ライフサイエンスコーパス: sedimentation velocity

1 eniently expressed as a fraction of the cell sedimentation velocity.

2 other mRNAs by sedimentation equilibrium or sedimentation velocity.

3 ced tubulin spiral formation, as measured by sedimentation velocity.

4 attering, N-terminal protein sequencing, and sedimentation velocity.

5 analytical size exclusion chromatography and sedimentation velocity.

6 ROPRO were compared with those determined by sedimentation velocity.

7 cells also exhibited the largest amyloplast sedimentation velocities.

8 added U4 RNA that is associated with U6 RNA (sedimentation velocity 16 S) was significantly higher in

9 Sedimentation velocity analyses indicated that dimeric P

10 Size-exclusion chromatography and sedimentation velocity analyses indicated that the bulk

11 Sedimentation velocity analyses of detergent-solubilized

12 Gel filtration and sedimentation velocity analyses of in vitro synthesized

13 Size exclusion chromatography and sedimentation velocity analyses of the cytosolic fractio

14 gomeric state and shape of A3G, we conducted sedimentation velocity analyses of the pure enzyme under

15 Size exclusion chromatography and sedimentation velocity analyses revealed that FANCJ-WT e

16 Importantly, intrinsic fluorescence and sedimentation velocity analyses show that GroES is capab

17 bient temperature as shown by native gel and sedimentation velocity analyses.

18 Sedimentation velocity analysis indicated single sedimen

19 Sedimentation velocity analysis is a powerful tool for t

20 tion chromatography and fluorescence-adapted sedimentation velocity analysis of cell lysates, we coll

21 e and IQ sequence is demonstrated further by sedimentation velocity analysis of complexes of Mlc1p wi

22 A method for sedimentation velocity analysis of polyribosomes is pres

23 Sedimentation velocity analysis of translin indicates th

24 Analytical gel filtration chromatography and sedimentation velocity analysis revealed that a(NT(104-3

25 ed receptor by sedimentation equilibrium and sedimentation velocity analysis reveals a monodisperse p

26 Sedimentation velocity analysis showed that the polysacc

27 Sedimentation velocity analysis shows that the reconstit

28 By circular dichroism, gel filtration, and sedimentation velocity analysis, we determined that each

29 cies, and the overall capability of boundary sedimentation velocity analysis.

30 ble for BH3 peptide binding, as confirmed by sedimentation velocity analysis.

31 ange high-pressure liquid chromatography and sedimentation velocity analysis.

32 IPOD and JUNQ patterns of aggregation using sedimentation velocity analysis.

33 ity interactions using fluorescence detected sedimentation velocity analytical ultracentrifugation (F

34 Sedimentation velocity analytical ultracentrifugation (S

35 as circular dichroism (CD) spectroscopy and sedimentation velocity analytical ultracentrifugation (s

36 Sedimentation velocity analytical ultracentrifugation (S

37 ural characterization of the RAM linker with sedimentation velocity analytical ultracentrifugation an

38 Sedimentation velocity analytical ultracentrifugation co

39 Sedimentation velocity analytical ultracentrifugation eq

40 the past, both sedimentation equilibrium and sedimentation velocity analytical ultracentrifugation ha

41 Sedimentation velocity analytical ultracentrifugation is

42 he size-distribution analysis of polymers by sedimentation velocity analytical ultracentrifugation is

43 Sedimentation velocity analytical ultracentrifugation is

44 raction of Myo5a and Rab3A was determined by sedimentation velocity analytical ultracentrifugation us

45 Sedimentation velocity analytical ultracentrifugation wi

46 and DeltaTM-FAAH by chemical cross-linking, sedimentation velocity analytical ultracentrifugation, a

47 Sedimentation equilibrium and sedimentation velocity analytical ultracentrifugation, t

48 d AMPA receptors using fluorescence-detected sedimentation velocity analytical ultracentrifugation.

49 purified proteins and their interactions is sedimentation velocity analytical ultracentrifugation.

50 on of nanoparticles and macromolecules using sedimentation velocity analytical ultracentrifugation.

51 ell as a weaker Nank self-association, using sedimentation velocity analytical ultracentrifugation.

52 n of long-standing interest in the theory of sedimentation velocity analytical ultracentrifugation.

