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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
41                                        Using density gradient centrifugation, a subcellular compartme
42  heat gave only two fractions on equilibrium density gradient centrifugation: a fraction comprised of
43                                              Density gradient centrifugation, affinity purification,
44 ffectively separated from each other by CsCl density gradient centrifugation alone.
45 partitioned to the cytoplasmic fraction, and density gradient centrifugation analysis demonstrated th
46                       Using a combination of density gradient centrifugation and agarose gel electrop
47 ated through multiple rounds of differential density gradient centrifugation and analyzed by immunoel
48                                Using sucrose density gradient centrifugation and antibody pulldowns,
49 Triton X-100 extraction followed by OptiPrep density gradient centrifugation and cholera toxin beta-s
50                             Instead, sucrose density gradient centrifugation and electron microscopy
51               Together with the results from density gradient centrifugation and fluorescence correla
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-
67 ion, native gel electrophoresis, and sucrose density gradient centrifugation assays.
68 ected in outer membranes produced by sucrose density gradient centrifugation, but it is sarcosyl solu
69         Moreover, chemical cross-linking and density gradient centrifugation demonstrate that there i
70                              Cesium chloride density gradient centrifugation demonstrated banding of
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
73                     Physical partitioning by density gradient centrifugation did not separate phyllos
74 le proteins from the melanosome fractions by density gradient centrifugation does not diminish organe
75  centrifugation (DC) and equilibrium buoyant density gradient centrifugation (EBDC).
76  away from mosquito salivary gland debris by density gradient centrifugation eliminated salivary glan
77                                   Continuous density gradient centrifugation enriched NEP activity in
78                           On the other hand, density gradient centrifugation experiments suggested a
79             A comparison of proteins in CsCl density gradient centrifugation fractions from supernata
80                 A cell fraction separated by density gradient centrifugation from blood had TSC2 LOH
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
84                                      Sucrose density gradient centrifugation, immunoblot, and immunoh
85                    Enzymatic assays, sucrose density gradient centrifugation, immunoprecipitation, do
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
88                                         CsCl density gradient centrifugation indicated that almost al
89                                              Density gradient centrifugation indicated that, unlike s
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
92                                      Sucrose density gradient centrifugation of a maize mitochondrial
93                                        After density gradient centrifugation of a microsomal fraction
94                                      Sucrose density gradient centrifugation of A6 cell detergent ext
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
97                                In agreement, density gradient centrifugation of heated and nonheated
98 in subcellular fractions obtained by sucrose density gradient centrifugation of human umbilical vein
99                                              Density gradient centrifugation of IgG1 molecules indica
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                                   By sucrose density gradient centrifugation of membranes, however, m
104 oluble membrane fraction prepared by sucrose density gradient centrifugation of postnuclear fraction
105                                      Sucrose density gradient centrifugation of postnuclear supernata
106                           Similarly, sucrose density gradient centrifugation of purified MAO B exhibi
107                                              Density gradient centrifugation of subcellular organelle
108                                      Sucrose density gradient centrifugation of the culture medium re
109                                      Sucrose density gradient centrifugation of the ribosomal fractio
110                                              Density gradient centrifugation of Triton X-100 lysates
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
114                                              Density gradient centrifugation procedures reduce the le
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
118                        Discontinuous sucrose density gradient centrifugation revealed NET in the lipi
119                                              Density gradient centrifugation revealed that in the ini
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
124                                      Sucrose density gradient centrifugation reveals two major forms
125 tems, were calculated from isopycnic banding density gradient centrifugation runs.
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
130                                      Sucrose density gradient centrifugation showed that exposure of
131                                              Density gradient centrifugation showed that secreted apo
132 eparation of purified E1 proteins by sucrose density gradient centrifugation showed that the wild-typ
133                                      Sucrose density-gradient centrifugation showed that the oleosins
134 he transducing particles by equilibrium CsCl density-gradient centrifugation showed that the particle
135                    Correspondingly, glycerol density gradient centrifugation shows that at neutral pH
136                                              Density gradient centrifugation studies reveal that thes
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
139                                Using sucrose density gradient centrifugation, this study evaluated wh
140                                Using sucrose density gradient centrifugation to analyze ribosome comp
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
143                                      We used density gradient centrifugation to isolate LDL in plasma
144 ed onto WBC isolation media and subjected to density gradient centrifugation to measure WBC-associate
145      Livers were removed and fractionated by density gradient centrifugation to obtain endosomal and
146                               Using alkaline density-gradient centrifugation to separate repaired DNA
147 uorescent labeling, ultracentrifugation, and density gradient centrifugation, virtually all CD46 was
148                         Isopycnic banding by density gradient centrifugation was used to measure dens
149 sting and osmotic lysis, followed by sucrose density gradient centrifugation, which separated OMs fro
150                          As shown by sucrose density gradient centrifugation, WT gamma-PAK, S490A, an
151  membranes with DodGlc2, followed by sucrose density gradient centrifugation, yielded a super complex

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