ライフサイエンスコーパス: red shift

1 -state lifetime and a corresponding spectral red shift.

2 s, whereas a classical model only predicts a red shift.

3 the fluorescence intensity decreases with a red shift.

4 The fluorescence emission of 1a film/NPs is red-shifted (~17 nm) compared with that of 1a solution i

5 C, enhanced charge transfer results in large red shifting (+40 nm) of its excitation/emission maxima.

6 Mito-MPVQ showed large red shifts (68 nm) and selective ratiometric signal upon

7 photoacoustic imaging, BphP1, with the most red-shifted absorption among genetically encoded probes.

8 These sulfones possess red-shifted absorption and emission spectra relative to

9 ituted or 2,12-disubstituted porphyrins with red-shifted absorption and emission spectra.

10 The BODIPYs 2b and 2c show red-shifted absorption and emission with higher fluoresc

11 n of a localized charge transfer state, with red-shifted absorption and emission.

12 l and chloride aerosol substrates exhibits a red-shifted absorption band ( approximately 450-650 nm)

13 nly F(-), AcO(-), and H2PO4(-) induced a new red-shifted absorption band that was attributed to a dep

14 mbled nanocomposites exhibited broadened and red-shifted absorption bands of AuNRs in nIR region due

15 entified to date, with Chl f having the most red-shifted absorption maximum because of a C2(1)-formyl

16 ChR variants with a red-shifted absorption maximum, such as the modified Vol

17 The npCOO(-) complexes exhibit red-shifted absorption profiles extending into the near-

18 he I- and B-forms (the former has a slightly red-shifted absorption relative to the latter) are based

19 d and synthesized with the goal of providing red-shifted absorption spectra relative to previously sy

20 m Chlamydomonas augustae (CaChR1) exhibits a red-shifted absorption spectrum as compared to Channelrh

21 n conducting ChR, now renamed PsACR1, with a red-shifted absorption suited for multicolor optogenetic

22 em by wavelengths that overlap only with the red-shifted absorption tails of anilines in frozen sampl

23 he substitution of acceptor on the C4 led to red-shifted absorption, while that on C7 retarded the ch

24 pounds containing 2,7-substitution exhibited red-shifted absorption, while the chromophore loading on

25 reate a pathway to synthesize complexes with red-shifted absorptions that possess long-lived, redox-a

26 This analogue red-shifted all of the rhodopsin variants tested, accomp

27 Remarkably, the same red-shifting amino acid changes occurred after the dupli

28 We therefore investigated the effect of red-shifting analogues of retinal, combined with red-shi

29 to the DBC ligands in DBC-UiO led to a 13 nm red shift and an 11-fold increase in the extinction coef

30 olid-state absorption spectra reveal further red shifts and increased relative intensities of DACT ba

31 ng of approximately 20 chains, which exhibit red-shifted and broadened PL compared to single-chain ag

32 , based on a resorufin scaffold, is the most red-shifted and FA sensitive in this series in terms of

33 IR) absorptions and metal insertion leads to red-shifted and intensified absorption features.

34 charge-transfer visible absorptions that are red-shifted and more intense than those of the parent W(

35 e isotopologues display Raman peaks that are red-shifted and spectrally resolved from the originally

36 tution of hexaphenylbutadiene, absorption is red-shifted and stability under ambient light is even mo

37 Dispersion images clearly depict the red-shifting and also broadening of the front side featu

38 dipole modes of the nanocarrots show a clear red shift, and the EELS maps show an asymmetric distribu

39 the highly conjugated quinoxalenediynes were red-shifted approximately 100-200 nm relative to those o

40 trol experiments, we propose that these peak red shifts are a consequence of the delocalization of co

41 re added to the nanostars, which resulted in red shifts as large as 51 nm and a limit of detection as

42 d an intense luminescence emission, slightly red-shifted as compared to the free AuNCs.

43 nd maximum emission (478 nm) which is 170 nm red-shifted as compared to uridine.

