ライフサイエンスコーパス: titration curve

1 the two folding transitions gives a complex titration curve.

2 te to +/- 0.1 pH unit at the midpoint of the titration curve.

3 near 7.5 and has a well-defined, single-pKa titration curve.

4 fication of fragment K(D) values from ligand titration curves.

5 lmer (MSV) equation for fitting fluorescence titration curves.

6 in calculating and interpreting complicated titration curves.

7 ammerhead RNA give very different isothermal titration curves.

8 ins the observed complex and varied spectral titration curves.

9 approximately described the observed (1) pH titration curve, (2) Ca, Mg, and Mn concentration by cat

10 -4) M), two peaks were observed in the force titration curve (adhesion force versus pH) at pH 4.5 and

11 We predict that such titration curves, along with accurate mass measurements,

12 The titration curves also indicate that the binding is anti-

13 cide with the midpoint of the far-UV CD acid titration curve and suggest that the protonation of one

14 d from the midpoint and slope of the calcium titration curve and the concentration of membrane bindin

15 te-Seq, that is capable of measuring binding titration curves and corresponding affinities for thousa

16 Simulations of titration curves and line shapes show that a primary dis

17 Calculations of titration curves and pH-stability profiles are presented

18 m electrostatic techniques, we calculate the titration curves and the stability of dimer and tetramer

19 nd some residues will have anomalous thermal titration curves and unusual baseline behaviour monitore

20 Potentiometric titration curves are analyzed using the NICA equations a

21 The titration curves are demonstrated to be pH-independent a

22 resis as unfolding and refolding equilibrium titration curves are non-coincident even after equilibra

23 For all three cases, the experimental pH titration curves are notably more consistent with the X-

24 Chemical shift-pH titration curves are obtained from cross-peaks for repor

25 )(2) [d(pGpG)] adduct exhibit pH-independent titration curves, attributable to the added effect of th

26 A significant difference in the titration curves between the holo and apo forms of the W

27 quilibrium concentrations of typical binding titration curves, but also the lineshapes of NMR spectra

28 Potentiometric acid-base titration curves collected on humic (nano)particles as a

29 The values, when plotted against pH, fit a titration curve corresponding to a pKa of 8.4 +/- 0.1.

30 be defined as the point of singularity in a titration curve, corresponding to the solution pH value

31 Second, by numerical integration of H(+) titration curves (Delta) measured potentiometrically und

32 The measurement of titration curves eliminates the confounding effects of a

33 tead, proton transport activity followed the titration curve for Asp-97, with an apparent pK(a) of 7.

34 A titration curve for the LCC was generated that showed th

35 Analysis of the theoretical microscopic titration curves for all of the ionizable residues of th

36 f CD, Trp fluorescence, and Soret absorbance titration curves for all the variants requires a six-sta

37 ection against co-transfection, showing that titration curves for commonly-used regulators agree betw

38 Titration curves for His 55 and the two other histidines

39 ) a simple procedure to measure and position titration curves for humic substances (HS) versus salt c

40 While the titration curves for most of the side-chain carboxyl res

41 Titration curves for two biological warfare agents, Baci

42 e measured potentials were used to produce a titration curve from which the end point of a reaction w

43 The titration curves gave dissociation binding constants for

44 Titration curves in the presence of BSA and micelles are

45 hibition, as measured by the slope of linear titration curves in this system, was observed with PA, G

46 Peptide titration curves indicated that this effect was not due

47 the biggest contributor to the shape of the titration curve, indicating that the formation of this s

48 side chains give rise to two- or three-step titration curves, indicative of the influence of multipl

49 per, a general expression for solute-protein titration curves is predicted, using an indirect mechani

50 h increasing pH in the manner expected for a titration curve model in which deprotonation of the hist

51 The resultant titration curve (normalized fluorescence intensity vs. l

52 However, the triphasic titration curve obtained from the ITC study suggests tha

53 The titration curves obtained by differential excitation usi

54 the 1:1 binding model, separate analyses of titration curves obtained while varying either P450 or C

55 Titration curves, obtained by fitting the donor's emissi

56 We demonstrate that the titration curve of a site in a group of interacting site

57 arlo (neMD/MC) simulations provided the full titration curve of active site Lys, explaining the need

58 The titration curve of an individual site in the molecule is

59 As follows from the fit of the titration curve of Asp-85, deprotonation of X' increases

60 ependent and correlated with the theoretical titration curve of the imidazole group.

