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1 ynamics of density gradient formation in the ultracentrifuge.
2 opseudomonas sphaeroides using an air-driven ultracentrifuge.
3 ticles were studied as a population using an ultracentrifuge.
4 reparative scale equipment to the air-driven ultracentrifuge allows the rapid isolation of ICM vesicl
5 locity/equilibrium methods in the analytical ultracentrifuge and by immunoprecipitation using an anti
6                                  Equilibrium ultracentrifuge and circular dichroism (CD) studies of a
7 esulted in about 15 years of research on the ultracentrifuge and its application to the study of biol
8  sedimentation equilibrium in the analytical ultracentrifuge and model-independent SEDFIT-MSTAR analy
9             iSCA v1.0 requires the use of an ultracentrifuge, and only about half of the nucleic acid
10 ssing MTP, HepG2 cells, and mouse liver were ultracentrifuged, and MTP was visualized in different de
11 cco mosaic virus led to our investigating an ultracentrifuge anomaly and the construction of a synthe
12 The mutant actin sediments in the analytical ultracentrifuge as a homogeneous monomeric species of 3.
13 d brain myosin V sediments in the analytical ultracentrifuge at 14 S as opposed to 11 S in the presen
14 Escherichia coli cells are centrifuged in an ultracentrifuge at high speed, 5-20% of the enzyme II ac
15                                   Plasma was ultracentrifuged at 17,000g for 60 minutes, and the micr
16 were adjusted to a density of 1.03 g/mL, and ultracentrifuged at 42,000 rpm and 37 degrees C for 13 h
17 luorescence detector for the XL-I analytical ultracentrifuge (AU-FDS) enables two different types of
18                               The analytical ultracentrifuge (AUC) and the modern field of analytical
19 angle X-ray scattering (SAXS) and analytical ultracentrifuge (AUC) techniques were applied to determi
20 ent sedimentation velocity in the analytical ultracentrifuge (AUC).
21 canning system of the Optima XL-I analytical ultracentrifuge can exhibit time-invariant noise compone
22 need to be excluded from the analysis due to ultracentrifuge cell end effects.
23 g also demonstrated formation of vesicles in ultracentrifuged Ch-unsaturated model bile (cholesterol
24     Sedimentation velocity in the analytical ultracentrifuge combined with calibrated gel chromatogra
25                                   Analytical ultracentrifuge data indicate that the hybrids have pred
26 S) that they are cleared from the analytical ultracentrifuge even at low speed (1500 rpm).
27                            The far-UV CD and ultracentrifuge experiments, however, indicated relative
28 nder AU conditions) in the time frame of our ultracentrifuge experiments.
29            A new generation of compact, fast ultracentrifuges facilitates the rapid and fully informa
30 ydrates significantly decreased the size and ultracentrifuge flotation rate of the major LDL and the
31 romatography of biles (TC/(TC + EYPC) = 0.7) ultracentrifuged for various durations showed a progress
32     Velocity sedimentation in the analytical ultracentrifuge gave a single sedimenting species with a
33 and sedimentation velocity in the analytical ultracentrifuge glargine was shown to be primarily dimer
34                        CAJ/Mnt mixtures were ultracentrifuged in order to separate them into supernat
35 s been developed based on the structural and ultracentrifuge information.
36 n addition, the purification method using an ultracentrifuge is tedious and labor-intensive.
37 ng cells by the conventional method using an ultracentrifuge, it resulted in a low yield.
38 apsed time in data files from the analytical ultracentrifuge, leading to overestimates of the sedimen
39                                              Ultracentrifuged material derived from sonicates of IFN-
40                 We present a simple and fast ultracentrifuge method here for two platinum compounds a
41  little inflammation as that obtained by the ultracentrifuge method.
42  sedimentation equilibrium in the analytical ultracentrifuge of (3.0 0.1) kDa and (4.2 0.2) kDa for s
43  Sedimentation equilibrium in the analytical ultracentrifuge of a dilute solution of protein (0.4 mg/
44 m HIV-infected individuals was collected and ultracentrifuged over 20% sucrose to isolate virions fro
45                                  Add-back of ultracentrifuge pellets (enriched in EVs but possibly ot
46  pol, and env regions of RNAs, prepared from ultracentrifuged pellets of filtered supernatants, indic
47                                              Ultracentrifuge results indicate the presence of three o
48 dimentation-diffusion equilibrium analytical ultracentrifuge (SE-AUC) to demonstrate that the suppres
49  sedimentation equilibrium in the analytical ultracentrifuge (SEDFIT, SEDFIT-MSTAR and MULTISIG analy
50 oligomeric state of dynamin II by analytical ultracentrifuge sedimentation equilibrium measurements a
51 ng size exclusion chromatography, analytical ultracentrifuge sedimentation, circular dichroism, trans
52 g the UV absorption optics of the analytical ultracentrifuge.Selective monitoring of SinR in mixtures
53 n equilibrium measurements in the analytical ultracentrifuge show that both wild-type and C14S Sml1p
54                                   Analytical ultracentrifuge studies on Smad3 and Smad4 protein const
55           In addition, the SPI1-MSPalphabeta ultracentrifuge studies reveal a low abundance 2:2 compl
56                                   Analytical ultracentrifuge studies revealed that in solution, the r
57 lls isolated from ascites, and the cell-free ultracentrifuged supernatant.
58 es: sedimentation velocity in the analytical ultracentrifuge (SV-AUC), dynamic light scattering (DLS)
59 tion of the Rayleigh interferometer onto the ultracentrifuge that had the greatest impact on our furt
60 ng in conjunction with the latest analytical ultracentrifuge, the Optima AUC by Beckman Coulter.
61 n site was investigated using the analytical ultracentrifuge to analyze heterodimers formed from reco
62  sedimentation equilibrium in the analytical ultracentrifuge to describe self-association under nonid
63                   iCM-conditioned medium was ultracentrifuged to collect mitochondria-rich EVs (M-EVs
64                              This sample was ultracentrifuged to obtain a lipoprotein density distrib
65 Serial bronchoalveolar lavage specimens were ultracentrifuged to obtain the exosomal pellet for RNA e
66  sedimentation equilibrium in the analytical ultracentrifuge together with capillary (rolling ball) v
67 rescence detection system for the analytical ultracentrifuge, we examined allosteric changes in PDE6
68  a recent study comparing various analytical ultracentrifuges, we showed that external calibration of
69 ation velocity experiments in the analytical ultracentrifuge were performed to identify different PAI
70                   By equipping an analytical ultracentrifuge with a novel multi-wavelength detector,
71 and sedimentation velocity in the analytical ultracentrifuge with viscometry.