ライフサイエンスコーパス: PAGE

1 PAGE analysis suggests that SlpB is produced at lower le

2 edium rare prepared beef were assessed by 2D PAGE for the comparison of protein profiles.

3 2D-PAGE images showed that proteins in the biocake (S3) at

4 ional polyacrylamide gel electrophoresis (2D-PAGE) separation and matrix-assisted laser desorption/io

5 Using 2D-PAGE, we demonstrate that mutant alpha-tropomyosinslow w

6 ect of O2 when exposed to UV, resulting in a PAGE-in-PDMS device.

7 Using microscopy and PAGE analysis, we show that Kdo-N3 is localized to the o

8 lsilane)-b-poly(allyl glycidyl ether) (PFS-b-PAGE) decorated with triethylene glycol (TEG), abbreviat

9 Upon analyses by blue native (BN) PAGE, two major types of cruciferin complexes of approxi

10 units showed loss of NDUFB8, confirmed by BN-PAGE analysis of CI assembly and IHC using an alternativ

11 ) in schizophrenia OFC were identified by BN-PAGE.

12 Furthermore, by combining BN-PAGE with protein interaction assays we show that AtFtsZ

13 ative polyacrylamide gel electrophoresis (BN-PAGE) from digitonin-solubilized thylakoids were similar

14 ative polyacrylamide gel electrophoresis (BN-PAGE) indicates that PP4 holoenzyme complexes, like thos

15 ative polyacrylamide gel electrophoresis (BN-PAGE) to demonstrate BbHtrA oligomeric structures that w

16 ative polyacrylamide gel electrophoresis (BN-PAGE).

17 s during blue native gel electrophoresis (BN-PAGE).

18 demonstrated by complexome profiling from BN-PAGE.

19 In BN-PAGE, the SNARE heterotrimer was identified as a 150-kDa

20 Finally, blue native PAGE (BN-PAGE) revealed that under nondenaturing conditions, P66

21 1 domain to peanut allergens was assessed by PAGE and Western analysis with anti-Ara h 1, 2, and 3 an

22 triggered assembly behavior was examined by PAGE analysis, and the morphologies of the grown dendrim

23 ypass polymerases kappa and eta, followed by PAGE-based assays to determine the catalytic efficiency

24 Nfo), the analysis of cleavage fragments by PAGE and MALDI-TOF/MS show that the G*[C8-N3]T* lesions

25 expressed spots, which were collected in 2-D PAGE gels and identified via mass spectrometry (nESI-QTO

26 -SR-B1 cells were analyzed by non-denaturing PAGE, size-exclusion chromatography, and the distributio

27 16 proteins were detected with 2-dimensional PAGE in combination with liquid chromatography/tandem ma

28 tions and examined by means of 2-dimensional PAGE.

29 Two-dimensional PAGE analysis shows that acidic forms of FANCL, some of

30 Two-dimensional PAGE and Phos-tag gel analysis of stress-stimulated STMN

31 other proteins as judged by two-dimensional PAGE of metabolically labeled/immunoprecipitated PMEL an

32 Using two-dimensional PAGE we resolved eight rather than the two previously re

33 A proteomic (two-dimensional PAGE with mass spectrometric analysis) comparison betwee

34 l time quantitative RT-PCR and 2-dimensional-PAGE showed that gamma-tubulin-1 is the dominant isotype

35 ns as both a molecular sieving matrix during PAGE and a blotting scaffold during immunoprobing.

36 y native polyacrylamide gel electrophoresis (PAGE) and cryogenic electron microscopy (cryoEM) imaging

37 h native polyacrylamide gel electrophoresis (PAGE) and pore-limit electrophoresis (PLE) were studied

38 te (SDS)-polyacrylamide gel electrophoresis (PAGE) in a PDMS/glass microfluidic chip.

39 te (SDS)-polyacrylamide gel electrophoresis (PAGE) method for measuring the amount of SWNTs in lysate

40 Urea-polyacrylamide gel electrophoresis (PAGE) of partially dephosphorylated beta-casein showed a

41 bsequent polyacrylamide gel electrophoresis (PAGE) of the single-cell lysate.

