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

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

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

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

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

5 <3kDa fractions were further fractionated by size exclusion chromatography.

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

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

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

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

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

11 hown by fluorescence confocal microscopy and size exclusion chromatography.

12 r ribozyme-fusion transcription by automated size exclusion chromatography.

13 m Saccharomyces cerevisiae are determined by size exclusion chromatography.

14 ained by exploiting molecular confinement on size exclusion chromatography.

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

16 formation via gel mobility shift assays and size exclusion chromatography.

17 soluble protein oligomers prefractionated by size exclusion chromatography.

18 roism, differential scanning calorimetry, or size exclusion chromatography.

19 d depolymerization mechanism as evidenced by size exclusion chromatography.

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

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

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

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

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

25 r-molecular-weight species, as determined by size-exclusion chromatography.

26 coprotein (HRG) in mouse and human plasma by size-exclusion chromatography.

27 ge-like nanoparticles was 81% as examined by size-exclusion chromatography.

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

29 high molecular weight complexes generated by size exclusion chromatography, although the detergent-sp

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

31 Based on size exclusion chromatography analyses, the peak molecul

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

33 We used size exclusion chromatography analysis of recombinant HA

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

35 Using size exclusion chromatography, analytical ultracentrifug

36 Here, using size-exclusion chromatography, analytical ultracentrifug

37 This homotrimer was further confirmed with size-exclusion chromatography, analytical ultracentrifug

38 Size exclusion chromatography and a simple intrinsic flu

39 Plasma CMPs were isolated via size exclusion chromatography and analyzed using global

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

41 Using size exclusion chromatography and blue native gel electr

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

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

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

45 a novel protocol involving a combination of size exclusion chromatography and differential centrifug

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

47 y, multiangle laser light scattering-coupled size exclusion chromatography and dynamic light scatteri

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

49 Size exclusion chromatography and Fourier transform ion

50 oss of double helix content was supported by size exclusion chromatography and FT-IR data, respective

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

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

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

54 Using size exclusion chromatography and native polyacrylamide

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

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

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

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

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

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

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

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

63 Size exclusion chromatography and Western blotting data

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

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

66 is monomeric in solution as demonstrated by size-exclusion chromatography and analytical ultracentri

67 s are loaded to kinetochores, we carried out size-exclusion chromatography and analyzed Bub3-containi

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

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

70 Results from size-exclusion chromatography and multi-angle light scat

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

72 Size-exclusion chromatography and SAXS experiments revea

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

74 Exosomes were isolated by size-exclusion chromatography and their morphology, size

75 Using size-exclusion chromatography and three distinct measure

76 w cytometry and evaluating GPCR stability by size-exclusion chromatography and UV absorbance measurem

77 Proteins were isolated using size-exclusion-chromatography and identified by mass spe

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

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

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

81 n chromatography, Superdex peptide 10/300 GL size exclusion chromatography, and liquid chromatography

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

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

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

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

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

87 phorylation and refolding assays, analytical size-exclusion chromatography, and hydrogen/deuterium ex

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

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

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

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

92 Aggregation was measured using size-exclusion chromatography, and PTM levels were calcu

93 Here, using hydrogen-deuterium exchange MS, size-exclusion chromatography, and sedimentation velocit

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

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

96 s purified using a tandem immunoaffinity and size-exclusion chromatography approach to obtain monomer

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

98 ng kinase assays, microscale thermophoresis, size exclusion chromatography, as well as site-directed

99 ystems, including membrane permeabilization, size-exclusion chromatography-based oligomer, and retrot

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

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

102 determine intracellular Ca(2+) exchange and size-exclusion chromatography; blue native page and immu

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

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

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

106 patible conditions are injected onto a short size-exclusion chromatography column.

107 Ion exchange and size exclusion chromatography combined with mass spectro

108 Size exclusion chromatography confirmed intrinsic viscos

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

110 Here we conclusively demonstrate using size exclusion chromatography coupled multi-angle light

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

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

113 paration to data interpretation using online size exclusion chromatography coupled to native IM mass

114 Size exclusion chromatography coupled to small-angle X-r

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

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

117 Size exclusion chromatography coupled with multiangle st

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

119 tration calorimetry, sedimentation velocity, size-exclusion chromatography coupled to multi-angle lig

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

121 H 4 as shown by multiple techniques, such as size-exclusion chromatography coupled to multiangle ligh

122 ding interactions, which was demonstrated by size-exclusion chromatography coupled with differential

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

124 rometry, analytical ultracentrifugation, and size-exclusion chromatography coupled with multi-angle l

125 Using size-exclusion chromatography coupled with small-angle X

126 Size-exclusion chromatography-coupled right-angled light

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

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

129 ative polyacrylamide gel electrophoresis and size exclusion chromatography demonstrated a defect in T

130 Analysis of cytosolic extracts by size-exclusion chromatography detected by an online indu

131 Size exclusion chromatography determines the molecular w

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

133 Using size-exclusion chromatography, differential scanning and

134 Using physical size exclusion chromatography/differential refractometry

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

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

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 e aggregates can be observed using SDS-PAGE, 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 Size-exclusion chromatography employing aqueous mobile p

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

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

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

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

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

149 Size exclusion chromatography fractionated the gluten pr

150 we have compared synaptotoxic activities in size-exclusion chromatography fractioned protein samples

151 large HDL, were isolated by high-resolution size exclusion chromatography from study subjects.

