ライフサイエンスコーパス: ultracentrifugation

1 oluble Htt-polyQ aggregates using analytical ultracentrifugation.

2 by solution NMR spectroscopy and analytical ultracentrifugation.

3 Released EVs were isolated by differential ultracentrifugation.

4 subjects or patients with CKD by sequential ultracentrifugation.

5 ical properties following iodixanol gradient ultracentrifugation.

6 ects, as well as mouse HDL, were isolated by ultracentrifugation.

7 in solution, as revealed through analytical ultracentrifugation.

8 ddition of sI-Pht, as assessed by analytical ultracentrifugation.

9 AA80, and further confirm this by analytical ultracentrifugation.

10 2 +/- 10 mol/mol as determined by analytical ultracentrifugation.

11 multi-angle light scattering, and analytical ultracentrifugation.

12 ro study using gel filtration and analytical ultracentrifugation.

13 ion of hydrodynamic parameters in analytical ultracentrifugation.

14 ules using sedimentation velocity analytical ultracentrifugation.

15 on chromatography and equilibrium analytical ultracentrifugation.

16 ing and stochiometric analysis by analytical ultracentrifugation.

17 he CC and the NTD as monitored by analytical ultracentrifugation.

18 ter purification by sucrose density gradient ultracentrifugation.

19 ) ( approximately 10(6) IU/ml), even without ultracentrifugation.

20 at can be purified by immunoprecipitation or ultracentrifugation.

21 re sacrificed and plasma MP were isolated by ultracentrifugation.

22 size exclusion chromatography and analytical ultracentrifugation.

23 confirmed to exist in solution by analytical ultracentrifugation.

24 wn by fluorescence anisotropy and analytical ultracentrifugation.

25 ysis of supernatants and pellets obtained by ultracentrifugation.

26 nsmission electron microscopy and analytical ultracentrifugation.

27 butions to homodimer stability by analytical ultracentrifugation.

28 e prepared by sequential ultrafiltration and ultracentrifugation.

29 ious chromatography resins and by analytical ultracentrifugation.

30 pendent proteins), based on density gradient ultracentrifugation.

31 e-detected sedimentation velocity analytical ultracentrifugation.

32 those from solution studies using analytical ultracentrifugation.

33 cell-culture supernatant fluids by isopycnic ultracentrifugation.

34 dimentation-diffusion analysis by analytical ultracentrifugation.

35 nal hydrodynamic information from analytical ultracentrifugation.

36 tions, as analyzed by sedimentation velocity ultracentrifugation.

37 lation Kit or by differential centrifugation/ultracentrifugation.

38 Exosomes were prepared using ultracentrifugation.

39 ligonucleotide-binding assays and analytical ultracentrifugation.

40 (1) analysis of Lp(a) fractions isolated by ultracentrifugation; (2) immunoprecipitation of plasma u

41 Analytical ultracentrifugation analyses show that the individual pe

42 Buoyant density ultracentrifugation analyses showed that NO2-Tyr(166)-ap

43 size exclusion chromatography and analytical ultracentrifugation analyses.

44 angle X-ray scattering (SAXS) and analytical ultracentrifugation analysis of the EcoP15I holoenzyme a

45 Analytical ultracentrifugation analysis reveals that the maturation

46 onal cryo-electron microscopy and analytical ultracentrifugation analysis, we determined the structur

47 In this study, we used sucrose gradient ultracentrifugation and a genome-wide microarray approac

48 uman cytotrophoblasts (CTBs) by differential ultracentrifugation and characterized them using transmi

49 Analytical ultracentrifugation and circular dichroism experiments s

50 bjected to further analysis using analytical ultracentrifugation and circular dichroism.

51 Analytical ultracentrifugation and clear native PAGE analysis show

52 Gel filtration analyses, analytical ultracentrifugation and co-immunoprecipitation experimen

53 Using ultracentrifugation and confocal microscopy, we found th

54 d several domain constructs using analytical ultracentrifugation and correlated VAI binding and PKR i

55 th size-exclusion chromatography, analytical ultracentrifugation and cross-linking experiments.

56 arance with and without exosomes isolated by ultracentrifugation and determined exosome-induced amylo

57 of PGR in solution as measured by analytical ultracentrifugation and dynamic light scattering.