53 -linking, size-exclusion chromatography, and sedimentation-velocity analytical ultracentrifugation we

54 However, BPI can enhance both the sedimentation velocity and apparent size of LPS aggregat

55 In analyses by sedimentation velocity and by cross-linking, both protei

56 odextrin DE17 causing a greater reduction in sedimentation velocity and compressibility of sediment f

57 ional AUC data obtained from analytical band sedimentation velocity and density gradient sedimentatio

58 oncentrations of salt (up to 13.4 M NaBr) by sedimentation velocity and diffusion experiments, becaus

59 For both IRPs, sedimentation velocity and dynamic light-scattering expe

60 protein complexes have been characterised by sedimentation velocity and EMSA using native and mutant

61 Sedimentation velocity and equilibrium analyses were use

62 t ratio (f/f(0)) of 1.28 calculated from the sedimentation velocity and equilibrium data is close to

63 Sedimentation velocity and equilibrium experiments and s

64 Sedimentation velocity and equilibrium experiments have

65 Additionally, sedimentation velocity and equilibrium experiments indic

66 ced, allowing the global analysis of several sedimentation velocity and equilibrium experiments.

67 ar dichroism, analytical ultracentrifugation sedimentation velocity and equilibrium methods, and sequ

68 Sedimentation velocity and equilibrium results establish

69 Sedimentation velocity and equilibrium studies conducted

70 Sedimentation velocity and equilibrium studies revealed

71 -B dimerization was examined by carrying out sedimentation velocity and equilibrium studies under hig

72 re (5-35 degrees C; pH 8.3) using analytical sedimentation velocity and equilibrium techniques, and f

73 Sedimentation velocity and equilibrium ultracentrifugati

74 ow micromolar monomer concentration range by sedimentation velocity and equilibrium ultracentrifugati

75 uring detergent environments was assessed by sedimentation velocity and equilibrium.

76 MutL and its binding to DNA using analytical sedimentation velocity and equilibrium.

77 Global analysis combining sedimentation velocity and fluorescence anisotropy yield

78 the DnaB helicase have been performed using sedimentation velocity and fluorescence energy transfer

79 Together with sedimentation velocity and fluorescence polarization ass

80 Furthermore, sedimentation velocity and gel filtration showed that NE

81 Sedimentation velocity and gel-filtration analysis showe

82 Sedimentation velocity and isothermal titration calorime

83 Sedimentation velocity and limited proteolysis experimen

84 c analysis by analytical ultracentrifugation sedimentation velocity and native mass spectrometry reve

85 complete CcO dimerization can be verified by sedimentation velocity and sedimentation equilibrium aft

86 and both are monomeric based on results from sedimentation velocity and sedimentation equilibrium cen

87 In contrast, sedimentation velocity and sedimentation equilibrium exp

88 o contains octamers and hexamers, using both sedimentation velocity and sedimentation equilibrium exp

89 A combination of sedimentation velocity and sedimentation equilibrium in

90 he energetics of PR-B self-association using sedimentation velocity and sedimentation equilibrium met

91 Sedimentation velocity and sedimentation equilibrium stu

92 ric human kinesin constructs, as measured by sedimentation velocity and sedimentation equilibrium, an

93 of the catalytic cycle were characterized by sedimentation velocity and small-angle X-ray scattering

94 wo subsets of complexes that differ in their sedimentation velocity and their association with cytosk

95 ANT-ADP, have been examined using analytical sedimentation velocity and time-dependent fluorescence a

96 Our sedimentation velocity and transmission electron microsc

97 dependent conformational changes detected in sedimentation velocity and/or fluorescence anisotropy me

98 Sedimentation-velocity and coimmunoprecipitation experim

99 Differential sedimentation-velocity and gel electrophoresis reveal th

100 on column multiangle laser light scattering, sedimentation velocity, and circular dichroism (CD) were

101 ction by using small-angle x-ray scattering, sedimentation velocity, and computational modeling techn

102 re analyzed by electrophoretic shift assays, sedimentation velocity, and electron microscopy.

