ライフサイエンスコーパス: sedimentation equilibrium

1 ding to a 3'-(dT)(20)-18 bp DNA substrate by sedimentation equilibrium.

2 gin-1 associates as a dimer when analyzed by sedimentation equilibrium.

3 ight scattering, sedimentation velocity, and sedimentation equilibrium.

4 r interference or absorbance measurements at sedimentation equilibrium.

5 f a dimerizing system in chemical as well as sedimentation equilibrium.

6 nce profiles acquired during the approach to sedimentation equilibrium.

7 ized by isothermal titration calorimetry and sedimentation equilibrium.

8 association of the peptides were measured by sedimentation equilibrium.

9 ansmembrane helices during the time-scale of sedimentation equilibrium.

10 7 +/- 4) kDa, a value confirmed by low-speed sedimentation equilibrium.

11 tistically different from values acquired by sedimentation equilibrium.

12 nd compared to values measured previously by sedimentation equilibrium.

13 detection, fluorescence quench titration, or sedimentation equilibrium.

14 l electrophoresis, isoelectric focusing, and sedimentation equilibrium.

15 the application to expedite the approach to sedimentation equilibrium.

16 with the equilibrium constant determined by sedimentation equilibrium.

17 his hypothesis was examined rigorously using sedimentation equilibrium.

18 n moiety in the protein/detergent complex by sedimentation equilibrium; (2) measurement of the appare

19 ed by disassociation constants determined by sedimentation equilibrium: 6.62 x 10(-6) M (rbetaA3), 0.

20 an be verified by sedimentation velocity and sedimentation equilibrium after correction for bound det

21 Sedimentation equilibrium analyses confirmed that Purbet

22 Sedimentation equilibrium analyses of con-G show that Ca

23 acentrifugation, sedimentation velocity, and sedimentation equilibrium analyses of the native dirigen

24 g of about 13 tubulin units as determined by sedimentation equilibrium analyses.

25 Sedimentation equilibrium analysis also indicates that d

26 Sedimentation equilibrium analysis by analytical ultrace

27 Sedimentation equilibrium analysis demonstrates that sel

28 Sedimentation equilibrium analysis in 0.1 M potassium ph

29 ree paramyxovirus F proteins was analyzed by sedimentation equilibrium analysis in detergent and buff

30 Sedimentation equilibrium analysis indicated that ClpA p

31 Sedimentation equilibrium analysis indicates an alpha 4

32 r organization in solution, we carried out a sedimentation equilibrium analysis of arrestin at both c

33 of this protein in solution, we carried out sedimentation equilibrium analysis of ATIC over a broad

34 Sedimentation equilibrium analysis of the recombinant hu

35 Sedimentation equilibrium analysis of TM domains contain

36 Sedimentation equilibrium analysis revealed that CsA beh

37 nce chemical shift perturbation mapping, and sedimentation equilibrium analysis show that KIX binds a

38 Sedimentation equilibrium analysis shows that Ms-Lon ass

39 Sedimentation equilibrium analysis shows that Tax and th

40 applied a method described previously, using sedimentation equilibrium analysis to calculate the cont

41 esidue long N-terminal fragment was shown by sedimentation equilibrium analysis to form a dimer with

42 Sedimentation equilibrium analysis using purified protei

43 Sedimentation equilibrium analysis was also used to esta

44 Sedimentation equilibrium analysis was used to compare t

45 Sedimentation equilibrium analysis yielded a weight-aver

46 on protein, a novel dye-label technique, and sedimentation equilibrium analysis, we directly and conc

47 Through sedimentation equilibrium analysis, we show that the enz

48 Using both protein cross-linking and sedimentation equilibrium analysis, we showed that the A

49 This was confirmed by sedimentation equilibrium analysis, which also revealed

50 a single predominant oligomeric species, and sedimentation equilibrium analysis-derived mass values i

51 n, high affinity heterodimers were formed in sedimentation equilibrium analysis.

52 examined as determined by gel permeation and sedimentation equilibrium analysis.

53 e reliability of the results obtained from a sedimentation equilibrium analysis.

54 igands in self-association was studied using sedimentation equilibrium analysis.