58 Mutational analysis coupled with analytical ultracentrifugation and equilibrium denaturations showed

59 A series of ultracentrifugation and Exoquick isolation kit were firs

60 Analytical ultracentrifugation and fluorescence anisotropy methods

61 rat brain alphabeta-tubulin using analytical ultracentrifugation and fluorescence anisotropy, observi

62 Assays based on analytical ultracentrifugation and fluorescence binding indicate th

63 TP protofilaments was observed by analytical ultracentrifugation and fluorescence correlation spectro

64 293T cell EVs isolated by flotation gradient ultracentrifugation and from exosomes containing the tet

65 Analytical ultracentrifugation and hydrogen deuterium exchange mass

66 BP2 self-association, as shown by analytical ultracentrifugation and in vivo cross-linking.

67 m purified human platelets, were isolated by ultracentrifugation and labeled with biotin or PKH67.

68 Analytical ultracentrifugation and liquid chromatography-ultraviole

69 of our OmpW-micelle complex using analytical ultracentrifugation and molecular dynamics simulations.

70 Analytical ultracentrifugation and native mass spectrometry were us

71 inker with sedimentation velocity analytical ultracentrifugation and NMR spectroscopy reveals that th

72 Ultracentrifugation and size exclusion chromatography in

73 m spectra, as well as equilibrium analytical ultracentrifugation and size exclusion chromatography.

74 We determined by means of analytical ultracentrifugation and small angle x-ray scattering ana

75 e of truncated M. sexta sGC using analytical ultracentrifugation and small-angle X-ray scattering (SA

76 Analytical ultracentrifugation and small-angle X-ray scattering sol

77 ution structure of native FHR5 by analytical ultracentrifugation and small-angle X-ray scattering.

78 Size separation of the urine by ultracentrifugation and sodium dodecyl sulfate polyacryl

79 lar lysate fractionation by density gradient ultracentrifugation and subsequent analysis by proteome-

80 20 and 400 nm from human serum and FBS using ultracentrifugation and sucrose gradient centrifugation.

81 Ultracentrifugation and virion assembly assays indicated

82 tions in relation to C3b and C3u, analytical ultracentrifugation and x-ray and neutron scattering stu

83 nd temperatures was determined by analytical ultracentrifugation and X-ray and neutron scattering.

84 zinc with C3 was quantified using analytical ultracentrifugation and x-ray scattering.

85 pattern of multimers observed in analytical ultracentrifugation, and a concentration dependence of a

86 size-exclusion chromatography and analytical ultracentrifugation, and also binds to its putative rece

87 tein/lipid ratio shown by isopycnic gradient ultracentrifugation, and are small in size with a mean d

88 gle particle electron microscopy, analytical ultracentrifugation, and bio-layer interferometry, we pr

89 Precipitation, analytical ultracentrifugation, and chemical cross-linking experime

90 amagnetic relaxation enhancement, analytical ultracentrifugation, and DEER EPR, indicate that the tra

91 ing small-angle x-ray scattering, analytical ultracentrifugation, and dynamic light scattering techni

92 tallography, solution scattering, analytical ultracentrifugation, and electron microscopy we determin

93 d to multiangle light scattering, analytical ultracentrifugation, and electron paramagnetic resonance

94 oblot, immunoprecipitation, density gradient ultracentrifugation, and enzyme-linked immunosorbent ass

95 NMR, analytical ultracentrifugation, and fluorescence studies suggest th

96 tures, Ca(2+) binding capacities, analytical ultracentrifugation, and light-scattering profiles of th

97 ntified by NMR spectroscopy, SPR, analytical ultracentrifugation, and microcalorimetry glycopeptides

98 NMR chemical shift perturbation, analytical ultracentrifugation, and native electrospray ionization

99 entary surface plasmon resonance, analytical ultracentrifugation, and native mass spectrometry experi

100 tical gel filtration, sedimentation-velocity ultracentrifugation, and negative-stain electron microsc

101 egates and Abeta monomers using differential ultracentrifugation, and purifying them >6000 fold by du

102 sm and fluorescence spectroscopy, analytical ultracentrifugation, and semi-native gel electrophoresis

103 we used native mass spectrometry, analytical ultracentrifugation, and size-exclusion chromatography c

104 using microscale thermophoresis, analytical ultracentrifugation, and size-exclusion chromatography s

105 tering, dynamic light scattering, analytical ultracentrifugation, and small angle X-ray scattering ea

106 graphy, dynamic light scattering, analytical ultracentrifugation, and small angle x-ray scattering ex

107 spectroscopy, FTIR spectroscopy, analytical ultracentrifugation, and thioflavin T assays.

