ライフサイエンスコーパス: self-quenching

1 centration and low resonance energy transfer self-quenching.

2 are mainly due to evaporation, hence causing self-quenching.

3 495 nm could be correlated with the level of self-quenching.

4 desired fluorescence characteristics such as self-quenching.

5 m far enough away from each other to prevent self-quenching.

6 addition of ssDNA yields insight into C*...C self-quenching.

7 ence of isolated monomers and the absence of self-quenching.

8 highly labeled oligomer was decreased due to self-quenching.

9 by the relief of octadecyl rhodamine B (R18) self-quenching.

10 probe-labeled Q132C apoA-I showed rhodamine self-quenching.

11 of the rhodamine dimers, which abolishes the self-quenching and consequently leads to an approximatel

12 transduction and combining both fluorescence self-quenching and energy-transfer mechanisms to enhance

13 ptimized conditions, where there is no probe self-quenching and minimum PCT, efficient signal amplifi

14 tly coupling distance-dependent fluorescence self-quenching and/or resonant-energy transfer to the pr

15 probes with each other (absorption spectra, self-quenching) and reduced nonspecific interactions wit

16 (1) In the scheme using fluorescence self-quenching as a signal-transduction mechanism, the f

17 e up water was measured using a fluorescence self-quenching assay under both oxygen/glucose deprivati

18 A fluorescence self-quenching assay was used to monitor the transfer of

19 sistent with those obtained using the DPHpPC self-quenching assay, while lipid mixing rates measured

20 tion of membrane leakage mechanisms from dye self-quenching assays; and 4), evaluation of nanodomain

21 ion or on aggregation, with the former often self-quenching at high concentrations, and the latter fa

22 to a low concentration of fluorescein due to self-quenching at high concentrations.

23 ence activation strategy is proposed whereby self-quenching avidin-rhodamine X, which has affinity fo

24 interaction, with concomitant relief of dye self-quenching; (b) fluorescence energy transfer from th

25 exhibit nonadditivity due to such things as self-quenching behavior or exciplex formation.

26 more efficiently in ssDNA than dsDNA, while self-quenching between 6-MI bases is enhanced in dsDNA.

27 of the two apt-DAR NPs are both weak due to self-quenching, but they increase inside the cells as a

28 consistent with diffusion-limited bimetallic self-quenching by electron transfer.

29 Amp or Lys(Mca) and thus has less chance of self-quenching, (c) Adp has a relatively high quantum yi

30 We found that most of the self-quenching can be partially eliminated by proximity

31 Self-quenching concentrations of lipid dye were placed i

32 fluorescent protein (EGFP) and labeled with self-quenching concentrations of R18 membrane dye were u

33 When R18 was in the bilayer at high, self-quenching concentrations, voltage pulses led to vol

34 One difficulty with fluorescein is its self-quenching due to resonance energy transfer between

35 lower poly(vinyl alcohol) layer contains the self-quenching dye carboxyfluorescein.

36 Self-quenching effects were determined by measuring thei

37 bases (length 1-4 monomers) showed moderate self-quenching except xC, which showed enhancement of Ph

38 Measurements of fluorescein self-quenching (fluorescent efficiency as a function of

39 One is based on the redistribution of a self-quenching fluorophore, whereas the second depends o

40 entration, causing fluorescence dimming from self-quenching for high but not low fluorescein concentr

41 e resonance energy transfer and fluorescence self-quenching from dye-labeled gramicidin channels, we

42 To avoid self-quenching from multiple fluorophores installed in c

43 otein (131 aa, 15 kDa) by using fluorescence self-quenching in combination with fluorescence correlat

44 unusually low buffer fluorescence is due to self-quenching in sedimentable aggregates or micelles wh

45 ratio imaging method involving fluorescence self-quenching indicated a 2.5-fold increase in volume d

46 In vitro measurements confirm that self-quenching is a function of the number of fluorophor

47 These results demonstrate that self-quenching is a sensitive and fast gas-phase probe o

48 r fluorescence resonance energy transfer and self-quenching is widely distributed, which reflects a b

49 s led to improvements of responsiveness, but self-quenching limited their brightness.

50 A self-quenching mechanism due to the aggregation of QDs i

51 We report an efficient triplet state self-quenching mechanism in crystals of eight benzopheno

52 The immunoconjugate is composed of self-quenching, near-infrared chromophores loaded onto a

53 explained by the effects of evaporation and self quenching of fluorescein; the latter is expected to

54 Self-quenching of adjacent fluorescein labels, which imp

55 sed on the effect of concentration-dependent self-quenching of covalently bound fluorophores upon DNA

56 A nonlinear coverage-dependent self-quenching of emission from surface-bound fluorescen

57 rat liver microsomal membranes by monitoring self-quenching of entrapped carboxyfluorescein (CF).

58 ng of basic peptides to vesicles produces no self-quenching of fluorescent monovalent acidic lipids.

59 lipid demixing is obtained from fluorescence self-quenching of labeled lipid and from natural abundan

60 beneficial substitution in terms of reducing self-quenching of luminescence.

61 X moieties, which effectively suppresses the self-quenching of PpIX, leading to significantly enhance

62 The intermolecular self-quenching of rhodamine observed when the peptide wa

63 e efficiency of photoinactivation because of self-quenching of the dye.

64 Although self-quenching of tryptophan resonances that was induced

65 on in concentrated solutions without showing self-quenching or aggregation phenomena.

66 secondary channel is tentatively assigned to self-quenching or triplet-triplet annihilation.

67 For 6MI in PTRA, this QSSQ "quasi-static self-quenching" or "dark" component represents approxima

68 llustrates a unique approach to limiting the self-quenching ordinarily exhibited at the high concentr

69 We have designed novel self-quenching photo-induced electron transfer (PET) flu

70 i LPS (B5), or cholesterol, were loaded with self-quenching probes and exposed to native or oxidative

71 veloped a linker cleavage assay by using the self-quenching property of this fluorophore.

72 on accessibility after physical mapping with self-quenching reporter molecules (SQRM).

73 To this end, we have developed stem-loop self-quenching reporter molecules (SQRMs) as probes for

74 mRNA mapping strategy employing fluorescent self-quenching reporter molecules (SQRMs) that facilitat

75 labeled, and the concentration dependence of self-quenching, supported this conclusion.

76 The self-quenching was mostly eliminated when this oligomer

77 e crowding of the pheophorbide molecules and self-quenching were kept to a minimum.

78 of the photoluminescence (PL) efficiency via self-quenching when the BT units are absent and increase

79 One difficulty with fluorescein is its self-quenching, which results in decreased intensities w