ライフサイエンスコーパス: size exclusion chromatography

1 ual to that of the protein (as determined by size exclusion chromatography).

2 zation techniques ((1)H NMR, MALDI-HRMS, and size-exclusion chromatography).

3 ified the resulting proteins by affinity and size exclusion chromatography.

4 e favorably compared with those derived from size exclusion chromatography.

5 und to coelute with antibody products during size exclusion chromatography.

6 d to analysis of total protein, SDS-PAGE and size exclusion chromatography.

7 hown by fluorescence confocal microscopy and size exclusion chromatography.

8 tion mass spectrometry (ESI MS) coupled with size exclusion chromatography.

9 m Saccharomyces cerevisiae are determined by size exclusion chromatography.

10 ained by exploiting molecular confinement on size exclusion chromatography.

11 on is also directly demonstrated in vitro by size exclusion chromatography.

12 uilibrium analytical ultracentrifugation and size exclusion chromatography.

13 2 lipopeptide ternary complex as measured by size exclusion chromatography.

14 both intact albumin and its fragments using size exclusion chromatography.

15 reas BiFae1B is a dimer in solution based on size exclusion chromatography.

16 a 1kDa cut-off membrane and fractionated by size exclusion chromatography.

17 y on the basis of hydrodynamic volume, using size exclusion chromatography.

18 <3kDa fractions were further fractionated by size exclusion chromatography.

19 dialysis and further into 94 fractions using size exclusion chromatography.

20 ration in high molecular weight fractions in size exclusion chromatography.

21 e fractions were isolated by high resolution size-exclusion chromatography.

22 s with 96% to 98% radiochemical purity after size-exclusion chromatography.

23 high molecular weight (HMW) on nondenaturing size-exclusion chromatography.

24 trated H(2)O(2) followed by purification via size-exclusion chromatography.

25 f Euphorbia neriifolia by anion exchange and size-exclusion chromatography.

26 nantly as 36mers in solution as estimated by size-exclusion chromatography.

27 uman plasma and eluted with plasma miRNAs in size-exclusion chromatography.

28 purified with a combination of affinity and size-exclusion chromatography.

29 It migrated as a dimeric protein during size-exclusion chromatography.

30 tion of anion-exchange, charge-transfer, and size-exclusion chromatographies.

31 nvolves isolation of wine polysaccharides by size exclusion chromatography, acid hydrolysis, eliminat

32 In size exclusion chromatography active SiaDW-135 migrated

33 Using anion-exchange and size exclusion chromatography, an inhibitory protein whi

34 ESI-HRMS, MALDI-HRMS, NMR, and size exclusion chromatography analyses indicated the for

35 Based on size exclusion chromatography analyses, the peak molecul

36 and Thr(68) are important for catalysis, and size exclusion chromatography analysis and x-ray crystal

37 We used size exclusion chromatography analysis of recombinant HA

38 ed to characterize the constructs, including size exclusion chromatography, analytical ultracentrifug

39 Using size exclusion chromatography, analytical ultracentrifug

40 These complexes have been characterized by size exclusion chromatography, analytical ultracentrifug

41 Results of size exclusion chromatography and 8-anilinonaphthalene-1

42 Size exclusion chromatography and a simple intrinsic flu

43 dimer formation in solution was supported by size exclusion chromatography and analytical ultracentri

44 omeric state in solution as characterized by size exclusion chromatography and analytical ultracentri

45 In addition, by combining the size exclusion chromatography and atomic force microscop

46 Using size exclusion chromatography and atomic force microscop

47 Using size exclusion chromatography and blue native gel electr

48 In this study, we utilized size exclusion chromatography and blue native polyacryla

49 h were isolated from C. fleckeri venom using size exclusion chromatography and cation exchange chroma

50 In cultured podocytes, size exclusion chromatography and confocal microscopy sh

51 utant (G42R) of Galphai1-GDP, as observed by size exclusion chromatography and differential hydrogen/

52 Our new method based on size exclusion chromatography and fluorescence measures

53 in mitochondrial transcription by performing size exclusion chromatography and immunoprecipitation ex

54 Biochemical (SDS-PAGE, Size exclusion chromatography and LC-MS/MS) and immunolo

55 work nodes in solution and analyzing them by size exclusion chromatography and light scattering.