152 transmembrane protein CD63 were isolated by size-exclusion chromatography from cell culture media.

153 candidates were confirmed in EVs isolated by size-exclusion chromatography from nasal lavages of chil

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

155 combinantly expressed enzyme was analyzed by size-exclusion chromatography, gas-phase electrophoretic

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

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

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

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

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

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

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

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

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

165 Bead-assisted depletion and size-exclusion chromatography improved specificity of Qd

166 We used size-exclusion chromatography in line with small-angle X

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

168 Size-exclusion chromatography, in combination with absor

169 Ultracentrifugation and size exclusion chromatography indicated that both PPOs o

170 Speciation was investigated by size-exclusion chromatography - inductively coupled plas

171 Size exclusion chromatography, mass spectrometry, X-ray

172 , we report a novel and sensitive mixed mode size exclusion chromatography (MM SEC) coupled with mult

173 analytical method, which couples mixed-mode size exclusion chromatography (mmSEC) with online native

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

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

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

177 techniques (circular dichroism spectroscopy, size-exclusion chromatography-multiangle laser light sca

178 Size-exclusion chromatography-multiangle light scatterin

179 re, using alphaSN aggregation, fibrillation, size-exclusion chromatography-multiangle light scatterin

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

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

182 a robust, quantitative, and automated online size-exclusion chromatography-native mass spectrometry (

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

184 r PrPC when monomeric fractions derived from size exclusion chromatography of normal brain homogenate

185 Size exclusion chromatography of purified AAC3 in dodecy

186 Using size exclusion chromatography of the MW2 supernatant, fo

187 ATPase assays and size exclusion chromatography of the trans-variants FlrC

188 Size-exclusion chromatography of human plasma has shown

189 Size-exclusion chromatography of Lys-C-digested native D

190 Size-exclusion chromatography of the CTD monomer showed

191 Size-exclusion chromatography of the isolated targeting

192 Size-exclusion chromatography of the lysates from mutant

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

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

195 in binding profiles of the ASO-conjugates by size-exclusion chromatography revealed distinct and spec

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

197 Size-exclusion chromatography revealed that oligomeric (

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

199 Size exclusion chromatography (SEC) and ion pair chromat

200 chromatography (IEC) column in tandem with a size exclusion chromatography (SEC) column to efficientl

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

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

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

204 e developed a method based on sequencing the size exclusion chromatography (SEC) fractions of nonvesi

205 Size exclusion chromatography (SEC) is a favored method

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

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

208 Size exclusion chromatography (SEC) was used to characte

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

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

211 hilic interaction chromatography (HILIC) and size exclusion chromatography (SEC) with the parallel de

212 he development of a new technology combining size exclusion chromatography (SEC), a commonly used EV

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

214 compatible solvent and conditions, combining size exclusion chromatography (SEC), ion-pair reversed p

215 those observed by conventional techniques of size exclusion chromatography (SEC), microflow imaging (

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

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

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

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

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

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

222 s done using ammonium bicarbonate buffer and size exclusion chromatography (SEC-ICP-sfMS), with possi

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

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

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

226 ng activity for four sites was discovered in size-exclusion chromatography (SEC) fractions >= 670 kDa

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

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

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

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

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

232 Subsequently, size-exclusion chromatography (SEC) with an MS-compatibl

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

234 by the knob and hole mutations, we combined size-exclusion chromatography (SEC), differential scanni

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

236 Coupling two-dimensional size-exclusion chromatography (SEC)-cIEF to ESI-MS/MS en

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

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

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

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

241 als, through either dialysis or low-pressure size-exclusion chromatography (SEC).

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

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

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

245 Size exclusion chromatography showed the full-length aCR

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

247 Size exclusion chromatography shows that trimer 4(F20Cha

248 horesis, analytical ultracentrifugation, and size-exclusion chromatography small angle x-ray scatteri

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

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

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

252 re, we directly combine MS-compatible serial size exclusion chromatography (sSEC) fractionation with

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

254 top-down proteomics platform coupling serial size exclusion chromatography (sSEC) to reversed-phase c

255 Size exclusion chromatography suggested for EMRE- and MC

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

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

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

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

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

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

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

263 of these tandem fused ACPs was determined by size exclusion chromatography to be higher (21 kDa, 36 k

264 his hydrolysate was subsequently purified by size exclusion chromatography to obtain fractions sorted

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

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

267 Size-exclusion chromatography, two-dimensional gel elect

268 Rs = 2.7) by UHP-SEC (ultra-high-performance size exclusion chromatography) under nondenaturing condi

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

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

271 A sequential two-step purification by size exclusion chromatography was carried out to fractio

272 Size-exclusion chromatography was used to characterize t

273 By size exclusion chromatography we demonstrate stable comp

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

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

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

277 ing monomeric PrP (mM1000) generated through size exclusion chromatography were found to harbor acute

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

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

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

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

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

283 Kinetic size exclusion chromatography with mass spectrometry det

284 Size exclusion chromatography with multi-angle light sca

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

286 Size exclusion chromatography with multiangle laser ligh

287 utility of an integrated approach, including size exclusion chromatography with multiangle light scat

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

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

290 hains followed by the product analysis using size exclusion chromatography with online mass spectrome

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

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

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

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

295 NMR and size-exclusion chromatography with light scattering reve

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

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

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

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

300 ected in the same colloidal size fraction by size-exclusion chromatography with multielement detectio