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

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

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

3 the resulting proteins by affinity and size exclusion chromatography.

4 orably compared with those derived from size exclusion chromatography.

5 ctions were isolated by high resolution size-exclusion chromatography.

6 o coelute with antibody products during size exclusion chromatography.

7 h 96% to 98% radiochemical purity after size-exclusion chromatography.

8 analysis of total protein, SDS-PAGE and size exclusion chromatography.

9 by fluorescence confocal microscopy and size exclusion chromatography.

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

11 charomyces cerevisiae are determined by size exclusion chromatography.

12 by exploiting molecular confinement on size exclusion chromatography.

13 also directly demonstrated in vitro by size exclusion chromatography.

14 rium analytical ultracentrifugation and size exclusion chromatography.

15 opeptide ternary complex as measured by size exclusion chromatography.

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

17 intact albumin and its fragments using size exclusion chromatography.

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

19 Da cut-off membrane and fractionated by size exclusion chromatography.

20 d H(2)O(2) followed by purification via size-exclusion chromatography.

21 horbia neriifolia by anion exchange and size-exclusion chromatography.

22 y as 36mers in solution as estimated by size-exclusion chromatography.

23 tracer was determined using quantitative gel exclusion chromatography.

24 plasma and eluted with plasma miRNAs in size-exclusion chromatography.

25 fied with a combination of affinity and size-exclusion chromatography.

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

27 fractions were further fractionated by size exclusion chromatography.

28 sis and further into 94 fractions using size exclusion chromatography.

29 n in high molecular weight fractions in size exclusion chromatography.

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

31 es isolation of wine polysaccharides by size exclusion chromatography, acid hydrolysis, elimination o

32 In size exclusion chromatography active SiaDW-135 migrated as a

33 Ion-exclusion chromatography allows recovery of the ionic li

34 Using anion-exchange and size exclusion chromatography, an inhibitory protein which ex

35 ESI-HRMS, MALDI-HRMS, NMR, and size exclusion chromatography analyses indicated the formatio

36 Based on size exclusion chromatography analyses, the peak molecular we

37 hr(68) are important for catalysis, and size exclusion chromatography analysis and x-ray crystallogra

38 We used size exclusion chromatography analysis of recombinant HA ecto

39 Using size exclusion chromatography, analytical ultracentrifugation

40 se complexes have been characterized by size exclusion chromatography, analytical ultracentrifugation

41 characterize the constructs, including size exclusion chromatography, analytical ultracentrifuge sed

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

43 Results of size exclusion chromatography and 8-anilinonaphthalene-1-sulf

44 Size exclusion chromatography and a simple intrinsic fluoresc

45 rs with no or two APOL1 risk alleles by size-exclusion chromatography and analysis of immunopurified

46 ive but were monomeric as determined by size-exclusion chromatography and analytical ultracentrifugat

47 formation in solution was supported by size exclusion chromatography and analytical ultracentrifugat

48 c state in solution as characterized by size exclusion chromatography and analytical ultracentrifugat

49 d prefibrillar species were isolated by size-exclusion chromatography and analyzed by STEM, dynamic l

50 In addition, by combining the size exclusion chromatography and atomic force microscopy (AF

51 Using size exclusion chromatography and atomic force microscopy, we

52 Using size exclusion chromatography and blue native gel electrophor

53 Size-exclusion chromatography and blue native polyacrylamide

54 In this study, we utilized size exclusion chromatography and blue native polyacrylamide

55 e isolated from C. fleckeri venom using size exclusion chromatography and cation exchange chromatogra

56 In cultured podocytes, size exclusion chromatography and confocal microscopy showed

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

58 presence of ATP and ADP, as assayed by size-exclusion chromatography and equilibrium analytical ultr

59 Fluorescence-detection size-exclusion chromatography and fluorescence anisotropy all

60 Our new method based on size exclusion chromatography and fluorescence measures solub

61 We studied the assembly using size-exclusion chromatography and fluorescence spectroscopy,

62 folded protein molecule was isolated by size-exclusion chromatography and had full enzymatic activity

63 tochondrial transcription by performing size exclusion chromatography and immunoprecipitation experim