103 COS-1 cells as assessed by Western blotting, sedimentation velocity, and immunofluorescence microscop

104 Gel filtration, sedimentation velocity, and immunoprecipitation experime

105 ES, intrinsic fluorescence, bis-ANS binding, sedimentation velocity, and limited proteolysis, we show

106 Analytical ultracentrifugation, sedimentation velocity, and sedimentation equilibrium an

107 ntitative fluorescence titration, analytical sedimentation velocity, and sedimentation equilibrium te

108 on, as measured by dynamic light scattering, sedimentation velocity, and sedimentation equilibrium.

109 Protein expression, disulfide bonding, sedimentation velocity, and subcellular localization of

110 ssayed by nonreducing Western blot analysis, sedimentation velocity, and subcellular localization.

111 o fill this gap, we report crystallographic, sedimentation-velocity, and kinetics data for human PYCR

112 the analysis of protein self-association by sedimentation velocity are developed, their statistical

113 , provided that the suspension viscosity and sedimentation velocity are scaled appropriately, and tha

114 Sedimentation velocity assays suggest that the expanded

115 Here, we use a combination of sedimentation velocity, atomic force microscopy and nucl

116 Analytical ultracentrifugation-sedimentation velocity (AUC-SV) is emerging as an import

117 urther insight was gained by analyzing EI by sedimentation velocity, by near UV CD spectroscopy, and

118 Polyribosome sedimentation velocity centrifugation can be used to ide

119 crosslinked and mildly sheared chromatin to sedimentation velocity centrifugation followed by size-f

120 s determined to be approximately 0.81 MDa by sedimentation velocity combined with dynamic light scatt

121 R-measured spin lattice relaxation rates and sedimentation velocity compared to those of the wild-typ

122 of the HMM molecule as judged by its slower sedimentation velocity compared with that in EGTA.

123 partial boundary modeling (PBM) to simplify sedimentation velocity data analysis by excluding specie

124 Static light scattering and sedimentation velocity data are consistent with the form

125 Sedimentation velocity data coupled with time-derivative

126 Sedimentation velocity data fit a model where PKR monome

127 Analysis of sedimentation velocity data for a 15 muM solution of ERK

128 partial specific volume and molar mass from sedimentation velocity data for cases where the anisotro

129 In this work we show how the analysis of sedimentation velocity data from the AUC equipped with a

130 Time-derivative approaches to analyzing sedimentation velocity data have proven to be highly suc

131 Kinetic analysis of the sedimentation velocity data indicated that holoBirA dime

132 Consistent with this idea, sedimentation velocity data reveal that the apo- and Mg(

133 tation coefficient distribution, g(s*), from sedimentation velocity data that was developed by Walter

134 A method for fitting experimental sedimentation velocity data to finite-element solutions

135 We analyzed the sedimentation velocity data using the van Holde-Weischet

136 , a method of globally analyzing multisignal sedimentation velocity data was introduced by Schuck and

137 Direct fitting of sedimentation velocity data with numerical solutions of

138 For the detailed analysis of sedimentation velocity data, the consideration of radial

139 ared with other current methods of analyzing sedimentation velocity data.

140 xtures is demonstrated via MWL evaluation of sedimentation velocity data.

141 apsid proteins are lost from the RTC and its sedimentation velocity decreases further.

142 er an external field and move with different sedimentation velocities dictated by their Svedberg coef

143 ing nonlinear least-squares curve-fitting of sedimentation velocity distributions to the Lamm equatio

144 a combination of native gel electrophoresis, sedimentation velocity, electron microscopy, and a recen

145 sphatidylcholine, PCPS) were evaluated using sedimentation velocity/equilibrium methods in the analyt

146 ed mass of the 3.3 S fragment estimated from sedimentation velocity/equilibrium studies; while the co

147 riment followed by a high-speed short-column sedimentation velocity experiment can result in sediment

148 ance analysis can increase the capacity of a sedimentation velocity experiment in ultracentrifugation

149 Sedimentation velocity experiments also show that additi

150 Sedimentation velocity experiments at low speeds and ele

151 1H NMR and sedimentation velocity experiments carried out with thei

152 Sedimentation velocity experiments confirm the presence

153 Sedimentation velocity experiments confirm the transient

154 Sedimentation velocity experiments confirmed that dimeri

155 Sedimentation velocity experiments confirmed the presenc

156 Dynamic light scattering and sedimentation velocity experiments demonstrated that HMG

157 Sedimentation velocity experiments demonstrated that the

158 Sedimentation velocity experiments determined that the M

159 Sedimentation velocity experiments gave a sedimentation

160 To test this hypothesis, sedimentation velocity experiments in the analytical ult

161 Results of sedimentation velocity experiments in the presence of sa

162 Sedimentation velocity experiments indicate that ELP[V5G

163 In agreement with the crystal structure, sedimentation velocity experiments indicate that L7D2 is

164 y, protease sensitivity, gel filtration, and sedimentation velocity experiments indicate that Nup2p i

