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1 and eventually to monomers as separated on a sucrose density gradient.
2 lex that sedimented at approximately 5S in a sucrose density gradient.
3 so be detected by co-sedimentation through a sucrose density gradient.
4 isolated between 1.17 and 1.21 g/cm(3) in a sucrose density gradient.
5 remains bound to liposomes centrifuged on a sucrose density gradient.
6 was detected only in the CRD fractions of a sucrose density gradient.
7 by centrifugation and further purified by a sucrose density gradient.
8 t detergent treatment, using a discontinuous sucrose density gradient.
9 se (RT) activity that banded at 1.15 g/ml in sucrose density gradients.
10 nit that is immature and migrates at 45 S in sucrose density gradients.
11 tudy (<380 nM), as judged by its mobility in sucrose density gradients.
12 insoluble protein recovered at the bottom of sucrose density gradients.
13 lexes toward the uncoiled lariat position in sucrose density gradients.
14 d with non-polysomal, but dense fractions on sucrose density gradients.
15 pulina hyodysenteriae by using discontinuous sucrose density gradients.
16 R1 by flotation of CHAPS lysates of cells in sucrose density gradients.
17 and comigrates with the outer dynein arm in sucrose density gradients.
18 lipid membranes as assessed by floatation in sucrose density gradients.
19 tionic lipid was confirmed and quantified on sucrose density gradients.
20 ts with known cytoplasmic dynein proteins in sucrose density gradients.
21 icated by aqueous two-phase partitioning and sucrose density gradients.
22 containing a known glycoprotein in flotation sucrose density gradients.
23 atalytically active following isolation from sucrose density gradients.
24 cofractionates with the outer dynein arm in sucrose density gradients.
25 M Na(2)CO(3) buffer and fractionated through sucrose density gradients.
26 associated with liposomes and aggregated on sucrose density gradients.
27 5 M KI, and copurifies with radial spokes in sucrose density gradients.
28 and fractionation of retinal lysates, using sucrose density gradients.
29 of 1.07 to l.14 as defined by flotation into sucrose density gradients.
30 ent; cores were isolated by sedimentation in sucrose density gradients.
31 o-sedimenting with caveolin and flotillin on sucrose density gradients.
40 d with normal prostate epithelial cells, and sucrose density gradient analysis showed co-sedimentatio
44 -free cytoplasmic complexes that copurify in sucrose density gradients and are stable in nonionic det
45 into the vesicle compartment as confirmed by sucrose density gradients and confocal immunofluorescent
46 as isolated as a low buoyant density band on sucrose density gradients and exhibited an increase in l
48 fferent PCDH15 and VLGR1 variants along with sucrose density gradients and the use of vesicle traffic
50 resh bovine brain and size fractionated on a sucrose density gradient, and a size-fractionated bovine
52 Deriphat-polyacrylamide gel electrophoresis, sucrose density gradients, and isolated PSII particles,
53 GN/endosome-resident SNAREs cofractionate in sucrose density gradients, and show similar solubility o
54 ist in membranes that float on discontinuous sucrose density gradients, and that methyl-beta-cyclodex
55 is found in the same fraction as 125I-Tf on sucrose density gradients, and this fraction can be spec
56 hia coli TonB was found to be distributed in sucrose density gradients approximately equally between
57 ibosome profiles upon centrifugation through sucrose density gradients, association of mutant 30 S su
58 high-speed centrifugation and sedimented in sucrose density gradients at the same bouyant density as
60 y Triton insoluble membranes that floated in sucrose density gradients but was recruited to these mem
61 h these proteins and comigrated with them on sucrose density gradients, but it did not colocalize, co
62 ower sedimentation rate than native virus on sucrose density gradients, but the particles retained al
63 ndicated by immunofluorescence localization, sucrose density gradients, cell fractionation, and yeast
64 However, the splitting was observed with sucrose density gradient centrifugation (SDGC) without I
67 ner and outer membranes were fractionated by sucrose density gradient centrifugation and identified b
