ライフサイエンスコーパス: SDS-PAGE

1 SDS-PAGE analyses indicated the formation of hydrolysate

2 SDS-PAGE analysis of the dry-enriched protein fractions

3 SDS-PAGE analysis showed high degree of protein polymeri

4 SDS-PAGE analysis showed that salt addition contributes

5 SDS-PAGE analysis showed that the band intensity of trop

6 SDS-PAGE and immunoassay analysis with rabbit polyclonal

7 SDS-PAGE and MS analysis revealed that the sheared archa

8 SDS-PAGE and SEM analyses were also carried out to compa

9 SDS-PAGE and Western blot analyses indicated that covale

10 SDS-PAGE and Western blot techniques were used to identi

11 SDS-PAGE coupled to LC-MS analysis of sand fly saliva, b

12 SDS-PAGE electrophoresis qualitatively detected three ma

13 SDS-PAGE gels stained for catecholase activity showed mu

14 SDS-PAGE gels were used to determine abundance of the CO

15 SDS-PAGE in non-reducing and reducing conditions reveale

16 SDS-PAGE of both roe protein concentrates showed protein

17 SDS-PAGE of pure CPC yielded two bands corresponding to

18 SDS-PAGE patterns show distinctive bands for each kind o

19 SDS-PAGE profile of PPI revealed major bands ranging fro

20 SDS-PAGE results revealed a reduction in the casein and

21 SDS-PAGE showed that annonacinone inhibited formation of

22 SDS-PAGE showed that collagens extracted with different

23 SDS-PAGE showed that the molecular mass of purified enzy

24 SDS-PAGE showed that the protein bands corresponding to

25 SDS-PAGE showed that the purified protein had molecular

26 SDS-PAGE shows the presence of a well separated protein

27 SDS-PAGE under reducing and non-reducing conditions did

28 SDS-PAGE was carried out for all collagens extracted und

29 SDS-PAGE was performed on type I collagen cross-linked i

30 SDS-PAGE, DLS, and TEM were used to confirm and characte

31 SDS-PAGE, surface hydrophobicity, circular dichroism, FT

32 SDS-PAGE, Western blots, bite blots, and immunization vi

33 tyrosine immunoprecipitations followed by 1D SDS-PAGE and mass spectrometry.

34 OF) spectra of fifteen bands separated by 1D SDS-PAGE.

35 The 2D SDS-PAGE separation demonstrated the presence of a few p

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

37 A SDS-PAGE analysis suggested that Dps should be a substra

38 e the astringency of red wines by means of a SDS-PAGE based-method.

39 After SDS-PAGE of the partially purified material, two separat

40 d a single polypeptide band of 83.1kDa after SDS-PAGE.

41 (T.u.) were analyzed by immunoblotting after SDS-PAGE and Urea-PAGE using polyclonal antibodies (PABs

42 Although SDS-PAGE did not show any differences for either the num

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

44 hange affects migration of the protein on an SDS-PAGE gel, and appears to alter secondary structure o

45 We used an SDS-PAGE-based screen to select peptides that dimerize b

46 Two different analysis methods were used: an SDS-PAGE based assay to detect IgG cleavage products and

47 UV absorbance and SDS-PAGE analyses were used to monitor MR progression du

48 d they were also subjected to amino acid and SDS-PAGE analysis.

49 Proteomic analysis and SDS-PAGE electrophoresis of the extracted proteome sugge

50 ultrahigh pressure liquid chromatography and SDS-PAGE gels.

51 Gel filtration chromatography and SDS-PAGE revealed that the enzyme is monomeric with a mo

52 aration, lectin affinity chromatography, and SDS-PAGE.

53 X-ray crystallography and SDS-PAGE further show that trimer 4(F20Cha), a covalentl

54 can be observed by X-ray crystallography and SDS-PAGE.

