TRITC
| Strukturformel | |||||||||||||||||||
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| Allgemeines | |||||||||||||||||||
| Name | TRITC | ||||||||||||||||||
| Andere Namen |
5(6)-Tetramethylrhodaminisothiocyanat | ||||||||||||||||||
| Summenformel | C25H21N3O3S | ||||||||||||||||||
| Kurzbeschreibung |
Feststoff[1] | ||||||||||||||||||
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| Eigenschaften | |||||||||||||||||||
| Molare Masse | 443,52 g·mol−1 | ||||||||||||||||||
| Aggregatzustand |
fest[1] | ||||||||||||||||||
| Löslichkeit | |||||||||||||||||||
| Sicherheitshinweise | |||||||||||||||||||
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| Wenn nicht anders vermerkt, gelten die angegebenen Daten bei Standardbedingungen (0 °C, 1000 hPa). | |||||||||||||||||||
TRITC ist ein Kupplungsreagenz aus der Gruppe der Isothiocyanate des Tetramethylrhodamins. 5(6)-TRITC wird als oranger Farbstoff zur Fluoreszenzmarkierung von Proteinen und Nukleinsäuren verwendet.[2][3] Bei einem FRET dient TRITC oftmals als Fluoreszenz-Akzeptor.
Einzelnachweise
- ↑ a b c d e Datenblatt 5(6)-Tetramethylrhodamine isothiocyanate bei Alfa Aesar, abgerufen am 22. Oktober 2016 (Seite nicht mehr abrufbar).
- ↑ Greg T. Hermanson: Bioconjugate Techniques. Academic Press, 2013, ISBN 978-0-12-382240-6, S. 409.
- ↑ A. Pedone, J. Bloino, S. Monti, G. Prampolini, V. Barone: Absorption and emission UV-Vis spectra of the TRITC fluorophore molecule in solution: a quantum mechanical study. In: Physical Chemistry Chemical Physics. Band 12, Nummer 4, Januar 2010, S. 1000–1006, doi:10.1039/b920255b, PMID 20066385.
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