68 wing both ATP-sensitive microtubule affinity/sucrose density gradient centrifugation and immunoprecip
69 ocytosis" into the light vesicle fraction in sucrose density gradient centrifugation assays, as did t
74 onocytogenes 100S ribosomes were observed by sucrose density gradient centrifugation of bacterial ext
75 Viral core-like complexes were isolated by sucrose density gradient centrifugation of detergent-tre
76 to ET-1 in subcellular fractions obtained by sucrose density gradient centrifugation of human umbilic
79 gent-insoluble membrane fraction prepared by sucrose density gradient centrifugation of postnuclear f
85 Characterization of the circulating mRNAs by sucrose density gradient centrifugation revealed that th
88 se of internal ribosome entry mechanisms and sucrose density gradient centrifugation showed that BC1-
92 dily detected in outer membranes produced by sucrose density gradient centrifugation, but it is sarco
96 nd when subjected to size-exclusion HPLC and sucrose density gradient centrifugation, in the presence
97 fferent approaches including gel filtration, sucrose density gradient centrifugation, pull-down of di
99 pheroplasting and osmotic lysis, followed by sucrose density gradient centrifugation, which separated
101 enriched membranes with DodGlc2, followed by sucrose density gradient centrifugation, yielded a super
115 wever, we show by chemical cross-linking and sucrose density-gradient centrifugation that in the abse
116 amination by aqueous two-phase partitioning, sucrose density-gradient centrifugation, and immunoelect
117 roteins by size exclusion chromatography and sucrose-density gradient centrifugation revealed that th
118 performed gel filtration chromatography and sucrose density gradient centrifugations in H(2)O and D(
119 We have used immunogold localization and sucrose density gradient cosedimentation analyses to con
120 Subcellular fractionation using equilibrium sucrose density gradients demonstrated decreased hyperph
129 f epitope-tagged versions of Upf proteins by sucrose density gradient fractionation of soluble lysate
136 form of CD39L4 by measuring the activity of sucrose density gradient fractions of monomers and parti
137 asts, as well as subcellular fractionations, sucrose density gradients, immunocytochemical labeling,
138 at Pixie associates with the 40 S subunit on sucrose density gradients in an ATP-dependent manner.
139 FP-modified Rab5 as a larger mass complex on sucrose density gradients indicates that it binds to oth
140 ediments with the product of the LF1 gene in sucrose density gradients, indicating that these protein
143 radiolabeling with [(3)H]palmitic acid, and sucrose density gradient membrane partitioning studies.
145 65 recognized a protein of roughly 65 kDa in sucrose density gradient-purified HHV-7 preparations; tr
146 al detergent extraction and fractionation in sucrose density gradients revealed TcdB-induced redistri
147 as released from infected cells; analysis on sucrose density gradients revealed that the precursor se
148 ntact sites were analyzed using a continuous sucrose density gradient, revealing an apparent heteroge
152 ere expressed in COS-1 cells and analyzed by sucrose density gradient sedimentation and gel filtratio
155 on X-100 in combination with gel filtration, sucrose density gradient sedimentation, and gel electrop
158 enzyme was constructed and characterized by sucrose-density gradient sedimentation, size-exclusion c
165 s of LIV during rate-zonal centrifugation in sucrose density gradients, suggesting that the enzyme is
166 er proteins as its sedimentation behavior in sucrose density gradient suggests an association with th
167 ments (L and R-DNA-gp3) sedimented faster in sucrose density gradients than their proteinase K-treate
168 branes were subfractionated on discontinuous sucrose density gradients to equilibrium or under nonequ
169 study, we used equilibrium sedimentation in sucrose density gradients to separate PrP(Sc) aggregates
173 mmunoprecipitation, confocal microscopy, and sucrose density gradient ultracentrifugation in mice.
174 ligomeric state of the purified complexes by sucrose density gradient ultracentrifugation revealed th
177 combination of both confocal microscopy and sucrose density gradient ultracentrifugation, we show th
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