55 ial immunopurification, deglycosylation, and SDS-PAGE separation of FPRs is sufficient to identify C-

56 ra h 6 were determined by sandwich ELISA and SDS-PAGE, and the allergenicities of treated peanuts wer

57 performance liquid chromatography (HPLC) and SDS-PAGE subunit analysis reveal that the first step of

58 aluated through the degree of hydrolysis and SDS-PAGE profiles.

59 abeling, followed by immunoprecipitation and SDS-PAGE, and in vitro transcription, translation and pr

60 ssfully compared to references: Kjeldahl and SDS-PAGE densitometry for the determination of the propo

61 the current reference methods, Kjeldahl and SDS-PAGE electrophoresis.

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

63 olecular weight estimated by NATIVE-PAGE and SDS-PAGE electrophoresis was approximately 60 kDa.

64 ent protein band appeared on native-PAGE and SDS-PAGE implying that the mPPO is a monomeric protein w

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

66 roscopy, secondary ion mass spectrometry and SDS-PAGE indicate that Cba. tepidum biogenic S(0) globul

67 ted using a combination of spectroscopic and SDS-PAGE assays.

68 Spectroscopic and SDS-PAGE binding assays of Sin a 2 and Ara h 1 with diff

69 Fluorescence spectroscopy and SDS-PAGE techniques were employed to explore quantitativ

70 total reflection-FTIR, CD spectroscopy, and SDS-PAGE.

71 ersisted under cell and lysate treatment and SDS-PAGE conditions that are expected to have suppressed

72 btained by electrophoretic technique such as SDS-PAGE.

73 om the sera of patients with diabetes before SDS-PAGE.

74 Biochemical (SDS-PAGE, Size exclusion chromatography and LC-MS/MS) an

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

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

77 By SDS-PAGE, two forms of NS5A with distinct apparent molec

78 cytic plaques are diagnostic of CBD(7,8); by SDS-PAGE, so too are detergent-insoluble, 37 kDa fragmen

79 The protein fractions analysed by SDS-PAGE showed similar bands, indicating different solu

80 Supernatants from each step were analysed by SDS-PAGE, ELISA, and Western blots.

81 om 0 to 240 min and subsequently analysed by SDS-PAGE, quantitative LC-MS/MS, untargeted LC-MS/MS and

82 t, the samples were dialyzed and analyzed by SDS-PAGE and for OA content.

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

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

85 s were noticeably different when analyzed by SDS-PAGE.

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

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

88 as isolated with high purity, as assessed by SDS-PAGE and native-PAGE zymogram, appearing as a single

89 IgG molecular integrity was assessed by SDS-PAGE immunoblotting.

90 fflux assay; protein content was assessed by SDS-PAGE Western blot.

91 gomers were reduced (-70.5%), as assessed by SDS-PAGE.

92 ysis of AS-48 digestion fragments in bulk by SDS-PAGE, RP-HPLC, and MALDI-TOF proves that the previou

93 n-tumor brain and neural progenitor cells by SDS-PAGE, immunoblot, mass spectrometry and reverse tran

94 lyzed the structure of recombinant CLEC3A by SDS-PAGE and immunoblot, glycan analysis, matrix-assiste

95 d 6.64mgg(-1)) were analysed and compared by SDS-PAGE, showing differences in their electrophoretic p

96 ysates with high specificity as confirmed by SDS-PAGE analysis with a phosphoprotein-specific stain a

97 their triple-helical structure, confirmed by SDS-PAGE and FTIR.

98 y introducing kansui, which was confirmed by SDS-PAGE, FTIR, and HPLC results.

99 Peak homogeneity was confirmed by SDS-PAGE.

100 Peptides were detected by SDS-PAGE and GC-MS was used to determine carbohydrate co

101 itional major peptide bands were detected by SDS-PAGE treatments as compared to the solar or freeze d

102 (molecular weight <15 kDa) as determined by SDS-PAGE and MALDI-TOF/MS analyses.

103 gliadins and glutenins profiling was done by SDS-PAGE.

104 lous migration of the cross-linked enzyme by SDS-PAGE.

