ライフサイエンスコーパス: density gradient

1 n centrifugation and from entering a Percoll density gradient.

2 zone characterized by a steeper-than-normal density gradient.

3 bound to liposomes centrifuged on a sucrose density gradient.

4 racentrifugation using a BiEDTA complex as a density gradient.

5 ected only in the CRD fractions of a sucrose density gradient.

6 Dnmt3b specifically with Hdac2 in a glycerol density gradient.

7 s to a more buoyant lipid raft fraction in a density gradient.

8 rifugation and further purified by a sucrose density gradient.

9 ent treatment, using a discontinuous sucrose density gradient.

10 fusion-like contribution that increases with density gradient.

11 the genome from the E protein in a tartrate density gradient.

12 thin a 3-h period of time without the use of density gradients.

13 and is usually mitigated through the use of density gradients.

14 ionates with the outer dynein arm in sucrose density gradients.

15 colocalizes with its G protein effectors on density gradients.

16 nuclear fractions are obtained using Percoll density gradients.

17 O(3) buffer and fractionated through sucrose density gradients.

18 ted with liposomes and aggregated on sucrose density gradients.

19 tivating factor (PAF) acetylhydrolase on KBr density gradients.

20 cron fractions with no need of salt or sugar density gradients.

21 and copurifies with radial spokes in sucrose density gradients.

22 d, followed by purification using continuous-density gradients.

23 d liver humanized FRG mice were separated by density gradients.

24 ctionation of retinal lysates, using sucrose density gradients.

25 nd ER fractions recovered from sucrose (Suc) density gradients.

26 to l.14 as defined by flotation into sucrose density gradients.

27 es were isolated by sedimentation in sucrose density gradients.

28 nting with caveolin and flotillin on sucrose density gradients.

29 olumn stability via enhanced salinity-driven density gradients.

30 rgent-resistant membranes (DRMs) in OptiPrep density gradients.

31 ers, and patients with COPD by using Percoll density gradients.

32 is immature and migrates at 45 S in sucrose density gradients.

33 detected large clusters that contain several density gradients.

34 on-polysomal, but dense fractions on sucrose density gradients.

35 ke; plasma was collected and fractionated by density gradients.

36 based on their MUC5AC and VAMP-8 content by density gradients.

37 shment of a capillary plexus that displays a density gradient across the myocardial wall, being highe

38 Sucrose density gradient analyses revealed formation of a stable

39 Sucrose density gradient analyses revealed that depletion of U3

40 Sucrose density gradient analysis detected AP1B predominantly in

41 Sucrose density gradient analysis indicates that a significant f

42 Sorbitol density gradient analysis of membrane compartments showe

43 Furthermore, sucrose density gradient analysis revealed significantly more al

44 ormal prostate epithelial cells, and sucrose density gradient analysis showed co-sedimentation of AR

45 Sucrose density gradient analysis showed that 96% of the circula

46 Density gradient analysis showed that BoNT serotypes A a

47 High-resolution sucrose density gradient analysis showed that, while mutating fa

48 sediment with pre-60S ribosomal particles in density gradient analysis.

49 lular compartments were separated on Percoll density gradients analyzed with T cells.

50 nse DNA polymer brushes on a biochip along a density gradient and directly measured the collective ex

51 ice were isolated by initial separation on a density gradient and then cultured as adherent cells on

52 orida Straits to show that the cross-current density gradient and vertical current shear of the Gulf

53 uinea pig liver by centrifugation on Percoll density gradients and compared to Percoll-purified in vi

54 vesicle compartment as confirmed by sucrose density gradients and confocal immunofluorescent co-loca

55 mbrane substructures of the AJC in iodixanol density gradients and define their protein constituents.

