ライフサイエンスコーパス: fluorescence fluctuation

1 ng correlation analysis of extrinsic oxazine fluorescence fluctuations.

2 hrough the evanescent wave contribute to the fluorescence fluctuations.

3 separations, we find significant long-lived fluorescence fluctuations among discrete levels originat

4 (PCH) analysis describes the distribution of fluorescence fluctuation amplitudes due to populations o

5 Here, we used fluorescence fluctuation analyses to quantitatively expl

6 Our approach is based on the application of fluorescence fluctuation analysis (FFA) and multiangle l

7 atography for the isolation and a model-free fluorescence fluctuation analysis for the investigation

8 Moreover, individual-eisosome fluorescence fluctuation analysis shows that eisosomes i

9 le RNA and protein detection with two-photon fluorescence fluctuation analysis to measure the average

10 Here we show that fluorescence-fluctuation analysis of raster scans at var

11 In this work we used fluorescence fluctuation analytical methods to determine

12 dsorbed on a semiconductor NP surface showed fluorescence fluctuations and blinking, with time consta

13 ugmented iFCS with an analysis of moments of fluorescence fluctuations and used it to measure stages

14 hrough the evanescent wave contribute to the fluorescence fluctuations, and when fluorescent and nonf

15 ions microscopy, and we also briefly address fluorescence fluctuation approaches, notably raster imag

16 Using different fluorescence fluctuation approaches, we established that

17 e fluorescence observation volume from which fluorescence fluctuations are measured, even at relative

18 eo microscopy experiments allow detection of fluorescence fluctuations at the timescales approaching

19 The fluorescence fluctuation autocorrelation function depend

20 An expression for the fluorescence fluctuation autocorrelation function in the

21 Theoretical expressions for the fluorescence fluctuation autocorrelation function when b

22 Fluorescence fluctuation autocorrelation functions were

23 Here, we present an analysis of resonance fluorescence fluctuations based on photon counting stati

24 Through these quantities, we build a fluorescence-fluctuation-based diffusion tensor that con

25 a novel tool for extracting quantities from fluorescence fluctuation data, i.e., the measured photon

26 Using simulated fluorescence fluctuation data, we find the BCa method to

27 We introduce a new analysis technique for fluorescence fluctuation data.

28 onstrate that the theory successfully models fluorescence fluctuation data.

29 a DNA hairpin in gels, we directly observed fluorescence fluctuations due to conformational intercon

30 The fluorescence fluctuation dynamics were found to be inhom

31 milarly, the autocorrelation function of the fluorescence fluctuations exhibited unexpected changes w

32 Most dual-color fluorescence fluctuation experiments are performed on fl

33 Brightness analysis of fluorescence fluctuation experiments has been used to su

34 alysis and identify the optimal position for fluorescence fluctuation experiments in the capillary.

35 A novel technique for the analysis of fluorescence fluctuation experiments is introduced.

36 that the contribution of autofluorescence to fluorescence fluctuation experiments is negligible at EG

37 Lastly, we performed fluorescence fluctuation experiments on cells expressing

38 The photon counting histogram of fluorescence fluctuation experiments, in which few molec

39 at describes the effects of sampling time on fluorescence fluctuation experiments.

40 analyzing the fluctuation amplitude g(0) of fluorescence fluctuation experiments.

41 ross-correlation function was applied to the fluorescence fluctuation from these two positions to cap

42 t of an approach in which the pixel-to-pixel fluorescence fluctuations from a single fluorescence ima

43 xes based on the analysis of single molecule fluorescence fluctuations from laser scanning confocal i

44 technique is based on brightness analysis of fluorescence fluctuations from three fluorescent protein

45 Fluorescence fluctuations, generated by trans-cis isomer

46 nescent wave, in solution, contribute to the fluorescence fluctuations have been published previously

47 Here we describe an enhanced fluorescence fluctuation imaging analysis, which employs

48 Fluorescence fluctuation imaging is a powerful means to

49 ight's behavior, including millisecond-scale fluorescence fluctuations in single molecules as well as

50 The intensity distribution of these fluorescence fluctuations is experimentally captured by

51 We report fluorescence fluctuation measurements of enhanced GFP (E

52 opy with advanced image-processing tools and fluorescence fluctuation methods and distinguished three

53 We introduce fluorescence fluctuation methods to determine, at high s

54 We used a unique method based on 2-photon fluorescence fluctuation microscopy to measure directly,

55 ng coimmunoprecipitation, cross-linking, and fluorescence fluctuation microscopy, we show that HS doe

56 ctional GFP-Mrr fusion protein using in vivo fluorescence fluctuation microscopy.