42 Using polyacrylamide gel electrophoresis (PAGE) to separate monomeric from dimeric (boron-bridged)

43 ility of polyacrylamide gel electrophoresis (PAGE), we develop a technique for fabrication of PAGE mo

44 /MS) and polyacrylamide gel electrophoresis (PAGE).

45 rchitecture using Genomics and Epidemiology (PAGE) Consortium, we examined evidence for heterogeneity

46 rchitecture using Genomics and Epidemiology (PAGE) studies: the Multiethnic Cohort Study (1993-2006)

47 rchitecture using Genomics and Epidemiology (PAGE) Study (2008-2012).

48 rchitecture Using Genomics and Epidemiology (PAGE) study is a consortium of multi-ancestry, populatio

49 rchitecture using Genomics and Epidemiology (PAGE) study, we identify susceptibility loci and investi

50 rchitecture using Genomics and Epidemiology (PAGE) study.

51 rchitecture using Genomics and Epidemiology (PAGE) study.

52 rchitecture using Genomics and Epidemiology (PAGE) study.

53 By applying FDF-PAGE, we provide evidence that both strands of viral sma

54 To address this problem, we established FDF-PAGE (fully-denaturing formaldehyde polyacrylamide gel e

55 Comparing non-denaturing conditions to FDF-PAGE uncovered extensive sequestration of miRNAs in mode

56 toggles from an "enclosed" microchannel for PAGE and blotting to an "open" PA gel lane for immunopro

57 Proteomic analysis of aggregate bands from PAGE gels reveal an abundance of Gly/Ala/Ser/Thr repeats

58 AGE)-LA ICP MS, and, in duplicate, by 2D IEF-PAGE.

59 ical lysis of cells in each microwell; (iii) PAGE of each single-cell lysate; (iv) exposure of the ge

60 In studies of the covalent mechanism, PAGE fluorography showed labeling of GLP-1R in immunopre

61 parable reproducibility to glass microdevice PAGE.

62 ding the application and use of microfluidic PAGE without the need for a glass microfabrication infra

63 Multimer-PAGE provides a simple inexpensive biochemical technique

64 resembled those observed following multimer-PAGE.

65 ed linearly with protein input into multimer-PAGE, suggesting to some extent, multimers were also for

66 Here we developed a method, termed "multimer-PAGE," that combines in-gel chemical cross-linking with

67 Once the multimer-PAGE technique was validated, relative stoichiometric co

68 dant soluble multimer detection via multimer-PAGE.

69 Native PAGE demonstrated that this ASADH tetramerization is app

70 on, cross-linking, and denaturing and native PAGE analyses of Gal80 in vitro and fluorescence imaging

71 ng, size exclusion chromatography and native PAGE show that Hs11S is assembled in different oligomeri

72 Finally, blue native PAGE (BN-PAGE) revealed that under nondenaturing conditi

73 Here we used Blue Native PAGE (BNP) and Western blots to study native htt in huma

74 Blue native PAGE analyses verify the presence of a SecYEG-PpiD compl

75 Blue native PAGE analysis identified high molecular weight complexes

76 Blue native PAGE and FRET assays revealed 1% n-dodecyl beta-d-maltos

77 RE1alpha complexes in cells with blue native PAGE immunoblotting.

78 Analyses by SEC, blue native PAGE, SDS-PAGE, and dynamic light scattering indicated t

79 We investigated these species by Blue Native PAGE, Suc density gradient centrifugation, 77K fluoresce

80 on under native conditions using blue native PAGE.

81 Blue-native PAGE analysis showed that the variant TatC proteins prod

82 ing on mammalian synapses we use blue-native PAGE and 'gene-tagging' of GluN1 to report the first bio

83 cles and migrated as a trimer by blue-native PAGE.

84 h unprocessed 12S globulin by 2D blue-native PAGE/SDS-PAGE indicated that the nhx5 nhx6 knockouts sho

85 By native PAGE, it was possible to detect formation of a complex b

86 ric by size exclusion chromatography, native PAGE, and small angle x-ray scattering.