105 The subunit molecular mass estimated by SDS-PAGE was 93 kDa for both strains, while the molecula

106 adation during in vitro GID was evaluated by SDS-PAGE and by measuring the nitrogen content of ultraf

107 ethod, Ara h 1 and Ara h 2 were evaluated by SDS-PAGE and sandwich ELISA.

108 d by recombinant techniques and evaluated by SDS-PAGE, size exclusion chromatography, circular dichro

109 Examination by SDS-PAGE followed by protein staining revealed protein p

110 tiparallel affinity purification followed by SDS-PAGE analysis is more predictive for expression scre

111 NH(2)-terminal I-like ectodomain followed by SDS-PAGE and microsequencing using electrospray (ISI-Q-T

112 s analysed by mass spectrometry, followed by SDS-PAGE and subsequent immunoblotting with antibodies d

113 uorescent penicillin BOCILLIN FL followed by SDS-PAGE shows that they are active for acylation by sub

114 ysis of clarified culture fluid fractions by SDS-PAGE and mass spectrometry revealed that the CTD was

115 e with previous studies it was identified by SDS-PAGE and MALDI-TOF-MS that ZnPP formation takes plac

116 few dimerizing sequences were identified by SDS-PAGE.

117 A covalently cross-linked dimer isolated by SDS-PAGE and mass analysis showed that dityrosine dimer

118 a molecular mass of approximately 85 kDa by SDS-PAGE, it elutes in fractions corresponding to approx

119 fractions from felodipine treated lenses by SDS-PAGE in conjunction with mass spectrometry and immun

120 nalysis of human postmortem brain lysates by SDS-PAGE and Western blot reveals htt as full-length and

121 based on this concept, we first measured by SDS-PAGE and confocal microscopy the level of inclusion

122 Circular dichroism, heat modifiability by SDS-PAGE, Triton X-114 phase partitioning and liposome i

123 Circular dichroism, heat modifiability by SDS-PAGE, Triton X-114 phase partitioning, and liposome

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

125 ultimerization were consistently observed by SDS-PAGE, Western blotting, and mass spectrometry.

126 haseolin-polyphenol complexation obtained by SDS-PAGE on a 10% polyacrylamide gel, it was observed th

127 Chemical analysis was performed by SDS-PAGE and mass spectrometry.

128 ntification of the small cleavage product by SDS-PAGE.

129 Analysis of the protein by SDS-PAGE revealed two subunits with molecular masses of

130 orm 1, which migrates as a 61-kDa protein by SDS-PAGE, is expressed in human islets and pancreatic in

131 (1-2 h); investigate SMALP protein purity by SDS-PAGE analysis and estimate protein concentration (4

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

133 rporation into receptor subunits resolved by SDS-PAGE, there was etomidate-inhibitable labeling by [(

134 ferent polypeptide profiles were revealed by SDS-PAGE between exposed and nonexposed pollen, but the

135 ds were detected in purified portal rings by SDS-PAGE under nonreducing conditions.

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

137 After deglycosylation and separation by SDS-PAGE, excised Coomassie Blue-staining bands ( approx

138 le enzymatic treatments under sonication, by SDS-PAGE, western blot and ELISA, with serum IgE of alle

139 ct of OT upon these laccases were studied by SDS-PAGE.

140 A 28 kDa (apparent molecular weight by SDS-PAGE analysis) soybean protein has been isolated by

141 ysis, differential scanning fluorimetry, CD, SDS-PAGE, and immunoblotting with conformation-dependent

142 on of USP20 correlates with a characteristic SDS-PAGE mobility shift of the protein, blocks its deubi

143 vector followed by affinity chromatography, SDS-PAGE, and identification of protein bands evident on

144 es, including size exclusion chromatography, SDS-PAGE, mass spectrometry, and cell stimulation follow

145 binatorial peptide ligand libraries (CPLLs), SDS-PAGE, nLC-ESI-MS/MS, and database search, permitted

