ライフサイエンスコーパス: fluorescence decay

1 e lifetimes by decreasing radiative rates of fluorescence decay.

2 olysis products, furan, were responsible for fluorescence decay.

3 of anthocyanins in solution shortened their fluorescence decay.

4 of the brief lifetime component of the qBBr fluorescence decay.

5 g to noninducing conditions and by measuring fluorescence decay.

6 for the previously described monoexponential fluorescence decay.

7 onential terms describing the time-dependent fluorescence decay.

8 intermediates were observed from femtosecond fluorescence decays.

9 spectroscopy based on statistical fitting of fluorescence decays, 2D FCS can resolve species whose fl

10 Fluorescence decay after photoactivation (FDAP) and fluo

11 Ts in axon-like processes, we used a refined fluorescence decay after photoactivation approach and si

12 e, we observed by quantitative imaging using fluorescence decay after photoactivation recordings of p

13 ed in earlier work have little effect on the fluorescence decay and appear to occur away from the try

14 igated by experimental measurements of Trp37 fluorescence decay and compared with theoretical measure

15 troscopy revealed a strong dependence of the fluorescence decay and electron-transfer/charge-recombin

16 ntly fluorogen dissociation, leading to fast fluorescence decay and fluorogen-concentration-dependent

17 Q6H2 was found to prevent both fluorescence decay and generation of lipid peroxides (LO

18 The greater fluorescence decay and more rapid breakup for the high c

19 nce of LHCBM9 resulted in faster chlorophyll fluorescence decay and reduced production of singlet oxy

20 c studies (emission quenching, time-resolved fluorescence decay, and transient absorption spectroscop

21 The in-plane depolarized fluorescence decays are described by a stretched exponen

22 nce decays, 2D FCS can resolve species whose fluorescence decays are linked by the rate constants in

23 dsRed fluorescence decays as a single exponential with a 3.65

24 of Corti, we show that the time constants of fluorescence decay at the basolateral pole of IHCs and a

25 sion is spectrally isolated, analysis of the fluorescence decay can distinguish changes in membrane f

26 This was followed by a biexponential fluorescence decay containing fast and slow components,

27 In agreement with our conclusions, the fluorescence decay curves of 6-fluorotryptophan-containi

28 Fluorescence decay curves of each are monoexponential ex

29 Fluorescence decay curves were measured with high precis

30 r time divided by that of an earlier image), fluorescence decay curves, fluorescence decay rates, and

31 Time-resolved fluorescence decay data for the Cu(I)-saturated probe in

32 ng global analysis to simultaneously fit the fluorescence decay data of all pixels in an image or dat

33 allows us to fit both the prompt and delayed fluorescence decay data quantitatively.

34 Fitting of the fluorescence decay data using the method of least square

35 (E), based on three-exponential fits to the fluorescence decay data, is 2.5 +/- 0.7% (SEM, N = 12).

36 icability of a rotamer model to describe the fluorescence decay data.

37 In monellin, the fluorescence decay displays multiexponential character w

38 The fluorescence decay due to photobleaching of the immobile

39 Fluorescence decay due to tangential flow would be expec

40 uire an accurate subnanosecond time-resolved fluorescence decay every 0.1 ms after stopped flow.

41 uorescence recovery after photobleaching and fluorescence decay experiments, we find that the stable

42 uch slower in the native rubredoxin; the Trp fluorescence decay extends to 10 ps and longer, reflecti

43 ed four kinetic components: an initial, fast fluorescence decay, followed by a transient increase, an

44 ingle crystals, we have established that the fluorescence decay function of AP shows a pronounced, ch

45 Analysis of the AP fluorescence decay function reveals conformational heter

46 The fluorescence decay functions of individual, specifically

47 sicle containing solutions, multiexponential fluorescence decays imply separate solute populations in

48 n the amplitude of the 60-70 ps component of fluorescence decay in open Chl b-containing PS II center

49 However, fluorescence decay in the presence of DCMU, which monito

50 Dual exponential fluorescence decay is assigned to the two conformers of

51 ly suggest that the extent of nonexponential fluorescence decay is governed primarily by the efficien

52 However, chlorophyll fluorescence decay kinetics after a single saturating fl

53 ins lacking photosystem I did not change the fluorescence decay kinetics after illumination, and ther

54 fer process was examined mechanistically via fluorescence decay kinetics and fluorescence anisotropy

55 The actual fluorescence decay kinetics can be fit to one exponentia

56 Fluorescence decay kinetics in the absence of DCMU indic

57 Fluorescence decay kinetics in the presence of DCMU indi

58 Trp4 fluorescence decay kinetics measured for the F4W protein

59 II (PSII), exhibits complex multiexponential fluorescence decay kinetics that for decades has been as

60 In this study, we have used fluorescence decay kinetics to quantitatively probe Phot

61 al processor allows extraction of the sample fluorescence decay kinetics without distortions which ca

62 ophan residue that exhibits multiexponential fluorescence decay kinetics, was also examined as a more

63 tensity by up to 500% and induce complicated fluorescence decay kinetics.

64 fast and slow components of the flash-probe fluorescence decay kinetics.