87 Gel filtration, native PAGE, and protein cross-linking were used to analyze the

88 abilize higher-order Bak oligomers on native PAGE, suggesting an important role in the Bak oligomeric

89 omatography and analyzed by SDS-PAGE, native PAGE, and Western immunoblot analysis.

90 We used native PAGE to follow the activity of Cif from the human pathog

91 ar mass estimated, using SDS-PAGE and native-PAGE electrophoresis, to be 86kDa.

92 Blue native-PAGE analysis revealed defects in the organization of CI

93 Although Blue Native-PAGE, total internal reflection fluorescence microscopy,

94 oximate molecular weight estimated by NATIVE-PAGE and SDS-PAGE electrophoresis was approximately 60 k

95 le prominent protein band appeared on native-PAGE and SDS-PAGE implying that the mPPO is a monomeric

96 capabilities of T-oligo using nondenaturing PAGE, nuclear magnetic resonance, and immunofluorescence

97 ), we develop a technique for fabrication of PAGE molecular sieving gels in PDMS microchannel network

98 abrication method compatible with performing PAGE protein separations in a composite PDMS-glass micro

99 en alpha1/alpha2 ratio was determined by SDS PAGE and by qRT-PCR in ex-vivo bone explants.

100 fate polyacrylamide gel electrophoresis (SDS PAGE)-LA ICP MS, and, in duplicate, by 2D IEF-PAGE.

101 OS system and comparative 2D blue native/SDS PAGE analyses using isolated mitochondria.

102 demonstrated by glycoprotein staining of SDS PAGE gels.

103 SDS-PAGE analyses indicated the formation of hydrolysates an

104 SDS-PAGE analysis showed that salt addition contributes to h

105 SDS-PAGE and immunoassay analysis with rabbit polyclonal ser

106 SDS-PAGE and Western blot analyses indicated that covalent i

107 SDS-PAGE electrophoresis qualitatively detected three major

108 SDS-PAGE gels stained for catecholase activity showed multip

109 SDS-PAGE gels were used to determine abundance of the CO2 -f

110 SDS-PAGE in non-reducing and reducing conditions revealed th

111 SDS-PAGE of pure CPC yielded two bands corresponding to alph

112 SDS-PAGE patterns show distinctive bands for each kind of ho

113 SDS-PAGE showed that annonacinone inhibited formation of PAI

114 SDS-PAGE showed that collagens extracted with different meth

115 SDS-PAGE showed that the molecular mass of purified enzyme w

116 SDS-PAGE showed that the protein bands corresponding to the

117 SDS-PAGE showed that the purified protein had molecular weig

118 SDS-PAGE shows the presence of a well separated protein band

119 SDS-PAGE was carried out for all collagens extracted under d

120 spectra of fifteen bands separated by 1D SDS-PAGE.

121 The 2D SDS-PAGE separation demonstrated the presence of a few prote

122 Large aggregates unable to enter a 4% SDS-PAGE gel were formed at pH 6.5 and 8.5, which became sol

123 A SDS-PAGE analysis suggested that Dps should be a substrate f

124 single polypeptide band of 83.1kDa after SDS-PAGE.

125 Although SDS-PAGE did not show any differences for either the number

126 Samples are then run on an SDS-PAGE gel and isolated bands are submitted for mass spect

127 e affects migration of the protein on an SDS-PAGE gel, and appears to alter secondary structure of th

128 UV absorbance and SDS-PAGE analyses were used to monitor MR progression during

129 using a combination of spectroscopic and SDS-PAGE assays.

130 Spectroscopic and SDS-PAGE binding assays of Sin a 2 and Ara h 1 with differen

131 sted under cell and lysate treatment and SDS-PAGE conditions that are expected to have suppressed the

132 Proteomic analysis and SDS-PAGE electrophoresis of the extracted proteome suggested

133 ular weight estimated by NATIVE-PAGE and SDS-PAGE electrophoresis was approximately 60 kDa.