44 gths of maximum absorption and emission were red-shifted as pi conjugation was systematically extende

45 al characterization clearly shows increasing red-shifts as a function of extended conjugation within

46 from laser-induced fluorescence that occurs red-shifted at approximately 780 nm.

47 were simultaneously measured by correlating red-shifts at distinct resonance peaks caused by specifi

48 bate N identical withC vibrational frequency red-shifts back toward that of the free molecule upon in

49 to the aromatic linking unit, resulting in a red-shifted band above the valence-band edge of MIL-125.

50 The analogous amides did not show a nuN-H red-shifted band, as the electron donor orbital in the a

51 f 2a-d together with the appearance of a new red-shifted band.

52 In contrast, the absorption maximum of the red-shifted beta-carotene was attributed to two differen

53 The giant red shift between solution and bulk films arises from en

54 ansfer (CT) states that give rise to a large red-shift between absorption and emission in these molec

55 It has a red-shifted bioluminescence emission maximum at 600 nm a

56 This emission is the most red-shifted bioluminescence reported without using a res

57 Red-shifted bioluminescence reporters are desirable for

58 nt of beetle luciferin analogues that elicit red-shifted bioluminescence with firefly luciferase (Flu

59 Red-shifted bioluminescent emitters allow improved in vi

60 nescence near the absorption edge, we find a red-shifted, broadband (full-width at half-maximum of ab

61 Chrimson's excitation spectrum is red shifted by 45 nm relative to previous channelrhodops

62 viously reported six-porphyrin ring, but are red-shifted by approximately 300 cm(-1), reflecting incr

63 e generates a photoluminescence peak that is red-shifted by as much as 254 meV from the nanotube's or

64 e in the near-IR region with a substantially red-shifted (by more than 100 nm) lambda(max) at 790 nm

65 We conclude that the red-shifted Ca2+ indicator Cal-590 is well suited for in

66 We also find that the enhanced red-shift cannot be explained without accounting for sol

67 ic inputs using ChR2 together with ReaChR, a red-shifted channelrhodopsin.

68 A red-shifted charge-transfer resonance is observed, consi

69 a capable of performing photosynthesis using red-shifted chlorophylls, chlorophyll d and f, reduces c

70 nts and faster kinetics compared to existing red-shifted ChRs.

71 While modified azobenzene cores with a red-shifted cis-to-trans isomerization have been previou

72 an reproduce Halpha line profiles with large red-shifts closely matching those observed in a C1.5 fla

73 th maximum emission at 642 +/- 3 nm, a 10 nm red shift compared with the fluorescence of 1a film.

74 a long-lived emission that is significantly red-shifted compared to the band gap.

75 R) band positions for these nanocrystals are red-shifted compared to those for pristine silver partic

76 absorbance peaks at 350 and ~504 nm that are red-shifted compared to those of 1a dissolved in solutio

77 spectra have split Soret bands, including a red-shifted component characteristic of a P450-carbene c

78 We present a red-shifted cruxhalorhodopsin, Jaws, derived from Haloar

79 nm; D380N, lambdamax = 506 nm) and one with red-shifted (D380E, lambdamax = 533 nm) absorption maxim

80 etry of the trion PL peak and resulting peak red-shift depends both on the trion size and a temperatu

81 cross phase modulation with soliton fission, red-shifted dispersive waves were generated which led to

82 NR undergoes a shock-induced red-shift due to an increase both in density and in poly

83 n the SWCNT bandgap emission (E11) and a new red-shifted emission (E11(-)) were observed in the prese

84 er with the sandwich complexes producing new red-shifted emission and absorption bands.

