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largely(passive) are ... influencedFluorescence spectra
exposure to solvent and or quenchers present in the dissolver(passive) are largely influenced byFluorescence spectra
exposure to solvent and or quenchers present in the solvent(passive) are mostly influenced byFluorescence spectra
not to substantially overlap any excitation spectra of the fluorescent substances(passive) are setEmission spectra of the fluorescent substances
surface plasmonscould influenceluminescence emission spectra
of sharp ZPLs and broad intensity distributions(passive) are composedFluorescence spectra
the reabsorption of the tissue(passive) are influenced byFluorescence emission spectra
a combination of the orientational dipolar solvent - solute relaxation and the hydrogen bond interaction(passive) is caused bythe perturbation of protic solvents on the fluorescence spectra
pullulan and cyclodextrins(passive) caused byfluorescence spectra
different rates of metabolismresultin different fluorescence emission spectra
x(passive) is influenced byFluorescence spectra
from excitation of the H bandoriginatedfrom excitation of the H band
from interactions between DOX - labeled MSNs - SS - DMSA and varied concentrations of GSH for 1 h ( a ) andresultedfrom interactions between DOX - labeled MSNs - SS - DMSA and varied concentrations of GSH for 1 h ( a ) and
rhodamine moieties with a fluorescence maximum at 579 nm in aqueous media in aqueous HEPES ( 2-[4-(2-hydroxy- ethyl)-1-piperazinyl]ethanesulfonic acid ) buffer ( 0.01 Moriginatedrhodamine moieties with a fluorescence maximum at 579 nm in aqueous media in aqueous HEPES ( 2-[4-(2-hydroxy- ethyl)-1-piperazinyl]ethanesulfonic acid ) buffer ( 0.01 M
to aggregation ... on a silicon substrate for 488 nm and 532 nm excitation and also find a red - shift in λem for longer excitation wavelengthsleadsto aggregation ... on a silicon substrate for 488 nm and 532 nm excitation and also find a red - shift in λem for longer excitation wavelengths
from population of single rovibronic levels in the A1Π(v 0 = 3 , 4 ) bands for 12C 16O and the A1Π(v 0 = 3 ) bands for 13C 16Oresultingfrom population of single rovibronic levels in the A1Π(v 0 = 3 , 4 ) bands for 12C 16O and the A1Π(v 0 = 3 ) bands for 13C 16O
to their easy identification and quantificationleadsto their easy identification and quantification
from the accumulation of dyes in single cellsresultingfrom the accumulation of dyes in single cells
from interactions of the high energy x - rays with a patient 's body which provide information regarding tissue propertiesresultingfrom interactions of the high energy x - rays with a patient 's body which provide information regarding tissue properties
mainly of the emissions of extracellular proteins and that the differences in the intensity of their emissions reveal the changes in the tissue structure and morphologyare composedmainly of the emissions of extracellular proteins and that the differences in the intensity of their emissions reveal the changes in the tissue structure and morphology
into its effect on emissions and performance of an engineresultinginto its effect on emissions and performance of an engine
from levels populated by VET after excitation of states in the OHoriginatingfrom levels populated by VET after excitation of states in the OH