134 ahigh pressure liquid chromatography and SDS-PAGE gels.

135 tests (SPTs), specific IgEs (sIgEs) and SDS-PAGE immunoblotting.

136 protein band appeared on native-PAGE and SDS-PAGE implying that the mPPO is a monomeric protein with

137 opy, secondary ion mass spectrometry and SDS-PAGE indicate that Cba. tepidum biogenic S(0) globules c

138 ted through the degree of hydrolysis and SDS-PAGE profiles.

139 Gel filtration chromatography and SDS-PAGE revealed that the enzyme is monomeric with a molecu

140 immunopurification, deglycosylation, and SDS-PAGE separation of FPRs is sufficient to identify C-term

141 ormance liquid chromatography (HPLC) and SDS-PAGE subunit analysis reveal that the first step of ther

142 tease showed a single band on native and SDS-PAGE with a molecular weight of 24kDa on SDS-PAGE.

143 al reflection-FTIR, CD spectroscopy, and SDS-PAGE.

144 ion, lectin affinity chromatography, and SDS-PAGE.

145 ned by electrophoretic technique such as SDS-PAGE.

146 he sera of patients with diabetes before SDS-PAGE.

147 Biochemical (SDS-PAGE, Size exclusion chromatography and LC-MS/MS) and im

148 Analyses by two-dimensional BN/SDS-PAGE revealed that both types of complexes are composed

149 h); investigate SMALP protein purity by SDS-PAGE analysis and estimate protein concentration (4 h);

150 rallel affinity purification followed by SDS-PAGE analysis is more predictive for expression screenin

151 es with high specificity as confirmed by SDS-PAGE analysis with a phosphoprotein-specific stain and m

152 Human retinal proteins were separated by SDS-PAGE and 2D gel electrophoresis (2-DE) and sera from AR

153 ion during in vitro GID was evaluated by SDS-PAGE and by measuring the nitrogen content of ultrafiltr

154 he samples were dialyzed and analyzed by SDS-PAGE and for OA content.

155 r triple-helical structure, confirmed by SDS-PAGE and FTIR.

156 Peptides were detected by SDS-PAGE and GC-MS was used to determine carbohydrate conten

157 d the structure of recombinant CLEC3A by SDS-PAGE and immunoblot, glycan analysis, matrix-assisted la

158 ree of LPO purification was monitored by SDS-PAGE and its R(z) (A(412)/A(280)) value.

159 ovalently cross-linked dimer isolated by SDS-PAGE and mass analysis showed that dityrosine dimer was

160 d, Ara h 1 and Ara h 2 were evaluated by SDS-PAGE and sandwich ELISA.

161 Identification of proteins resolved by SDS-PAGE depends on robust in-gel protein digestion and effi

162 Examination by SDS-PAGE followed by protein staining revealed protein profi

163 ctions from felodipine treated lenses by SDS-PAGE in conjunction with mass spectrometry and immunoblo

164 olin-polyphenol complexation obtained by SDS-PAGE on a 10% polyacrylamide gel, it was observed that t

165 The protein fractions analysed by SDS-PAGE showed similar bands, indicating different solubili

166 nal major peptide bands were detected by SDS-PAGE treatments as compared to the solar or freeze dryin

167 time-of-flight mass spectrometry and by SDS-PAGE using biotinylated PGA1 (PGA1-B).

168 After deglycosylation and separation by SDS-PAGE, excised Coomassie Blue-staining bands ( approximat

169 mor brain and neural progenitor cells by SDS-PAGE, immunoblot, mass spectrometry and reverse transcri

170 olecular mass of approximately 85 kDa by SDS-PAGE, it elutes in fractions corresponding to approximat

171 -exchange chromatography and analyzed by SDS-PAGE, native PAGE, and Western immunoblot analysis.

172 of AS-48 digestion fragments in bulk by SDS-PAGE, RP-HPLC, and MALDI-TOF proves that the previous pe

173 64mgg(-1)) were analysed and compared by SDS-PAGE, showing differences in their electrophoretic prote

174 ers show multiple bands when analyzed by SDS-PAGE, suggesting that they may be oligomeric.

