ライフサイエンスコーパス: emission spectrum

1 th resulting color changes and shifts in the emission spectrum.

2 bsorption spectrum of the cell and the solar emission spectrum.

3 was recorded at 535 nm, the peak of the YFP emission spectrum.

4 at a single wavelength near the peak of the emission spectrum.

5 ncrease in the magnitude of the fluorescence emission spectrum.

6 also the dominant fluorophore of the native emission spectrum.

7 on in the Lamb-Dicke regime with sub-Doppler emission spectrum.

8 m red-shifted intrinsic protein fluorescence emission spectrum.

9 by a blue shift in the band position of the emission spectrum.

10 of ligand binding and return to the initial emission spectrum.

11 ing there a 'squeezed' narrowband near-field emission spectrum.

12 al (3D) imaging for four dyes 10 nm apart in emission spectrum.

13 aphene and substrate can be used to tune the emission spectrum.

14 ent, allowing for wavelength shifting of the emission spectrum.

15 otein pair and alteration of the fluorescent emission spectrum.

16 mostly depolarized over the majority of the emission spectrum.

17 the PpIX spectral signature in the collected emission spectrum (0.014-0.041 mug/ml in phantoms), and

18 random lasers often have a relatively broad emission spectrum, a random laser that utilizes vibratio

19 ed from hot objects is to tailor the thermal emission spectrum according to the desired application.

20 ganic light emitting diode (OLED), having an emission spectrum adapted to algal absorption spectrum a

21 m with the blue most spectral feature of the emission spectrum allows an unambiguous assignment of th

22 A 4 nm blue-shifted fluorescence emission spectrum and a 25% increase in ellipticity at 2

23 nocrystals have a narrow, tunable, symmetric emission spectrum and are photochemically stable.

24 n to be topotecan from the similarity of the emission spectrum and decay times observed for one-photo

25 substitutions are commonly used to shift the emission spectrum and optimize luminescent properties, b

26 bstrate binding leads to a blue shift in the emission spectrum and reduction in accessibility to pola

27 nt, Arg-144 --> Lys cause a red-shift in the emission spectrum and render the fluorophore more access

28 ngths near voltage-sensitive portions of the emission spectrum and shifts in the complete emission sp

29 nt of novel thermal sources that control the emission spectrum and the angular emission pattern is of

30 solar cells, the mismatch between the Sun's emission spectrum and the cells' absorption profile limi

31 The device emission spectrum and the chemical structure of Pt-16 ar

32 c properties of nile red to extract both the emission spectrum and the position of each dye molecule

33 Receptor 2 exhibits a dual monomer-excimer emission spectrum and undergoes a remarked ratiometry in

34 e redox potential of the ferrocene unit, the emission spectrum, and a noticeable color change from ye

35 reened for relative light output, a shift in emission spectrum, and glow-type light emission kinetics

36 vibronic progression in the low-temperature emission spectrum, and solvent dependence.

37 py, quantum yield, and center of mass of the emission spectrum are consistent with the movement of th

38 nt and a 2 nm blue-shift in the fluorescence emission spectrum are consistent with tryptophan residue

39 The peak wavelength and shape of the emission spectrum are not altered by either of these eff

40 The emission spectrum around 511 kiloelectronvolts shows cle

41 to use their characteristic, size-dependent emission spectrum as optical barcode but so far there is

42 aging has been hampered by its 481 nm peaked emission spectrum, as blue wavelengths are strongly atte

43 e effectively, with lamps that have a narrow emission spectrum at 311 +/- 2 nm.

44 rs exhibit a strong room-temperature near-IR emission spectrum at 950 nm.

45 simultaneous measurement of the fluorescence emission spectrum at all sample points.

46 ation at 547 nm yields a glutamate-dependent emission spectrum between 550 and 700 nm that can be exp

47 g emission in the fluorescence line-narrowed emission spectrum can be accounted for, in part, by the

48 micontinuous films, and thus the fluorescent emission spectrum, can be controlled and significantly i

49 referencing, pH-sensitive dye SNAFL-1, whose emission spectrum changes at lambda = 550 in response to

50 the remaining pools also had a blue-shifted emission spectrum consistent with immobilized NADH.