85 Red-shifted emission bands, band broadening, and large S

86 plant light-harvesting complex explains the red-shifted emission by strong localization of the excit

87 to the CDs, the particle aggregation-induced red-shifted emission enables the development of the CD-b

88 ns of the imine XFs in different solvents, a red-shifted emission is detected, resulting in an altere

89 donor-acceptor pyrazoles display remarkably red-shifted emission maxima and pronounced positive solv

90 for many other desirable features, such as a red-shifted emission spectrum or enhanced photostability

91 The tetrasubstituted derivatives displayed red-shifted emission when compared to the monosubstitute

92 e PAS only or no Cys residues at all exhibit red-shifted emission with shorter lifetimes.

93 Probes with novel properties, such as red-shifted emission, large Stokes shifts, and high phot

94 and fuming of a solid sample gave blue- and red-shifted emissions, respectively.

95 display remarkable binding affinity toward a red-shifted environment-sensitive merocyanine derivative

96 ese phosphors feature an extremely broad and red-shifted Eu(2+) emission band; however, convincing ex

97 used for in vivo neurophysiology, GECIs with red-shifted excitation and emission spectra have advanta

98 Neptune, whereas the third, mCardinal, has a red-shifted excitation spectrum without reduction in bri

99 The red-shifted features only emerge when the ion pairs olig

100 The excess red-shift first appeared with 0.8 km.s(-1) impacts.

101 he far-red/infrared and exhibit the furthest red-shifted fluorescence emission thus far reported for

102 h CL is reported to produce a characteristic red-shifted fluorescence emission.

103 ter autonomously, thereby unmasking intense, red-shifted fluorescence emission.

104 vatofluorochromic behavior and significantly red-shifted fluorescence in solvents of high polarity an

105 We describe a red-shifted fluorescence resonance energy transfer (FRET

106 Here, we tested the red-shifted fluorescent Ca2+ indicator Cal-590 for deep

107 to increase the imaging depth is the use of red-shifted fluorescent dyes, as scattering of photons i

108 diate over mesoscopic distances and induce a red-shifted fluorescent emission from appropriate fluoro

109 ast few years a large series of the advanced red-shifted fluorescent proteins (RFPs) has been develop

110 Compared to conventional GFP-like red-shifted fluorescent proteins, iRFP670 and iRFP720 de

111 Here we report a red-shifted fluorescent substrate for ALDH, AldeRed 588-

112 he 8-silyloxyquinoline scaffold, producing a red-shifted fluoride probe (4) capable of detecting 50 m

113 drin, resulting in a more pH independent and red-shifted fluorophore.

114 rgent micelles and in liposomes, and contain red-shifted fluorophores that are suitable for high-thro

115 cter of the DTDKP core was demonstrated by a red shift following the electron-donating strength of th

116 s for the reducing gases, H(2) and CO, and a red shift for the oxidizing gas, NO(2).

117 green FP-based voltage indicators, a bright red-shifted FP-based voltage indicator has the intrinsic

118 Raman spectra show a significant and gradual red shift from 383 cm(-1) to 372 cm(-1) when the doping

119 ion of the coumarin ring results in a strong red-shift from 330 to 370 nm when the pH of solution is

120 on respond to light with maximal sensitivity red-shifted from 360 to 420 nm, consistent with an alter

121 inolinone displayed an absorption wavelength red-shifted from 470 to 540 nm (Deltalambda = 70 nm) wit

122 de backbone-can quench fluorophores that are red-shifted from intrinsic protein fluorescence, such as

123 ximum emission at about 637 +/- 4 nm, ~20 nm red-shifted from its fluorescence, while the ECL spectru

124 37 nm), the major LSPR band is progressively red-shifted from that of the gold cores with increasing

125 Since thioamides quench some fluorophores red-shifted from those naturally occurring in proteins,

126 ) = 480 nm, lambdaemis(report) = 640 nm) are red-shifted from those of the DCM-Cys probe (lambdaabs(p

127 hat the peak of the internal photon spectrum red-shifts from 765 to >/=800 nanometers.

