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

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

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

3 HP genotype was determined by polyacrylamide gel electrophoresis.

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

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

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

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

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

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

10 be used as a general SDS replacement in SDS-polyacrylamide gel electrophoresis.

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

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

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

14 labeled substrates followed by analysis with polyacrylamide gel electrophoresis.

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

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

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

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

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

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

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

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

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

24 immunohistochemical analysis and blue native polyacrylamide gel electrophoresis.

25 id chromatography and sodium dodecyl sulfate polyacrylamide gel electrophoresis.

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

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

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

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

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

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

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

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

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

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

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

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

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

39 ish species was separated by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), and the to

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

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

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

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

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

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

46 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis demonstrated

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

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

49 Blue native-polyacrylamide gel electrophoresis analysis showed that

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

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

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

53 Blue Native polyacrylamide gel electrophoresis, analytical ultracent

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

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

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

57 Native polyacrylamide gel electrophoresis and analytical gel fi

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

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

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

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

62 Two-dimensional blue native polyacrylamide gel electrophoresis and coimmunoprecipita

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

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

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

66 ceable separation on sodium dodecyl sulphate-polyacrylamide gel electrophoresis and high-performance

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

68 lysis, using combined sodium dodecyl sulfate-polyacrylamide gel electrophoresis and high-performance

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

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

71 Sodium dodecyl sulfate polyacrylamide gel electrophoresis and image densitometr

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

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

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

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

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

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

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

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

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

81 osin alpha-4 chain (TPM4) by two-dimensional polyacrylamide gel electrophoresis and mass spectrometry

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

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

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

85 Native 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 Native polyacrylamide gel electrophoresis and size exclusion ch

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

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 d is introduced that is based on Blue Native Polyacrylamide Gel Electrophoresis (BN-PAGE) and dot imm

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

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

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

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

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

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

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

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

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

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 torage were identified using two-dimensional polyacrylamide gel electrophoresis coupled with matrix-a

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

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

139 Sodium dodecyl sulfate polyacrylamide gel electrophoresis demonstrated that 60%

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

141 Polyacrylamide gel electrophoresis demonstrated that the

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

143 3 bp DNA fragment, as observed by denaturing polyacrylamide gel electrophoresis (dPAGE).

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

145 using a combined approach of non-denaturing polyacrylamide gel electrophoresis, dynamic light scatte

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

147 bination of in vitro techniques (TWJ-screen, polyacrylamide gel electrophoresis, fluorescence resonan

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

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

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

151 One-dimensional polyacrylamide gel electrophoresis followed by nanocapil

152 ng (to quantify total (32)P-activity) and by polyacrylamide gel electrophoresis followed by phosphori

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

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

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

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

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

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

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

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

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

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

163 Blue native polyacrylamide gel electrophoresis, gel filtration, and

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

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

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

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

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

169 Blue native polyacrylamide gel electrophoresis identified PCFT dimer

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

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

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

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

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

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

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 g metal ion contaminant sweeping-blue native-polyacrylamide gel electrophoresis (MICS-BN-PAGE).

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

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

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

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

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

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

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

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

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

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

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

193 Blue native-polyacrylamide gel electrophoresis of mitochondrial extr

194 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of proteins associate

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

196 Moreover, polyacrylamide gel electrophoresis of the enriched extra

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

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

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

200 thoroughly characterized such DNA motifs by polyacrylamide gel electrophoresis (PAGE) and fluorescen

201 Polyacrylamide Gel Electrophoresis (PAGE) and Latex Aggl

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 olding and PTMs is difficult because routine polyacrylamide gel electrophoresis (PAGE) methods lack t

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

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

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

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

213 Using polyacrylamide gel electrophoresis (PAGE) to separate mo

214 Native polyacrylamide gel electrophoresis (PAGE) was integrated

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

216 rovide high mobilities of glycoconjugates on polyacrylamide gel electrophoresis (PAGE), as compared w

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

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

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

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

221 Sodium dodecyl sulfate-polyacrylamide gel electrophoresis profiles of transglut

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

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

224 Based on native MS and polyacrylamide gel electrophoresis results, the abundanc

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 The sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis o

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

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

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 ity was determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and matrix

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

268 bilized trypsin using 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 on cell wall composition, we used GC-MS and polyacrylamide gel electrophoresis to measure cell-wall

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

285 Nondenaturing polyacrylamide gel electrophoresis verified that apoA-V(

286 Native polyacrylamide gel electrophoresis was used to analyze m

287 Blue native polyacrylamide gel electrophoresis was used to isolate a

288 ing size exclusion chromatography and native polyacrylamide gel electrophoresis we demonstrated that

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 a, which migrates on sodium dodecyl sulphate polyacrylamide gel electrophoresis with a molecular weig

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