55 A new sedimentation equilibrium analytical procedure shows the

56 analytical size-exclusion chromatography and sedimentation equilibrium analytical ultracentrifugation

57 he core of the protein were studied by using sedimentation equilibrium analytical ultracentrifugation

58 Sedimentation equilibrium analytical ultracentrifugation

59 e have used alanine-scanning mutagenesis and sedimentation equilibrium analytical ultracentrifugation

60 Sedimentation equilibrium analytical ultracentrifugation

61 Sedimentation equilibrium analytical ultracentrifugation

62 ducing single-alanine substitutions and used sedimentation equilibrium analytical ultracentrifugation

63 We have used sedimentation equilibrium analytical ultracentrifugation

64 Sedimentation equilibrium analytical ultracentrifugation

65 Using SDS-PAGE analysis and sedimentation equilibrium analytical ultracentrifugation

66 Utilizing sedimentation equilibrium analytical ultracentrifugation

67 into stable monomers in solution as shown by sedimentation equilibrium and CD and formed an intrachai

68 Sedimentation equilibrium and chemical cross-linking exp

69 Sedimentation equilibrium and circular dichroism studies

70 Sedimentation equilibrium and cross-linking data demonst

71 Using sedimentation equilibrium and cross-linking methods, we

72 have been measured in the absence of DNA by sedimentation equilibrium and gel filtration chromatogra

73 As shown by sedimentation equilibrium and gel-filtration experiments

74 chemical and biophysical analyses, including sedimentation equilibrium and scanning transmission elec

75 In the past, both sedimentation equilibrium and sedimentation velocity ana

76 Sedimentation equilibrium and sedimentation velocity ana

77 f the octylglucoside-solubilized receptor by sedimentation equilibrium and sedimentation velocity ana

78 cterized and compared using a combination of sedimentation equilibrium and sedimentation velocity in

79 d S3/S4 half-operator oligonucleotides using sedimentation equilibrium and sedimentation velocity mea

80 Using analytical ultracentrifugation in both sedimentation equilibrium and sedimentation velocity mod

81 have established that C-tau is a monomer by sedimentation equilibrium and sedimentation velocity ult

82 Based on sedimentation equilibrium and size exclusion chromatogra

83 tion constant (Ka) of 2-4 x 10(8) M-1, using sedimentation equilibrium and size exclusion chromatogra

84 Stoicheometric analyses, coupled with sedimentation equilibrium and size exclusion chromatogra

85 The pH dependence of both the sedimentation equilibrium and the oxygen binding of the

86 The sedimentation equilibrium and velocity data indicate tha

87 single-headed myosin-She3p complex, based on sedimentation equilibrium and velocity data.

88 Sedimentation equilibrium and velocity runs revealed oli

89 Recent sedimentation equilibrium and velocity studies show that

90 ar UV CD spectroscopy, thermal denaturation, sedimentation equilibrium and velocity, and intrinsic fl

91 Affinities were determined by sedimentation equilibrium and/or surface plasmon detecti

92 Dynamic light scattering, sedimentation equilibrium, and circular dichroism measur

93 echniques, including sedimentation velocity, sedimentation equilibrium, and dynamic light scattering

94 ircular dichroism, dynamic light scattering, sedimentation equilibrium, and fluorescence experiments

95 eport the results of sedimentation velocity, sedimentation equilibrium, and gel-filtration experiment

96 We have used NMR spectroscopy, sedimentation equilibrium, and intrinsic fluorescence to

97 n explored by analytical gel chromatography, sedimentation equilibrium, and oxygen binding experiment

98 he techniques of intensity light scattering, sedimentation equilibrium, and radiation inactivation we

99 forms a very stable trimer as determined by sedimentation equilibrium, and the concentration depende

100 assembly in these mutants were monitored by sedimentation equilibrium, and the conformational states

101 s, as measured by sedimentation velocity and sedimentation equilibrium, and the tryptic cleavage patt

102 now shown unambiguously by light scattering, sedimentation equilibrium, and titration calorimetry tha

103 chemical methods including light scattering, sedimentation equilibrium, and titration calorimetry, we

104 the "Smc2/4 complex," which upon analysis by sedimentation equilibrium appears to reversibly self-ass

105 Sedimentation equilibrium assays indicate that the Ig3 d

106 en measured under a variety of conditions by sedimentation equilibrium at pH 7.5 and 4 and 20 degrees

107 nfirmed by analytical ultracentrifugation to sedimentation equilibrium by which a 1:1 complex was obt

108 d on results from sedimentation velocity and sedimentation equilibrium centrifugation as well as anal

109 of the self-association state of hDlg using sedimentation equilibrium centrifugation, matrix-assiste

110 oresis, isoelectric focusing, and analytical sedimentation equilibrium centrifugation.