128 We observed a red-shifted ground-state intermediate (GSI) that we assi

129 We discovered a subset of red-shifted GRs that exhibit high levels of fluorescence

130 .0, 7.0, and 9.0 as evident by the extensive red shift (>350 nm) of the wavelength of maximum tryptop

131 The red-shifted H1 tautomer is strongly favored in matched (

132 ssion, but struggle to reproduce closely the red-shifted Halpha lines.

133 Cyanobutadienyl corannulenes 5-8 show red-shifted ICT absorptions with end-absorptions approac

134 e simulation-derived vibrational spectrum to red shift in a manner that reproduces the red-shift prev

135 4-c]chromene-6,7-diones caused a significant red shift in both the absorption and emission maxima, an

136 tution in green fluorescent protein causes a red shift in emission to yield a class of mutants known

137 allization event that can be traced with the red shift in Ge K edge energy which is also identified b

138 confirmed that unencapsulated TPT exhibits a red shift in its spectrum as pH is increased.

139 l lacking both Tyr and Trp residues causes a red shift in NEIL1's intrinsic Trp-specific fluorescence

140 he WO(3) matrix, contributed to the observed red shift in optical absorption.

141 Optical measurements showed a progressive red shift in plasmonic behavior between Au NPs, Au NPPs,

142 ouble mutant, inducing an astonishing 200 nm red shift in the absorbance maximum.

143 lectronic characterization showed a dramatic red shift in the absorption and the emission and a reduc

144 -dependent optical signal characterized by a red shift in the carotenoid peak of the triplet-minus-si

145 i) shorter fluorescence lifetimes, and (iii) red shift in the emission spectra, compared with the hyd

146 e detection of cysteine was accompanied by a red shift in the fluorescence maximum of PBI, from 532 t

147 Glycine also caused a red shift in the OH stretch region, whereas betaine mini

148 individual dimers which reveal a significant red shift in the plasmonic resonance peaks, consistent w

149 V absorption maximum undergoes a significant red shift in the presence of acetate anions, providing a

150 group did not lead to a significant further red shift in these spectra.

151 ution of the mixture of VK1 and heparin show red shifts in both the channels on changing the concentr

152 of up to +80 nm that can be transcribed into red shifts in emission of up to +140 nm by Forster reson

153 and solid-ordered (So) membranes results in red shifts in excitation of up to +80 nm that can be tra

154 he chromophores can result in either blue or red shifts in the absorbance and emission spectra.

155 ne and thiophene rings, which results in the red-shift in absorption upon substitution of tellurium f

156 ry target strand, thereby effecting a 330 nm red-shift in cluster absorption and a background-limited

157 solutions of 1-4 was observed as seen by the red-shift in ECL maxima relative to their corresponding

158 sters and the extents of the UV-vis spectrum red-shift in lambdamax have a strong positive correlatio

159 SWS2, including two changes known to cause a red-shift in light absorption, and is favored in blackwa

160 The red-shift in low-energy absorption is likely due to both

161 mponent in these cationic NBGCPEs leads to a red-shift in the absorption spectra and to a modificatio

162 olecules, in comparison to the corresponding red-shift in the individual ligand.

163 The red-shift in the low-energy transition leads to optical

164 eals that heavy atom substitution leads to a red-shift in the low-energy transition, while the high-e

165 uning is due to the cumulative effect of the red-shift in the LSP energy and the electrostatic field

166 olved in toluene and exhibited a significant red-shift in the optical properties toward the infrared

167 ilar spectral color (or peak position) but a red-shift in the peak positions by same amount relative

168 The red-shift in the plasmon absorption spectra of fructose

169 ed microorganisms exhibited a characteristic red-shift in the spectra.

170 t the ground state UV-vis absorption of 7 is red-shifted in comparison to the parent NDI 1.

171 u(2+) and CaAlSiN3:Eu(2+), are commonly more red-shifted in photoluminescence and have better thermal

172 changes in the absorption spectra, which is red-shifted, in 1:1 or 1:2 (sensor/anion) stoichiometry.

