ライフサイエンスコーパス: fluorescence yield

1 cules, which confer on them a high intrinsic fluorescence yield.

2 d for independent assessment of PSI and PSII fluorescence yield.

3 nitro group, consistent with changes of NS1 fluorescence yield.

4 nts by monitoring the decline in chlorophyll fluorescence yield.

5 d in the reconstitution alters the resulting fluorescence yield.

6 not change the kinetics of the decay of the fluorescence yield.

7 ation pulse-induced changes in chlorophyll a fluorescence yield.

8 th the observed increase in the steady-state fluorescence yield.

9 d in invertebrate systems, mostly due to low fluorescence yields.

10 red in resulting strains through chlorophyll fluorescence yields.

11 The relationship between the fluorescence yield and P(+) (fraction of closed RC) show

12 Fluorescence yield and partial electron yield measuremen

13 on period four oscillations in both maximum fluorescence yield and the relative contribution of QA-

14 The spatial pattern of fluorescence yields and lifetimes strongly suggests that

15 singlet and triplet excitation energies and fluorescence yields and lifetimes; conformational proper

16 n STED microscopy can be slowed down and the fluorescence yield be enhanced by scanning with high spe

17 The fluorescence yield characteristics of Synechocystis sp.

18 has excited-state characteristics (lifetime, fluorescence yield) comparable (within approximately 10%

19 tion coefficient and improving the resulting fluorescence yield compared to a classical single-fluoro

20 In this work, the fluorescence yield concomitant with the oxidized dimer (

21 e(III)] and is accompanied by a delay in the fluorescence yield decay kinetics attributed to the slow

22 eat shock protein 101 had identical rates of fluorescence yield decline as nontransgenic cotton.

23 The rate of fluorescence yield decline during the elevated respirato

24 the time course and magnitude of chlorophyll fluorescence yield decline in samples from irrigated and

25 ield to the maximum (OJIP transient), or the fluorescence yield decrease during reoxidation of plasto

26 l intensity and spectral shift of tryptophan fluorescence yielded distinctly different kinetics and a

27 temperatures, respectively, a dimer with low fluorescence yield dominates, which cannot be extended t

28 Collectively, the fluorescence yields, excited-state lifetimes, oxidation

29 Variable fluorescence yield experiments demonstrated that this mu

30 Both immunological analysis and variable fluorescence yield experiments indicated that E339Q asse

31 tly, compared to that parent arenes, but the fluorescence yields fall by at least 1 order of magnitud

32 This study uses partial fluorescence yield Fe L-edge X-ray absorption spectrosco

33 yields, Ft ) and saturation pulses (maximal fluorescence yields, Fm ).

34 m)' is prone to underestimation, the maximum fluorescence yield following brief cessation of actinic

35 These fluorescent Holliday junctions improve fluorescence yields for both single-domain and full-size

36 Total variable fluorescence yields for the R342S mutant indicated that

37 e of actinic light intensities (steady-state fluorescence yields, Ft ) and saturation pulses (maximal

38 on modes, namely total electron yield (TEY), fluorescence yield (FY), and scanning transmission X-ray

39 maps of nucleic acid mass, protein mass and fluorescence yield in unlabeled cells.

40 ype accounted for more than 30% of the total fluorescence yield, in the mutant it accounted for less

41 s individual fluorophores at reasonably high fluorescence yields, including IR-125, quantum dots, met

42 for trapping the excited state leads to the fluorescence yield increase observed experimentally, and

43 Analysis of the variable fluorescence yield indicated that the mutant accumulated

44 Measurements of the variable fluorescence yield indicated that the mutant assembled f

45 Measurements of total variable fluorescence yield indicated that this mutant assembled

46 Measurements of total variable fluorescence yield indicated that this mutant assembled

47 Measurements of total variable fluorescence yield indicated that this mutant assembled

48 had absorption maxima at 635 nm and very low fluorescence yields, indicating they contained the more

49 utilization of the excitation, the measured fluorescence yield is informed by the migration of the e

50 fect of scanning speed on photobleaching and fluorescence yield is more remarkable at higher levels o

51 ding and by equilibrium measurements of DC6C fluorescence yielded KD values of 2-4 microM for the des

52 Total fluorescence yield measurements indicated that all of th

53 Fluorescence yield measurements indicated that both the

54 Fluorescence yield measurements reveal no energy change

55 Fluorescence yield measurements were obtained within min

56 I) membranes has been studied by flash-probe fluorescence yield measurements.

57 The small variable fluorescence yield observed after a single saturating fl

58 The maximum fluorescence yield observed under steady-state actinic i

59 Optimal total fluorescence yield occurred at 6 attomoles of IR-786 per

60 The assay selectively monitors the fluorescence yield of 5-hydroxytryptophan by exciting th

61 rease in intrinsic Trp fluorescence, and the fluorescence yield of a pyrene at Cys374 is decreased.

62 The fluorescence yield of bound 2'(3')-O-[N-methylanthranilo

63 roduce the concept of optical control of the fluorescence yield of CdSe quantum dots through plasmon-

64 his mode of data collection by measuring the fluorescence yield of fluorescein dye molecules in aqueo

65 The chlorophyll fluorescence yield of purified photosystem II light-harv

66 M with C28W(1b) results in a decrease in the fluorescence yield of the fluorophore, allowing the kine

67 results suggest that the delayed decline in fluorescence yield of water-stressed tissue exposed to p

68 ions at residue D1-H118 had no effect on Chl fluorescence yield or quenching kinetics.

69 for the periodicity of four in both maximum fluorescence yield pattern and flash-dependent changes i

70 red region (lambda = 398, 626 nm), a modest fluorescence yield (Phi f approximately 0.11), a long si

71 hort, P+), are known to be quenchers of Chla fluorescence yield (phi f) of photosystem II.

72 sight into the relationship of variable Chla fluorescence yield (phi f) to the concentration of the t

73 , (z), and dL, affect x-ray reflectivity and fluorescence yield profiles as an aid in their interpret

74 In this work, Pb L(alpha) fluorescence yield profiles for samples equilibrated wit

75 s found that the kinetics of the decrease in fluorescence yield robustly fitted a second-order kineti

76 Flash-number dependence of Chla fluorescence yield shows either a period 4, due to the f

77 s with satellite retrievals of solar-induced fluorescence yields suggests that the mean values of the

78 For comparison, standard total fluorescence yield (TFY) XAS and nonresonant XES data we

79 ubstrate, PS, producing an adduct with lower fluorescence yield than that of PE.

80 sion protein, and thus result in higher cell fluorescence, yielded the pspA gene encoding phage shock

81 such as the rise from the basic dark-adapted fluorescence yield to the maximum (OJIP transient), or t

82 robe bis-ANS showed a pronounced increase in fluorescence yield upon binding to alpha-crystallin from

83 n (CMCN-NBD-MPE = 4 microM), reached maximum fluorescence yield upon the addition of taurodeoxycholat

84 Measurements of the kinetics of fluorescence yield verify that Q(A)(-) to Q(B) electron

85 e components is detected based on changes in fluorescence yield, viewed by a maxi Imaging-Pulse-Ampli

86 than in the control strain, and the variable fluorescence yield was quenched.

87 The fluorescence yields were quantified by photodensitometry

88 High pressure affected the tryptophan fluorescence yield, which decreased by about 37% at 480

89 d will inevitably lead to a dip in the total-fluorescence-yield X-ray absorption spectrum.