111 luble CD4 molecule, as determined by ITC and sedimentation equilibrium centrifugation.

112 tracentrifugation data confirmed this, where sedimentation equilibrium curve fits gave a mean molecul

113 Sedimentation equilibrium curve fits gave a mean molecul

114 Sedimentation equilibrium data (obtained at 4.8-11.2 muM

115 Global analysis of the sedimentation equilibrium data demonstrated that PR-B se

116 Global analysis of the sedimentation equilibrium data has enabled us to determi

117 tein concentrations, and good global fits to sedimentation equilibrium data require a positive value

118 Our sedimentation equilibrium data show that, in the presenc

119 Sedimentation equilibrium data showed that SCR-1/5 is mo

120 Sedimentation equilibrium data suggest at a minimum, a m

121 vely, in agreement with their sequences, and sedimentation equilibrium data supported these determina

122 Global fitting of sedimentation equilibrium data under native solution con

123 Sedimentation equilibrium data were interpreted in terms

124 he recombinant protein by gel filtration and sedimentation equilibrium demonstrate a dimer-tetramer s

125 ons, static light scattering, and analytical sedimentation equilibrium, demonstrate that Ud NS1A ED f

126 Sedimentation equilibrium demonstrated that both echista

127 Sedimentation equilibrium-derived mass values for both f

128 Whereas sedimentation equilibrium distributions for phosphorylas

129 l allowance for thermodynamic nonideality in sedimentation equilibrium distributions reflecting solut

130 Analysis of sedimentation-equilibrium distributions obtained at 15 0

131 Sedimentation equilibrium, dynamic light scattering, ele

132 he approach to equilibrium in a short-column sedimentation equilibrium experiment followed by a high-

133 in after start of a conventional long-column sedimentation equilibrium experiment.

134 rization of C167PM has been characterized in sedimentation equilibrium experiments (K(d) approximatel

135 e prolonged stability needed in conventional sedimentation equilibrium experiments and it can increas

136 Results from sedimentation equilibrium experiments are consistent wit

137 ce optical data acquisition system, allowing sedimentation equilibrium experiments at loading concent

138 To clarify this discrepancy, sedimentation equilibrium experiments by analytical ultr

139 Sedimentation equilibrium experiments by analytical ultr

140 Sedimentation equilibrium experiments confirm that the E

141 Sedimentation equilibrium experiments confirmed that the

142 Sedimentation equilibrium experiments demonstrated that

143 Sedimentation equilibrium experiments establish that the

144 ce the number of SCR domains compared to CR2 Sedimentation equilibrium experiments gave a mean molecu

145 sedimentation velocity and density gradient sedimentation equilibrium experiments in CsCl with UV de

146 Analytical gel filtration and sedimentation equilibrium experiments indicate that doub

147 Sedimentation equilibrium experiments indicate that thes

148 Sedimentation equilibrium experiments of pRB/Ad5 E1A and

149 iments and it can increase the efficiency of sedimentation equilibrium experiments of previously unch

150 Sedimentation equilibrium experiments on each subunit an

151 Sedimentation equilibrium experiments show that an alani

152 In contrast, sedimentation velocity and sedimentation equilibrium experiments show that full-len

153 Sedimentation equilibrium experiments show that single-c

154 dI is found to form a homodimer of 16.7 kDa; sedimentation equilibrium experiments show that the dime

155 Sedimentation equilibrium experiments show that the tetr

156 Sedimentation equilibrium experiments showed that a cons

157 slinking, size-exclusion chromatography, and sedimentation equilibrium experiments shows that the mos

158 Sedimentation equilibrium experiments suggest that bindi

159 6 E7 and Ad5 E1A oligomerization properties, sedimentation equilibrium experiments were performed wit

160 Sedimentation equilibrium experiments with EcoRuvA showe

161 Their oligomerization was confirmed in sedimentation equilibrium experiments, which also establ

162 K(A) = 5.6 and 5.1 [M(-1)], respectively, in sedimentation equilibrium experiments.

163 nder nondenaturing conditions as measured by sedimentation equilibrium experiments.