173 This red shift indicates formation of H-bonds to the alphaKG

174 a of as-prepared nanostructures were largely red-shifted, indicating J-type aggregation for all mater

175 vel bacteriochlorins demonstrated remarkably red-shifted intense Q(y) absorption bands observed in th

176 ment undergoes a photocycle with a prominent red-shifted intermediate whose formation and decay kinet

177 CO2 in the polymer displayed a red-shifted IR absorption spectrum and a shorter vibrati

178 ited state deactivation dynamics of the most red-shifted iRFPs: iRFP702, iRFP713 and iRFP720.

179 We find that the experimentally observed red-shift is consistent with identifying the emissive st

180 amin A2, eliminating the animal's ability to red-shift its photoreceptor spectral sensitivity and red

181 One (alpha) is the functional pigment that red-shifts its spectral properties upon trimer formation

182 bdamax = 1476 nm (P2), which is the farthest red-shifted lambdamax reported to date for a soluble pro

183 nd emission spectral bands are significantly red-shifted (lambdamax = 495-590 nm, lambdaem = 533-683

184 'Red-shifted' luciferases, which emit light of longer wav

185 We describe the development of red-shifted luciferins based on synthetic coelenterazine

186 The LSPR red shift magnitude is linearly proportional to the incr

187 uorescent acceptor ShadowG for mTFP1 and the red-shifted mKate2 for LSSmOrange.

188 uted evenly along the retinal molecule while red-shifting mutations were clustered near the residue K

189 shifting analogues of retinal, combined with red-shifting mutations, on the spectral properties and p

190 gth of this hydrogen bond results in a large red shift, nearly 189 cm(-1), on the alcohol stretching

191 show the hydrated electron has a broader and red-shifted O-H stretching band compared with bulk water

192 ltaneous formation of two pi-hydrogen bonds (red-shifting O-H...pi and blue-shifting ortho-C-H...pi)

193 of the systems, which is in agreement with a red-shifting observed for the lambdamax of the substitut

194 A red shift of 18.7 nm in resonance wavelength is recorded

195 structures: The solvent- and pH-independent red shift of absorption and emission of push-pull fluoro

196 gregation on addition of cerium indicated by red shift of SPR peak followed by complete precipitation

197 n lowering of the band gap, which leads to a red shift of the absorption spectrum in these benzothiad

198 The aggregation of AuNPs results in a red shift of the AuNP plasmonic spectrum, or a color cha

199 Poorly basic anions (Cl(-), Br(-)) cause a red shift of the emission band(s).

200 ssociated with the two terms are distinct; a red shift of the H(A) ground-state bleaching is observed

201 noncavity model can capture the experimental red shift of the hydrated electron's absorption spectrum

202 es an increase in the intensity and a steady red shift of the longitudinal surface plasmon resonance

203 ed, electron-releasing substituents induce a red shift of the low-energy absorption allowing excitati

204 ental and calculated far-IR spectra showed a red shift of the low-frequency peaks upon peptide bindin

205 the anthracene sidewalls leads to a smaller red shift of the squaraine absorption and emission bands

206 omotive scaling of electron temperature, and red shifting of emitted second-harmonic.

207 ngle tuning mutations that incurred blue and red shifts of 42nm and 22nm, respectively, that did not

208 ochemical mechanism accounting for the Raman red shifts of phenylalanine and thymine in response to (

209 f the negatively charged carboxylates causes red shifts of the absorption maximum.

210 Pressure-induced blue and red shifts of the corresponding vibrational modes indica

211 for the fluorescence emission intensity and red shifts of the emission wavelength of r-betaLg sugges

212 Large red shifts of the UV/vis absorption bands evidence effic

213 n the visible and NIR region, with a further red-shift of about 90 and 60 nm, respectively, compared

214 We observed a reproducible red-shift of an adenine-related marker band from 733 to

215 In the symmetric complexes the red-shift of the 0-0 peak with increasing |J(0)|, as wel

216 e the processing key to a drastic change and red-shift of the absorption characteristics.

