TRITC
| Structural formula | |||||||||||||||||||
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| General | |||||||||||||||||||
| Surname | TRITC | ||||||||||||||||||
| other names |
5 (6) tetramethylrhodamine isothiocyanate |
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| Molecular formula | C 25 H 21 N 3 O 3 S | ||||||||||||||||||
| Brief description |
Solid |
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| properties | |||||||||||||||||||
| Molar mass | 443.52 g mol −1 | ||||||||||||||||||
| Physical state |
firmly |
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| solubility |
soluble in DMSO or methanol |
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| safety instructions | |||||||||||||||||||
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| As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . | |||||||||||||||||||
TRITC is a coupling reagent from the group of isothiocyanates of tetramethylrhodamine . 5 (6) -TRITC is used as an orange dye for fluorescent labeling of proteins and nucleic acids . In a FRET , TRITC often serves as a fluorescence acceptor.
Individual evidence
- ↑ a b c d e data sheet 5 (6) -Tetramethylrhodamine isothiocyanate from AlfaAesar, accessed on October 22, 2016 ( PDF )(JavaScript required) .
- ↑ Greg T. Hermanson: Bioconjugate Techniques. Academic Press, 2013, ISBN 978-0-12-382240-6 , p. 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 . Volume 12, Number 4, January 2010, pp. 1000-1006, doi: 10.1039 / b920255b , PMID 20066385 .