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1 th a fluorophore (fluorescein) and quencher (dabcyl).
2 contain a donor/acceptor FRET pair (FITC and DABCYL).
3 ents a superior alternative to the much-used dabcyl.
4      In comparison with the organic quencher Dabcyl (4,4'-dimethylaminophenyl azo benzoic acid), meta
5 peptide flanked by the FRET fluorophore pair DABCYL and EDANS.
6 nd 4-(4-dimethylaminophenylazo)benzoic acid (DABCYL) are attached to the N-terminus and the lysyl sid
7 (4-(4-dimethylaminophe nyl azo)benzoic acid (DABCYL))-Arg and (7-methoxycoumarin-4-yl)acetyl (MCA))-S
8  4-(4'-dimethylaminophenylazo) benzoic acid (DABCYL) as a quencher.
9 und to be superior to the corresponding Cy3B/DABCYL Beacon.
10  substrate DNA modified with the fluorescein/dabcyl couple allowed to measure AA concentration within
11  1-Pyreneacetamide, 1-pyrenecarboxamide, and DABCYL derivatives have been used in preparation of mole
12 ophenylazo)benzoyl and 5-carboxyfluorescein (Dabcyl/Fam) pair and are based on known cleavage sequenc
13 e nucleic acid was modified with fluorescein/dabcyl FRET pair across the cleavage site.
14 dimethylamino)phenyl)azo) benzoic acid (FITC/DABCYL) FRET pair to produce a signal upon substrate cle
15 ing tested than with more traditional (EDANS/DABCYL) FRET protease substrates.
16 Ala-Arg peptide bond separates the quencher, DABCYL, from the donor, EDANS, and results in a large in
17 l-permeable FRET substrate SM-P124 (Ac-GRRRK(Dabcyl)-GGAANC(MeOBn)RMGG-fluorescein).
18 te stimulation, depends on the presence of a DABCYL group on the peptide N terminus.
19                    The CD23-based substrate, Dabcyl-His-Gly-Asp-Gln-Met-Ala-Gln-Lys-Ser-Lys(Fam)-NH2,
20            The advantage of hydrodabcyl over dabcyl is exemplarily demonstrated for the cleavage of t
21                       Therefore, fluorescein-Dabcyl-labeled Foerster resonance energy transfer (FRET)
22 TPs as the IAEDANS comes into contact with a Dabcyl-labeled, one-base gapped DNA.
23     The precursor TNF-alpha-based substrate, Dabcyl-Leu-Ala-Gln-Ala-Homophe-Arg-Ser-Lys(Fam)-NH2, is
24 annealed to a complementary 18-nucleotide 5'-Dabcyl-modified DNA.
25      Thus, the standard peptides contain the dabcyl moiety for determination of the amount in a sampl
26 e selected beacons was located adjacent to a DABCYL moiety in the capture oligonucleotide; addition o
27 rene monomers on the 5' end and the quencher DABCYL on the 3' end, were engineered and employed for r
28    A fluorescent donor (Edans) and quencher (Dabcyl) pair was added to the C- and N-termini of a supp
29 orin structure and further conjugated with a dabcyl quencher.
30 poration of a bulky gamma-phosphate-O-linker-dabcyl substituent.
31 ic acid (IAEDANS) and the DNA substrate with Dabcyl, we are able to observe rapid fingers closing in
32 A very popular dark fluorescence quencher is dabcyl, which is a hydrophobic azobenzene derivative.
33 onfirmed that the best substrate, FRET-P2 [K(Dabcyl)YRVAFQKLAE(Edans)K], was approximately 100-fold m