ライフサイエンスコーパス: basic pH

1 was also found to be extremely sensitive to basic pH.

2 as increased by illumination, Zn2+ ions, and basic pH.

3 fferent crystal forms obtained at acidic and basic pH.

4 d exchange becomes the dominant mechanism at basic pH.

5 und to occur for the molecular analog in the basic pH.

6 by the electron-withdrawing groups or highly basic pH.

7 at 280 K for the protein at both acidic and basic pH.

8 ins the B-sheet structure both at acidic and basic pH.

9 fluorimetric techniques in physiological and basic pH.

10 within a matter of hours, even at neutral to basic pH.

11 e in aqueous medium, which becomes faster at basic pH.

12 decreases by 4 kcal/mol between neutral and basic pH.

13 l and basic pH and Asn(16)-Gly(17) rather at basic pH.

14 exchange in residues other than histidine at basic pH.

15 stable, particularly at a neutral to a more basic pH.

16 dation of hydroquinone to quinone by O(2) at basic pH.

17 = 7 and decreases sharply at more acidic or basic pH.

18 een generated in water at neutral and mildly basic pH.

19 ows the current to activate at slightly more basic pH.

20 ionality, and optimal DNA cleavage occurs at basic pH.

21 aggregation-prone in vitro, particularly at basic pH.

22 t acidic pH or by fluid phase endocytosis at basic pH.

23 ees C at acidic pH and 32 to 37 degrees C at basic pH.

24 increased beta-sheet content at neutral and basic pH.

25 water-exchangeable proton on the protein at basic pHs.

26 (hydro)peroxo ligand of the intermediate at basic pHs.

27 cidic (pH 1) and lose red color in extremely basic (pH 13) medium, showing negative halochromism.

28 es not change significantly at the extremely basic pH = 13 or acidic pH = 1 conditions, suggesting th

29 nd 4.58, respectively) and under "acidic and basic" pH (2.8 and 8.0) conditions.

30 On the other hand, the less basic PH(2)(-) has a weaker stabilizing interaction with

31 Emollient (with either basic pH 8.5 or pH 5.5) was applied double-blinded twice

32 mol Blue distinguished samples with slightly basic pH (8.0) from samples with slightly acidic pH (6.5

33 4 M urea or 2 M guanidine hydrochloride) and basic pH (8.0), reduced mPrP(23-231) refolds to the nati

34 Mucilage activity was greater in weakly basic (pH 9) and weakly acidic (pH 5.5) pH.

35 At slightly basic pH, 9.0, scrambling of the Cys5-Cys22 disulfide bo

36 h blue light (lambda = 450 nm) in neutral to basic pH, a [2 + 2] photocycloaddition can be triggered

37 Strand invasion was efficient at neutral to basic pH, a wide range of temperatures (0-65 degrees C),

38 ignificant decreases in Cerenkov emission at basic pH and allowed the estimation of absolute pH in vi

39 deamidated spontaneously at near-neutral and basic pH and Asn(16)-Gly(17) rather at basic pH.

40 ular modifications was mostly observed after basic pH and high temperatures treatments, together with

41 transition by up to several pH units toward basic pH and induce substantial protonation-independent

42 improved in shorter chain lipids, with more basic pH and low ionic strength; it is hindered by unsat

43 age activity is greatly stimulated at mildly basic pH and requires divalent cations.

44 s conditions of high ionic strength, neutral/basic pH, and low temperatures (26 degrees C) and is sti

45 ne and dichloronitromethane were detected at basic pH, and the mass balance was initially poor at neu

46 d with the uptake of approximately 2 H(+) at basic pH, and this value increases with decreasing pH.

47 ediate, which is sensitive to hydroxylamine, basic pH, and treatments with ATP or ADP.

48 tion constant) of the potentiation to a more basic pH as compared with P2X(2) and revealed a substant

49 While exposure to acidic and basic pHs, as well as iron-free medium, had no significa

50 ral pseudostationary phase in neutral pH and basic pH background electrolytes.

51 ng the sensitivity of a vma-1 null mutant to basic pH but did not correct the morphological defects.

52 with diffusion-limited complex formation at basic pH but rapid dissociation under acidic conditions.

53 eptide can form a triple helix at acidic and basic pH, but is insoluble around neutral pH.

54 Both acute barrier disruption and topical basic pH challenges accelerate reacidification of SKH2/J

55 At basic pH cis-12-OH-TBOH decayed quickly via hydroxide/wa

56 h with monoclonal antibodies incubated under basic pH conditions and on antibodies isolated from huma

57 generated by thermolysis of persulfate under basic pH conditions and perfluoroalkyl acid (PFAA) precu

58 cemic compounds at very acidic, neutral, and basic pH conditions in micellar electrokinetic chromatog

59 Under basic pH conditions, the heavy chain 220-light chain 214

60 nnulus, making it more fragile under neutral/basic pH conditions.

61 (VI) is effective under acidic, neutral, and basic pH conditions.

62 was 2-fold higher at pH 6.5-7 than at a more basic pH, consistent with the formation and transport of

63 At neutral to basic pH, deamidation proceeds by the initial formation

64 At 20 degrees C and slightly basic pH, derivatives 4 and 5 undergo amide cleavage wit

65 ne complexes and facilitate their release at basic pH for subsequent quantification.

66 , was increased in the presence of an inward basic pH gradient.