57 Fluorescence fluctuations occurring between two FRET sta

58 ) at equilibrium on a local scale, analyzing fluorescence fluctuations of individual pH-sensitive flu

59 Such fluorescence fluctuation patterns may contain informatio

60 f particle brightness and concentration from fluorescence-fluctuation photon-counting statistics usin

61 The brightness of fluorescence fluctuations provides information about pro

62 This work investigates the use of fluorescence fluctuation spectroscopy (FFS) as a tool fo

63 rom immobile sources present a challenge for fluorescence fluctuation spectroscopy (FFS) because the

64 Fluorescence fluctuation spectroscopy (FFS) has recently

65 of bright particles at low concentrations by fluorescence fluctuation spectroscopy (FFS) is challengi

66 ubtypes and their G-proteins using two-color fluorescence fluctuation spectroscopy (FFS) of mouse MIN

67 Fluorescence fluctuation spectroscopy (FFS) quantifies i

68 Fluorescence fluctuation spectroscopy (FFS) quantifies t

69 In this study, we used fluorescence fluctuation spectroscopy (FFS) to evaluate

70 tein mCherry is of considerable interest for fluorescence fluctuation spectroscopy (FFS), because the

71 Here, we present results of fluorescence fluctuation spectroscopy analyses indicatin

72 escence cumulant analysis (TIFCA) to analyze fluorescence fluctuation spectroscopy data.

73 Fluorescence fluctuation spectroscopy determines the bri

74 Fluorescence fluctuation spectroscopy has become an impo

75 In particular, dual-color, z-scan fluorescence fluctuation spectroscopy in conjunction wit

76 of protein heterointeractions by dual-color fluorescence fluctuation spectroscopy in living cells.

77 In addition, using fluorescence fluctuation spectroscopy in single living c

78 nsity scan through the sample, followed by a fluorescence fluctuation spectroscopy measurement at eac

79 Dual-color fluorescence fluctuation spectroscopy provides a general

80 Fluorescence fluctuation spectroscopy provides informati

81 Here, we use a newly developed multipoint fluorescence fluctuation spectroscopy technique to study

82 internal reflection fluorescence microscopy, fluorescence fluctuation spectroscopy techniques, and th

83 in living human embryonic kidney cells using fluorescence fluctuation spectroscopy techniques, namely

84 ultipoint moment analysis (TIMMA), a form of fluorescence fluctuation spectroscopy that is capable of

85 ) Gag protein expressed in COS-1 cells using fluorescence fluctuation spectroscopy to determine the s

86 Here, we used fluorescence fluctuation spectroscopy to directly detect

87 Here, we applied fluorescence fluctuation spectroscopy to quantitatively

88 report the first experimental realization of fluorescence fluctuation spectroscopy under high pressur

89 Fluorescence fluctuation spectroscopy utilizes the signa

90 ocorrelation function, traditionally used in fluorescence fluctuation spectroscopy, which separates a

91 ion-dependent dimerization of p85alpha using fluorescence fluctuation spectroscopy.

92 ging environment for brightness studies with fluorescence fluctuation spectroscopy.

93 otropy, and in living cells using two-photon fluorescence fluctuation spectroscopy.

94 ed phenomena may be of broader importance in fluorescence fluctuation spectroscopy.

95 In contrast, three established fluorescence fluctuation techniques (FCS, FCCS, and PCH)

96 Using fluorescence fluctuation techniques (photon-counting his

97 of a tBid monomer, measured separately using fluorescence fluctuation techniques.

98 We attribute fluorescence fluctuations to the interfacial ET reaction

99 Correlation analysis of single-molecule fluorescence fluctuations uncovered site-dependent nanos

100 We argue that spatiotemporal analysis of fluorescence fluctuations using multiple detection chann

101 protein-protein interactions into changes in fluorescence fluctuations, which are quantifiable throug

102 Finally, we observe fluorescence fluctuations with a correlation time of ove

103 ume and analyze the temporal behavior of the fluorescence fluctuations within the stationary observat