108 easured after vertical spin density-gradient ultracentrifugation, and triglycerides were directly mea

109 higher sedimentation velocities in gradient ultracentrifugations, and a longer incubation time in an

110 We have combined EM and analytical ultracentrifugation approaches to show that RECQ1 can fo

111 ent, sonication and sucrose density-gradient ultracentrifugation are subsequently used to isolate the

112 pared with direct binding measurements using ultracentrifugation as a reference.

113 Further, by using gradient ultracentrifugation assay, we show that the smaller aggr

114 er-dimer transition, as probed by analytical ultracentrifugation at various [TK].

115 in LDL cholesterol, as measured by means of ultracentrifugation, at week 52.

116 id testing by vertical spin density gradient ultracentrifugation (Atherotech, Birmingham, Alabama) fr

117 profiling by vertical spin density gradient ultracentrifugation (Atherotech, Birmingham, Alabama) fr

118 Here, we show how two techniques, analytical ultracentrifugation (AUC) and total organic carbon analy

119 ces in instrumentation have moved analytical ultracentrifugation (AUC) closer to a possible validatio

120 Analytical ultracentrifugation (AUC) has proven to be a powerful to

121 Sedimentation velocity (SV) analytical ultracentrifugation (AUC) is a classic technique for the

122 Sedimentation equilibrium (SE) analytical ultracentrifugation (AUC) is a gold standard for the rig

123 Analytical ultracentrifugation (AUC) is especially useful for the c

124 Analytical ultracentrifugation (AUC) studies of formation of the N-

125 ission Electron Microscopy (TEM), Analytical Ultracentrifugation (AUC), and UV/Vis spectroscopy.

126 systems (NDDSs) by making use of analytical ultracentrifugation (AUC).

127 e report the novel application of Analytical Ultracentrifugation (AUCF) to characterise the polymeric

128 on agrees quantitatively with our analytical ultracentrifugation-based measurements and previously pu

129 01Bio, Wako and iZON along with conventional ultracentrifugation-based method for exosome yield, puri

130 Ultracentrifugation-based single-copy assays are sensiti

131 ne has shown that isopycnic density gradient ultracentrifugation can produce structurally and electro

132 ochron iButton) that can be inserted into an ultracentrifugation cell assembly and spun at low rotor

133 ing small-angle x-ray scattering, analytical ultracentrifugation, circular dichroism, x-ray fiber dif

134 These data and analytical ultracentrifugation compaction analyses are used herein

135 d molecular weights determined by analytical ultracentrifugation confirm the SAXS model.

136 Analytical ultracentrifugation confirmed the presence of Ig domain

137 veolar lavage fluid of asthmatic subjects by ultracentrifugation contained TF.

138 Ultracentrifugation converted the purified 3F7.A10 mAb i

139 mers to a single compact dimer by analytical ultracentrifugation, coupled with a >30 A decrease in ma

140 tive polyacrylamide gel electrophoresis, and ultracentrifugation data show that the dimer is in equil

141 s validated against gold-standard analytical ultracentrifugation data.

142 this protocol describes sample preparation, ultracentrifugation, data acquisition, and data analysis

143 Evidence from NMR and analytical ultracentrifugation demonstrates that the carnosic acid

144 The recent application of density gradient ultracentrifugation (DGU) for structural sorting of sing

145 ation of (13)C labeling and density gradient ultracentrifugation (DGU) to produce an array of (13)C-l

146 m estuarine sediments using density gradient ultracentrifugation (DGU), followed by online flow-throu

147 and metallic SWCNTs through density gradient ultracentrifugation (DGU).

148 Analytical ultracentrifugation disclosed that IgG2 is monomeric wit

149 biophysical approaches, including analytical ultracentrifugation, dynamic light scattering, and therm

150 nts (FtsZ-GTP) as demonstrated by analytical ultracentrifugation, dynamic light scattering, fluoresce

151 ns below 30 muM, as determined by analytical ultracentrifugation, dynamic light scattering, size excl

152 d as a tetramer, as determined by analytical ultracentrifugation, electron microscopy, and electrospr

153 methods that includes sedimentation velocity ultracentrifugation, electron microscopy, and hydrodynam

154 Using surface plasmon resonance, ultracentrifugation, ELISA, and reporter cell assays, we

155 Sedimentation velocity analytical ultracentrifugation equipped with fluorescence detection

156 Analytical ultracentrifugation establishes that the isolated regula

157 orm complexes that can be precipitated using ultracentrifugation, even without prior heating.