67 Our results indicate that basic pH (>/=8.5), low NaCl concentrations (</=50 mm), a

68 At acidic and basic pH, however, we again observed the trimer conforma

69 Their activity at acidic and basic pH in vivo makes them promising templates for biom

70 rted mostly in acidic solutions and a few at basic pHs in mixed organic aqueous solutions, visible-li

71 At basic pH increasing the salt concentration reduced the T

72 lipophilic, electrically charged, and highly basic pH indicator, which is used for the readout in abs

73 unfractionated protein digest is infused at basic pH into an electrospray mass spectrometer at a flo

74 s IgG in acidic endosomes and releases it at basic pH into blood.

75 rs a strong competitive fitness advantage at basic pH, it confers a reduced advantage under neutral c

76 due to the stimulation of efflux, whereas at basic pH, it is due to the inhibition of influx.

77 reduced with increasing lipid chain length, basic pH, low salt, the incorporation of negatively char

78 le to promote water oxidation under neutral, basic (pH < 13), and acidic conditions (pH > 1).

79 g and endocytosis occurred at acidic but not basic pH, mimicking pH-dependent uptake of IgG by FcRn.

80 Conversely, at basic pH, NO3- uptake by NO3- and NO2(-)-induced and uni

81 endosomes and ligand release at the slightly basic pH of blood.

82 idic pH of endosomes and releases IgG at the basic pH of blood.

83 esicles (pH </= 6.5) and releases IgG at the basic pH of the bloodstream (pH approximately 7.4).

84 sicles and releases IgG upon exposure to the basic pH of the bloodstream.

85 inding events, respectively, at the slightly basic pH of the cell surface (pH 7.4), but undetectable

86 that soluble TfR and HFE bind tightly at the basic pH of the cell surface, but not at the acidic pH o

87 The action of A22 and MP265 is enhanced by basic pH of the culture medium.

88 e gE-gI, which binds Fcgamma at the slightly basic pH of the extracellular milieu but not at the acid

89 cs of imino proton exchange as a function of basic pH or added ammonia catalyst are used to measure t

90 ns (30 microg/ml) was rapidly inactivated at basic pH or in the presence of formate under anaerobic c

91 At very basic pH, PL quenching was observed independent of surfa

92 Fe(VI)) were investigated over the acidic to basic pH range.

93 n exhibits distinct structures at acidic and basic pH, reflecting changes upon binding or release of

94 The molecular dynamic study of MD3 at mildly basic pH reveals that reactive ground state conformers (

95 nalysis of peptides fractionated off-line by basic pH reversed-phase (bRP) chromatography.

96 vior is especially observable at neutral and basic pH's in water and in organic solvents like dimethy

97 not strictly associated with freezing while basic pH shifts in the core more consistently followed b

98 From neutral to basic pH, TAML activators with H2O2 efficiently degrade

99 s found to be much higher at near neutral or basic pH than at acidic pH.

100 pH but undergoes a conformational change at basic pH that disrupts the site.

101 ther, at this oxidation state at neutral and basic pH, the Ru complex undergoes the coordination of a

102 At basic pHs, the thiolate mini-heme protein can catalyze O

103 or water addition and increased with NaCl or basic pH; thus, T(2) and WHC best correlated when each f

104 rom cyclase to aromatic prenyltransferase at basic pH to generate prenylindoles.

105 tured from plasma were chemically reduced at basic pH to release the linker-drug, followed by self-im

106 At more basic pH values (>or=9.6), however, adsorbed PDDA molecu

107 killing P. aeruginosa and S. epidermidis at basic pH values (pH = 9) compared to acidic pH values (p

108 cs was slow at low Cu(2+) concentrations and basic pH values (up to several hours), while the unquenc

109 showed increased activity rate at relatively basic pH values of 7.9 and 8.5.

110 were almost completely unquenched, while at basic pH values significant quenching (85-90%) was obser

111 on was carried out in solutions of different basic pH values to study the effect of hydrogen ion conc

112 p formation and is gradually shifted to more basic pH values when the length of the linker domain is

113 activity with a sharp decline at relatively basic pH values which is accompanied by a drastic change

114 he particle surface that signals neutral and basic pH values with a green fluorescence.

115 ady-state desensitization is induced at more basic pH values, and Big Dynorphin sensitivity is enhanc

116 tures higher than 100 degrees C, at slightly basic pH values, and with an activation energy of about

117 erved in the presence of oxygen, at slightly basic pH values, depended on time, temperature, and the

118 At both acidic and slightly basic pH values, PfAPP efficiently hydrolyzed the amino-

119 aining the red and blue colors at acidic and basic pH values, suggesting a higher resistance to pH va

120 )yl thioureas is only relevant at neutral to basic pH values.

121 etention of chitinase activity at acidic and basic pH values.

122 ing a homogeneous negative charge density at basic pH were initially coated with a two-domain recombi

123 e to intramolecular charge transfer (ICT) in basic pH were well explained by the time-dependent densi

124 The reducing capacity of FeS was greatest at basic pH where surface-mediated FeS oxidation dominated.

125 in water, at room temperature, and at mildly basic pH, which makes them a suitable platform for furth

126 duction activity of the enzyme at neutral or basic pH with higher product specificity.

127 ores predominantly to multimer or monomer at basic pH with or without Ca2+, respectively.