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1 PHB-containing bacteria were concentrated by density gradient centrifugation.
2 riched membrane fractions as seen by sucrose density gradient centrifugation.
3 and size fractionation were purified by CsCl density gradient centrifugation.
4 nate without detergent), followed by sucrose density gradient centrifugation.
5 preparation was purified by cesium chloride density gradient centrifugation.
6 reitol (DTT)-mediated reduction, and buoyant density gradient centrifugation.
7 erol were incubated and subjected to sucrose density gradient centrifugation.
8 papain and DNase digestion, trituration, and density gradient centrifugation.
9 ed from cells and from membrane fragments by density gradient centrifugation.
10 Oocysts were initially isolated by sucrose density gradient centrifugation.
11 nts with lysosomal enzyme markers by Percoll density gradient centrifugation.
12 iltration column but were made visible after density gradient centrifugation.
13 suspension-cultured cells following sucrose density gradient centrifugation.
14 consistent with previous measurements using density gradient centrifugation.
15 olated by collagenase-pronase-perfusion, and density gradient centrifugation.
16 ith centrosome fractions isolated by sucrose density gradient centrifugation.
17 psin population was isolated and purified by density gradient centrifugation.
18 hromatographic matrices followed by glycerol density gradient centrifugation.
19 to be an outer membrane protein by isopycnic density gradient centrifugation.
20 fferent fractions by detergent treatment and density gradient centrifugation.
21 llagenase digestion of the liver followed by density gradient centrifugation.
22 additional separation using cesium chloride density gradient centrifugation.
23 te, and in particulate fractions obtained by density gradient centrifugation.
24 lubilized oligomers was confirmed by sucrose density gradient centrifugation.
25 and/or membrane fractionation using OptiPrep density gradient centrifugation.
26 of detergent extraction and differential and density gradient centrifugation.
27 to insulin binding as determined by sucrose density gradient centrifugation.
28 ble membranes then were separated by sucrose density gradient centrifugation.
29 heir light buoyant densities through sucrose density gradient centrifugation.
30 s and luminal contents were subjected to KBr density gradient centrifugation.
31 disruption and initial separation by sucrose density gradient centrifugation.
32 ticks by velocity centrifugation and Percoll density gradient centrifugation.
33 of gel filtration chromatography and sucrose density gradient centrifugation.
34 g low- and high-salt extractions followed by density gradient centrifugation.
35 Mucins were separated by cesium chloride density gradient centrifugation.
36 Mouse BMCs were isolated by density-gradient centrifugation.
37 from stationary-phase (SP) yeast cultures by density-gradient centrifugation.
38 genase perfusion of the liver and subsequent density-gradient centrifugation.
39 rbon source, can be resolved from 12C-DNA by density-gradient centrifugation.
40 gated these species by Blue Native PAGE, Suc density gradient centrifugation, 77K fluorescence, circu
42 heat gave only two fractions on equilibrium density gradient centrifugation: a fraction comprised of
45 partitioned to the cytoplasmic fraction, and density gradient centrifugation analysis demonstrated th
47 ated through multiple rounds of differential density gradient centrifugation and analyzed by immunoel
49 Triton X-100 extraction followed by OptiPrep density gradient centrifugation and cholera toxin beta-s
52 l-enriched LRs were isolated from Giardia by density gradient centrifugation and found to be sensitiv
53 outer membranes were fractionated by sucrose density gradient centrifugation and identified by appear
54 h ATP-sensitive microtubule affinity/sucrose density gradient centrifugation and immunoprecipitation
55 cogen selection/screening regimen of buoyant density gradient centrifugation and iodine vapor colony
56 ance of hydrodynamically large structures in density gradient centrifugation and native gel electroph
57 -purify with high density lipoprotein during density gradient centrifugation and subsequent gel filtr
58 re isolated from adult mice via Ficoll-Paque density-gradient centrifugation and cultured in the pres
59 e wild-type helper virus by CsCl equilibrium density-gradient centrifugation and used to superinfect
60 homogeneity by a combination of elutriation, density gradient centrifugation, and 48-hour culture.