56 ted as a low buoyant density band on sucrose density gradients and exhibited an increase in light sca

57 parietal cortex blocks were fractionated by density gradients and further enriched for neurons by an

58 copurifies with outer arm dynein in sucrose density gradients and is missing only in those strains c

59 PCDH15 and VLGR1 variants along with sucrose density gradients and the use of vesicle trafficking inh

60 exosome preparations by electron microscopy, density gradient, and immunoblotting, we determined that

61 ed by gravimetry using kerosene-bromobenzene density gradients, and from wet/dry weight measurements.

62 -polyacrylamide gel electrophoresis, sucrose density gradients, and isolated PSII particles, we found

63 e same fractions as H-RasWT on four types of density gradients, and remained fully membrane-bound.

64 ome-resident SNAREs cofractionate in sucrose density gradients, and show similar solubility or insolu

65 embranes that float on discontinuous sucrose density gradients, and that methyl-beta-cyclodextrin tre

66 rmed by cofractionation of these proteins in density gradients, as well as by coimmunoprecipitation.

67 Density gradient assays demonstrated that several of the

68 ctions form a sharp band in potassium iodide density gradients at 1.195 g/cm3 and the 16 K protein is

69 Islets are purified on density gradients, but procedures currently used have li

70 imentation rate than native virus on sucrose density gradients, but the particles retained all of the

71 We show that a useful density gradient can be formed within a few hours beginn

72 n contrast, do not introduce interference if density gradients can be avoided and they resolve lipopr

73 we report that the use of tailored nonlinear density gradients can significantly improve density-grad

74 In addition to redox-MHD, density gradients caused by the redox reactions also pla

75 10 mum/s above the electrodes as a result of density gradients caused by the redox reactions and foll

76 The efficiency of custom density gradients (CDGs) to recover high islet yield was

77 by immunofluorescence localization, sucrose density gradients, cell fractionation, and yeast two-hyb

78 ver, the splitting was observed with sucrose density gradient centrifugation (SDGC) without IF3 if RR

79 partitioned to the cytoplasmic fraction, and density gradient centrifugation analysis demonstrated th

80 Using a combination of density gradient centrifugation and agarose gel electrop

81 ated through multiple rounds of differential density gradient centrifugation and analyzed by immunoel

82 Using sucrose density gradient centrifugation and antibody pulldowns,

83 Triton X-100 extraction followed by OptiPrep density gradient centrifugation and cholera toxin beta-s

84 Instead, sucrose density gradient centrifugation and electron microscopy

85 Together with the results from density gradient centrifugation and fluorescence correla

86 l-enriched LRs were isolated from Giardia by density gradient centrifugation and found to be sensitiv

87 ance of hydrodynamically large structures in density gradient centrifugation and native gel electroph

88 -purify with high density lipoprotein during density gradient centrifugation and subsequent gel filtr

89 Physical partitioning by density gradient centrifugation did not separate phyllos

90 away from mosquito salivary gland debris by density gradient centrifugation eliminated salivary glan

91 A comparison of proteins in CsCl density gradient centrifugation fractions from supernata

92 A cell fraction separated by density gradient centrifugation from blood had TSC2 LOH

93 d mononuclear cells (PBMCs) were isolated by density gradient centrifugation from the blood of patien

94 ents from infected cells by differential and density gradient centrifugation further indicated that P

95 CsCl density gradient centrifugation indicated that almost al

96 Density gradient centrifugation indicated that, unlike s

97 enes 100S ribosomes were observed by sucrose density gradient centrifugation of bacterial extracts du

98 Density gradient centrifugation of isolated exosomes rev

99 Density gradient centrifugation of L1 ribonucleoprotein

100 Sucrose density gradient centrifugation of large ribosomal subun

101 Sucrose density gradient centrifugation of the culture medium re

102 Density gradient centrifugation of Triton X-100 lysates

103 o exclude nonviable cells require the use of density gradient centrifugation or antibody-based cell s

104 Density gradient centrifugation procedures reduce the le

105 Discontinuous sucrose density gradient centrifugation revealed NET in the lipi

106 Density gradient centrifugation revealed that in the ini

107 rization of the circulating mRNAs by sucrose density gradient centrifugation revealed that the liver-