61 The acoustic titration curves of 160 bp DNA revealed three stages of

62 stified by the observation that the biphasic titration curves of D85E and Y185F are converted to mono

63 Ca(2+) titration curves of day 6 myofibrils showed two distinct

64 ively low Mg2+ concentration, the normalized titration curves of DNA mobility were well fit by Mannin

65 Titration curves of hyperimmune sera were included on as

66 The titration curves of lambda(max) for mutants on the EF lo

67 ent pKa values were also determined from the titration curves of phase angles and modulations versus

68 NMR titration curves of residues in the Ca(2+)-binding regio

69 Titration curves of sera from rabbits immunized with P.

70 The titration curves of several known HIV-RT inhibitors have

71 Titration curves of the Fe-His frequency against pH are

72 ng sites can be accurately reconstructed, if titration curves of the other sites are known.

73 ed by integrating the difference between the titration curves of the two species.

74 Comparison of the titration curves of the unliganded enzyme with that obta

75 a pK value (defined as the mid-point of the titration curve) of 7.1 and a slope of 0.6.

76 o have a pH dependence, which was fit with a titration curve (pKa = 7.7), suggesting the protonation

77 The form of the titration curve predicted from this lateral pressure mec

78 Titration curves predicted significant differences in ch

79 ad to relatively broad histograms and broad "titration" curves, providing clear evidence for kinetic

80 Establishing a titration curve requires several steps, i.e., blank subt

81 amino acid position 623 (E623Q) displayed a titration curve shifted to the left relative to wild typ

82 Propidium iodide titration curves showed that rewinding of DNA supercoils

83 The FT Raman spectra and the acid titration curves suggest that the 391 nm form of the chr

84 he presence of urea show curved or sigmoidal titration curves suggestive of direct urea binding.

85 ve CD band near 200 nm, and biphasic thermal titration curves that reflect varied stability of these

86 rs, percentages probabilities, and slopes of titration curves, that can be more accurately quantified

87 The shape of the equilibrium binding titration curve, the effects on the 2Fe-2S EPR spectrum,

88 as a function of the midpoint of the calcium titration curve, the Hill coefficient, and the concentra

89 We show that theoretical microscopic titration curves (THEMATICS) can be used to identify act

90 The power of theoretical microscopic titration curves (THEMATICS), when coupled with a statis

91 labeled peptide for binding to NCS-1 shifted titration curves to higher NCS-1 concentrations, suggest

92 fitting of the resultant equilibrium binding titration curves to the Adair-Pauling equations, and mod

93 Nonlinear curve fitting of metal titration curves using the multiple independent binding

94 A biphasic fluorescence titration curve was observed, confirming the previous ob

95 Parallelism in titration curves was observed in the III-HSA but not in

96 l, to our knowledge, approach to analyze NMR titration curves was proposed.

97 f the effects of ionic strength on the force titration curves, we discuss the applicability of JKR th

98 Chemical shift-pH titration curves were obtained for the lysine side-chain

99 Resulting EPR titration curves were simulated assuming different redox

100 cases, up to three steps in the fluorescence titration curves were visible, which were fit to apparen

101 epentaacetate (DTPA) exhibiting nonmonotonic titration curves, where it gives an excellent fit to exp

102 -treated solutions increased, resulting in a titration curve, which was used to determine the amount

103 rin was strikingly pH-sensitive, producing a titration curve with a midpoint at pH 6.8.

104 llowing conclusions: 1) Asp-85 has a complex titration curve with two values of pKa; in addition to a

105 ss than 100 fg DNA or 10(2) CFU/ml in serial titration curves with pure bacteria.

106 owever, block was not complete; the best-fit titration curves yielded an acid pH asymptote of 10-15%,

107 Fitting of the normalized titration curves yields an apparent pKa = 7.16(+/-0.02)