51 The emission spectrum contains 6 lines at 320, 400, 490, 560

52 The change in emission spectrum correlated with a loss in the ability

53 d on assembly state-dependent changes in the emission spectrum demonstrated cell proliferation rate-d

54 The shape of the prodan emission spectrum detected both liquid-solid and order-d

55 ort ground-based observations of the dayside emission spectrum for HD 189733b between 2.0-2.4 microm

56 ctam ring in CCF2, changing its fluorescence emission spectrum from green (520 nm) to blue (447 nm) a

57 ed-E5, a fluorescent protein that shifts its emission spectrum from green to red over time, was expre

58 Time-resolved measurements of the emission spectrum have been extended to a six decade tim

59 formed from above two reactions a bright CL emission spectrum having two peaks (518 nm for fluoresce

60 site, DC6C displayed a strongly blue-shifted emission spectrum, higher intrinsic fluorescence, and we

61 F80W:V21K also shows a shifted fluorescence emission spectrum in both di(C18:1)PC and di(C18:1)PA an

62 ction phenotype, and a shift in fluorescence emission spectrum in di(C18:1)PC not reversed in di(C18:

63 t in a significant shift in the fluorescence emission spectrum in dioleoylphosphatidylcholine [di(C18

64 units of AA Tauri possesses a rich molecular emission spectrum in the mid-infrared, indicating a high

65 nifit displays a GABA-dependent fluorescence emission spectrum in the range of 500-700 nm that permit

66 scence lifetime, good photostability, and an emission spectrum in the visible region.

67 The encoded bead emission spectrum indicates that the peak position of th

68 max) = 499 nm) matches the photoluminescence emission spectrum, indicating that the emission is from

69 External control of the emission spectrum is also achieved, highlighting the fle

70 The dye's fluorescence emission spectrum is blue-shifted 60 nm in liquid-ordere

71 The emission spectrum is characterised by multiple peaks wit

72 The emission spectrum is characterized by a broad band cente

73 This shift in emission spectrum is due to the transfer of the absorbed

74 uorescent fatty acid analogue Laurdan, whose emission spectrum is sensitive to structural differences

75 laced by a dye molecule (coumarin 102) whose emission spectrum is sensitive to the local electric fie

76 ation of both TPrA and Al(HQS)3, and the ECL emission spectrum (lambda(max) = 499 nm) matches the pho

77 Our data show an anomalous dependence of emission spectrum, lifetimes, and quantum yield (QY) on

78 For example, whereas the emission spectrum of 10(-3) M N-hexyl-N-methyl-3-(pyren-

79 The emission spectrum of 2 is found to depend on the nature

80 to unassembled tubulin was observed, but the emission spectrum of 2-AB-PT in the presence of the tubu

81 Exploiting the gamma-emission spectrum of 99mTc, increased uptake of Tc-Q58 i

82 nt changes in the intensity and shape of the emission spectrum of [K(7)(NBD),Nle(12)] alpha-factor du

83 Further, the emission spectrum of a blend of singly doped nanoparticl

84 ploit this 'self-mixing' effect to infer the emission spectrum of a semiconductor laser using a laser

85 When corrected for scattering, the emission spectrum of a thick lipofuscin deposit or intra

86 The shape of the emission spectrum of a thick sample of lipofuscin granul

87 on of individual granules also resembles the emission spectrum of A2E, but the spectrum of individual

88 The bioluminescence emission spectrum of both mutants was normal, and both y

89 ovide a possible explanation for the unusual emission spectrum of C5 protein.

90 d characteristic changes in the fluorescence emission spectrum of dansyl-calmodulin, and had an appar

91 ed characteristic shifts in the fluorescence emission spectrum of dansyl-CaM, with apparent affinitie

92 The fluorescence emission spectrum of Dauda bound to KcsA in bilayers of

93 n shows good agreement with the fluorescence emission spectrum of DSBFNPC.

94 Using intrinsic tryptophan fluorescence emission spectrum of ECD2 polypeptide and fluorescence a

95 or substitutions that alter the fluorescence emission spectrum of environmentally sensitive fluoresce

96 canning by exploiting the position-dependent emission spectrum of fluorophores above a simple biocomp

97 We detect in NGC 1333-IRAS 4B a rich emission spectrum of H2O, at wavelengths 20-37 microm, w

98 The ability to tailor the emission spectrum of high-temperature sources may find a

99 Trp17 dominates the emission spectrum of IL-1ra, while Trp120 is quenched pr

100 The emission spectrum of individual RPE molecules also displ

101 The emission spectrum of internalized A2E was also determine

102 An excimer peak was present in the emission spectrum of labeled S265C F-actin and in the la

103 The emission spectrum of LAURDAN was examined by two-photon

104 iloelectronvolts has long been sought in the emission spectrum of microquasars as evidence for the ex

105 The results show that the uncorrected emission spectrum of pyrene-poly(C) decreases by a facto

106 e components (dark, shot, and flicker), (ii) emission spectrum of the analyte, (iii) emission spectru

107 ylation resulted in an 8-nm red-shift of the emission spectrum of the attached IAANS probe and a redu

108 The emission spectrum of the btIr- and btpIr-based devices (

109 ce of Mg(2+); in the presence of Mg(2+), the emission spectrum of the CheA(F455W):ATP complex was red

110 charge-coupled device detector monitors the emission spectrum of the coil, which includes the dark l

111 using 100 discrete energy points in the beta-emission spectrum of the different radionuclides.