108 by size exclusion chromatography and sucrose-density gradient centrifugation revealed that the phosph

109 amination of lipid rafts isolated by sucrose density gradient centrifugation revealed the constitutiv

110 f the Golgi complex into two fractions using density gradient centrifugation showed effects of aged A

111 ternal ribosome entry mechanisms and sucrose density gradient centrifugation showed that BC1-mediated

112 Sucrose density gradient centrifugation showed that exposure of

113 Density gradient centrifugation studies reveal that thes

114 Using sucrose density gradient centrifugation to analyze ribosome comp

115 Triton X-100 at 4 degrees C and subjected to density gradient centrifugation to isolate DRMs from the

116 We used density gradient centrifugation to isolate LDL in plasma

117 gated these species by Blue Native PAGE, Suc density gradient centrifugation, 77K fluorescence, circu

118 Density gradient centrifugation, affinity purification,

119 volunteers (n=7) were isolated using Ficoll density gradient centrifugation, and plated on fibronect

120 analyzed purified MUC2-N by gel filtration, density gradient centrifugation, and transmission electr

121 Sucrose density gradient centrifugation, immunoblot, and immunoh

122 Enzymatic assays, sucrose density gradient centrifugation, immunoprecipitation, do

123 to known proteoglycans; purified using CsCl density gradient centrifugation, molecular sieve, and io

124 approaches including gel filtration, sucrose density gradient centrifugation, pull-down of differenti

125 od mononuclear cells were isolated by Ficoll density gradient centrifugation, separated into cellular

126 Using sucrose density gradient centrifugation, this study evaluated wh

127 sting and osmotic lysis, followed by sucrose density gradient centrifugation, which separated OMs fro

128 As shown by sucrose density gradient centrifugation, WT gamma-PAK, S490A, an

129 olated by collagenase-pronase-perfusion, and density gradient centrifugation.

130 ith centrosome fractions isolated by sucrose density gradient centrifugation.

131 psin population was isolated and purified by density gradient centrifugation.

132 hromatographic matrices followed by glycerol density gradient centrifugation.

133 to be an outer membrane protein by isopycnic density gradient centrifugation.

134 fferent fractions by detergent treatment and density gradient centrifugation.

135 llagenase digestion of the liver followed by density gradient centrifugation.

136 additional separation using cesium chloride density gradient centrifugation.

137 te, and in particulate fractions obtained by density gradient centrifugation.

138 lubilized oligomers was confirmed by sucrose density gradient centrifugation.

139 and/or membrane fractionation using OptiPrep density gradient centrifugation.

140 of detergent extraction and differential and density gradient centrifugation.

141 to insulin binding as determined by sucrose density gradient centrifugation.

142 ble membranes then were separated by sucrose density gradient centrifugation.

143 heir light buoyant densities through sucrose density gradient centrifugation.

144 s and luminal contents were subjected to KBr density gradient centrifugation.

145 PHB-containing bacteria were concentrated by density gradient centrifugation.

146 iltration column but were made visible after density gradient centrifugation.

147 suspension-cultured cells following sucrose density gradient centrifugation.

148 consistent with previous measurements using density gradient centrifugation.

149 heat gave only two fractions on equilibrium density gradient centrifugation: a fraction comprised of

150 re isolated from adult mice via Ficoll-Paque density-gradient centrifugation and cultured in the pres

151 n by aqueous two-phase partitioning, sucrose density-gradient centrifugation, and immunoelectron micr

152 Mouse BMCs were isolated by density-gradient centrifugation.

153 genase perfusion of the liver and subsequent density-gradient centrifugation.

154 from stationary-phase (SP) yeast cultures by density-gradient centrifugation.