64 Biochemical (SDS-PAGE, Size exclusion chromatography and LC-MS/MS) and immunological

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

66 Further analysis by size exclusion chromatography and mass spectrometry indicated

67 Analysis of GHT by a combination of size exclusion chromatography and mass spectrometry revealed

68 While HvJAMM1 was inhibited by size exclusion chromatography and metal chelators, its activi

69 Dynamic light scattering, size exclusion chromatography and native PAGE show that Hs11S

70 bination of classical chemical methods, size exclusion chromatography and NMR spectroscopy, was the o

71 emonstrated, which are characterized by size exclusion chromatography and NMR spectroscopy.

72 Size-exclusion chromatography and particle sizing by dynamic

73 Hydrolysates were separated by size exclusion chromatography and purified fractions were ana

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

75 ta-cell antigens, we applied sequential size exclusion chromatography and reverse-phase high-performa

76 Size-exclusion chromatography and SAXS experiments reveal tha

77 Size exclusion chromatography and sedimentation velocity anal

78 nd NCAD12, were studied with analytical size exclusion chromatography and sedimentation velocity.

79 With size exclusion chromatography and small angle x-ray scatterin

80 only minor conformational changes while size-exclusion chromatography and small angle X-ray scatterin

81 ent with the crystallography data, both size exclusion chromatography and small angle x-ray scatterin

82 By size exclusion chromatography and small-angle X-ray scatterin

83 lgae were isolated and characterized by size exclusion chromatography and Solid-state NMR spectroscop

84 hydrodynamic volume close to 2000kDa by size exclusion chromatography and the exocarp and mesocarp pr

85 Using size-exclusion chromatography and three distinct measures of

86 Size exclusion chromatography and Western blotting data obtai

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

88 aturing gel electrophoresis techniques, size-exclusion chromatography, and an oligomer-specific ELISA

89 and circular dichroism spectroscopies, size exclusion chromatography, and analytical ultracentrifuga

90 ultiangle light scattering coupled with size exclusion chromatography, and bacterial two-hybrid data

91 ctrophoretic mobility gel shift assays, size-exclusion chromatography, and electron microscopy, we an

92 The concentrate was fractionated by size exclusion chromatography, and fractions were then screen

93 i plants by nuclear magnetic resonance, size-exclusion chromatography, and gas chromatography-mass sp

94 the heterocomplex formation with ELISA, size-exclusion chromatography, and immunoblotting using both

95 ng mutagenesis, chemical cross-linking, size exclusion chromatography, and native polyacrylamide gel

96 Results from circular dichroism, size-exclusion chromatography, and NMR demonstrate that the S

97 n species in AD brains by custom ELISA, size-exclusion chromatography, and nondenaturing/denaturing i

98 Bovine hemolysate was purified by size exclusion chromatography, and one high molecular weight

99 Differential centrifugation, size-exclusion chromatography, and proteinase K treatment of

100 romatography-mass spectrometry (LC-MS), size exclusion chromatography, and quantitative RT-PCR, we pr

101 Analyses by non-reducing SDS-PAGE, size exclusion chromatography, and sedimentation velocity rev

102 s were analyzed by non-denaturing PAGE, size-exclusion chromatography, and the distribution of apoAI,

103 is separated by molecular weight using size exclusion chromatography, and the response of each molec

104 bination with dynamic light scattering, size-exclusion chromatography, and transmittance electron mic

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

106 gh purity in milligram quantities using size exclusion chromatography, as evidenced by mass spectrome

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

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

109 tRNA synthetase, co-eluted with sRNA by size exclusion chromatography, but resolved from met-tRNAi by

110 6), Furthermore, we demonstrate that size-exclusion chromatography can be a suitable method for es

111 cessfully demonstrated that quantitative gel exclusion chromatography can be used to follow diffusion

112 t techniques and evaluated by SDS-PAGE, size exclusion chromatography, circular dichroism spectra, EL

113 ation time-of-flight mass spectrometry, size-exclusion chromatography, circular dichroism spectroscop

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

115 Ion exchange and size exclusion chromatography combined with mass spectrometry

116 Size exclusion chromatography confirmed intrinsic viscosity m

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

118 modulating beta-lactamase activity, and size exclusion chromatography confirmed that the integral fus