146 ced by HPP, this processing modified the 1-D SDS-PAGE sarcoplasmic patterns in a direct-dependent man

147 al assays (thioflavin T, circular dichroism, SDS-PAGE, size exclusion chromatography, surface plasmon

148 If second dimension SDS-PAGE followed BNP, the 180-kDa mutant htt was absent

149 he complex was confirmed by second dimension SDS-PAGE, Western blotting, mass spectrometry, and the u

150 A combination of one-dimensional SDS-PAGE and semi-quantitative mass spectrometry identif

151 Two-dimensional SDS-PAGE of the purified active fraction revealed a sing

152 rom the migration pattern on two-dimensional SDS-PAGE, the majority of plasma CL-K1 was found in comp

153 ation and nonreduced/reduced two-dimensional SDS-PAGE, we detected CL-K1 and CL-L1 in disulfide bridg

154 rmation of complexes that were stable during SDS-PAGE.

155 sulfate poly acrylamide gel electrophoreses (SDS-PAGE) indicated that the integrity of major myofibri

156 l sulfate-polyacrylamide gel electrophoresis SDS-PAGE-immunoblotting with patient sera and rabbit ser

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

158 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis of the OM revealed a high molecular m

159 Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) analysis revealed the localization of phosviti

160 sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and matrix-assisted laser desorption/ionizatio

161 sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) combined with principal component analysis (PC

162 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) fiber typing and one for Western blot protein

163 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gel containing a copolymerized protein substra

164 sulfate polyacrylamide gel electrophoresis (SDS-PAGE) helped the separation of these misfolded prote

165 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) is a widely used technique for protein separat

166 sulfate- polyacrylamide gel electrophoresis (SDS-PAGE) or capillary gel electrophoresis (CGE) toward

167 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) protocol is described.

168 w proteins separated by gel electrophoresis (SDS-PAGE) to be detected as peptides by mass spectrometr

169 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was used during the CE-SDS peak characterizati

170 naturing polyacrylamide gel electrophoresis (SDS-PAGE) was used to separate proteins.

171 sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and enables SDS-PAGE and subsequent immuno-pr

172 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), oxidative damage to amino acids, and changes

173 sulfate polyacrylamide gel electrophoresis (SDS-PAGE), which was eliminated by phosphatase treatment

174 sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).

175 ulphate-polyaccrylamide gel electrophoresis (SDS-PAGE).

176 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

177 sulphate polyacrylamide gel electrophoresis (SDS-PAGE).

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

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

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

181 ing-mass spectrometry MYDGF assay, employing SDS-PAGE-based protein fractionation to deplete high-abu

182 gel electrophoresis (SDS-PAGE), and enables SDS-PAGE and subsequent immuno-probing in an automated m

183 ssays carried out included sugar estimation, SDS-PAGE, GPC, color, FT-IR, DSC, thermal stability, sol

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

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

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

187 d appearance of small protein fragments from SDS-PAGE in dry-aged samples compared to the unaged.

188 The results from SDS-PAGE illustrated that the most adsorbed quantity amo

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

190 ional changes (surface hydrophobicity, FTIR, SDS-PAGE and thiol content) of gluten in relation to its

191 Furthermore, SDS-PAGE analysis showed high similarity among the prote

192 try (MALDI-TOF MS), gas chromatography (GC), SDS-PAGE, Toll-like receptor 4 (TLR4) stimulation, and i

193 130-140- and >150-kDa complexes by gradient SDS-PAGE analysis.

194 y two-dimensional isoelectric focusing (IEF)/SDS-PAGE not only revealed different alpha and beta isof

195 IEF/SDS-PAGE examination of irradiated tadpole brain homogen

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

197 ccurately, with distinctive protein bands in SDS-PAGE at 140 kDa and 110 kDa for bovine and porcine s

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

199 de sequence, a 76-kDa moiety was detected in SDS-PAGE without reducing agent and heat inactivation.