61 from normal human subjects with Ficoll-Paque density gradient centrifugation, and adherent cells were
62 volunteers (n=7) were isolated using Ficoll density gradient centrifugation, and plated on fibronect
63 were purified by negative viscosity-positive density gradient centrifugation, and their component pro
64 analyzed purified MUC2-N by gel filtration, density gradient centrifugation, and transmission electr
65 n by aqueous two-phase partitioning, sucrose density-gradient centrifugation, and immunoelectron micr
66 " into the light vesicle fraction in sucrose density gradient centrifugation assays, as did the wild-
68 ected in outer membranes produced by sucrose density gradient centrifugation, but it is sarcosyl solu
71 Immunoblotting of rafts isolated by sucrose density gradient centrifugation demonstrated recruitment
72 r, pulse-chase studies employing metrizamide density gradient centrifugation demonstrated that the gl
74 le proteins from the melanosome fractions by density gradient centrifugation does not diminish organe
76 away from mosquito salivary gland debris by density gradient centrifugation eliminated salivary glan
81 d mononuclear cells (PBMCs) were isolated by density gradient centrifugation from the blood of patien
82 ents from infected cells by differential and density gradient centrifugation further indicated that P
83 Mutant viral particles, purified by sucrose density gradient centrifugation, had low infectivity and
86 ed gel filtration chromatography and sucrose density gradient centrifugations in H(2)O and D(2)O, and
87 subjected to size-exclusion HPLC and sucrose density gradient centrifugation, in the presence of DodG
90 the native enzyme when subjected to glycerol density gradient centrifugation, indicating that they fo
91 to known proteoglycans; purified using CsCl density gradient centrifugation, molecular sieve, and io
95 enes 100S ribosomes were observed by sucrose density gradient centrifugation of bacterial extracts du
96 core-like complexes were isolated by sucrose density gradient centrifugation of detergent-treated vir
98 in subcellular fractions obtained by sucrose density gradient centrifugation of human umbilical vein
104 oluble membrane fraction prepared by sucrose density gradient centrifugation of postnuclear fraction
111 fractionated into two subpopulations by Suc density gradient centrifugation: one subpopulation of bu
112 o exclude nonviable cells require the use of density gradient centrifugation or antibody-based cell s
113 solated from peripheral blood by a series of density-gradient centrifugations or magnetic bead separa
115 veolin-containing lipid-rich fraction during density gradient centrifugation, properties that are con
116 approaches including gel filtration, sucrose density gradient centrifugation, pull-down of differenti
117 When yeast cell lysates are fractionated by density gradient centrifugation, Qsr1p separates from or
120 rization of the circulating mRNAs by sucrose density gradient centrifugation revealed that the liver-
121 by size exclusion chromatography and sucrose-density gradient centrifugation revealed that the phosph
122 tion of organelles in the pellet fraction by density gradient centrifugation revealed that VLCS activ
123 amination of lipid rafts isolated by sucrose density gradient centrifugation revealed the constitutiv
126 ver, the splitting was observed with sucrose density gradient centrifugation (SDGC) without IF3 if RR
127 od mononuclear cells were isolated by Ficoll density gradient centrifugation, separated into cellular
128 f the Golgi complex into two fractions using density gradient centrifugation showed effects of aged A
129 ternal ribosome entry mechanisms and sucrose density gradient centrifugation showed that BC1-mediated
132 eparation of purified E1 proteins by sucrose density gradient centrifugation showed that the wild-typ
134 he transducing particles by equilibrium CsCl density-gradient centrifugation showed that the particle
137 e HbE/beta thalassemia; this is confirmed by density-gradient centrifugation studies that show no dec
138 e show by chemical cross-linking and sucrose density-gradient centrifugation that in the absence of b
141 we have combined pulse-chase techniques with density gradient centrifugation to identify, isolate, an
142 Triton X-100 at 4 degrees C and subjected to density gradient centrifugation to isolate DRMs from the
144 ed onto WBC isolation media and subjected to density gradient centrifugation to measure WBC-associate
147 uorescent labeling, ultracentrifugation, and density gradient centrifugation, virtually all CD46 was
149 sting and osmotic lysis, followed by sucrose density gradient centrifugation, which separated OMs fro
151 membranes with DodGlc2, followed by sucrose density gradient centrifugation, yielded a super complex
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