56 Further analysis by size exclusion chromatography and mass spectrometry indi

57 Analysis of GHT by a combination of size exclusion chromatography and mass spectrometry reve

58 While HvJAMM1 was inhibited by size exclusion chromatography and metal chelators, its a

59 Dynamic light scattering, size exclusion chromatography and native PAGE show that

60 e combination of classical chemical methods, size exclusion chromatography and NMR spectroscopy, was

61 een demonstrated, which are characterized by size exclusion chromatography and NMR spectroscopy.

62 Hydrolysates were separated by size exclusion chromatography and purified fractions wer

63 fy beta-cell antigens, we applied sequential size exclusion chromatography and reverse-phase high-per

64 Size exclusion chromatography and sedimentation velocity

65 D12 and NCAD12, were studied with analytical size exclusion chromatography and sedimentation velocity

66 With size exclusion chromatography and small angle x-ray scat

67 nsistent with the crystallography data, both size exclusion chromatography and small angle x-ray scat

68 By size exclusion chromatography and small-angle X-ray scat

69 own algae were isolated and characterized by size exclusion chromatography and Solid-state NMR spectr

70 ed a hydrodynamic volume close to 2000kDa by size exclusion chromatography and the exocarp and mesoca

71 Size exclusion chromatography and Western blotting data

72 uccessful elimination of PB was confirmed by size-exclusion chromatography and (1)H NMR spectroscopy.

73 donors with no or two APOL1 risk alleles by size-exclusion chromatography and analysis of immunopuri

74 y active but were monomeric as determined by size-exclusion chromatography and analytical ultracentri

75 ilized prefibrillar species were isolated by size-exclusion chromatography and analyzed by STEM, dyna

76 Size-exclusion chromatography and blue native polyacryla

77 Sedimentation velocity, size-exclusion chromatography and cryo-electron microsco

78 n the presence of ATP and ADP, as assayed by size-exclusion chromatography and equilibrium analytical

79 Fluorescence-detection size-exclusion chromatography and fluorescence anisotrop

80 We studied the assembly using size-exclusion chromatography and fluorescence spectrosc

81 The folded protein molecule was isolated by size-exclusion chromatography and had full enzymatic act

82 Size-exclusion chromatography and particle sizing by dyn

83 ions in sputum were measured with the use of size-exclusion chromatography and refractometry.

84 Size-exclusion chromatography and SAXS experiments revea

85 uced only minor conformational changes while size-exclusion chromatography and small angle X-ray scat

86 Using size-exclusion chromatography and three distinct measure

87 operties validated by x-ray crystallography, size exclusion chromatography, and activity assay.

88 sible and circular dichroism spectroscopies, size exclusion chromatography, and analytical ultracentr

89 is, multiangle light scattering coupled with size exclusion chromatography, and bacterial two-hybrid

90 The concentrate was fractionated by size exclusion chromatography, and fractions were then s

91 Using mutagenesis, chemical cross-linking, size exclusion chromatography, and native polyacrylamide

92 Bovine hemolysate was purified by size exclusion chromatography, and one high molecular we

93 id chromatography-mass spectrometry (LC-MS), size exclusion chromatography, and quantitative RT-PCR,

94 Analyses by non-reducing SDS-PAGE, size exclusion chromatography, and sedimentation velocit

95 , BrC is separated by molecular weight using size exclusion chromatography, and the response of each

96 d denaturing gel electrophoresis techniques, size-exclusion chromatography, and an oligomer-specific

97 g electrophoretic mobility gel shift assays, size-exclusion chromatography, and electron microscopy,

98 T-RNAi plants by nuclear magnetic resonance, size-exclusion chromatography, and gas chromatography-ma

99 ssed the heterocomplex formation with ELISA, size-exclusion chromatography, and immunoblotting using

100 Results from circular dichroism, size-exclusion chromatography, and NMR demonstrate that

101 phaSyn species in AD brains by custom ELISA, size-exclusion chromatography, and nondenaturing/denatur

102 Differential centrifugation, size-exclusion chromatography, and proteinase K treatmen

103 cells were analyzed by non-denaturing PAGE, size-exclusion chromatography, and the distribution of a