165 Sedimentation velocity experiments indicate that the bif

166 Analytical ultracentrifugation sedimentation velocity experiments indicate that these S

167 Results of laser light scattering and sedimentation velocity experiments indicated that Purbet

168 Sedimentation velocity experiments of titrated stoichiom

169 Sedimentation velocity experiments reveal that Ms-Lon mo

170 Size-exclusion chromatography and sedimentation velocity experiments revealed that the Aal

171 Sedimentation velocity experiments show that apo-SOD1 di

172 Sedimentation velocity experiments show that the deliver

173 For C3d, X-ray scattering and sedimentation velocity experiments showed that it exists

174 Size-distribution analyses in sedimentation velocity experiments showed that monomeric

175 Sedimentation velocity experiments showed that this dime

176 eous protein was adenylated as isolated, and sedimentation velocity experiments suggested that the en

177 ment of the spinning rotor during high-speed sedimentation velocity experiments up to 60,000rpm.

178 Sedimentation velocity experiments using the g*(s) deriv

179 Sedimentation velocity experiments using the time deriva

180 A method for fitting sedimentation velocity experiments using whole boundary

181 Sedimentation velocity experiments were also performed o

182 Sedimentation velocity experiments were employed to show

183 the determination of size-distributions from sedimentation velocity experiments were examined and dev

184 Sedimentation velocity experiments with gp59 protein and

185 Sedimentation velocity experiments yielded an estimate o

186 strated with double-sector and single-sector sedimentation velocity experiments, and with analytical

187 against noncognate tRNA was also observed in sedimentation velocity experiments, which showed that a

188 of 4.2 was calculated for the dimer based on sedimentation velocity experiments.

189 ecently described for the direct modeling of sedimentation velocity experiments.

190 tation and diffusion constants obtained from sedimentation velocity experiments.

191 and hydrodynamic properties determined from sedimentation velocity experiments.

192 ent in the analysis of boundary spreading in sedimentation velocity experiments.

193 Sedimentation-velocity experiments provided insight into

194 Fluorescence detected sedimentation velocity (FDS-SV) has emerged as a powerfu

195 We used sedimentation velocity, fluorescence anisotropy, and sur

196 mentation experiments showed a transition in sedimentation velocity from 7.2 to 4.2 S with a transiti

197 evealed similar results with a transition in sedimentation velocity from 7.9 to 4.4 S with a T(m) of

198 Sedimentation velocity gave a sedimentation coefficient

199 he shapes of the reaction boundaries and the sedimentation velocity gradients have been predicted by

200 sents practical limitations on the number of sedimentation velocity gradients that can be run simulta

201 Time resolved fluorescence anisotropy and sedimentation velocity has been used to study the rotati

202 dissociation of four subunits as detected by sedimentation velocity, high-performance ion-exchange ch

203 assessed easily by common techniques such as sedimentation velocity, HPLC, gel electrophoresis, and d

204 n altered resistance to Proteinase K, higher sedimentation velocities in gradient ultracentrifugation

205 Using dynamic light scattering and sedimentation velocity in the analytical ultracentrifuge

206 d oligomers were studied with time-dependent sedimentation velocity in the analytical ultracentrifuge

207 combination of sedimentation equilibrium and sedimentation velocity in the analytical ultracentrifuge

208 Sedimentation velocity in the analytical ultracentrifuge

209 Sedimentation velocity is a classical method for measuri

210 Sedimentation velocity measurements demonstrated that bo

211 Our sedimentation velocity measurements of the DnaB protein-

212 Determined from sedimentation velocity measurements on the lipid-free pr

213 Sedimentation velocity measurements show that recombinan

214 Here, we describe methods to configure sedimentation velocity measurements using fluorescence d

215 leotides using sedimentation equilibrium and sedimentation velocity measurements.

