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1  unbound plasma concentration (determined by equilibrium dialysis).
2 Daptomycin protein binding was determined by equilibrium dialysis.
3 g affinity was measured quantitatively using equilibrium dialysis.
4 s between a protein and a small ion based on equilibrium dialysis.
5  the point at which it cannot be measured by equilibrium dialysis.
6 t flavocytochrome was normal, as measured by equilibrium dialysis.
7  manner, both in a protein blot assay and by equilibrium dialysis.
8 of those nucleotides for Rad51 determined by equilibrium dialysis.
9 hylene ATP (Ap(CH2)pp), was also detected by equilibrium dialysis.
10 itaxel in patient ascites were studied using equilibrium dialysis.
11  assess the bioavailability of calcium using equilibrium dialysis after simulated gastric digestion m
12 rase A3-3 (mGSTA3-3) has been measured using equilibrium dialysis and a direct fluorescence quenching
13 ) binding capacity of cCSQ was checked using equilibrium dialysis and atomic absorption spectroscopy,
14 e formyltransferase (rmGARFT) was studied by equilibrium dialysis and by steady-state kinetics using
15 aramagnetic resonance (EPR) spectroscopy and equilibrium dialysis and isothermal titration calorimetr
16  were investigated using in vitro digestion, equilibrium dialysis and kinetic analyses.
17                                              Equilibrium dialysis and pre-steady-state kinetic analys
18 hyroxine and several thyroxine analogs using equilibrium dialysis and quenching of tryptophan 214 flu
19 ding of thyroxine to these HSA species using equilibrium dialysis and quenching of tryptophan 214 flu
20              Results from ICP analysis after equilibrium dialysis and relaxation assays with limiting
21                                   We present equilibrium dialysis and saturation transfer difference
22 ants using isothermal titration calorimetry, equilibrium dialysis and scintillation proximity assays.
23  8.5 +/- 2.6 microm for AcCoA obtained using equilibrium dialysis and to the K(i) (inhibition constan
24                                              Equilibrium dialysis and turbidity measurements showed t
25 and labor efficient compared to conventional equilibrium dialysis and ultrafiltration methods.
26 teins were characterized by a combination of equilibrium dialysis and UV/visible, EPR, and hyperfine-
27 nts of substrate/product binding affinities (equilibrium dialysis), and a pre-steady-state quench-flo
28     We use fluorescence, circular dichroism, equilibrium dialysis, and activity measurements to demon
29 a(2+) in a cooperative manner as assessed by equilibrium dialysis, and its circular dichroism spectru
30 ivo reporter and in vitro expression assays, equilibrium dialysis, and northern analysis, we show tha
31 ommon substrate 1-chloro 2,4-dinitrobenzene, equilibrium dialysis, and tryptophan quenching.
32  and defined using controlled trypsinolysis, equilibrium dialysis at low temperature, and kinetic ana
33                                           In equilibrium dialysis, BAD-1 bound 45Ca2+ with an affinit
34                                              Equilibrium dialysis confirmed that mutant rFV(a2)-C2 do
35                                              Equilibrium dialysis demonstrated that the equilibrium d
36 idovudine, and the results were confirmed by equilibrium dialysis determinations.
37 cribed here enables the user to customize an equilibrium dialysis device to fit their own experiments
38      The liposome dialyzer is a small-volume equilibrium dialysis device, built from commercially ava
39 a(2+) was removed from the proteins prior to equilibrium dialysis, E3CaG-2 bound 22-27 Ca(2+), CaG-2
40                                          The equilibrium dialysis experiments and kinetic data suppor
41 nd TMEi4-6 (Val345-Cys462) were prepared for equilibrium dialysis experiments by exhaustive dialysis
42                                              Equilibrium dialysis experiments detected binding of 4,
43                                              Equilibrium dialysis experiments identified three Mn2+-
44                                              Equilibrium dialysis experiments indicate a binding stoi
45 e spectroscopy, DNA winding, viscometry, and equilibrium dialysis experiments indicate that the napht
46                                              Equilibrium dialysis experiments provide an estimated bi
47                                              Equilibrium dialysis experiments show that purified MobB
48                                              Equilibrium dialysis experiments suggested one bound lig
49                                              Equilibrium dialysis experiments were performed using oc
50 OPC:POPE:cholesterol lipid vesicles (LUV) in equilibrium dialysis experiments.
51  only one binding site/dimer was detected in equilibrium dialysis experiments.