65 pseudo-first-order rate constant describing fluorescence decay (kobs) increases linearly with [cytoc

66 ce peak intensity at 390 nm (I(375)/I(390)), fluorescence decay lifetime (tau), or rotational correla

67 Independent fluorescence decay lifetime and rotational dynamics para

68 hat the bases are stacked; at the same time, fluorescence decay lifetimes are heterogeneous, indicati

69 rescent protein (GFPuv) that exhibit altered fluorescence decay lifetimes.

70 According to variable fluorescence decay measurements in DCMU-treated cells, c

71 ient absorption spectroscopy, and picosecond fluorescence decay measurements permits detailed analysi

72 Time-resolved fluorescence decay measurements upon Chl excitation show

73 differs between different dyes; the initial fluorescence decay mirrors the loss of granule contents

74 ns typically entails fitting data to complex fluorescence decay models but such experiments are frequ

75 ich occurs within the mixing time; and 2), a fluorescence decay occurring between approximately 100 a

76 explanation for the unusual monoexponential fluorescence decay of 5-fluorotryptophan (5FTrp) in sing

77 We have analyzed the fluorescence decay of anthocyanins by fluorescence lifet

78 , a linear correlation was found between the fluorescence decay of BODIPY 581/591 C11 and the concent

79 tive component (deltagamma(r)(-1)(t)) of the fluorescence decay of chromophores in proteins also is e

80 Oxidation-induced fluorescence decay of diphenylhexatriene-labeled phospha

81 Western blot analysis indicated that the fluorescence decay of EGFP-MODC-(422-461) was correlated

82 d relaxation of protein water to explain the fluorescence decay of monellin.

83 The fluorescence decay of Rev M11 delta 14 was resolved into

84 The fluorescence decay of the cis-W3 zwitterion was biexpone

85 The time-resolved fluorescence decay of the donor in each labeled junction

86 Fluorescence decay of the solute molecules is collected

87 provide compelling evidence that the complex fluorescence decay of the tryptophan zwitterion originat

88 Analysis of the donor fluorescence decay of the unfolded subpopulation of both

89 The fluorescence decay of Trp246 is a triple exponential wit

90 The fluorescence decay of Trp45 in wild-type Rev was resolve

91 the origin of the ubiquitous nonexponential fluorescence decay of tryptophan in proteins.

92 The fluorescence decays of all five peptides and Rev M9 delt

93 Analysis of the fluorescence decays of DNA-EB quenched by Cu(2+) and Ni(

94 In this paper, the best model for the fluorescence decays of solute molecules is selected with

95 The analysis of fluorescence decay poses a challenging problem for the c

96 Rather, heterogeneity in fluorescence decay processes was accommodated by the bre

97 e model should display the same trend as the fluorescence decay profiles when an experimental conditi

98 Fluorescence decay rate for the low concentration condit

99 roscopy furnishes radiative and nonradiative fluorescence decay rates in various solvent polarities.

100 n earlier image), fluorescence decay curves, fluorescence decay rates, and histograms of estimated te

101 these states do not directly impact NAD(P)H fluorescence decay rates.

102 otected from such surface quenching, and its fluorescence decay reflects reacidification kinetics.

103 Analysis of the fluorescence decay resolved two lifetimes, corresponding

104 Fluorescence decay signals from PSII reconstituted with

105 nt and incompetent states that have distinct fluorescence decay signatures indicating different base

106 The fluorescence decay spanned a full three orders of magnit

107 Changes in the fluorescence decay suggest that FAD can exist in four co

108 of oxygen from solution lowered the rate of fluorescence decay, suggesting strategies that can be em

109 The apparent half-time for fluorescence decay (t(1/2)) in PSII(-Mn) increased from

110 to screen the different membrane phases via fluorescence decay time analysis, making this new probe

111 n solution and in gas phase by measuring the fluorescence decay time and ion-neutral collision cross

112 2AP does not exhibit the long fluorescence decay time characteristic of the free nucle

113 The absorption spectrum and fluorescence decay time components of the complex at roo

114 d emission spectra (TRES) indicate that this fluorescence decay time should be ascribed to a highly q

115 ervations: the scaling of the characteristic fluorescence decay time with the vesicle diameter and th

116 roperties, such as high solubility and short fluorescence decay time, could be obtained from fluoroph

117 Nonlinear fitting of the fluorescence decay times provides activation parameters

118 of different complexes led to variations in fluorescence decay times.

119 o for 15 ms to 1000 s and then to follow the fluorescence decay upon chemical dilution into excess ac

120 The initial, fast fluorescence decay was assigned to DC6C dissociation fro

121 However, the identical fluorescence decay waveforms for saturating amounts of d

122 Kinetic circular dichroism and fluorescence decays were measured simultaneously to moni

123 he electron donor, measured by time-resolved fluorescence decay, were positively correlated with the

124 at AppAwt and Y21F mutant protein exhibits a fluorescence decay with a lifetime of 0.6 ns.

125 ior to data collection shows monoexponential fluorescence decay with a lifetime of 1.0 ns.

126 ted AppAwt but not Y21F also exhibits slower fluorescence decay with a lifetime of 1.7 ns.

127 Trp fluorescence decay with the onset of solvation dynamics

128 yields of 0.04-0.24, and triple exponential fluorescence decays with lifetimes of 4.4-6.6, 1.4-3.2,

129 its a respectable quantum yield and a simple fluorescence decay, with marginal amounts of dark specie