200 appearance of a 160 kDa myosin-4 fragment in SDS-PAGE, further decreased water-holding of myofibrils

201 d corresponding to the tetramer (152 kDa) in SDS-PAGE, suggesting that the MGAT2 enzyme primarily fun

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

203 ew mecA homolog, showed aberrant mobility in SDS-PAGE, structural instability and loss of activity at

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

205 r O-linked glycans from proteins resolved in SDS-PAGE gels for subsequent analysis by mass spectromet

206 Rather, confocal microscopy, SDS-PAGE, and intrinsic fluorescence measurements indica

207 OXPHOS system and comparative 2D blue native/SDS PAGE analyses using isolated mitochondria.

208 h molecular-weight complexes and Blue Native/SDS-PAGE and isoelectric focusing demonstrated that diff

209 on after immunoprecipitation and blue native/SDS-PAGE.

210 a discrete "jump" in mobility by nonreducing SDS-PAGE, suggesting formation of at most a few final pa

211 esonance energy transfer (FRET), nonreducing SDS-PAGE, and strategic mutation of the Ab hinge region

212 ic enzymes are first resolved in nonreducing SDS-PAGE on a gel without protein substrate.

213 The observed SDS-PAGE bands did not show any evidence of zein crossli

214 as demonstrated by glycoprotein staining of SDS PAGE gels.

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

216 Proteomics tools based on image analysis of SDS-PAGE protein gels and protein identification by tand

217 his method has been used as a replacement of SDS-PAGE for purity analysis of adeno-associated virus (

218 The results of SDS-PAGE gel and Western blot indicated that CRANAD-17 w

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

220 On SDS-PAGE analysis the composition of cortical fiber cell

221 On SDS-PAGE, AML-1 showed an apparent molecular mass of 27

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

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

224 nized by the alphaOEP80(325-337) antibody on SDS-PAGE.

225 conditions than under reducing conditions on SDS-PAGE.

226 d by these fibroblasts was mildly delayed on SDS-PAGE gel, suggesting some overmodification of collag

227 cated shoulder proteins that are detected on SDS-PAGE as faster-migrating shoulder bands designated L

228 In line with the migration shift detected on SDS-PAGE of cell culture collagen, extracts of bone coll

229 a-lg) present in cheese whey is difficult on SDS-PAGE due to their close proximity during electrophor

230 t molecular mass of approximately 150 kDa on SDS-PAGE and did not contain Gbeta5 Mass spectrometry an

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

232 banding patterns from whole-cell lysates on SDS-PAGE gels, by direct staining and/or immunoblotting,

233 actually TFPIbeta based on (1) migration on SDS-PAGE before and after deglycosylation, (2) the lack

234 revealed the same abnormal chain pattern on SDS-PAGE with an overabundance of a gamma112 cross-linke

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

236 Cell lysates were resolved on SDS-PAGE and analyzed by Western blot.

237 myosin super-family members were revealed on SDS-PAGE.

238 ax exhibits a slight molecular mass shift on SDS-PAGE as compared with recombinant Bax, which suggest

239 The anomalous migration of SNORC on SDS-PAGE was due to its primary polypeptide features, su

240 which resolved to a single 65-kDa species on SDS-PAGE.

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

242 ned in vitro by laying labeled bacteria over SDS-PAGE-separated salivary proteins.

243 Analyses by SEC, blue native PAGE, SDS-PAGE, and dynamic light scattering indicated that th

244 rocessed 12S globulin by 2D blue-native PAGE/SDS-PAGE indicated that the nhx5 nhx6 knockouts showed c

245 ition, Blue Native-PAGE and Blue Native-PAGE/SDS-PAGE 2D analyses demonstrated co-existence of the al

246 ECs) was determined by semiquantitative PCR, SDS-PAGE/Western blotting, and immunofluorescence staini

247 llected and freeze-dried in order to perform SDS-PAGE and immunoblotting tests.

248 In this article, we present SDS-PAGE differential mobility studies combined with flu

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

250 ish species were estimated by a quantitative SDS-PAGE.