104 n combination with dynamic light scattering, size-exclusion chromatography, and transmittance electro

105 We used differential centrifugation and size-exclusion chromatography as orthogonal approaches t

106 in high purity in milligram quantities using size exclusion chromatography, as evidenced by mass spec

107 show that commercially available bind-elute size exclusion chromatography (BE-SEC) columns purify EV

108 Fractions were obtained by size exclusion chromatography, before and after enzymati

109 ular domains of RAE-1 and m152 and performed size exclusion chromatography binding assays as well as

110 acyl tRNA synthetase, co-eluted with sRNA by size exclusion chromatography, but resolved from met-tRN

111 6), Furthermore, we demonstrate that size-exclusion chromatography can be a suitable method f

112 binant techniques and evaluated by SDS-PAGE, size exclusion chromatography, circular dichroism spectr

113 ionization time-of-flight mass spectrometry, size-exclusion chromatography, circular dichroism spectr

114 ing (R53H) and domain swapping (A39P), using size-exclusion chromatography, circular dichroism, and h

115 Ion exchange and size exclusion chromatography combined with mass spectro

116 Size exclusion chromatography confirmed intrinsic viscos

117 vitro protein-protein interaction assays and size exclusion chromatography confirmed that PYL4(A194T)

118 for modulating beta-lactamase activity, and size exclusion chromatography confirmed that the integra

119 We optimized a hyphenated system based on size exclusion chromatography coupled to a microwave/UV

120 e cytoplasmatic and extracellular fractions (size exclusion chromatography coupled to ICP-MS) reveale

121 The method is based on size exclusion chromatography coupled to inductively cou

122 characterize beta-glucans in beer wort using size exclusion chromatography coupled with a triple-dete

123 characterization of metal biomolecules using size exclusion chromatography coupled with inductively c

124 Size exclusion chromatography coupled with light-scatter

125 Size exclusion chromatography coupled with multiangle st

126 Speciation analysis by size-exclusion chromatography coupled to inductively cou

127 We analyzed the samples with size-exclusion chromatography coupled to molecular absor

128 omers were evaluated by ultracentrifugation, size-exclusion chromatography coupled to multiangle lase

129 were IdeS digested, reduced, and analyzed by size-exclusion chromatography coupled with mass spectrom

130 tructure of the ZmPPR10: ATPH: complex using size-exclusion chromatography-coupled synchrotron small-

131 blot analysis and comparisons with published size exclusion chromatography data and the masses of kno

132 The size-exclusion chromatography data further indicate that

133 by a combination of techniques, such as NMR, size exclusion chromatography, differential scanning cal

134 Using physical size exclusion chromatography/differential refractometry

135 Since standard analytical tools such as size-exclusion chromatography do not provide realistic m

136 h the wild-type enzyme is active as a dimer, size exclusion chromatography, dynamic and quasi-elastic

137 rved as a tetramer in the crystal lattice by size exclusion chromatography, dynamic light scattering,

138 Through size exclusion chromatography, dynamic light scattering,

139 well-defined Pt(II) -SCNPs was evidenced by size exclusion chromatography, dynamic light scattering,

140 On size exclusion chromatography, EcChiP had an apparent na

141 ding measurements, dynamic light scattering, size-exclusion chromatography, electron microscopy, and

142 Size exclusion chromatography, ELISA, and surface plasmo

143 anging from n = 1 to >100 units of Tau using size exclusion chromatography, fluorescence correlation

144 umatins were extensively characterised using size exclusion chromatography for homogeneity, reversed-

145 Here, we used ultrafiltration and size-exclusion chromatography for the isolation and a mo

146 Here, we combine size-exclusion chromatography, Forster resonance energy

147 in T fluorescence, dynamic light scattering, size exclusion chromatography, Fourier transform infrare

148 Size exclusion chromatography fractionated the gluten pr

149 However, analysis of size exclusion chromatography fractions demonstrated tha

150 ient transfection and fluorescence-detection size-exclusion chromatography (FSEC) experiments using a

151 ultracentrifugation, gel electrophoresis and size-exclusion chromatography), hollow-fiber flow FFF co

152 tection, used together with high performance size exclusion chromatography (HPSEC) of carbohydrates,

153 nic matter (DOM) determined by high pressure size exclusion chromatography (HPSEC) using measurements

154 Here high-performance size exclusion chromatography (HPSEC) was coupled to flu

155 High Pressure Size Exclusion Chromatography (HPSEC) was used to monito

156 weight fraction (HMW) using high-performance size-exclusion chromatography (HPSEC) and volatile compo

157 rches were characterized by high-performance size-exclusion chromatography (HPSEC) equipped with stat

158 opectin determination using High-Performance-Size-Exclusion-Chromatography (HPSEC).