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

120 oplasmatic and extracellular fractions (size exclusion chromatography coupled to ICP-MS) revealed not

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

122 Speciation analysis by size-exclusion chromatography coupled to inductively coupled

123 We analyzed the samples with size-exclusion chromatography coupled to molecular absorbance

124 were evaluated by ultracentrifugation, size-exclusion chromatography coupled to multiangle laser lig

125 cterize beta-glucans in beer wort using size exclusion chromatography coupled with a triple-detector

126 cterization of metal biomolecules using size exclusion chromatography coupled with inductively couple

127 Size exclusion chromatography coupled with light-scattering a

128 IdeS digested, reduced, and analyzed by size-exclusion chromatography coupled with mass spectrometry

129 Size exclusion chromatography coupled with multiangle static

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

131 analysis and comparisons with published size exclusion chromatography data and the masses of known co

132 The size-exclusion chromatography data further indicate that the

133 combination of techniques, such as NMR, size exclusion chromatography, differential scanning calorime

134 Using physical size exclusion chromatography/differential refractometry (SEC

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

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

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

138 Through size exclusion chromatography, dynamic light scattering, and

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

140 On size exclusion chromatography, EcChiP had an apparent native

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

142 Size exclusion chromatography, ELISA, and surface plasmon res

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

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

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

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

147 fluorescence, dynamic light scattering, size exclusion chromatography, Fourier transform infrared spe

148 Size exclusion chromatography fractionated the gluten protein

149 However, analysis of size exclusion chromatography fractions demonstrated that the

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

151 centrifugation, gel electrophoresis and size-exclusion chromatography), hollow-fiber flow FFF coupled

152 t fraction (HMW) using high-performance size-exclusion chromatography (HPSEC) and volatile compounds

153 were characterized by high-performance size-exclusion chromatography (HPSEC) equipped with static li

154 on, used together with high performance size exclusion chromatography (HPSEC) of carbohydrates, gave

155 atter (DOM) determined by high pressure size exclusion chromatography (HPSEC) using measurements made

156 Here high-performance size exclusion chromatography (HPSEC) was coupled to fluoresc

157 High Pressure Size Exclusion Chromatography (HPSEC) was used to monitor cha

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

159 phosphate and silicate in seawater using ion exclusion chromatography (IEC) coupled with sector field

160 l Si standards were determined by online ion exclusion chromatography (IEC) multicollector inductivel

161 ured Hrd1 complexes from these cells by size-exclusion chromatography, immunodepletion, and absolute

162 NMR spectroscopy, as well as analytical size exclusion chromatography, imply that Abeta is maintained

163 Size-exclusion chromatography, in combination with absorbance

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

165 Ultracentrifugation and size exclusion chromatography indicated that both PPOs occur

166 state-of-the-art speciation analysis by size-exclusion chromatography inductively coupled plasma mass

167 Size exclusion chromatography, mass spectrometry, X-ray cryst

168 sue surfaces and then analyzed by using size exclusion chromatography/mass spectrometry (SEC-MS).

169 The results from analytical size-exclusion chromatography, Mn(II) competition titrations,

170 loyed a series of techniques, including size-exclusion chromatography-multi-angle light scattering, d

171 Size exclusion chromatography, multiangle light scattering, s

172 Here, using size exclusion chromatography-multiangle laser light scatteri

173 e of the chaperonin, as demonstrated by size-exclusion chromatography, native gel electrophoresis and

174 D. rerio alphaE-catenin is monomeric by size exclusion chromatography, native PAGE, and small angle x

175 d using analytical ultracentrifugation, size-exclusion chromatography, NMR relaxation studies, dynami

176 Size exclusion chromatography of detergent solubilized, purif

177 Size exclusion chromatography of hRNR or alpha alone with ClF

178 Size-exclusion chromatography of human plasma has shown PCSK9

179 Size exclusion chromatography of purified AAC3 in dodecyl mal

180 Size-exclusion chromatography of the CTD monomer showed that

181 Using size exclusion chromatography of the MW2 supernatant, followe

182 SDS-gel electrophoresis and analytical size exclusion chromatography of the recombinant protein reve

183 e of the hydrolysates as analysed using size exclusion chromatography, or the antioxidant activity (P

