ライフサイエンスコーパス: equilibrium dialysis

1 unbound plasma concentration (determined by equilibrium dialysis).

2 s between a protein and a small ion based on equilibrium dialysis.

3 Daptomycin protein binding was determined by equilibrium dialysis.

4 g affinity was measured quantitatively using 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 assess the bioavailability of calcium using equilibrium dialysis after simulated gastric digestion m

11 rase A3-3 (mGSTA3-3) has been measured using equilibrium dialysis and a direct fluorescence quenching

12 ) binding capacity of cCSQ was checked using equilibrium dialysis and atomic absorption spectroscopy,

13 e formyltransferase (rmGARFT) was studied by equilibrium dialysis and by steady-state kinetics using

14 aramagnetic resonance (EPR) spectroscopy and equilibrium dialysis and isothermal titration calorimetr

15 Equilibrium dialysis and pre-steady-state kinetic analys

16 hyroxine and several thyroxine analogs using equilibrium dialysis and quenching of tryptophan 214 flu

17 ding of thyroxine to these HSA species using equilibrium dialysis and quenching of tryptophan 214 flu

18 Results from ICP analysis after equilibrium dialysis and relaxation assays with limiting

19 We present equilibrium dialysis and saturation transfer difference

20 ants using isothermal titration calorimetry, equilibrium dialysis and scintillation proximity assays.

21 8.5 +/- 2.6 microm for AcCoA obtained using equilibrium dialysis and to the K(i) (inhibition constan

22 Equilibrium dialysis and turbidity measurements showed t

23 teins were characterized by a combination of equilibrium dialysis and UV/visible, EPR, and hyperfine-

24 nts of substrate/product binding affinities (equilibrium dialysis), and a pre-steady-state quench-flo

25 We use fluorescence, circular dichroism, equilibrium dialysis, and activity measurements to demon

26 a(2+) in a cooperative manner as assessed by equilibrium dialysis, and its circular dichroism spectru

27 ivo reporter and in vitro expression assays, equilibrium dialysis, and northern analysis, we show tha

28 ommon substrate 1-chloro 2,4-dinitrobenzene, equilibrium dialysis, and tryptophan quenching.

29 and defined using controlled trypsinolysis, equilibrium dialysis at low temperature, and kinetic ana

30 In equilibrium dialysis, BAD-1 bound 45Ca2+ with an affinit

31 Equilibrium dialysis confirmed that mutant rFV(a2)-C2 do

32 Equilibrium dialysis demonstrated that the equilibrium d

33 idovudine, and the results were confirmed by equilibrium dialysis determinations.

34 cribed here enables the user to customize an equilibrium dialysis device to fit their own experiments

35 The liposome dialyzer is a small-volume equilibrium dialysis device, built from commercially ava

36 a(2+) was removed from the proteins prior to equilibrium dialysis, E3CaG-2 bound 22-27 Ca(2+), CaG-2

37 The equilibrium dialysis experiments and kinetic data suppor

38 nd TMEi4-6 (Val345-Cys462) were prepared for equilibrium dialysis experiments by exhaustive dialysis

39 Equilibrium dialysis experiments detected binding of 4,

40 Equilibrium dialysis experiments identified three Mn2+-

41 Equilibrium dialysis experiments indicate a binding stoi

42 e spectroscopy, DNA winding, viscometry, and equilibrium dialysis experiments indicate that the napht

43 Equilibrium dialysis experiments provide an estimated bi

44 Equilibrium dialysis experiments show that purified MobB

45 Equilibrium dialysis experiments suggested one bound lig

46 Equilibrium dialysis experiments were performed using oc

47 OPC:POPE:cholesterol lipid vesicles (LUV) in equilibrium dialysis experiments.

48 only one binding site/dimer was detected in equilibrium dialysis experiments.

49 NMR and equilibrium dialysis failed to demonstrate binding of le

50 te and (6R)-CH3-H4folate to MeTr by 13C NMR, equilibrium dialysis, fluorescence quenching, and proton

51 ded DNA, have been studied quantitatively by equilibrium dialysis, fluorescence spectroscopy, and cir

52 Equilibrium dialysis, fluorescent hydrophobic probe bind

53 Equilibrium dialysis indicated that the competitive inhi

54 n paramagnetic resonance (EPR) spectroscopy, equilibrium dialysis, intrinsic tryptophan fluorescence

55 Equilibrium dialysis is a simple and effective technique

56 binding site for forskolin was identified by equilibrium dialysis; its Kd (0.1 microM) corresponds to

57 ivity, circular dichroism, fluorescence, and equilibrium dialysis measurements on proteolytic and bio

58 bind 1.9 +/- 0.2 Ni(II) ions as assessed by equilibrium dialysis measurements, compared with the 6.0

59 ion constant) per UreD protomer according to equilibrium dialysis measurements.

60 was determined, using a specially developed equilibrium dialysis method.

61 y using isothermal titration calorimetry and equilibrium dialysis methods, suggesting that the ligand

62 In equilibrium dialysis, N-Gal-1 and V5D-Gal-1 bind N-acety

63 Equilibrium dialysis of constructs comprised of the adjo

64 Equilibrium dialysis of methionyl aminopeptidase from Es

65 Equilibrium dialysis of the soluble TM analogs in [45Ca2

66 ayed by atomic absorption spectroscopy or an equilibrium dialysis protocol in which Ca(2+) was remove

67 assays, limited proteolysis protection, and equilibrium dialysis, provide evidence that the amino-te

68 erestingly, the binding constant measured by equilibrium dialysis, rather than by monitoring a locali

69 tary approaches: a direct approach of Donnan equilibrium dialysis read out by atomic emission spectro

70 d by ITC are in good agreement with previous equilibrium dialysis results, after differences in pH an

71 NMR titration and equilibrium dialysis showed that both substrates and pro

72 Results from equilibrium dialysis, STD-NMR, and noncovalent mass spec

73 While X-ray crystallography and equilibrium dialysis suggested two sugar-combining sites

74 aphy/tandem mass spectrometry detection, the equilibrium dialysis technique that is conventionally us

75 ng of alpha 2m to IL-8 was measured using an equilibrium dialysis technique, and Kd was 30 nM.

76 mustine binding to tubulin was determined by equilibrium dialysis to be 23 +/- 5 mM.

77 nd phosphoribosylpyrophosphate were shown by equilibrium dialysis to bind to free PyrR (dissociation

78 We use fluorescence, circular dichroism, and equilibrium dialysis to demonstrate that (1) the FV C2 d

79 Using equilibrium dialysis to investigate binding of bis-ANS t

80 ization-defective RT proteins was studied by equilibrium dialysis, tryptophan fluorescence, and nativ

81 Analysis by equilibrium dialysis using (45)Ca and <400 microM free C

82 (K(i) = 4.6 mM) was observed as measured by equilibrium dialysis using 20 microM Ca2+ and 8 microM f

83 Equilibrium dialysis was used to study the binding of tw

84 the disaccharide to anti-Gal, as measured by equilibrium dialysis, was seven-fold lower than that of

85 By equilibrium dialysis we demonstrated that acetylation re

86 Equilibrium dialysis with (45)Ca(2+) revealed that recom

87 Equilibrium dialysis with (65)Zn(2+) revealed that Zn(2+

88 Equilibrium dialysis yields Adair constants of 4.2(0.1)