A Colorific and Fluorescent Dual Signal Probe for DNA

Tong Wu; Xiao Jun Peng

doi:10.4028/www.scientific.net/AMR.441.398

Paper Titles

Relationship between Various Chemical Treatments on the Mechanical, Anti-Felting and Dyeing Properties of Wool
p.376

Synthesis and Crystal Structure of the Complex of (R,R)-N,N’-bis(salicylal)-1,2-Cyclohexanediamine with Fe³⁺
p.382

Synthesis and Crystal Structure of a New Ni²⁺Complex¹
p.387

Synthesis and Transport of K⁺ Ions of Mono-Substituted Calix[4]arenes
p.392

A Colorific and Fluorescent Dual Signal Probe for DNA
p.398

Electrochemical Synthesis of Methoxy-Dimethylbenzene and its Application in Gasoline
p.403

A Novel Procedure for the Synthesis of 1,2:5,6-di-O-Isopropylidene-D-Glucofranose by Ultrasound
p.408

Effect of Gold Nanoparticles on Fluorescence Properties of Hyperbranched Poly(amido amine)s
p.413

Synthesis of Symmetrical N,N′-Alkylidene Bisamides Using Zinc Chloride as a Lewis Acid Catalyst
p.421

HomeAdvanced Materials ResearchAdvanced Materials Research Vol. 441A Colorific and Fluorescent Dual Signal Probe for...

A Colorific and Fluorescent Dual Signal Probe for DNA

Abstract:

The synthesis and characteristics of a new styryl colorific and fluorescent dual signal probe for DNA are described. Sty-HPy shows a high fluorescence enhancement (> 35-fold) in conjunction with a visible colorific change (45 nm red-shift) when bound to dsDNA. The large Stokes shift (140 nm) and sensitive colorific response to DNA are both attributed to the rational design of intramolecular charge transfer (ICT) intra Sty-HPy.

You might also be interested in these eBooks

Eco-Dyeing, Finishing and Green Chemistry

View Preview

Info:

Periodical:

Advanced Materials Research (Volume 441)

Pages:

398-402

DOI:

https://doi.org/10.4028/www.scientific.net/AMR.441.398

Citation:

Cite this paper

Online since:

January 2012

Authors:

Tong Wu, Xiao Jun Peng

Keywords:

Colorific Probe, Fluorescent DNA Probe, ICT, Styryl Dye

Export:

RIS, BibTeX

Price:

Permissions CCC:

Request Permissions

Permissions PLS:

Request Permissions

Сopyright:

Citation:

References

[1] L.J. Kricka and P. Fortina, