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1 nrelated extracellular vesicles with similar buoyant density.
2 lose and separated by rate sedimentation and buoyant density.
3 entry of HCV particles independent of their buoyant density.
4 iwall nanotubes through differences in their buoyant density.
5 les, and in membrane structures with a lower buoyant density.
6 form, also brings about a similar change in buoyant density.
7 ry granules and were similar to lysosomes in buoyant density.
8 h full-length genomes based on their lighter buoyant density.
9 d little or no impact on apoB28 secretion or buoyant density.
10 cal sedimentation coefficients and different buoyant densities.
11 apolipoprotein (apo) association as well as buoyant densities.
12 s in distribution of HCV in a broad range of buoyant densities.
13 ants to engineer subtle differences in their buoyant densities.
14 kinetics, higher peak titers, and increased buoyant densities.
15 ectious virus particles have low to very low buoyant densities.
16 were associated with a membrane fraction of buoyant density 1.10-1.14 g ml-1, which partially overla
18 zed in the OM, which contained areas of high buoyant density (1.21 to 1.24 g cm(-3)) and low buoyant
19 entation value of approximately 100S, have a buoyant density (1.28 g/ml) on cesium chloride similar t
20 ional analyses, including PCR amplification, buoyant density analysis in a CsCl gradient, and immunop
21 tinct populations of vesicles with different buoyant densities and sedimentation coefficients were de
23 lt, HCV virions display a characteristic low buoyant density and a deceiving coat, with host-derived
24 ed a membrane bilayer and displayed a higher buoyant density and a lower infectivity-to-HCV RNA ratio
26 -protein crosslinked material has an altered buoyant density and can be purified by banding in cesium
27 R were enriched on the basis of their unique buoyant density and composition of cholesterol, caveolin
28 EV subset was smaller and exhibited a higher buoyant density and distinct phospholipid composition co
29 opurified with RNA polymerase complexes, and buoyant density and polymerase studies suggest that C. p
30 in lysates had a surprising range of sizes, buoyant densities, and distinct relative amounts of enca
31 cholesterol and sphingolipids, have a light buoyant density, and function in both endocytosis and ce
32 for lacking cell attachment protein sigma1), buoyant density, and particle morphology by scanning cry
33 that have the sedimentation coefficient, the buoyant density, and the protein composition similar to
34 rticle complexes of progressively decreasing buoyant density, approaching the density of protein alon
35 esistant membranes (DRM-H) exhibits a higher buoyant density ( approximately 1.16 g/ml) because of as
36 (approximately 65 to 70 nm) but different in buoyant density (approximately 1.15 to 1.20 g/ml) from e
37 fied recombinant vesicles: (i) have the same buoyant density as mammalian caveolae; (ii) appear as ap
38 ent-resistant fraction was isolated as a low buoyant density band on sucrose density gradients and ex
39 4p were similar morphologically and in their buoyant density, but larger than normal COPII vesicles (
40 subunit of the rod CNG channel) with the low buoyant density, caveolin-1-enriched membranes was also
43 nlarged heteromorphic lamellar structures by buoyant density centrifugation and subsequent SDS-PAGE a
46 n-1 in ROS almost exclusively resides in low-buoyant-density, cholesterol-rich, detergent-resistant m
50 d two-surfactant micelle, leading to a large buoyant density difference between the electronic specie
51 radient centrifugation: one subpopulation of buoyant density equivalent to 22% to 28% (w/w) Suc; the
52 hes from a mixture of membranes with similar buoyant densities following Lubrol WX extraction or soni
54 disk membranes because detergent-treated low buoyant density fractions isolated from homogenates with
55 tched and caveolin-1 can be co-isolated from buoyant density fractions that represent caveolae/raft m
56 hout disinfection and at successively higher buoyant densities from monthly disposable contact lenses
58 A glycogen selection/screening regimen of buoyant density gradient centrifugation and iodine vapor
60 y of Golgi-derived or endosomal membranes in buoyant density gradients, although changes in ionic str
61 -tagged Och1p reside in a compartment with a buoyant density identical to that of wild-type Och1p and
62 MUC2, and MUC5AC mucins eluted mainly at low buoyant densities in extractions from lenses worn long t
64 gments (DRMs) that exhibit a relatively high buoyant density in sucrose (DRM-H; d approximately 1.16
67 ere enriched in a minor membrane fraction of buoyant density intermediate between that of cytoplasmic
68 fferent chromatin regions according to their buoyant density may bias chromatin immunoprecipitation r
69 ranes, since adenylyl cyclase targets to low buoyant density membrane fractions of HEK cells that lac
70 for enhancement of its association with low buoyant density membrane fractions, commonly termed lipi
71 Gp and Pex3p budded vesicles sediment as low-buoyant-density membranes on a Nycodenz gradient and cop
72 ntified in cell lysates; these particles had buoyant densities of 1.06 and 1.12 to 1.17 g/ml in sucro
73 features of beta-retroviruses sedimenting at buoyant densities of 1.12 to 1.18 g/mL in sucrose gradie
74 lucose or [12C,1H]glucose, respectively) had buoyant densities of 1.643 and 1.585 g ml-1, respectivel
75 us particles produced from the culture had a buoyant density of 1.13 to 1.15 g/ml in sucrose and coul
78 density gradient ultracentrifugation, had a buoyant density of 1.375 g/cm3 and consisted of a head (
81 The virus particles in the medium had the buoyant density of extracellular enveloped viruses (EEV)
83 since NP-40 did not significantly affect the buoyant density of HCV replication complexes or protease
85 In an equilibrium gradient, Tgl bands at the buoyant density of membranes and with the NADH-oxidase a
86 ficients as well as the molecular weight and buoyant density of rat mitochondrial ribosomes were dete
93 repares an insoluble membrane fraction whose buoyant density permits its flotation in discontinuous s
94 usage did not correlate with a change in the buoyant density profiles of the variants, suggesting an
96 le from the vesicles formed in vivo by their buoyant density, protein composition, topology, and morp
97 of PI4KIIalpha and its association with low buoyant density "raft" domains are critically dependent
98 man B lymphocytes, isolated as a function of buoyant density, require activation for up-regulation of
101 oped a novel approach based upon a selective buoyant density shift of the brain lysosomes in a mutant
102 insulator or boundary elements are found at buoyant densities similar to those of free protein and a
105 ese putative capsule mutants have dissimilar buoyant densities, suggesting different levels of capsul
106 (HCV) particles display a distinctly higher buoyant density than do secreted virus particles, sugges
107 V correlated with virions of a lower average buoyant density than HCVcc, suggesting that physical ass
108 subdomains separable by means of their light buoyant densities through sucrose density gradient centr
109 e 2B and 2C proteins, membranes identical in buoyant density to those observed during poliovirus infe
110 ecular-weight protein complexes shifts their buoyant density to values much lower then that of bulk c
113 t VLDL maturation (as assessed by changes in buoyant density) was associated with conformational chan
114 ious virus subpopulations differing in their buoyant densities, we show that these HCV particles util
115 dichalcogenides due to their high intrinsic buoyant densities when encapsulated with ionic small mol
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