155 ave used immunogold localization and sucrose density gradient cosedimentation analyses to confirm ass

156 from the star, the resulting temperature and density gradients create a complex chemical environment

157 ular fractionation using equilibrium sucrose density gradients demonstrated decreased hyperphosphoryl

158 sence of diffusion waves and the presence of density gradient driven natural convection.

159 ffusion is well understood, the influence of density gradient-driven natural convection on the mass t

160 short experimental times of tens of seconds, density gradient-driven natural convection significantly

161 Fluid density gradients due to the spatially varying reagent c

162 Result of the sucrose density gradient experiment suggests that Der interacts

163 Density gradient flotation assays demonstrated that ER-t

164 By using a detergent-free density gradient flotation technique, we found that 80%

165 iEDTA) and have investigated the dynamics of density gradient formation in the ultracentrifuge.

166 Discontinuous sucrose density gradient fractionation and immunoconfocal locali

167 Density gradient fractionation and immunoprecipitation a

168 Sucrose density gradient fractionation of cytoplasmic extracts f

169 Using discontinuous sucrose density gradient fractionation of post-nuclear supernata

170 rived Arabidopsis protoplasts, followed by a density gradient fractionation of the cellular content.

171 Sucrose density gradient fractionation of the culture medium and

172 After density gradient fractionation of the organelles, immuno

173 Sucrose density gradient fractionation of the purified complexes

174 nse vesicles, is responsible for the altered density gradient fractionation profile.

175 Sucrose density gradient fractionation reveals that loss of Hap1

176 In plasma samples subjected to density gradient fractionation, OxPL were present on pla

177 By density gradient fractionation, Soi3/Rav1p associated as

178 Using sorbitol density gradient fractionation, we show here that in kin

179 Quantification of HCV RNA throughout the density gradient fractions revealed that HCV(VLDF) rapid

180 BIG2, but not BIG1, appeared in density-gradient fractions containing TfnR, Rab11, and E

181 Density gradients have been long used to separate fragme

182 a suggest that using an iodixanol-controlled density gradient improves the islet recovery rate in hum

183 associates with the 40 S subunit on sucrose density gradients in an ATP-dependent manner.

184 es, and the presence or absence of adipocyte density gradients in the marrow space, all as a function

185 tion of the volutin granules using iodixanol density gradients indicated a preferential localization

186 with the product of the LF1 gene in sucrose density gradients, indicating that these proteins may fo

187 d, subsets of the BMV particles separated by density gradients into a pool enriched for RNA1 (B1) and

188 Axial density profiles and vertical density gradients localized the Sph 1-P response to tran

189 morphonuclear leukocytes were separated with density gradient media.

190 beling with [(3)H]palmitic acid, and sucrose density gradient membrane partitioning studies.

191 fractionated by modification of an iodixanol density gradient method previously used for acidocalciso

192 n mitochondria were obtained using a Percoll density gradient method.

193 ion of the enol crystal was facilitated by a density-gradient method.

194 cell separation occurs almost exclusively by density gradient methods and by fluorescence- and magnet

195 An adaptable density gradient multilayer polymerization (DGMP) method

196 When isolated using density gradients, myosin IIA-associated NK cell lytic g

197 rsity of Wisconsin solution to create linear density gradients of 1.065 to 1.095 g/mL.

198 NA) polymer phases, we fabricated continuous density gradients of binding sites for assembly on a pho

199 nts of both I(to,fast) and I(to,slow) and/or density gradients of either phenotype.

200 ibility best predicted prevalence across the density gradients of hosts and parasites, outperforming

201 We used sucrose density gradients of nucleosomes prepared by partial and

202 preparation and characterization of protein density gradients on solid supports.

203 ed the effectiveness of iodixanol-controlled density gradients on the islet purification step.

204 rode damage, and the impact of ionic current density gradients on velocity profiles over the anodes a

205 ke existing methods that are guided by local density gradients, our method is guided by correspondenc

206 ving arbitrary 3D topographies and definable density gradients over micrometer dimensions provide the

207 The cesium chloride (CsCl) density gradient profile of virus particles containing g

208 sue by enzymatic digestion and discontinuous density gradient purification.