164 amers, using both sedimentation velocity and sedimentation equilibrium experiments.

165 tion using cross-linking and mutagenesis and sedimentation equilibrium experiments.

166 molecular mass of 31.9 kDa, as determined by sedimentation equilibrium experiments.

167 Global sedimentation equilibrium fits indicated that a monomer-

168 ive site by means of sedimentation velocity, sedimentation equilibrium, fluorescence solute quenching

169 The suitability of sedimentation equilibrium for characterizing the self-as

170 his investigation indicates the potential of sedimentation equilibrium for the quantitative character

171 al offsets from interference optical data of sedimentation equilibrium gradients.

172 Using sedimentation equilibrium in C14 betaine micelles, we di

173 Sedimentation equilibrium in the analytical centrifuge r

174 lation) have been studied using short-column sedimentation equilibrium in the analytical ultracentrif

175 A combination of sedimentation velocity and sedimentation equilibrium in the analytical ultracentrif

176 Sedimentation equilibrium in the analytical ultracentrif

177 tail analytical solutions of expressions for sedimentation equilibrium in the analytical ultracentrif

178 0 Da as determined by neutron scattering and sedimentation equilibrium, in good agreement with the se

179 conformation is remarkably changed, and the sedimentation equilibrium indicates that the protein is

180 Sedimentation equilibrium is a powerful tool for the cha

181 Characterizing membrane proteins by sedimentation equilibrium is challenging because deterge

182 timate for SCF-sKit interaction, obtained by sedimentation equilibrium, is about 17 nm at 25 degrees

183 e assembly process have been dissected using sedimentation equilibrium measurements and DNaseI footpr

184 Sedimentation equilibrium measurements and scanning tran

185 of dynamin II by analytical ultracentrifuge sedimentation equilibrium measurements at high ionic str

186 Sedimentation equilibrium measurements confirmed the pen

187 Sedimentation equilibrium measurements in the analytical

188 Sedimentation equilibrium measurements indicate that PKR

189 Sedimentation equilibrium measurements indicated that a

190 Sedimentation equilibrium measurements of LC8 at pH 7 re

191 Sedimentation equilibrium measurements reveal that 11 of

192 Additionally, sedimentation equilibrium measurements reveal that coupl

193 Sedimentation equilibrium measurements reveal that pPKRm

194 Sedimentation equilibrium measurements show that the agg

195 Sedimentation equilibrium measurements show these protei

196 Sedimentation equilibrium measurements showed recombinan

197 Sedimentation equilibrium measurements showed the reduce

198 Sedimentation equilibrium measurements to determine the

199 From sedimentation equilibrium measurements, we determined th

200 The aggregation numbers determined by sedimentation equilibrium methods match those measured b

201 association using sedimentation velocity and sedimentation equilibrium methods.

202 Sedimentation equilibrium of a homogeneous 4.5 S populat

203 polysomes were separated from other mRNAs by sedimentation equilibrium or sedimentation velocity.

204 ants, SN228 and SR228, was also evaluated by sedimentation equilibrium over this same temperature ran

205 reduce the systematic errors in the measured sedimentation equilibrium profiles by more than an order

206 ading concentrations are calculated from the sedimentation equilibrium profiles.

207 the monomer-monomer interface is stabilized, sedimentation equilibrium results demonstrated that the

208 Sedimentation equilibrium results further suggest that t

209 Sedimentation equilibrium results show that the associat

210 usion (F) proteins interact as trimers using sedimentation equilibrium (SE) analysis.

211 Sedimentation equilibrium (SE) analytical ultracentrifug

212 The current study uses sedimentation equilibrium (SE), circular dichroism (CD),

213 and large molar mass profiles, confirmed by sedimentation equilibrium "SEDFIT MSTAR" analysis.

