ライフサイエンスコーパス: fluorescence spectrum

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1 differentiating fluorophores based on their fluorescence spectrum.

2 scribed here bind thioflavin T and shift its fluorescence spectrum.

3 pposite polarities in different parts of the fluorescence spectrum.

4 opens a pathway to in situ control over the fluorescence spectrum.

5 A 77 K fluorescence spectrum analysis of treated PSII membranes

6 From the fluorescence spectrum and from an inversion of the Debye

7 dye environment and dramatically altered the fluorescence spectrum and intensity, resulting in a stro

8 However, inspection of the fluorescence spectrum and LC-MS analysis of the reaction

9 transect in the Deltalambda = 25 synchronous fluorescence spectrum and with the preexponential terms

10 leptosperin not only displayed an identical fluorescence spectrum, but supplementation of leptosperi

11 Using an intracellular substrate whose fluorescence spectrum changes after hydrolysis by Bla, w

12 mophore exhibits a nonshifted absorption and fluorescence spectrum characteristic of its native, exte

13 s at megapixels per hour with the full X-ray fluorescence spectrum collected per pixel.

14 n olive oil gave a different but interesting fluorescence spectrum, composed of three bands: one low

15 e donor and acceptor even though the donor's fluorescence spectrum does not overlap with absorption s

16 The ability to measure the entire fluorescence spectrum from each sensor simultaneously du

17 We observe the UV fluorescence spectrum from naturally occurring tryptopha

18 r describes a method to measure the complete fluorescence spectrum from numerous fluorescent microsph

19 p, NFK and ArgP emission dominates the total fluorescence spectrum in both emulsified post-surgical h

20 orption spectrum and a red-shifted, quenched fluorescence spectrum, indicating aggregation of the con

21 ing cluster size (the onset of the PH(+)(aq) fluorescence spectrum is 600 nm and the maximum is 518 n

22 An unusual and highly quenched fluorescence spectrum is also observed for Trp 38.

23 ly impossible for both UV-vis absorption and fluorescence spectrum measurements.

24 The fluorescence spectrum observed after entrapping MgADP-fl

25 For example, the fluorescence spectrum of 7AW is sufficiently separated f

26 Here we simulate a time-resolved fluorescence spectrum of a dye in aqueous solution, the

27 The fluorescence spectrum of a solution of selected dyes all

28 e) bond is correlated with alteration of the fluorescence spectrum of the active PLP ketoenamine taut

29 cent quantum yields where the absorbance and fluorescence spectrum of the fluorophore was not affecte

30 It is clear from these results that the fluorescence spectrum of the introduced tryptophans in t

31 meric state, circular dichroism spectrum, or fluorescence spectrum of the sensor domain but do stabil

32 The blue-shift of the Citrine fluorescence spectrum resulting from the bending of the

33 Its fluorescence spectrum shows two major peaks at 718 and 7

34 from a denaturing polyacrylamide gel, has a fluorescence spectrum similar to that of activated NCS-c

35 erent from established UV-vis absorption and fluorescence spectrum techniques where large amounts of

36 a chemical system often creates a congested fluorescence spectrum that is difficult to interpret.

37 the active site gorge, shows changes in its fluorescence spectrum that reflect the fluorescent side

38 e process by comparison of the laser-induced fluorescence spectrum to the ultraviolet depletion spect

39 the component parts, while in each case the fluorescence spectrum upon illumination of the Zn porphy

40 The fluorescence spectrum was less intense and more red-shif

41 During refolding, the initial fluorescence spectrum was not that of native or unfolded

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