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

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

2 the resulting proteins by affinity and size exclusion chromatography.

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

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

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

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

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

8 fractions were further fractionated by size exclusion chromatography.

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

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

11 orably compared with those derived from size exclusion chromatography.

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

13 o coelute with antibody products during size exclusion chromatography.

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

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

16 by fluorescence confocal microscopy and size exclusion chromatography.

17 ozyme-fusion transcription by automated size exclusion chromatography.

18 charomyces cerevisiae are determined by size exclusion chromatography.

19 by exploiting molecular confinement on size exclusion chromatography.

20 also directly demonstrated in vitro by size exclusion chromatography.

21 ation via gel mobility shift assays and size exclusion chromatography.

22 ecular-weight species, as determined by size-exclusion chromatography.

23 le protein oligomers prefractionated by size exclusion chromatography.

24 tein (HRG) in mouse and human plasma by size-exclusion chromatography.

25 ke nanoparticles was 81% as examined by size-exclusion chromatography.

26 , differential scanning calorimetry, or size exclusion chromatography.

27 olymerization mechanism as evidenced by size exclusion chromatography.

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

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

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

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

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

33 We used size exclusion chromatography analysis of recombinant HA ecto

34 Here, using size-exclusion chromatography, analytical ultracentrifugation

35 s homotrimer was further confirmed with size-exclusion chromatography, analytical ultracentrifugation

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

37 Size exclusion chromatography and a simple intrinsic fluoresc

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

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

40 onomeric in solution as demonstrated by size-exclusion chromatography and analytical ultracentrifugat

41 loaded to kinetochores, we carried out size-exclusion chromatography and analyzed Bub3-containing co

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

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

44 Using size exclusion chromatography and blue native gel electrophor

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

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

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

48 vel protocol involving a combination of size exclusion chromatography and differential centrifugation

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

50 ltiangle laser light scattering-coupled size exclusion chromatography and dynamic light scattering me

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

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

53 Size exclusion chromatography and Fourier transform ion cyclo

54 f double helix content was supported by size exclusion chromatography and FT-IR data, respectively.

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

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

57 Results from size-exclusion chromatography and multi-angle light scatterin

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

59 Using size exclusion chromatography and native polyacrylamide gel e

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

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

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

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

64 Size-exclusion chromatography and SAXS experiments reveal tha

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

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

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

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

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

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

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

72 Using size-exclusion chromatography and three distinct measures of

73 ometry and evaluating GPCR stability by size-exclusion chromatography and UV absorbance measurements.

74 Size exclusion chromatography and Western blotting data obtai

75 Proteins were isolated using size-exclusion-chromatography and identified by mass spectrom

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

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

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

79 lation and refolding assays, analytical size-exclusion chromatography, and hydrogen/deuterium exchang

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

81 omatography, Superdex peptide 10/300 GL size exclusion chromatography, and liquid chromatography-elec

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

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

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

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

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

87 Aggregation was measured using size-exclusion chromatography, and PTM levels were calculated

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

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

90 , using hydrogen-deuterium exchange MS, size-exclusion chromatography, and sedimentation velocity, we

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

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

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

94 ified using a tandem immunoaffinity and size-exclusion chromatography approach to obtain monomeric fl

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

96 nase assays, microscale thermophoresis, size exclusion chromatography, as well as site-directed mutag

97 s, including membrane permeabilization, size-exclusion chromatography-based oligomer, and retrotransl

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

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

100 rmine intracellular Ca(2+) exchange and size-exclusion chromatography; blue native page and immunopre

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

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

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

104 le conditions are injected onto a short size-exclusion chromatography column.

105 Ion exchange and size exclusion chromatography combined with mass spectrometry

106 Size exclusion chromatography confirmed intrinsic viscosity m

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

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

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

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

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

112 on calorimetry, sedimentation velocity, size-exclusion chromatography coupled to multi-angle light sc

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

114 s shown by multiple techniques, such as size-exclusion chromatography coupled to multiangle light sca

115 ion to data interpretation using online size exclusion chromatography coupled to native IM mass spect

116 Size exclusion chromatography coupled to small-angle X-ray sc

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

118 interactions, which was demonstrated by size-exclusion chromatography coupled with differential hydro

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

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

121 ry, analytical ultracentrifugation, and size-exclusion chromatography coupled with multi-angle light

122 Size exclusion chromatography coupled with multiangle static

123 Using size-exclusion chromatography coupled with small-angle X-ray

124 Size-exclusion chromatography-coupled right-angled light scat

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

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

127 polyacrylamide gel electrophoresis and size exclusion chromatography demonstrated a defect in TRAPP

128 Analysis of cytosolic extracts by size-exclusion chromatography detected by an online inductive

129 Size exclusion chromatography determines the molecular weight

130 Using size-exclusion chromatography, differential scanning and isot

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

132 Using physical size exclusion chromatography/differential refractometry (SEC

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

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

135 Through size exclusion chromatography, dynamic light scattering, and

136 regates can be observed using SDS-PAGE, size-exclusion chromatography, dynamic light scattering, and

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

138 On size exclusion chromatography, EcChiP had an apparent native

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

140 Size exclusion chromatography, ELISA, and surface plasmon res

141 Size-exclusion chromatography employing aqueous mobile phases

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

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

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

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

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

147 Size exclusion chromatography fractionated the gluten protein

148 ave compared synaptotoxic activities in size-exclusion chromatography fractioned protein samples from

149 smembrane protein CD63 were isolated by size-exclusion chromatography from cell culture media.