214 nzyme have been obtained by using analytical sedimentation equilibrium, sedimentation velocity studie

215 Further analysis by sedimentation equilibrium showed that degludec exhibited

216 Sedimentation equilibrium shows the IDE mutants exhibit

217 Using sedimentation equilibrium, spontaneously inactivated HTb

218 Here, we report results from sedimentation equilibrium studies and two different subu

219 Gel permeation chromatography and sedimentation equilibrium studies confirm that the Fe(3+

220 nergy scale and free energy differences from sedimentation equilibrium studies for point mutants of t

221 Gel filtration chromatography and sedimentation equilibrium studies indicate that these an

222 Sedimentation equilibrium studies indicate that these HR

223 Sedimentation equilibrium studies indicated that 8% of t

224 However, sedimentation equilibrium studies indicated that the ina

225 Sedimentation equilibrium studies of CR2 SCR 1-2 gave mo

226 Sedimentation equilibrium studies of dilute solutions of

227 Sedimentation equilibrium studies of translin with an FI

228 Further, sedimentation equilibrium studies reveal that reconstitu

229 Sedimentation equilibrium studies reveal that under non-

230 In addition, sedimentation equilibrium studies revealed that HL had a

231 Sedimentation equilibrium studies show that scRPA is a s

232 Moreover, NMR and sedimentation equilibrium studies show that the activati

233 Sedimentation equilibrium studies show that the equilibr

234 Sedimentation equilibrium studies show that the Escheric

235 Sedimentation equilibrium studies show that the Escheric

236 Sedimentation equilibrium studies show that the regulato

237 Sedimentation equilibrium studies showed that in the abs

238 Sedimentation equilibrium studies showed very little ass

239 We now show by NMR and sedimentation equilibrium studies that a mutant protease

240 Sedimentation velocity and sedimentation equilibrium studies were performed.

241 Sedimentation equilibrium studies with purified proteins

242 By sedimentation equilibrium studies, we have found that pr

243 ly monomeric at 5 degrees C as determined by sedimentation equilibrium studies.

244 on calorimetry, biomolecular interaction, or sedimentation equilibrium studies.

245 ording to results from mass spectrometry and sedimentation equilibrium studies.

246 tion, analytical sedimentation velocity, and sedimentation equilibrium techniques.

247 , using isothermal titration calorimetry and sedimentation equilibrium techniques.

248 d CaM were determined by CD spectrometry and sedimentation equilibrium: their affinities were Cys(-)-

249 tions, isothermal titration calorimetry, and sedimentation equilibrium to determine whether scRPA can

250 However, sedimentation equilibrium ultracentrifugation data showe

251 However, a thermodynamic investigation using sedimentation equilibrium ultracentrifugation in deterge

252 In the present study, sedimentation equilibrium ultracentrifugation is employe

253 Sedimentation equilibrium ultracentrifugation showed tha

254 Sedimentation equilibrium ultracentrifugation shows that

255 Size-exclusion chromatography and sedimentation equilibrium ultracentrifugation studies sh

256 Clostridium thermoaceticum was determined by sedimentation equilibrium ultracentrifugation to be 300,

257 mples of enzyme were subjected to analytical sedimentation equilibrium ultracentrifugation to obtain

258 -domain interactions were investigated using sedimentation equilibrium ultracentrifugation, cross-lin

259 apoBCCP and apoBCCP87 were determined using sedimentation equilibrium ultracentrifugation.

260 hybrid peptides were studied in micelles by sedimentation equilibrium ultracentrifugation.

261 Analysis by sedimentation equilibrium unequivocally identified the o

262 ein-surfactant complexes are investigated by sedimentation equilibrium via analytical ultracentrifuga

263 The Mr determined by sedimentation equilibrium was 197,600+/-13,700 and the a

264 techniques, and additional studies in which sedimentation equilibrium was used show that the binding

265 By sedimentation equilibrium we determined that the main pl

266 Using sedimentation equilibrium, we show that yeast cTBP forms

267 ere a systematic study of K(a) determined by sedimentation equilibrium, which showed that it varied b

268 Sedimentation equilibrium yielded a molecular mass of 96