217 IR spectroscopic measurements showed a clear red-shift of the C identical withC and ferrocenyl ring =

218 The model successfully explains the red-shift of the CN stretch as a function of the dielect

219 ent oxidation, leading to an enhancement and red-shift of the gold surface plasmon resonance (SPR).

220 A significant red-shift of the PL peak for Eu(3+) was observed.

221 tion with dielectric liquids leads also to a red-shift of the plasma edge.

222 d optical response, as witnessed by a strong red-shift of the probe absorption bands, thus allowing t

223 Despite the spectral red-shift of their lowest absorption band, the fluoresce

224 via Langmuir-Blodgett deposition results in red-shifting of some, but not all, of the plasmon featur

225 the aggregation of the metallic cores and a "red-shift" of fluorescence.

226 ion and calcium imaging by coexpression of a red-shifted opsin and a genetically encoded calcium indi

227 eurons with single-cell precision, using the red-shifted opsin C1V1(T).

228 Poly(cyclosilane) has red-shifted optical absorbance relative to the monomer.

229 All examples exhibit red-shifted optical absorption, as well as solid-state o

230 charged states, characterized by remarkably red-shifted optical absorptions, extending beyond 2200 n

231 orin-like chromophores that possess slightly red-shifted optical spectra compared to the correspondin

232 m) and single-neuron photostimulation with a red-shifted optogenetic probe (C1V1, lambda = 1,064 +/-

233 the highest voltage sensitivity to date for red-shifted PeT-based voltage sensors, and is compatible

234 PsChR was 437 nm at neutral pH and exhibited red shifts (pKa values at 6.6 and 3.8) upon acidificatio

235 planar excited state, sulfide donors promote red-shifting polarization.

236 um heterocycle to construct a panel of novel red-shifted polymethine dyes, with emission wavelengths

237 ry to tumours, achieve deeper tissue PDT via red-shifted porphyrin Q-bands, energy transfer and sonod

238 to red shift in a manner that reproduces the red-shift previously reported experimentally.

239 m and emits at 675 nm that makes it the most red-shifted protein of the GFP-like protein family.

240 of fluorescence quantum yield and absorption red shift, provides high labeling selectivity.

241 port the synthesis and characterization of a red-shifted PTL, L-MAG0460, for the light-gated ionotrop

242 hore with, for the parent oxazolochlorin 12, red-shifted Q(x) band with enhanced oscillator strengths

243 isosbestic point at 473 nm, pKa of 7.5, and red shift relative to fluorescein.

244 tails into the near-IR and is significantly red-shifted relative to that of the related complex [Ru(

245 To our knowledge, this is by far the largest red shift reported for any retinal protein.

246 The peptide design is inspired by the red shift seen in the yellow fluorescent protein that re

247 regular pentamers (2 and 3) possessed a new, red-shifted shoulder structure that suggests the packing

248 The spectrum expands along the red shifted side of the spectrum faster than on the blue

249 CT bands in the 800-1100 nm NIR region and a red-shifted Soret band (lambdamax, 443 nm).

250 In addition, the red-shifted spectral profile of BeRST 1, relative to com

251 ts with augmented light sensitivity (ChR2+), red-shifted spectral sensitivity (ChR2-RED) or both (ChR

252 es (Cl(-), Br(-), I(-)) is evaluated through red shifted SPR along with continuous increase in absorb

253 d with 2D MXene yield a broad, significanlty red-shifted SPR band with a peak at 230 nm.

254 the band edge, and we observe a continuously red-shifting streak.

255 cale required for cellular imaging, but does red shift the emission maximum of probe 4 in comparison

256 The resulting increase in particle spacing red shifts the 2-D diffracted light.

257 drawing group at the meso position of BODIPY red shifts the absorption and emission with enhanced qua

258 n of InN nanocrystals with NOBF4 is found to red-shift the absorption onset to approximately 1.3 eV a

259 nd-capping with a diphenylamine unit further red-shifted the absorption and emission profiles and imp

260 Although red-shifting the absorption wavelength to enter the ther

261 lls increases the net refractive index, thus red-shifting the effective optical thickness (EOT).