251 Non-reducing SDS-PAGE confirms assembly of the predicted Cys(820)-lin

252 Congo red-positive fibrils, and non-reducing SDS-PAGE of M129C during fibrillation conditions at diff

253 Non-reducing SDS-PAGE shows two bands of about 38kDa exhibiting stron

254 Analyses by non-reducing SDS-PAGE, size exclusion chromatography, and sedimentati

255 n and neutralization process by non-reducing SDS-PAGE.

256 ty column, separated by nonreducing-reducing SDS-PAGE, and identified by mass spectrometry.

257 45 kDa in size when analysed under reducing SDS-PAGE.

258 r analysed by static laser light scattering, SDS-PAGE and optical-fluorescence microscopy.

259 ha modification with 10% fetal bovine serum; SDS-PAGE, sodium dodecyl sulfate-polyacrylamide gel elec

260 otein content was not altered significantly, SDS PAGE profiling exhibited minor modifications in the

261 recrystallization and they presented similar SDS-PAGE profiles, with bands close to 20 and 37 kDa.

262 Despite their structural similarity, SDS-PAGE stability assays and collision-induced dissocia

263 ation, as shown by a decrease in solubility, SDS-PAGE pattern, and Confocal Laser Scanning Microscopy

264 romatography coupled with mass spectrometry, SDS-PAGE and immunoassay.

265 5.0109, as documented by mass spectrometry, SDS-PAGE, isoelectric focusing, size-exclusion chromatog

266 also the high sensitivity of silver stained SDS-PAGE.

267 sensitivity is comparable to silver-stained SDS-PAGE.

268 Phos-tag SDS-PAGE coupled with MS analysis disclosed that SnRK1 i

269 SK protein was also detected by the Phos-tag SDS-PAGE method.

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

271 ly P amounts in cells determined by Phos-tag SDS-PAGE.

272 The SDS-PAGE pattern of A. mellifera proteins honey showed t

273 st degree of hydrolysis of HPIs by HT in the SDS-PAGE profiles.

274 Through SDS-PAGE analysis, an increased degree of hydrolysis wit

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

276 Acetone treatment of cocoa powder prior to SDS-PAGE led to losses of nitrogenous compounds.

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

278 Tricine SDS-PAGE revealed stepwise truncations of the O antigen

279 -lg by staining acrylamide gel after tricine SDS-PAGE using cationic 'stains all' dye.

280 t neutral pH by high resolution Tris-Tricine SDS-PAGE and matrix-assisted laser desorption ionization

281 hich is directly relevant to the widely-used SDS-PAGE based slab-gel Western blot, while saving sampl

282 Using SDS-PAGE, we found that Rsp profoundly affected cell sur

283 stimated to be approximately 62,000Da, using SDS-PAGE and 57151Da, based on mass spectrometry results

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

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

286 Hydrolysis profiles were displayed using SDS-PAGE.

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

288 of contractile proteins in human heart using SDS-PAGE and three detection methods: specific enzymatic

289 e hydrolysis profiles were illustrated using SDS-PAGE.

290 Indeed, using SDS-PAGE, mass spectrometry and western analyses, we sho

291 ed glycation endproducts were measured using SDS-PAGE gels and by ELISA whereas Amadori products were

292 These aggregates can be observed using SDS-PAGE, size-exclusion chromatography, dynamic light s

293 yzed before and after plasma treatment using SDS-PAGE, FTIR, UPLC-MS/MS and ELISA.

294 he hydrolysis profiles were visualised using SDS-PAGE.

295 scrambled forms is reversed on CE-SDS versus SDS-PAGE.

296 Via SDS-PAGE, most of the mutant c-monomers exhibited increa

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

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

299 ependent NF-kappaB responses; however, while SDS-PAGE analysis showed similar LPS ladder patterns for

300 lue native (BN) electrophorese combined with SDS-PAGE yielded NOX4 to reside in macromolecular comple