158 were synthesized and utilized in analytical ultracentrifugation experiments and demonstrate that MER

159 e bonds, NMR solution studies and analytical ultracentrifugation experiments are reported in addition

160 X-ray co-crystal structure analysis and ultracentrifugation experiments clearly demonstrate that

161 Kinetic and analytical ultracentrifugation experiments demonstrate that alloste

162 Analytical ultracentrifugation experiments demonstrate that CheR2 i

163 Analytical ultracentrifugation experiments indicated that Kindlin-3

164 thermal titration calorimetry and analytical ultracentrifugation experiments indicated that the preva

165 Analytical ultracentrifugation experiments show that mature caspase

166 Circular dichroism and analytical ultracentrifugation experiments show that this core regi

167 synchrotron x-ray scattering and analytical ultracentrifugation experiments showed that the carbohyd

168 enceforth referred to as VanS) in analytical ultracentrifugation experiments to study VanS oligomeric

169 c species, which was confirmed by analytical ultracentrifugation experiments.

170 embranes using fluorescence spectroscopy and ultracentrifugation experiments.

171 tion states by gel filtration and analytical ultracentrifugation experiments.

172 e detected sedimentation velocity analytical ultracentrifugation (FDS-SV).

173 Here we use analytical ultracentrifugation, fluorescence polarization and NMR-b

174 ptor (hPVR) using various techniques such as ultracentrifugation, fluorescence-activated cell sorting

175 icle and dissolved Ag fractions (ICPMS after ultracentrifugation), for the characterization of Ag-NP

176 Ultracentrifugation fractionation experiments revealed t

177 pplied to RNA extracted from EVs isolated by ultracentrifugation from the plasma of five healthy volu

178 er related methods (filter assay, analytical ultracentrifugation, gel electrophoresis and size-exclus

179 Analytical ultracentrifugation has long been considered a gold stan

180 ce of the sample cell assembly in analytical ultracentrifugation holds the sample solution between wi

181 Using analytical ultracentrifugation in both sedimentation equilibrium an

182 the proteins was determined using analytical ultracentrifugation in the absence or presence of high c

183 them (>70%) are retained even after extended ultracentrifugation in the preparations of vesicle-deple

184 X3 and AM HC-HA withstands four runs of CsCl ultracentrifugation in the presence of 4 m GnHCl.

185 ues (dynamic light scattering and analytical ultracentrifugation) in an attempt to provide the basis

186 ed on sedimentation velocity (SV) analytical ultracentrifugation, in combination with a novel multiwa

187 Analytical gel chromatography and ultracentrifugation indicated tetrameric structure of th

188 mutagenesis, gel filtration, and analytical ultracentrifugation indicated that dimers form the basic

189 Analytical ultracentrifugation indicated that SR1:3, SR4:6, and SR7

190 Sedimentation velocity (SV) analytical ultracentrifugation is a classical biophysical technique

191 Sedimentation velocity analytical ultracentrifugation is a classical biophysical technique

192 Although ultracentrifugation is commonly used for isolation of EV

193 d using SWCNTs separated by density gradient ultracentrifugation, it is found that the high-pressure

194 th placebo, evolocumab significantly reduced ultracentrifugation LDL cholesterol at 12 weeks by 30.9%

195 he primary endpoint was percentage change in ultracentrifugation LDL cholesterol from baseline at wee

196 12, LDL-C reduction measured by preparative ultracentrifugation (least squares mean [standard error

197 cal lipids were also analyzed using gradient ultracentrifugation, liquid chromatography-mass spectrom

198 oteins by Isotope Tagging after Differential ultraCentrifugation (LOPIT-DC) and compare this method t

199 ercentage change from baseline to week 12 in ultracentrifugation-measured LDL cholesterol.