112 The NaCl-induced change in the Trp-31 emission spectrum of the double mutant on the zwitterion

113 W subcomplex indicates that the fluorescence emission spectrum of the enzyme is maximally perturbed w

114 of the substrate overlapped the fluorescence emission spectrum of the enzyme, these abnormalities wer

115 The emission spectrum of the fluorescence of the tryptophan

116 In this assay system, changes in the emission spectrum of the fluorophore acrylodan, induced

117 diation has the same spectral profile as the emission spectrum of the fluorophores.

118 een reported that shifts in the fluorescence emission spectrum of the introduced tryptophans in the b

119 The emission spectrum of the laser-generated breakdown plasm

120 the tubulin-colchicine complex resembled the emission spectrum of the ligand bound to microtubules.

121 e that ET is not dependent on overlap in the emission spectrum of the luminophore and the absorption

122 A close to ideal overlap between the emission spectrum of the NanoLuciferase receptor tag and

123 (ii) emission spectrum of the analyte, (iii) emission spectrum of the optical background, and (iv) tr

124 extractions, the nature of the fluorescence emission spectrum of the PEG phase after extraction was

125 tion in a high-signal-to-noise, mid-infrared emission spectrum of the planet itself.

126 did not reveal the presence of water in the emission spectrum of the planet.

127 We found that the emission spectrum of the protonated form does not exhibi

128 - and far-UV CD spectra, in the fluorescence emission spectrum of the single tryptophan residue at po

129 intensity and blue-shift of the fluorescence emission spectrum of the single tryptophan residue of th

130 The fluorescence emission spectrum of the single tryptophan residue-conta

131 proach is the voltage-dependent shift in the emission spectrum of the voltage-sensitive dye di-8-buty

132 The fluorescence emission spectrum of this enzyme is quenched differentia

133 The emission spectrum of this initial species mirrors the ab

134 e (TL), OSL, radioluminescence (RL), and OSL emission spectrum of this new material and carried out a

135 The emission spectrum of this probe indicated that the C ter

136 In contrast, the emission spectrum of Trp-141, located on the NH2-termina

137 (i) The fluorescence emission spectrum of Trp-151 and fluorescence-quenching

138 a pronounced blue shift in the fluorescence emission spectrum of wild type MBP and a peak at about 2

139 ing produced a red shift in the fluorescence emission spectrum of wild type MBP and a sharp hypochrom

140 pendent KSV values as well as a blue-shifted emission spectrum on O2 addition.

141 er desirable features, such as a red-shifted emission spectrum or enhanced photostability.

142 h ultraviolet B from lamps that have a broad emission spectrum or, more effectively, with lamps that

143 e dynamical weather structures may alter the emission spectrum over time.

144 ties (including lifetime, quantum yield, and emission spectrum) over time or in different chemical en

145 iguing phenomena, such as the Mollow-triplet emission spectrum, photon antibunching and coherent phot

146 ters its intrinsic (tryptophan) fluorescence emission spectrum, providing a strong indication that li

147 We used QDs and emission spectrum scanning multiphoton microscopy to dev

148 large unilamellar lipid vesicles (LUVs), its emission spectrum shifts up to 30 nm to the blue with in

149 e, in the H117T mutant the 77-K fluorescence emission spectrum shows a much smaller amplitude at 695

150 metry of inhibition for thrombin and gave an emission spectrum that discriminated between native, cle

151 l below the peak wavelength of the blackbody emission spectrum, the radiative heat flux increases by

152 m to long lifetime species with blue-shifted emission spectrum; the activation energy for nonradiativ

153 from short lifetime species with red-shifted emission spectrum to long lifetime species with blue-shi

154 orescence emission significantly, shifts the emission spectrum to shorter wavelengths, and also induc

155 ly, accompanied by significant shifts in the emission spectrum to shorter wavelengths.

156 vity of unstructured metals, resulting in an emission spectrum useful for solar thermophotovoltaics.

157 th recordings, or from opposite sides of the emission spectrum, varied linearly with the amplitude of

158 served, but the low-temperature fluorescence emission spectrum was drastically altered in the mutants

159 emission spectrum and shifts in the complete emission spectrum were determined for emission from plas

160 apoA-I that exhibits a distinct fluorescence emission spectrum when in different states of lipid asso

161 sing absorption profiles coinciding with the emission spectrum, which together fundamentally limit th

162 Blue shifts in the emission spectrum with time after excitation and systema