52                                      NMR and equilibrium dialysis failed to demonstrate binding of le
53 te and (6R)-CH3-H4folate to MeTr by 13C NMR, equilibrium dialysis, fluorescence quenching, and proton
54 ded DNA, have been studied quantitatively by equilibrium dialysis, fluorescence spectroscopy, and cir
55                                              Equilibrium dialysis, fluorescent hydrophobic probe bind
56  developed mass spectrometry integrated with equilibrium dialysis for the discovery of allostery syst
57                                              Equilibrium dialysis indicated that the competitive inhi
58 n paramagnetic resonance (EPR) spectroscopy, equilibrium dialysis, intrinsic tryptophan fluorescence
59                                              Equilibrium dialysis is a simple and effective technique
60 binding site for forskolin was identified by equilibrium dialysis; its Kd (0.1 microM) corresponds to
61 ivity, circular dichroism, fluorescence, and equilibrium dialysis measurements on proteolytic and bio
62  bind 1.9 +/- 0.2 Ni(II) ions as assessed by equilibrium dialysis measurements, compared with the 6.0
63 ion constant) per UreD protomer according to equilibrium dialysis measurements.
64  was determined, using a specially developed equilibrium dialysis method.
65 y using isothermal titration calorimetry and equilibrium dialysis methods, suggesting that the ligand
66                                           In equilibrium dialysis, N-Gal-1 and V5D-Gal-1 bind N-acety
67                                              Equilibrium dialysis, native mass spectrometry, isotherm
68                                              Equilibrium dialysis of constructs comprised of the adjo
69                                              Equilibrium dialysis of methionyl aminopeptidase from Es
70                                              Equilibrium dialysis of the soluble TM analogs in [45Ca2
71 ayed by atomic absorption spectroscopy or an equilibrium dialysis protocol in which Ca(2+) was remove
72  assays, limited proteolysis protection, and equilibrium dialysis, provide evidence that the amino-te
73 erestingly, the binding constant measured by equilibrium dialysis, rather than by monitoring a locali
74 tary approaches: a direct approach of Donnan equilibrium dialysis read out by atomic emission spectro
75 d by ITC are in good agreement with previous equilibrium dialysis results, after differences in pH an
76                            NMR titration and equilibrium dialysis showed that both substrates and pro
77                        This was supported by equilibrium dialysis, STD-NMR experiments, and inhibitio
78                                 Results from equilibrium dialysis, STD-NMR, and noncovalent mass spec
79              While X-ray crystallography and equilibrium dialysis suggested two sugar-combining sites
80 aphy/tandem mass spectrometry detection, the equilibrium dialysis technique that is conventionally us
81 ng of alpha 2m to IL-8 was measured using an equilibrium dialysis technique, and Kd was 30 nM.
82                                              Equilibrium dialysis testing indicated a stronger bindin
83 mustine binding to tubulin was determined by equilibrium dialysis to be 23 +/- 5 mM.
84 nd phosphoribosylpyrophosphate were shown by equilibrium dialysis to bind to free PyrR (dissociation
85 We use fluorescence, circular dichroism, and equilibrium dialysis to demonstrate that (1) the FV C2 d
86                                        Using equilibrium dialysis to investigate binding of bis-ANS t
87     Here, we address this gap by using rapid equilibrium dialysis to measure the binding and f(unboun
88 ization-defective RT proteins was studied by equilibrium dialysis, tryptophan fluorescence, and nativ
89                                  Analysis by equilibrium dialysis using (45)Ca and <400 microM free C
90  (K(i) = 4.6 mM) was observed as measured by equilibrium dialysis using 20 microM Ca2+ and 8 microM f
91                                              Equilibrium dialysis was used to study the binding of tw
92 the disaccharide to anti-Gal, as measured by equilibrium dialysis, was seven-fold lower than that of
93                                           By equilibrium dialysis we demonstrated that acetylation re
94                                              Equilibrium dialysis with (45)Ca(2+) revealed that recom
95                                              Equilibrium dialysis with (65)Zn(2+) revealed that Zn(2+
96                                              Equilibrium dialysis yields Adair constants of 4.2(0.1)