis reveals significantly

231 nonreduced capillary sodium dodecyl sulfate polyacrylamide gel electrophoresis, reversed-phase high-

232 tract was realized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis SDS-PAGE-immunoblotti

233 trometry (ICP MS), 1D sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS PAGE)-LA ICP MS,

234 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analyses o

235 Sodium Dodecyl Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) analysis r

236 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis s

237 ced, and separated by sodium dodecyl sulfate/polyacrylamide gel electrophoresis (SDS-PAGE) and blots

238 and characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and electr

239 rins were assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and immuno

240 ation (IP) pattern on sodium docecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and simila

241 samples by utilising sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) combined w

242 two portions: one for sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) fiber typi

243 omprises non-reducing sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed b

244 es into a nonreducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gel contai

245 e as a 49-kDa band on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gels.

246 The use of sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) helped the

247 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) is a widel

248 ew method for on-chip sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) of protein

249 - and beta-tubulin by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) on minigel

250 h parallel capillary sodium dodecyl sulfate- polyacrylamide gel electrophoresis (SDS-PAGE) or capilla

251 A modified Laemmli sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) protocol i

252 Analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) revealed t

253 trategy that involves sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) separation

254 microscopy (AFM) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) to investi

255 raphy and preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) to obtain

256 In addition, when sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was used d

257 Denaturing polyacrylamide gel electrophoresis (SDS-PAGE) was used t

258 We have performed sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) with pepti

259 epletion method (with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)) achieved

260 sized proteins after sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and enabl

261 ("half-antibody") on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), in which

262 ich were confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), oxidative

263 c mobility (shift) in sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), which was

264 graphy (SE-HPLC) and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).

265 -IEF were analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE).

266 hip protein sizing by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

267 bilized trypsin using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

268 nate separated by 1-D sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

269 ere characterised by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE).

270 ion were verified via sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)/Western an

271 essed, they are separated via sodium dodecyl-polyacrylamide gel electrophoresis (SDS-PAGE, the second

272 Sodium dodecyl sulfate polyacrylamide gel electrophoresis showed modification w

273 Using two-dimensional Blue Native polyacrylamide gel electrophoresis/sodium dodecyl sulfat

274 Blue native polyacrylamide gel electrophoresis studies revealed that

275 By using blue native/Deriphat-polyacrylamide gel electrophoresis, sucrose density grad

276 Agarose and polyacrylamide gel electrophoresis systems for the molec

277 m spectroscopy, Dynamic Light Scattering and Polyacrylamide Gel Electrophoresis techniques were used

278 I, IV, and V were isolated using Blue Native polyacrylamide gel electrophoresis techniques.

279 esis method as an alternative to traditional polyacrylamide gel electrophoresis to characterize nucle

280 We used polyacrylamide gel electrophoresis to compare the extent

281 at the modified nucleotides, and analysis by polyacrylamide gel electrophoresis to determine the posi

282 '-radiolabeled DNA substrates and denaturing polyacrylamide gel electrophoresis to provide evidence f

283 shed FDF-PAGE (fully-denaturing formaldehyde polyacrylamide gel electrophoresis) to prevent annealing

284 Polyacrylamide gel electrophoresis under native and dena

285 Amino acid chromatographic analysis, polyacrylamide gel electrophoresis, UV-Vis spectrophotom

286 Nondenaturing polyacrylamide gel electrophoresis verified that apoA-V(

287 Native polyacrylamide gel electrophoresis was used to analyze m

288 Blue native polyacrylamide gel electrophoresis was used to isolate a

289 By using improved polyacrylamide gel electrophoresis we were able to visua

290 g, size exclusion chromatography, and native polyacrylamide gel electrophoresis, we demonstrate that

291 Using two dimensional polyacrylamide gel electrophoresis, we demonstrated that

292 oupled Sepharose affinity chromatography and polyacrylamide gel electrophoresis, we identified a 65-k

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

294 rosylated proteins resolved by 2-dimensional polyacrylamide gel electrophoresis were very similar in

295 l electrophoresis and sodium dodecyl sulfate-polyacrylamide gel electrophoresis Western blotting, rev

296 HRG was confirmed by sodium dodecyl sulphate polyacrylamide gel electrophoresis-Western blot and size

297 e molecular weight on sodium dodecyl sulfate-polyacrylamide gel electrophoresis, whether expressed in

298 d by migration during sodium dodecyl sulfate-polyacrylamide gel electrophoresis with an apparent mole

299 and analysis by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis with different concen

300 product comigrated in sodium dodecyl sulfate-polyacrylamide gel electrophoresis with the 58-kDa virio