262 These experiments showed that TMAO red-shifts the OH stretch of the IR spectrum via a mecha

263 dium increases when the laser wavelength was red shifted, the threshold laser power for reliable guid

264 lf-doping of SnO2-x nanocrystals with Sn(2+) red-shifts their absorption to the visible region and si

265 A red-shift to 380 nm was realized by addition of another

266 asmon resonance (SPR) band of Tyr-Au NPs was red-shifted to 596 and 616nm and the emission peak (Tyr)

267 ization microscopy dyes, and is sufficiently red-shifted to allow multicolor imaging.

268 the most interesting cases, the spectra were red-shifted to maximum absorbance at wavelengths longer

269 velength lambdamax band, bucking the general red-shifting trend expected for such linkages.

270 ed on their sensitivity to excess light, the red-shifted triplet-minus-singlet signal was tightly cor

271 lly indirect band gap, an important emission red shift up to the near-infrared region (730 nm) is obs

272 a upflows, and Halpha hydrogen emission with red shifts up to 1-4 A.

273 RNA structures exhibit excitonic transitions red-shifted up to 0.6 eV compared to the B-form of stack

274 ng a dominant J-type excitonic coupling with red-shifts up to 45 nm, exceptionally small line widths

275 ed photophysical properties, including large red-shifts (up to 82 nm) and stimuli-responsive behavior

276 An ultraviolet-visible spectral red shift upon OFX adsorption indicated formation of inn

277 ve rise to an intense, broad emission, which red shifts upon increasing the solvent polarity and stem

278 r transition in (Fe(II)/alphaKG)FIH which is red-shifted upon CAD binding.

279 he pure CE conformer in water has a slightly red-shifted UV spectrum with respect to that in the gas

280 We express CsChrimson, a red-shifted variant of channelrhodopsin, in specific che

281 0 H(2) per metal cation reveal that strongly red-shifted vibrational modes arise from isolated H(2) b

282 ions such as a slow light inactivation and a red-shifted visible absorption maximum as compared with

283 longwave retinal sensitivity is enhanced by red-shifted visual pigments, a longwave reflecting tapet

284 ally map action potential propagation with a red-shifted voltage sensitive dye in whole mouse hearts.

285 Occurring in ca. 10 ns, this NR red-shift was caused by the formation of an ion pair cre

286 A profound red-shift was observed in the absorption and fluorescenc

287 This new class of dyes displays red-shifted wavelengths of emission and greater sensitiv

288 Large red shifts were observed in the fluorescence emission ma

289 i(5-x)Al(x)N(8-x)O(x) lattices, leading to a red shift when the M = Ba and Sr host cations are larger

290 rly all absorption maxima were significantly red-shifted when compared to Prodan.

291 The computed absorption maximum is red-shifted when compared to the gas phase.

292 on wavelength of the photonic superstructure red-shifted, whereas its reverse process occurred upon i

293 nd phenol, NR showed an excess shock-induced red-shift with a distinct time dependence not present in

294 The frequencies of the AAD free-OH stretch red-shift with increasingly positive charge, consistent

295 H(3))(2)(G)Cl](+) at 1718 cm(-1), remarkably red-shifted with respect to an unperturbed C horizontal

296 e-emission ECL signal also appeared slightly red-shifted with respect to the main luminophore emissio

297 etonitrile solutions are on average 9 cm(-1) red-shifted with respect to unbiased gas-phase values.

298 It is found that the CN stretch frequency red-shifts with increasing dielectric constant.

299 The plasma frequency red-shifts with increasing lattice constant and blue-shi

300 = 1.6 muM), explaining previous reports of a red-shifted XplA Soret band in pure enzyme.