200 Analytical gel-filtration and ultracentrifugation measurements confirm that the protei

201 Analytical ultracentrifugation measurements suggest that aggregatio

202 solated through an optimized ultrafiltration/ultracentrifugation method and characterized with variou

203 This new generation of ultracentrifugation methods underscores a need to furthe

204 Ultracentrifugation methods, in contrast, do not introdu

205 by size exclusion chromatography, analytical ultracentrifugation, multiangle laser light scattering,

206 and software for multiwavelength analytical ultracentrifugation (MWL-AUC) experiments, demonstrating

207 s verified using a combination of analytical ultracentrifugation, native electrospray mass spectromet

208 termediates were characterized by analytical ultracentrifugation, native gel electrophoresis, and ele

209 amic and structural studies using analytical ultracentrifugation, NMR, and small-angle x-ray scatteri

210 We show here using analytical ultracentrifugation, NMR, size-exclusion chromatography

211 c assembly which are confirmed by analytical ultracentrifugation of both the crystallized domain and

212 Analytical ultracentrifugation of phospho-mimetic CENP-A nucleosome

213 l packing analysis, combined with analytical ultracentrifugation of Sonic Hh-GAG complexes, suggests

214 Analytical ultracentrifugation of the recombinant versions of Tp095

215 Dynamic light scattering and analytical ultracentrifugation on UNC-6 (with and without its C-dom

216 human plasma is a component of HDL either by ultracentrifugation or by lipid binding assays.

217 the need for less efficient methods such as ultracentrifugation or high-performance liquid chromatog

218 substrate for conversion, and attenuated by ultracentrifugation or incubation with SOD1 misfolding-s

219 ired purification of viral particles through ultracentrifugation or PEG precipitation, was PEG indepe

220 Using analytical ultracentrifugation, our results revealed that Asp(21) a

221 ority of studies to date have focused on the ultracentrifugation pellet, potentially losing a novel s

222 Analytical ultracentrifugation profiles of G-actin can be ascribed

223 techniques and compared them to traditional ultracentrifugation protocol.

224 ifugation, followed by a single small-volume ultracentrifugation purification step.

225 ix-free assay of co-sedimentation analytical ultracentrifugation, reinforced by dynamic light scatter

226 xclusion chromatography (SEC) and analytical ultracentrifugation, remain the default tools in charact

227 aining fraction could be however purified by ultracentrifugation resulting in the mitigation of MCPDE

228 small-angle X-ray scattering and analytical ultracentrifugation revealed that HC1 self-associates in

229 rified complexes by sucrose density gradient ultracentrifugation revealed that the three proteins for

230 lectron microscopy with data from analytical ultracentrifugation reveals the crucial role of kinetic

231 assays, PARP activity assays, and analytical ultracentrifugation sedimentation analysis, we found tha

232 Hydrodynamic analysis by analytical ultracentrifugation sedimentation velocity and native ma

233 from both GST pulldown assays and analytical ultracentrifugation show that GstDnaB1-300 is sufficient

234 fluorescence anisotropy decay and analytical ultracentrifugation show that the iM structure has a com

235 Analytical ultracentrifugation showed concentration-dependent self-

236 Analytical ultracentrifugation showed that 1K1 and NK1 were more st

237 Analytical ultracentrifugation showed that both antibodies were pre

238 Analytical ultracentrifugation showed that both IgG4 forms were pri

239 nce (NMR) spectroscopy as well as analytical ultracentrifugation, showing that they have a weight ave

240 Analytical ultracentrifugation shows one main complex, sedimenting

241 Hsp90 dimers and oligomers were evaluated by ultracentrifugation, size-exclusion chromatography coupl

242 eltaC) is further validated using analytical ultracentrifugation, size-exclusion chromatography, NMR

243 By combining analytical ultracentrifugation, small angle x-ray scattering, and c

244 We show using analytical ultracentrifugation, small angle x-ray scattering, and e

245 ng size-exclusion chromatography, analytical ultracentrifugation, small-angle X-ray scattering (SAXS)

246 ses including circular dichroism, analytical ultracentrifugation, small-angle x-ray scattering, and h

247 magnetic resonance spectroscopy, analytical ultracentrifugation, small-angle X-ray scattering, molec

248 and fluorescence spectroscopies, analytical ultracentrifugation, splicing assays, and cell microscop

249 centration was significantly reduced when an ultracentrifugation step preceded NTA.

250 ion, eliminating the need for time-consuming ultracentrifugation steps.