159 -captured Hrd1 complexes from these cells by size-exclusion chromatography, immunodepletion, and abso

160 and NMR spectroscopy, as well as analytical size exclusion chromatography, imply that Abeta is maint

161 lymers were in the range M(n) = 12-40 kDa by size exclusion chromatography in THF.

162 Dimers of MtHPP, determined by size exclusion chromatography, in the presence of CO2 or

163 Size-exclusion chromatography, in combination with absor

164 Ultracentrifugation and size exclusion chromatography indicated that both PPOs o

165 sing state-of-the-art speciation analysis by size-exclusion chromatography inductively coupled plasma

166 Size exclusion chromatography, mass spectrometry, X-ray

167 m tissue surfaces and then analyzed by using size exclusion chromatography/mass spectrometry (SEC-MS)

168 The results from analytical size-exclusion chromatography, Mn(II) competition titrat

169 e employed a series of techniques, including size-exclusion chromatography-multi-angle light scatteri

170 Size exclusion chromatography, multiangle light scatteri

171 Here, using size exclusion chromatography-multiangle laser light sca

172 that D. rerio alphaE-catenin is monomeric by size exclusion chromatography, native PAGE, and small an

173 ucture of the chaperonin, as demonstrated by size-exclusion chromatography, native gel electrophoresi

174 idated using analytical ultracentrifugation, size-exclusion chromatography, NMR relaxation studies, d

175 Size exclusion chromatography of detergent solubilized,

176 Size exclusion chromatography of hRNR or alpha alone wit

177 Size exclusion chromatography of purified AAC3 in dodecy

178 Using size exclusion chromatography of the MW2 supernatant, fo

179 more, SDS-gel electrophoresis and analytical size exclusion chromatography of the recombinant protein

180 Size-exclusion chromatography of human plasma has shown

181 Size-exclusion chromatography of the CTD monomer showed

182 ion of capsids can be measured in vitro with size exclusion chromatography or dynamic light scatterin

183 rofile of the hydrolysates as analysed using size exclusion chromatography, or the antioxidant activi

184 een starch molecular structures (obtained by size-exclusion chromatography, proton NMR and multiple-a

185 wall material, using phloroglucinolysis and size exclusion chromatography, provided quantitative and

186 Here, using size-exclusion chromatography, pulldown assays, and smal

187 Size exclusion chromatography revealed that non-phosphor

188 Size exclusion chromatography revealed the native LdUPRT

189 Finally, size exclusion chromatography revealed the presence of p

190 formulations, dynamic light scattering, and size-exclusion chromatography revealed only limited SCI

191 Size-exclusion chromatography revealed that oligomeric (

192 Through the online combination of size exclusion chromatography, SAXS, and refractometry,

193 a panel of biochemical approaches, including size exclusion chromatography, SDS-PAGE, mass spectromet

194 which were not observed using nonequilibrium size exclusion chromatography (SEC) analysis.

195 ar, and lower resolution techniques, such as size exclusion chromatography (SEC) and analytical ultra

196 In this work, we use size exclusion chromatography (SEC) and electrospray ion

197 Size exclusion chromatography (SEC) and ion pair chromat

198 ography, extracted proteins were analysed by size exclusion chromatography (SEC) coupled to inductive

199 lied to assess their functional quality: (i) size exclusion chromatography (SEC) demonstrated functio

200 D as a complementary analytical technique to size exclusion chromatography (SEC) for understanding pr

201 Size exclusion chromatography (SEC) is a favored method

202 Purified proteins were subjected to size exclusion chromatography (SEC) to characterize olig

203 phobic-interaction chromatography (HIC), and size exclusion chromatography (SEC) to isolate NL trimer