184 tarch molecular structures (obtained by size-exclusion chromatography, proton NMR and multiple-angle

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

186 Here, using size-exclusion chromatography, pulldown assays, and small ang

187 ulations, dynamic light scattering, and size-exclusion chromatography revealed only limited SCI self-

188 Size exclusion chromatography revealed that non-phosphorylate

189 Size-exclusion chromatography revealed that oligomeric (125)I

190 Size exclusion chromatography revealed the native LdUPRT to b

191 Finally, size exclusion chromatography revealed the presence of p30 in

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

193 el of biochemical approaches, including size exclusion chromatography, SDS-PAGE, mass spectrometry, a

194 The dimer fraction was separated by size-exclusion chromatography (SEC) after pre-fractionation o

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

196 nd lower resolution techniques, such as size exclusion chromatography (SEC) and analytical ultracentr

197 In this work, we use size exclusion chromatography (SEC) and electrospray ionizati

198 ctions were collected using preparative size-exclusion chromatography (SEC) and extensively character

199 Size exclusion chromatography (SEC) and ion pair chromatograp

200 ng analytical ultracentrifugation, NMR, size-exclusion chromatography (SEC) and multi-angle light sca

201 Size-exclusion chromatography (SEC) and small-angle X-ray sca

202 rs, combinations of interactive LC with size-exclusion chromatography (SEC) are especially useful for

203 hy, extracted proteins were analysed by size exclusion chromatography (SEC) coupled to inductively co

204 to assess their functional quality: (i) size exclusion chromatography (SEC) demonstrated functional c

205 a complementary analytical technique to size exclusion chromatography (SEC) for understanding protein

206 Size-exclusion chromatography (SEC) has been developed as a r

207 their size, with ultrahigh-performance size-exclusion chromatography (SEC) in the second dimension t

208 Size exclusion chromatography (SEC) is a favored method for s

209 g is addressed via a quintuple-detector size-exclusion chromatography (SEC) method consisting of mult

210 This article reports a size-exclusion chromatography (SEC) method that permits the h

211 However, size-exclusion chromatography (SEC) revealed that both non-en

212 Purified proteins were subjected to size exclusion chromatography (SEC) to characterize oligomeri

213 c-interaction chromatography (HIC), and size exclusion chromatography (SEC) to isolate NL trimers fro

214 erformance liquid chromatography (HPLC)-size exclusion chromatography (SEC) to online isotope ratio m

215 KSEC-MS utilizes the ability of size-exclusion chromatography (SEC) to separate any small mol

216 Size-exclusion chromatography (SEC) was used as a conservativ

217 In this study, size exclusion chromatography (SEC) was used in combination w

218 Size exclusion chromatography (SEC) was used to characterize

219 racterized by the second dimension (D2) size exclusion chromatography (SEC) with IR5 and LS detectors

220 preparations have been determined using size exclusion chromatography (SEC) with optical detection.

221 mpares three common laboratory methods, size-exclusion chromatography (SEC), (1)H nuclear magnetic re

222 lated analytes were well separated with size exclusion chromatography (SEC), and rutin and naringenin

223 sensitivity of conventional techniques, size-exclusion chromatography (SEC), microflow imaging (MFI),

224 pendent approaches including analytical size exclusion chromatography (SEC), SEC combined with multi-

225 Mn measured by other techniques such as size exclusion chromatography (SEC), vapor pressure osmometry

226 flow field-flow fractionation (AF4) and size-exclusion chromatography (SEC), which were online couple

227 ht mass spectrometry (MALDI-ToF MS) and size exclusion chromatography (SEC).

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

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

230 roximately 151,000 Da upon Superdex 200 size-exclusion chromatography (SEC).

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

232 ligomers are detectable by AFM, EM, and size-exclusion chromatography (SEC).

233 scence spectroscopy, UV-absorption, and size exclusion chromatography (SEC).