175 ation into receptor subunits resolved by SDS-PAGE, there was etomidate-inhibitable labeling by [(3)H]

176 By SDS-PAGE, two forms of NS5A with distinct apparent molecular

177 nzymatic treatments under sonication, by SDS-PAGE, western blot and ELISA, with serum IgE of allergic

178 merization were consistently observed by SDS-PAGE, Western blotting, and mass spectrometry.

179 rs were reduced (-70.5%), as assessed by SDS-PAGE.

180 re noticeably different when analyzed by SDS-PAGE.

181 migration of the cross-linked enzyme by SDS-PAGE.

182 and 2 h, the pellicles were analyzed by SDS-PAGE.

183 ication of the small cleavage product by SDS-PAGE.

184 f USP20 correlates with a characteristic SDS-PAGE mobility shift of the protein, blocks its deubiquit

185 tor followed by affinity chromatography, SDS-PAGE, and identification of protein bands evident only w

186 torial peptide ligand libraries (CPLLs), SDS-PAGE, nLC-ESI-MS/MS, and database search, permitted iden

187 by HPP, this processing modified the 1-D SDS-PAGE sarcoplasmic patterns in a direct-dependent manner

188 ssays (thioflavin T, circular dichroism, SDS-PAGE, size exclusion chromatography, surface plasmon res

189 omplex was confirmed by second dimension SDS-PAGE, Western blotting, mass spectrometry, and the use o

190 Two-dimensional SDS-PAGE of the purified active fraction revealed a single s

191 the migration pattern on two-dimensional SDS-PAGE, the majority of plasma CL-K1 was found in complex

192 n and nonreduced/reduced two-dimensional SDS-PAGE, we detected CL-K1 and CL-L1 in disulfide bridge-st

193 ion of complexes that were stable during SDS-PAGE.

194 hate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) analysis revealed the localization of phosvitin in

195 hate-polyacrylamide gel electrophoresis (SDS-PAGE) combined with principal component analysis (PCA).

196 fate-polyacrylamide gel electrophoresis (SDS-PAGE) is a widely used technique for protein separation,

197 oteins separated by gel electrophoresis (SDS-PAGE) to be detected as peptides by mass spectrometry in

198 ring polyacrylamide gel electrophoresis (SDS-PAGE) was used to separate proteins.

199 fate polyacrylamide gel electrophoresis (SDS-PAGE), and enables SDS-PAGE and subsequent immuno-probin

200 fate-polyacrylamide gel electrophoresis (SDS-PAGE), oxidative damage to amino acids, and changes in t

201 fate polyacrylamide gel electrophoresis (SDS-PAGE), which was eliminated by phosphatase treatment.

202 fate-polyacrylamide gel electrophoresis (SDS-PAGE).

203 hate polyacrylamide gel electrophoresis (SDS-PAGE).

204 hate-polyacrylamide gel electrophoresis (SDS-PAGE).

205 ate-polyaccrylamide gel electrophoresis (SDS-PAGE).

206 ecyl-polyacrylamide gel electrophoresis (SDS-PAGE, the second-D separation) on either a capillary gel

207 lfate-polyacrylamide gel electrophoresis SDS-PAGE-immunoblotting with patient sera and rabbit serum a

208 r proteins using OFFGEL electrophoresis, SDS-PAGE and protein identification by MALDI-TOF MS.

209 The simple approach employing SDS-PAGE and PCA reported in this paper may provide a useful

210 electrophoresis (SDS-PAGE), and enables SDS-PAGE and subsequent immuno-probing in an automated micro

211 s carried out included sugar estimation, SDS-PAGE, GPC, color, FT-IR, DSC, thermal stability, solubil

212 As expected, SDS-PAGE patterns were species-specific but differences, due

213 Seventeen protein bands from SDS-PAGE were analysed and 26 proteins were identified.

214 Moreover, 19 protein bands from SDS-PAGE were analyzed and a total of 45 different proteins

215 l changes (surface hydrophobicity, FTIR, SDS-PAGE and thiol content) of gluten in relation to its ant

216 identified as type-I collagens by FTIR, SDS-PAGE, and molecular weight distribution analyses.

