Chemical Communications 2003-04-21

A new dark quencher for use in genetic analysis.

Jonathan P May, Lynda J Brown, Ivo Rudloff, Tom Brown

Index: Chem. Commun. (Camb.) (8) , 970-1, (2003)

Full Text: HTML

Abstract

A novel, long-wavelength, non-fluorescent quencher (LQ), based on 1,4-diaminoanthraquinone, has been incorporated at the 3' and 5'-termini of oligonucleotides. The quencher has been used in Molecular beacons, efficiently quenching the long wavelength fluorophore, Cy5.

Related Compounds

  • 1,4-Diaminoanthraq...

Related Articles:

Sensitivity of the valence structure in diruthenium complexes as a function of terminal and bridging ligands.

2014-06-16

[Inorg. Chem. 53(12) , 6082-93, (2014)]

Vibrational analysis of 1,4-diaminoanthraquinone and 1,5-dichloroanthraquinone. A joint FTIR, FT-Raman and scaled quantum mechanical study.

2005-06-01

[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 61(8) , 1799-809, (2005)]

Speciation determination of chromium using 1,4-diaminoanthraquinone with spectrophotometric and spectrofluorometric methods.

2009-06-01

[Anal. Sci. 25(6) , 807-12, (2009)]

The mutagenic effect in bacteriophage T4D of a hair dye, 1,4 diaminoanthraquinone, and of two solvents, dimethylsulfoxide and ethanol.

1983-01-01

[Hereditas 99(2) , 209-13, (1983)]

Synthesis and antibacterial activity of some novel chiral fluorophoric biscyclic macrocycles.

2007-09-15

[Bioorg. Med. Chem. Lett. 17 , 5270-3, (2007)]

More Articles...