204 igh-performance liquid chromatography (HPLC)-size exclusion chromatography (SEC) to online isotope ra

205 In this study, size exclusion chromatography (SEC) was used in combinat

206 Size exclusion chromatography (SEC) was used to characte

207 n characterized by the second dimension (D2) size exclusion chromatography (SEC) with IR5 and LS dete

208 LMWH preparations have been determined using size exclusion chromatography (SEC) with optical detecti

209 capsulated analytes were well separated with size exclusion chromatography (SEC), and rutin and narin

210 independent approaches including analytical size exclusion chromatography (SEC), SEC combined with m

211 the Mn measured by other techniques such as size exclusion chromatography (SEC), vapor pressure osmo

212 -flight mass spectrometry (MALDI-ToF MS) and size exclusion chromatography (SEC).

213 lysis of polymers are critically revised for size exclusion chromatography (SEC).

214 luorescence spectroscopy, UV-absorption, and size exclusion chromatography (SEC).

215 formed between NEIL1 and PCNA (+/-DNA) using size exclusion chromatography (SEC).

216 The dimer fraction was separated by size-exclusion chromatography (SEC) after pre-fractionat

217 W fractions were collected using preparative size-exclusion chromatography (SEC) and extensively char

218 e using analytical ultracentrifugation, NMR, size-exclusion chromatography (SEC) and multi-angle ligh

219 Size-exclusion chromatography (SEC) and small-angle X-ra

220 olymers, combinations of interactive LC with size-exclusion chromatography (SEC) are especially usefu

221 Size-exclusion chromatography (SEC) has been developed a

222 ed on their size, with ultrahigh-performance size-exclusion chromatography (SEC) in the second dimens

223 coming is addressed via a quintuple-detector size-exclusion chromatography (SEC) method consisting of

224 This article reports a size-exclusion chromatography (SEC) method that permits

225 However, size-exclusion chromatography (SEC) revealed that both n

226 KSEC-MS utilizes the ability of size-exclusion chromatography (SEC) to separate any smal

227 Size-exclusion chromatography (SEC) was used as a conser

228 dy compares three common laboratory methods, size-exclusion chromatography (SEC), (1)H nuclear magnet

229 the sensitivity of conventional techniques, size-exclusion chromatography (SEC), microflow imaging (

230 ical-flow field-flow fractionation (AF4) and size-exclusion chromatography (SEC), which were online c

231 Oligomers were further separated by size-exclusion chromatography (SEC).

232 t approximately 151,000 Da upon Superdex 200 size-exclusion chromatography (SEC).

233 The digesta were analysed by size-exclusion chromatography (SEC).

234 the oligomers are detectable by AFM, EM, and size-exclusion chromatography (SEC).

235 This method is thus complementary to size-exclusion chromatography (SEC).

236 l suitability was evaluated and compared for size exclusion chromatography, (SEC), liquid chromatogra

237 tacticity in the first dimension coupled to size-exclusion chromatography separating according to mo

238 , fluorescence correlation spectroscopy, and size exclusion chromatography show that the sensor-clust

239 ChrR crystallized as a tetramer, and size exclusion chromatography showed that this is the ol

240 Size exclusion chromatography showed that Ub-CP was pres

241 Size exclusion chromatography showed that Zn(2+) stabili

242 Size exclusion chromatography showed the full-length aCR

243 Simultaneously, size-exclusion chromatography showed an increase of the

244 Size exclusion chromatography shows that the 3' recognit

245 Multiple experiments, including size exclusion chromatography, small-angle x ray scatter

246 tracentrifugation, dynamic light scattering, size exclusion chromatography, small-angle x-ray scatter

247 ons of full-length NEMO, we employed in-line size exclusion chromatography-small-angle X-ray scatteri

248 Herein, we developed a serial size exclusion chromatography (sSEC) strategy to enable

249 most proteins can be purified using a single size-exclusion chromatography step, immediately appropri

250 Size exclusion chromatography suggested for EMRE- and MC

251 Analysis of the purified protein by size-exclusion chromatography suggests that gpNu3 is hig

252 (thioflavin T, circular dichroism, SDS-PAGE, size exclusion chromatography, surface plasmon resonance