217 Furthermore, SDS-PAGE analysis showed high similarity among the protein f

218 o-dimensional isoelectric focusing (IEF)/SDS-PAGE not only revealed different alpha and beta isoforms

219 IEF/SDS-PAGE examination of irradiated tadpole brain homogenate

220 polyacrylamide gel electrophoresis (IEF/SDS-PAGE) and fluorescence measurements.

221 linked glycans from proteins resolved in SDS-PAGE gels for subsequent analysis by mass spectrometry (

222 form of Gdown1 with altered mobility in SDS-PAGE that appears during mitosis.

223 No fragmentation was observed in SDS-PAGE while transmission electron micrographs showed comp

224 70 generated products that comigrated in SDS-PAGE with the C1 and C2 forms, respectively, and mutatio

225 equence, a 76-kDa moiety was detected in SDS-PAGE without reducing agent and heat inactivation.

226 ecA homolog, showed aberrant mobility in SDS-PAGE, structural instability and loss of activity at 37

227 rresponding to the tetramer (152 kDa) in SDS-PAGE, suggesting that the MGAT2 enzyme primarily functio

228 lecular-weight complexes and Blue Native/SDS-PAGE and isoelectric focusing demonstrated that differen

229 fter immunoprecipitation and blue native/SDS-PAGE.

230 ance energy transfer (FRET), nonreducing SDS-PAGE, and strategic mutation of the Ab hinge region was

231 Herein, we describe the use of SDS-PAGE and microprobe Raman spectroscopy to detect and dis

232 method has been used as a replacement of SDS-PAGE for purity analysis of adeno-associated virus (AAV)

233 The results of SDS-PAGE gel and Western blot indicated that CRANAD-17 was c

234 Densitometry analysis of SDS-PAGE gels confirmed no size degradation (P>0.05) as a fu

235 teomics tools based on image analysis of SDS-PAGE protein gels and protein identification by tandem m

236 lecular mass of approximately 150 kDa on SDS-PAGE and did not contain Gbeta5 Mass spectrometry analys

237 d shoulder proteins that are detected on SDS-PAGE as faster-migrating shoulder bands designated LANA1

238 these fibroblasts was mildly delayed on SDS-PAGE gel, suggesting some overmodification of collagen d

239 ding patterns from whole-cell lysates on SDS-PAGE gels, by direct staining and/or immunoblotting, usi

240 ine with the migration shift detected on SDS-PAGE of cell culture collagen, extracts of bone collagen

241 ealed the same abnormal chain pattern on SDS-PAGE with an overabundance of a gamma112 cross-linked tr

242 ranes, ran as intact dimeric proteins on SDS-PAGE, and migrated as an approximately 1100-kDa band on

243 The enzyme preparation when analysed on SDS-PAGE, displayed a single protein band with Mr 33 kDa; Su

244 PAGE with a molecular weight of 24kDa on SDS-PAGE.

245 itions than under reducing conditions on SDS-PAGE.

246 as a dimer while migrating at 66 kDa on SDS-PAGE.

247 in super-family members were revealed on SDS-PAGE.

248 is not sufficient for regular SDS CGE or SDS-PAGE assay.

249 Analyses by SEC, blue native PAGE, SDS-PAGE, and dynamic light scattering indicated that the re

250 ssed 12S globulin by 2D blue-native PAGE/SDS-PAGE indicated that the nhx5 nhx6 knockouts showed compr

251 was determined by semiquantitative PCR, SDS-PAGE/Western blotting, and immunofluorescence staining.

252 ted and freeze-dried in order to perform SDS-PAGE and immunoblotting tests.

253 subjected to analysis of total protein, SDS-PAGE and size exclusion chromatography.

254 species were estimated by a quantitative SDS-PAGE.

