Complementary Methods of Processing diS-C3(3) Fluorescence Spectra Used for Monitoring the Plasma Membrane Potential of Yeast: Their Pros and Cons
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F14%3A10288249" target="_blank" >RIV/00216208:11320/14:10288249 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1007/s10895-013-1323-6" target="_blank" >http://dx.doi.org/10.1007/s10895-013-1323-6</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s10895-013-1323-6" target="_blank" >10.1007/s10895-013-1323-6</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Complementary Methods of Processing diS-C3(3) Fluorescence Spectra Used for Monitoring the Plasma Membrane Potential of Yeast: Their Pros and Cons
Popis výsledku v původním jazyce
Carbocyanine dye diS-C-3(3) was repeatedly employed in monitoring the plasma membrane potential of yeast and other living cells. Four methods of measuring and evaluating probe fluorescence signal were used in different studies, based on following fluorescence parameters: fluorescence intensity emitted within a certain spectral interval, F(580)/F(560) fluorescence emission ratio, wavelength of emissionspectrum maximum, and the ratio of respective fluorescence intensities corresponding to the diS-C-3(3) bound to cytosolic macromolecules and remaining dissolved in the aqueous cell medium (i.e., unbound, or free). We have shown that data corresponding to the three latter spectral assessments of diS-C-3(3) accumulation in cells is mutually convertible, which means that their alternative use cannot lead to ambiguities in the interpretation of the results of biological experiments.
Název v anglickém jazyce
Complementary Methods of Processing diS-C3(3) Fluorescence Spectra Used for Monitoring the Plasma Membrane Potential of Yeast: Their Pros and Cons
Popis výsledku anglicky
Carbocyanine dye diS-C-3(3) was repeatedly employed in monitoring the plasma membrane potential of yeast and other living cells. Four methods of measuring and evaluating probe fluorescence signal were used in different studies, based on following fluorescence parameters: fluorescence intensity emitted within a certain spectral interval, F(580)/F(560) fluorescence emission ratio, wavelength of emissionspectrum maximum, and the ratio of respective fluorescence intensities corresponding to the diS-C-3(3) bound to cytosolic macromolecules and remaining dissolved in the aqueous cell medium (i.e., unbound, or free). We have shown that data corresponding to the three latter spectral assessments of diS-C-3(3) accumulation in cells is mutually convertible, which means that their alternative use cannot lead to ambiguities in the interpretation of the results of biological experiments.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
BO - Biofyzika
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2014
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Fluorescence
ISSN
1053-0509
e-ISSN
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Svazek periodika
24
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
7
Strana od-do
541-547
Kód UT WoS článku
000334183100030
EID výsledku v databázi Scopus
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