209 show that a fraction of HBx colocalizes with density-gradient-purified mitochondria and associates wi

210 red before purification by the ATGS, and the density gradient range for islet purification in a COBE

211 iven slumping of the basin-scale north-south density gradient, resulting in a patchy bloom beginning

212 in fluid systems with initial, well-defined density gradients results in the formation of distinct l

213 Density gradients revealed the presence of membrane-asso

214 tes were analyzed using a continuous sucrose density gradient, revealing an apparent heterogeneity du

215 Sedimentation in sucrose density gradients reveals that large unilamellar vesicle

216 Using standard density gradient (SDG) ranges for human islet purificati

217 Density gradient sedimentation analysis of protein lysat

218 Biochemical analyses, including density gradient sedimentation and co-immunoprecipitatio

219 essed in COS-1 cells and analyzed by sucrose density gradient sedimentation and gel filtration for th

220 examined a virion-enriched band purified by density gradient sedimentation and observed that treatme

221 m analytical band sedimentation velocity and density gradient sedimentation equilibrium experiments i

222 Two-phase partitioning and sucrose density gradient sedimentation established that RPP1A re

223 e PIKfyveWT-containing fractions obtained by density gradient sedimentation of total membranes from P

224 in combination with gel filtration, sucrose density gradient sedimentation, and gel electrophoresis.

225 was constructed and characterized by sucrose-density gradient sedimentation, size-exclusion chromatog

226 into nascent virus particles isolated after density gradient sedimentation.

227 In adult density-gradient separated BMMNCs, canonical Wnt3a promo

228 ng using stable isotopes coupled either with density gradient separation (SIP) or with FISH-SIMS.

229 Worms were recovered by density gradient separation and examined using both cult

230 Sucrose density gradient separation and immunoblotting with know

231 nsity-distinct fractions by ultracentrifugal density gradient separation in CsBiEDTA.

232 pH outside the incubator with Hibernate and density gradient separation of neurons from debris.

233 P class in human serum with ultracentrifugal density gradient separation.

234 -100 microl of peripheral whole blood and no density-gradient separation, and the entire procedure fr

235 Sucrose density gradients show that EGO is not associated with r

236 Using sucrose density gradient, size-exclusion chromatography, and mat

237 d the development of a near-surface vertical density gradient (stratification) that inhibits vertical

238 behaves like a raft-associated protein on a density gradient supports this hypothesis.

239 Ficoll, or Percoll (Pharmacia) that formed a density gradient that allowed the cells to slowly settle

240 we used equilibrium sedimentation in sucrose density gradients to separate PrP(Sc) aggregates from th

241 In sucrose density gradients Trypanosoma brucei NOG1 co-sediments w

242 who underwent lipid testing by vertical spin density gradient ultracentrifugation (Atherotech, Birmin

243 o underwent lipid profiling by vertical spin density gradient ultracentrifugation (Atherotech, Birmin

244 lute systems for analysis of lipoproteins by density gradient ultracentrifugation (DGU) by varying bo

245 The recent application of density gradient ultracentrifugation (DGU) for structura

246 ein in well-defined density ranges using the density gradient ultracentrifugation (DGU) method.

247 utilize a combination of (13)C labeling and density gradient ultracentrifugation (DGU) to produce an

248 e semiconducting and metallic SWCNTs through density gradient ultracentrifugation (DGU).