251 ross-linking, gel filtration, and analytical ultracentrifugation studies aimed at evaluating interact

252 ecSecA dimerization based on our analytical ultracentrifugation studies of SecA L6A and shown to for

253 Analytical ultracentrifugation studies of the SPI1-MSPbeta interact

254 Analytical ultracentrifugation studies showed that p85alpha undergo

255 orescence, circular dichroism and analytical ultracentrifugation studies showed that POT1 binding is

256 Analytical ultracentrifugation studies support that MERS-CoV 3CL(pr

257 ng pull-down, gel filtration, and analytical ultracentrifugation studies, we show that the N-terminus

258 -dependent circular dichroism and analytical ultracentrifugation suggest that the htt(NT) sequence, w

259 h extracellular vesicles (EVs) and remain in ultracentrifugation supernatants of cell-conditioned med

260 ination of X-ray crystallography, analytical ultracentrifugation, surface plasmon resonance and doubl

261 oscopy and sedimentation velocity analytical ultracentrifugation (svAUC) to undertake initial structu

262 sorting method can be combined with existing ultracentrifugation SWCNT sorting methods to produce "or

263 this work, using a combination of analytical ultracentrifugation techniques and DNA binding experimen

264 , to show by NMR spectroscopy and analytical ultracentrifugation that at biologically relevant concen

265 by surface plasmon resonance and analytical ultracentrifugation, that individual HTH motifs of the B

266 Liposome suspensions were concentrated by ultracentrifugation; the pellets were reconstituted in w

267 ld-type proteins were assessed by analytical ultracentrifugation, thioflavin T binding, transmission

268 ng tissue or cell lysates using differential ultracentrifugation through sucrose gradients.

269 We employed analytical ultracentrifugation to demonstrate that dematin is monom

270 of site-directed mutagenesis and analytical ultracentrifugation to derive thermodynamic parameters f

271 Here we utilize analytical ultracentrifugation to determine the thermodynamic param

272 In this study, we employed analytical ultracentrifugation to establish that four transition me

273 interactions in solution, we used analytical ultracentrifugation to measure the dimerization constant

274 nia We used fluorescence-detected analytical ultracentrifugation to measure tubulin dissociation over

275 spectrometry, was complemented with density ultracentrifugation to reveal the colocalized, or dissoc

276 We use analytical ultracentrifugation to show that purified Blt1p is a tet

277 ng size exclusion chromatography, analytical ultracentrifugation, transmission electron, and atomic f

278 ENP isolation from the conditioned medium by ultracentrifugation (UC) can take ~3 d, the AF4 fraction

279 Density gradient ultracentrifugation (UC) is currently the only technique

280 EVs have traditionally been purified by ultracentrifugation (UC), however UC has limitations, in

281 gation behavior of AgNPs were examined using ultracentrifugation, ultrafiltration, and asymmetrical f

282 anotubes (SWNTs), sorted by density-gradient ultracentrifugation, undergo self-assembly using depleti

283 Lipid testing was performed by ultracentrifugation (Vertical Auto Profile, Atherotech,

284 Rapid ultracentrifugation was used to directly measure LDL-C c

285 Previously, analytical ultracentrifugation was utilized to demonstrate that iso

286 Analytical ultracentrifugation was utilized to determine hydrodynam

287 rential scanning calorimetry, and analytical ultracentrifugation, we demonstrate the AgamOBP48 dimeri

288 Using analytical ultracentrifugation, we determined a dissociation consta

289 gel filtration chromatography and analytical ultracentrifugation, we found that a fully functional co

290 small-angle X-ray scattering and analytical ultracentrifugation, we found that ClipCG12 adopts a lar

291 Using analytical ultracentrifugation, we found that pH-induced conformati

292 gle x-ray scattering analysis and analytical ultracentrifugation, we show that NaD1 forms dimers in s

293 ry human DC-secreted EV (DC-EV), isolated by ultracentrifugation, were characterized for their size,

294 size-exclusion chromatography and analytical ultracentrifugation, whereas other class III nucleotidyl

295 aracterization technique based on analytical ultracentrifugation, which demonstrates exceptional pote

296 In this study, we coupled ultracentrifugation with attenuated total reflectance-Fo

297 Sedimentation velocity analytical ultracentrifugation with fluorescence detection has emer

298 al cell fractionation using density gradient ultracentrifugation with multiplexed quantitative proteo

299 However, we show using analytical ultracentrifugation, X-ray crystallography, and enzyme k

300 ion structure by a combination of analytical ultracentrifugation, X-ray scattering and constrained mo