216 gation in both sedimentation equilibrium and sedimentation velocity modes, we studied the oligomeriza

217 Sedimentation velocities of protein-coated particles in

218 Nuclear-associated RTCs have a sedimentation velocity of 80S.

219 V RTCs isolated early after infection have a sedimentation velocity of approximately 560S.

220 We demonstrate that HMGN1 decreases the sedimentation velocity of nucleosomal arrays in low ioni

221 The sedimentation velocity of the RTC decreases during rever

222 Sedimentation velocity of varied ratios of LTbetaR to a

223 Sedimentation velocity provides the only direct evidence

224 Later, different species with a sedimentation velocity ranging from 350S to 100S appear.

225 eric structure, as measured by far UV-CD and sedimentation velocity, respectively.

226 ependently consistent with K2 estimates from sedimentation velocity results for vinblastine and vinor

227 is capable of providing precise and accurate sedimentation velocity results that are consistent with

228 Previous sedimentation velocity results with vinblastine have bee

229 SDS-PAGE, size exclusion chromatography, and sedimentation velocity revealed two native high Mr disul

230 Sedimentation velocity reveals a distribution of species

231 We demonstrate that a single sedimentation velocity run on an adenovirus sample can d

232 n and light scattering techniques, including sedimentation velocity, sedimentation equilibrium, and d

233 Here, we report the results of sedimentation velocity, sedimentation equilibrium, and g

234 ediate occupying the active site by means of sedimentation velocity, sedimentation equilibrium, fluor

235 combination of dynamic light scattering and sedimentation velocity showed that NTS1 was monomeric in

236 Sedimentation velocity shows that PYCR1 forms a concentr

237 Sedimentation velocity, size-exclusion chromatography an

238 Sedimentation velocity studies at neutral pH demonstrate

239 t micromolar concentrations of the receptor, sedimentation velocity studies demonstrate that PR-A und

240 Sedimentation velocity studies indicate that each polype

241 Sedimentation velocity studies of hormone-bound PR-B at

242 Moreover, sedimentation velocity studies of the ternary complex pr

243 Sedimentation velocity studies show that this repacking

244 Fluorescence spectra and sedimentation velocity studies showed that melittin boun

245 The results of sedimentation velocity studies were consistent with pred

246 using analytical sedimentation equilibrium, sedimentation velocity studies, and the rigorous fluores

247 Sedimentation velocity (SV) analytical ultracentrifugati

248 Sedimentation velocity (SV) analytical ultracentrifugati

249 Sedimentation velocity (SV) analytical ultracentrifugati

250 e introduce a new analytical method based on sedimentation velocity (SV) analytical ultracentrifugati

251 Sedimentation velocity (SV) is a method based on first p

252 port small-angle X-ray scattering (SAXS) and sedimentation velocity (SV) studies on the enzyme-DNA co

253 rates, has also been characterized using the sedimentation velocity technique.

254 by examining by dynamic light scattering and sedimentation velocity techniques the complexes formed w

255 Here, we establish by sedimentation velocity that the ATDs of GluR6 and KA2 co

256 the dimeric and tetrameric enzyme species by sedimentation velocity, this procedure has been used to

257 CAR-D1 is shown by sedimentation velocity to be monomeric at pH 3.0.

258 hysicochemical study described here, we used sedimentation velocity to compare vinorelbine- and vinfl

259 nt study, we have used fluorescence-detected sedimentation velocity to determine the effect of S-sulf

260 Similarly, sedimentation velocity ultracentrifugation experiments u

261 with a sedimentation coefficient of 4.8 S in sedimentation velocity ultracentrifugation experiments,

262 Urea denaturation, sedimentation velocity ultracentrifugation, and electron

263 using a combination of methods that includes sedimentation velocity ultracentrifugation, electron mic

264 s a monomer by sedimentation equilibrium and sedimentation velocity ultracentrifugation.

265 these monoclonal antibodies was analyzed by sedimentation velocity ultracentrifugation.

266 ological salt concentrations, as analyzed by sedimentation velocity ultracentrifugation.

267 Using analytical gel filtration, sedimentation-velocity ultracentrifugation, and negative

268 In this work, sedimentation velocity was employed to monitor the parti

269 Sedimentation velocities were converted to apparent aggr

270 Complementary sedimentation velocity with deuterated water gives a pic