249 Density gradient ultracentrifugation (DGUC) revealed tha

250 Density gradient ultracentrifugation analysis of plasma

251 Using sucrose density gradient ultracentrifugation and a sensitive ELI

252 ) that resemble nascent HDL were analyzed by density gradient ultracentrifugation and electron micros

253 Separation of VLDL was performed by density gradient ultracentrifugation and immunoaffinity

254 ectors in two steps: iodixanol discontinuous density gradient ultracentrifugation and size exclusion

255 Fractionation by density gradient ultracentrifugation and visualization b

256 Characterization by density gradient ultracentrifugation and visualization b

257 Here, we show how density gradient ultracentrifugation can be used to sepa

258 otubes and graphene has shown that isopycnic density gradient ultracentrifugation can produce structu

259 cipitation, confocal microscopy, and sucrose density gradient ultracentrifugation in mice.

260 c state of the purified complexes by sucrose density gradient ultracentrifugation revealed that the t

261 cal method that couples immunoseparation and density gradient ultracentrifugation to separate and dif

262 We also employed discontinuous sucrose density gradient ultracentrifugation to show that the LR

263 demonstrate the analytical power of linking density gradient ultracentrifugation with affinity separ

264 ombines biochemical cell fractionation using density gradient ultracentrifugation with multiplexed qu

265 eleased by high-salt buffer, fractionated by density gradient ultracentrifugation, and characterized

266 Immunoblot, immunoprecipitation, density gradient ultracentrifugation, and enzyme-linked

267 by nuclear magnetic resonance spectroscopy, density gradient ultracentrifugation, and gradient gel e

268 nigripalpus (CuniNPV) were purified by Ludox density gradient ultracentrifugation, and the proteins w

269 response observed using SWCNTs separated by density gradient ultracentrifugation, it is found that t

270 tern blotting of mitochondrial complexes and density gradient ultracentrifugation, we show that that

271 ins isolated from serum HDL collected from a density gradient ultracentrifugation-based separation.

272 use of any additional cosurfactant, through density gradient ultracentrifugation.

273 repared from mouse retina by differential or density gradient ultracentrifugation.

274 ssociation with lipid rafts as determined by density gradient ultracentrifugation.

275 on by agarose gel electrophoresis or sucrose density gradient ultracentrifugation.

276 ed from the protoplasmic cylinder by sucrose density gradient ultracentrifugation.

277 ture-grown HCV after purification by sucrose density gradient ultracentrifugation.

278 Carbonate treatment, sonication and sucrose density-gradient ultracentrifugation are subsequently us

279 nced lipoprotein testing using vertical-spin density-gradient ultracentrifugation did not improve pre

280 Density-gradient ultracentrifugation has recently emerge

281 structures, and has often required repeated density-gradient ultracentrifugation processing.

282 density gradients can significantly improve density-gradient ultracentrifugation separations.

283 Native gel electrophoresis, density-gradient ultracentrifugation, and chemical cross

284 s were directly measured after vertical spin density-gradient ultracentrifugation, and triglycerides

285 nced lipoprotein testing using vertical-spin density-gradient ultracentrifugation, traditional testin

286 e-walled carbon nanotubes (SWNTs), sorted by density-gradient ultracentrifugation, undergo self-assem

287 Using the scalable technique of density-gradient ultracentrifugation, we have isolated n

288 Subcellular distribution was determined by density-gradient ultracentrifugation.

289 om plasma of normal volunteers by sequential density-gradient ultracentrifugation.

290 n transmembrane receptors revealed a spatial density gradient underlying characteristic molecular den

291 suring their distribution pattern across the density gradient using amine-reactive isotope tagging an

292 cells by detergent insolubility, buoyancy on density gradients using two distinct approaches, and col

293 that mediate platelet interactions, albumin density gradient washed, gel-filtered platelets (3.5 x 1

294 Using sucrose density gradients we have found that human T cell beta(1

295 However, using sucrose density gradients, we demonstrate that the association o

296 Discontinuous sucrose density gradients were used for fractionation of Golgi m

297 Ludox density gradients were used to enrich for Escherichia co

298 Density gradients were used to track changes in reticulo

299 can be highly turbulent, since the vertical density gradient which suppresses turbulence is weak.

300 lications, including the characterization of density gradients, which are used to separate objects in