ライフサイエンスコーパス: density gradient

1 combination with the analysis of the reduced density gradient.

2 n centrifugation and from entering a Percoll density gradient.

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

4 ction can be changed by tuning the preplasma density gradient.

5 bound to liposomes centrifuged on a sucrose density gradient.

6 racentrifugation using a BiEDTA complex as a density gradient.

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

8 Dnmt3b specifically with Hdac2 in a glycerol density gradient.

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

10 rifugation and further purified by a sucrose density gradient.

11 fusion-like contribution that increases with density gradient.

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

13 detected large clusters that contain several density gradients.

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

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

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

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

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

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

20 colocalizes with its G protein effectors on density gradients.

21 nuclear fractions are obtained using Percoll density gradients.

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

23 ted with liposomes and aggregated on sucrose density gradients.

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

25 and copurifies with radial spokes in sucrose density gradients.

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

27 ctionation of retinal lysates, using sucrose density gradients.

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

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

30 es were isolated by sedimentation in sucrose density gradients.

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

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

33 olumn stability via enhanced salinity-driven density gradients.

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

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

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

37 e identified through analysis of the reduced density gradient, a fundamental parameter at the core of

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

39 Sucrose density gradient analyses revealed formation of a stable

40 Sucrose density gradient analyses revealed that depletion of U3

41 Sucrose density gradient analysis detected AP1B predominantly in

42 Sucrose density gradient analysis indicates that a significant f

43 Sorbitol density gradient analysis of membrane compartments showe

44 Furthermore, sucrose density gradient analysis revealed significantly more al

45 Plasma density gradient analysis revealed the presence of the n

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

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

48 Density gradient analysis showed that BoNT serotypes A a

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

50 titative polymerase chain reaction analysis, density gradient analysis, and Western blotting.

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

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

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

54 and monocytes were isolated by using Ficoll density gradient and magnetic bead separation and incuba

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

56 These HEVcc particles were characterized in density gradients and allowed the trans-complementation

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

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

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

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

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

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

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

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

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

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

67 Ts were found to form a separate band in the density gradient apart from the fluorescent SWCNTs.

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

69 Density gradient assays demonstrated that several of the

70 on (LOPIT-DC) and compare this method to the density gradient-based hyperLOPIT approach.

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

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

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

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

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

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

77 10 mum/s above the electrodes as a result of density gradients caused by the redox reactions and foll

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

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

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

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

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

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

84 Using sucrose density gradient centrifugation and antibody pulldowns,

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

86 Instead, sucrose density gradient centrifugation and electron microscopy

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

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

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

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

91 We compare our device against a density gradient centrifugation by processing 0.5 mL por

92 Cross-linking sucrose density gradient centrifugation demonstrated an associat

93 Physical partitioning by density gradient centrifugation did not separate phyllos

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

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

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

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

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

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

100 Density gradient centrifugation of isolated exosomes rev

101 Density gradient centrifugation of L1 ribonucleoprotein

102 Sucrose density gradient centrifugation of large ribosomal subun

103 Sucrose density gradient centrifugation of the culture medium re

104 Density gradient centrifugation of Triton X-100 lysates

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

106 Density gradient centrifugation procedures reduce the le

107 In 25 min of operating time, density gradient centrifugation recovers an average of 3

108 Discontinuous sucrose density gradient centrifugation revealed NET in the lipi

109 Density gradient centrifugation revealed that in the ini

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

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

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

113 Sucrose density gradient centrifugation showed that exposure of

114 llular fractionation analysis using OptiPrep density gradient centrifugation shows an increase of fun

115 Density gradient centrifugation studies reveal that thes

116 Using sucrose density gradient centrifugation to analyze ribosome comp

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

118 We used density gradient centrifugation to isolate LDL in plasma

119 ernal reflection fluorescence microscopy and density gradient centrifugation we found that mouse TRPA

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

121 Density gradient centrifugation, affinity purification,

122 llular granules were fractionated by Percoll density gradient centrifugation, and N- and O-glycans pr

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

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

125 Sucrose density gradient centrifugation, immunoblot, and immunoh

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

127 ocrine tissue and are difficult to purify by density gradient centrifugation, leading to poor islet r

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

129 Using sucrose density gradient centrifugation, this study evaluated wh

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

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

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

133 suspension-cultured cells following sucrose density gradient centrifugation.

134 consistent with previous measurements using density gradient centrifugation.

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

136 ith centrosome fractions isolated by sucrose density gradient centrifugation.

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

138 hromatographic matrices followed by glycerol density gradient centrifugation.

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

140 fferent fractions by detergent treatment and density gradient centrifugation.

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

142 additional separation using cesium chloride density gradient centrifugation.

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

144 lubilized oligomers was confirmed by sucrose density gradient centrifugation.

145 liac crest and cells were enriched by Ficoll density gradient centrifugation.

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

147 of detergent extraction and differential and density gradient centrifugation.

148 PHB-containing bacteria were concentrated by 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 from stationary-phase (SP) yeast cultures by density-gradient centrifugation.

152 Mouse BMCs were isolated by density-gradient centrifugation.

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

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

155 ular fractionation using equilibrium sucrose density gradients demonstrated decreased hyperphosphoryl

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

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

158 Fluid density gradients due to the spatially varying reagent c

159 omigrated with 50S ribosomal subunits in Suc density gradients, even after RNase treatment of stromal

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

161 Density gradient flotation assays demonstrated that ER-t

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

163 ed for a short period ex vivo before using a density gradient for schizont enrichment.

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

165 Here, we employ high-resolution density gradient fractionation and direct immunoaffinity

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 Sucrose density gradient fractionation reveals that loss of Hap1

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

176 By density gradient fractionation, Soi3/Rav1p associated as

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

178 isolated using differential centrifugation & density-gradient fractionation from bronchoalveolar lava

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 g, or ionizing environments, shock-waves and density gradients impart phase distortions that obscure

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

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

185 weakly-absorbing, low-Z materials, or steep density gradients in matter under extreme conditions.

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

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

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

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

190 The nature of the density gradient limits this approach to a small paramet

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

192 morphonuclear leukocytes were separated with density gradient media.

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

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

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

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

197 An adaptable density gradient multilayer polymerization (DGMP) method

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

214 Density gradients revealed the presence of membrane-asso

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

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

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

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

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

224 h monoribosomes and polyribosomes by sucrose density gradient sedimentation.

225 into nascent virus particles isolated after density gradient sedimentation.

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

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

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

229 Sucrose density gradient separation and immunoblotting with know

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

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

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

233 -100 microl of peripheral whole blood and no density-gradient separation, and the entire procedure fr

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

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

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

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

238 ese defects from the system by introducing a density gradient to create a configuration in a single s

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

240 e EDA wave spreads across a mesenchymal cell density gradient, triggering pattern formation by loweri

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 were isolated from estuarine sediments using density gradient ultracentrifugation (DGU), followed by

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

250 Density gradient ultracentrifugation (UC) is currently t

251 Density gradient ultracentrifugation analysis of plasma

252 Using sucrose density gradient ultracentrifugation and a sensitive ELI

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

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

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

256 is based on cellular lysate fractionation by density gradient ultracentrifugation and subsequent anal

257 Fractionation by density gradient ultracentrifugation and visualization b

258 Characterization by density gradient ultracentrifugation and visualization b

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

276 ed R-DeeP (RNA-dependent proteins), based on 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 n transmembrane receptors revealed a spatial density gradient underlying characteristic molecular den

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

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

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

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

294 In addition, fractions of the density gradient were also obtained for further analysis

295 Back-to-front MPA density gradients were controlled by higher cofilin-medi

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