255 Non-reducing SDS-PAGE confirms assembly of the predicted Cys(820)-linked

256 Non-reducing SDS-PAGE shows two bands of about 38kDa exhibiting strong ac

257 olumn, separated by nonreducing-reducing SDS-PAGE, and identified by mass spectrometry.

258 Analyses by non-reducing SDS-PAGE, size exclusion chromatography, and sedimentation v

259 kDa in size when analysed under reducing SDS-PAGE.

260 odification with 10% fetal bovine serum; SDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel electrop

261 tography coupled with mass spectrometry, SDS-PAGE and immunoassay.

262 109, as documented by mass spectrometry, SDS-PAGE, isoelectric focusing, size-exclusion chromatograph

263 o the high sensitivity of silver stained SDS-PAGE.

264 sitivity is comparable to silver-stained SDS-PAGE.

265 In this study, we used Phos-tag SDS-PAGE to determine the cellular level of phospho-FrzZ und

266 The SDS-PAGE pattern of A. mellifera proteins honey showed three

267 egree of hydrolysis of HPIs by HT in the SDS-PAGE profiles.

268 etone treatment of cocoa powder prior to SDS-PAGE led to losses of nitrogenous compounds.

269 form when cell lysates were subjected to SDS-PAGE under non-reducing conditions.

270 t was approximately 27.5kDa according to SDS-PAGE, shown a single band in zymography.

271 utral pH by high resolution Tris-Tricine SDS-PAGE and matrix-assisted laser desorption ionization tim

272 Tricine SDS-PAGE revealed stepwise truncations of the O antigen that

273 is directly relevant to the widely-used SDS-PAGE based slab-gel Western blot, while saving sample vo

274 ated to be approximately 62,000Da, using SDS-PAGE and 57151Da, based on mass spectrometry results.

275 Proteins were studied by using SDS-PAGE and immunoblotting with sera from patients with pea

276 of equal molecular mass estimated, using SDS-PAGE and native-PAGE electrophoresis, to be 86kDa.

277 ontractile proteins in human heart using SDS-PAGE and three detection methods: specific enzymatic con

278 lycation endproducts were measured using SDS-PAGE gels and by ELISA whereas Amadori products were ass

279 of in-depth sulfoglycomic analysis using SDS-PAGE resolved proteins.

280 drolysis profiles were illustrated using SDS-PAGE.

281 ydrolysis profiles were visualised using SDS-PAGE.

282 Hydrolysis profiles were displayed using SDS-PAGE.

283 -0.5 Pa/s and then further separated via SDS-PAGE in a 25 mm long channel.

284 influence of HD on BLG molecular weight SDS-PAGE was used.

285 native (BN) electrophorese combined with SDS-PAGE yielded NOX4 to reside in macromolecular complexes.

286 SDS/PAGE is universally used in biochemistry, cell biology,

287 SDS/PAGE, mass spectrometry, and Edman degradation identifie

288 nning sequences, we quantitate anomalous SDS/PAGE fractionation of helical membrane proteins by compa

289 ffect of acrylamide concentration on the SDS/PAGE mobility of a variety of natural membrane proteins.

290 teins are reliably determined from their SDS/PAGE mobility, most helical membrane proteins, which com

291 rmination of their molecular weights via SDS/PAGE.

292 nmodified proteins (PICUP) combined with SDS/PAGE, and NMR, we probed the mechanisms underlying CP-2'

293 We then characterize the PAGE separation performance.

294 ceride levels in European Americans from the PAGE study.

295 We see this PAGE-in-PDMS fabrication technique as expanding the appl

296 facilitates the protocol by eliminating two PAGE purification steps.

297 phoretic approaches [native, urea, acid urea PAGEs and isoelectric focusing (IEF)] as the first-dimen

298 ctive towards kappa-casein, analysed by Urea-PAGE and LC-ESI-MS, whereas the degradation of alpha and

299 tuguese PDO cheeses were analysed using Urea-PAGE and reverse phase-high performance liquid chromatog

300 Peptide mapping using Urea-PAGE followed by CA revealed two major clusters accordin