ライフサイエンスコーパス: fluorescence yield

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

2 nts by monitoring the decline in chlorophyll fluorescence yield.

3 d in the reconstitution alters the resulting fluorescence yield.

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

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

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

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

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

9 red in resulting strains through chlorophyll fluorescence yields.

10 Fluorescence yield and partial electron yield measuremen

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

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

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

14 The fluorescence yield characteristics of Synechocystis sp.

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

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

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

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

19 The rate of fluorescence yield decline during the elevated respirato

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

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

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

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

24 Variable fluorescence yield experiments demonstrated that this mu

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

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

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

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

29 Total variable fluorescence yields for the R342S mutant indicated that

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

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

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

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

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

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

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

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

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

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

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

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

42 Total fluorescence yield measurements indicated that all of th

43 Fluorescence yield measurements indicated that both the

44 Fluorescence yield measurements reveal no energy change

45 Fluorescence yield measurements were obtained within min

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 The fluorescence yields were quantified by photodensitometry

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

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