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

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

236 tability was evaluated and compared for size exclusion chromatography, (SEC), liquid chromatography u

237 icity in the first dimension coupled to size-exclusion chromatography separating according to molar m

238 orescence correlation spectroscopy, and size exclusion chromatography show that the sensor-cluster co

239 Simultaneously, size-exclusion chromatography showed an increase of the molec

240 ChrR crystallized as a tetramer, and size exclusion chromatography showed that this is the oligome

241 Size exclusion chromatography showed that Ub-CP was present a

242 Size exclusion chromatography showed that Zn(2+) stabilizes a

243 Size exclusion chromatography showed the full-length aCRY to

244 Size exclusion chromatography shows that the 3' recognition s

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

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

247 f full-length NEMO, we employed in-line size exclusion chromatography-small-angle X-ray scattering.

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

249 proteins can be purified using a single size-exclusion chromatography step, immediately appropriate f

250 Size exclusion chromatography suggested for EMRE- and MCU-con

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

252 flavin T, circular dichroism, SDS-PAGE, size exclusion chromatography, surface plasmon resonance, tra

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

254 We show by size-exclusion chromatography that both AtsB and anSMEcpe are

255 also present new experimental data from size exclusion chromatography that support our computational

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

257 ich agreed with the results obtained by size exclusion chromatography, that showed that wines with hi

258 ate species through electrophoresis and size-exclusion chromatography, the latter has been used in co

259 lecules in the asymmetric unit and from size-exclusion chromatography, the protein dimerizes in solut

260 NMR spectroscopies in conjunction with size exclusion chromatography to help rationalize the relativ

261 scein Diacetate Succinimidyl Ester, and size exclusion chromatography to remove unconjugated label.

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

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

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

265 Size-exclusion chromatography, two-dimensional gel electropho

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

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

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

269 Size-exclusion chromatography was used to characterize the in

270 By size exclusion chromatography we demonstrate stable complex f

271 id, co-precipitation, cross-linking and size exclusion chromatography we show that Slc1 (SycE-like ch

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

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

274 Utilizing size-exclusion chromatography, we separated primary preparati

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

276 d (56)Fe elution profiles, observed via size-exclusion chromatography, were highly correlated (averag

277 asted experimentally with multidetector size-exclusion chromatography, where, even under extremely ge

278 stributions were determined by coupling size exclusion chromatography with a multi-angle light scatte

279 rein we report a facile method based on size exclusion chromatography with fluorescence detection (SE

280 3.3-H4, using coimmunoprecipitation and size-exclusion chromatography with highly purified components

281 EM, small angle X-ray scattering, size exclusion chromatography with inline multiangle light sc

282 st in a monomeric state as confirmed by size exclusion chromatography with inline multiangle static l

283 NMR and size-exclusion chromatography with light scattering reveal th

284 ometry, SDS-PAGE, isoelectric focusing, size-exclusion chromatography with light scattering, circular

285 solve this problem, we present kinetic size-exclusion chromatography with mass spectrometry detectio

286 Kinetic size exclusion chromatography with mass spectrometry detectio

287 SEC-MALLS (size-exclusion chromatography with multi-angle laser light sc

288 Size-exclusion chromatography with multi-angle laser light sc

289 ing a fluorescence thermal shift assay, size-exclusion chromatography with multi-angle light scatteri

290 ospray ionization mass spectrometry and size-exclusion chromatography with multi-angle light scatteri

291 btained by native mass spectrometry and size exclusion chromatography with multi-angle light scatteri

292 ted the multimeric nature of Spd1 using size-exclusion chromatography with multi-angle light scatteri

293 Size exclusion chromatography with multi-angle light scatteri

294 Size exclusion chromatography with multiangle laser light sca

295 ted NOM was 23,300 g/mol, determined by size exclusion chromatography with multiangle light scatterin

296 s from circular dichroism spectroscopy, size exclusion chromatography with multiangle light scatterin

297 roach for identifying plant SABPs using size-exclusion chromatography with radiolabeled SA, as these

298 polymers determined by high performance-size exclusion chromatography with refractometric detection (

299 p of solid phase extraction (SPE) using size exclusion chromatography with Sephadex LH-20 without the

300 n vitro by dynamic light scattering and size exclusion chromatography with subsequent cholesterol and