150 dates were confirmed in EVs isolated by size-exclusion chromatography from nasal lavages of children

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

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

153 nantly expressed enzyme was analyzed by size-exclusion chromatography, gas-phase electrophoretic mobi

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

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

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

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

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

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

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

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

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

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

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

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

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

167 Size-exclusion chromatography, in combination with absorbance

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

169 Ultracentrifugation and size exclusion chromatography indicated that both PPOs occur

170 Speciation was investigated by size-exclusion chromatography - inductively coupled plasma ma

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

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

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

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

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

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

177 iques (circular dichroism spectroscopy, size-exclusion chromatography-multiangle laser light scatteri

178 Size-exclusion chromatography-multiangle light scattering (SE

179 sing alphaSN aggregation, fibrillation, size-exclusion chromatography-multiangle light scattering (SE

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

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

182 ust, quantitative, and automated online size-exclusion chromatography-native mass spectrometry (SEC-n

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

184 Size-exclusion chromatography of human plasma has shown PCSK9

185 Size-exclusion chromatography of Lys-C-digested native DMBT1

186 C when monomeric fractions derived from size exclusion chromatography of normal brain homogenates (mN

187 Size exclusion chromatography of purified AAC3 in dodecyl mal

188 Size-exclusion chromatography of the CTD monomer showed that

189 Size-exclusion chromatography of the isolated targeting seque

190 Size-exclusion chromatography of the lysates from mutant p53-

191 Using size exclusion chromatography of the MW2 supernatant, followe

192 ATPase assays and size exclusion chromatography of the trans-variants FlrC(C)-Y

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

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

195 nding profiles of the ASO-conjugates by size-exclusion chromatography revealed distinct and species-s

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

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

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

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

200 Size exclusion chromatography (SEC) and ion pair chromatograp

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

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

203 atography (IEC) column in tandem with a size exclusion chromatography (SEC) column to efficiently sep

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

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

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

207 tivity for four sites was discovered in size-exclusion chromatography (SEC) fractions >= 670 kDa, whi

208 eloped a method based on sequencing the size exclusion chromatography (SEC) fractions of nonvesicular

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

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

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

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

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

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

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

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

217 Size exclusion chromatography (SEC) was used to characterize

218 Subsequently, size-exclusion chromatography (SEC) with an MS-compatible mob

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 interaction chromatography (HILIC) and size exclusion chromatography (SEC) with the parallel detecti

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

223 velopment of a new technology combining size exclusion chromatography (SEC), a commonly used EV purif

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

225 he knob and hole mutations, we combined size-exclusion chromatography (SEC), differential scanning ca

226 tible solvent and conditions, combining size exclusion chromatography (SEC), ion-pair reversed phase

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

228 observed by conventional techniques of size exclusion chromatography (SEC), microflow imaging (MFI),

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

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

231 Coupling two-dimensional size-exclusion chromatography (SEC)-cIEF to ESI-MS/MS enabled

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

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

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

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

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

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

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

239 through either dialysis or low-pressure size-exclusion chromatography (SEC).

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

241 e using ammonium bicarbonate buffer and size exclusion chromatography (SEC-ICP-sfMS), with possible a

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

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

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

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

246 Size exclusion chromatography showed the full-length aCRY to

247 Size exclusion chromatography shows that trimer 4(F20Cha) for

248 is, analytical ultracentrifugation, and size-exclusion chromatography small angle x-ray scattering.

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

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

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

252 e directly combine MS-compatible serial size exclusion chromatography (sSEC) fractionation with 12 T

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

254 own proteomics platform coupling serial size exclusion chromatography (sSEC) to reversed-phase chroma

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

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

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

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

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

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

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

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

263 ese tandem fused ACPs was determined by size exclusion chromatography to be higher (21 kDa, 36 kDa an

264 ydrolysate was subsequently purified by size exclusion chromatography to obtain fractions sorted by s

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

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

267 Size-exclusion chromatography, two-dimensional gel electropho

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

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

270 o 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 fractionate

272 Size-exclusion chromatography was used to characterize the in

273 By size exclusion chromatography we demonstrate stable complex f

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

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

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

277 onomeric PrP (mM1000) generated through size exclusion chromatography were found to harbor acute syna

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

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

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

281 3.3-H4, using coimmunoprecipitation and size-exclusion chromatography with highly purified components

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

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

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

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

286 Kinetic size exclusion chromatography with mass spectrometry detectio

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

288 Size exclusion chromatography with multi-angle light scatteri

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 Size exclusion chromatography with multiangle laser light sca

293 ty of an integrated approach, including size exclusion chromatography with multiangle light scatterin

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

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

296 in the same colloidal size fraction by size-exclusion chromatography with multielement detection.

297 followed by the product analysis using size exclusion chromatography with online mass spectrometry d

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