253 An anomaly in 10E8v4 size exclusion chromatography that appeared to be relate

254 We also present new experimental data from size exclusion chromatography that support our computati

255 from NMR, small angle x-ray scattering, and size exclusion chromatography that were used to generate

256 We show by size-exclusion chromatography that both AtsB and anSMEcp

257 e, which agreed with the results obtained by size exclusion chromatography, that showed that wines wi

258 alladate species through electrophoresis and size-exclusion chromatography, the latter has been used

259 wo molecules in the asymmetric unit and from size-exclusion chromatography, the protein dimerizes in

260 , and NMR spectroscopies in conjunction with size exclusion chromatography to help rationalize the re

261 luorescein Diacetate Succinimidyl Ester, and size exclusion chromatography to remove unconjugated lab

262 sulfate precipitation followed by desalting size exclusion chromatography) to get purified napins.

263 Examining the mutant heart, native size-exclusion chromatography, transmission electron mic

264 In blue native gels and size exclusion chromatography, TRPM1 migrated with a mob

265 Size-exclusion chromatography, two-dimensional gel elect

266 from soluble and insoluble aggregates using size exclusion chromatography, under nondenaturing condi

267 Further analysis using pulldowns and size-exclusion chromatography underscored the critical r

268 own to elute, mainly near the void volume by size-exclusion chromatography, using Bio-Gel P6 (1-6kDa)

269 Size-exclusion chromatography was used to characterize t

270 By size exclusion chromatography we demonstrate stable comp

271 -hybrid, co-precipitation, cross-linking and size exclusion chromatography we show that Slc1 (SycE-li

272 raction of Arabidopsis thaliana leaves using size exclusion chromatography, we identified hundreds of

273 lycol precipitation, iodixanol gradient, and size-exclusion chromatography, we obtained from HCV-sero

274 Utilizing size-exclusion chromatography, we separated primary prep

275 ilibrium and stopped-flow binding assays and size exclusion chromatography were compatible with a two

276 Pb and (56)Fe elution profiles, observed via size-exclusion chromatography, were highly correlated (a

277 contrasted experimentally with multidetector size-exclusion chromatography, where, even under extreme

278 ss distributions were determined by coupling size exclusion chromatography with a multi-angle light s

279 Herein we report a facile method based on size exclusion chromatography with fluorescence detectio

280 EM, small angle X-ray scattering, size exclusion chromatography with inline multiangle lig

281 o exist in a monomeric state as confirmed by size exclusion chromatography with inline multiangle sta

282 Kinetic size exclusion chromatography with mass spectrometry det

283 lts obtained by native mass spectrometry and size exclusion chromatography with multi-angle light sca

284 Size exclusion chromatography with multi-angle light sca

285 Size exclusion chromatography with multiangle laser ligh

286 tionated NOM was 23,300 g/mol, determined by size exclusion chromatography with multiangle light scat

287 esults from circular dichroism spectroscopy, size exclusion chromatography with multiangle light scat

288 TAG polymers determined by high performance-size exclusion chromatography with refractometric detect

289 e step of solid phase extraction (SPE) using size exclusion chromatography with Sephadex LH-20 withou

290 zed in vitro by dynamic light scattering and size exclusion chromatography with subsequent cholestero

291 axx-H3.3-H4, using coimmunoprecipitation and size-exclusion chromatography with highly purified compo

292 NMR and size-exclusion chromatography with light scattering reve

293 pectrometry, SDS-PAGE, isoelectric focusing, size-exclusion chromatography with light scattering, cir

294 To solve this problem, we present kinetic size-exclusion chromatography with mass spectrometry det

295 SEC-MALLS (size-exclusion chromatography with multi-angle laser lig

296 Size-exclusion chromatography with multi-angle laser lig

297 Using a fluorescence thermal shift assay, size-exclusion chromatography with multi-angle light sca

298 lectrospray ionization mass spectrometry and size-exclusion chromatography with multi-angle light sca

299 stigated the multimeric nature of Spd1 using size-exclusion chromatography with multi-angle light sca

300 l approach for identifying plant SABPs using size-exclusion chromatography with radiolabeled SA, as t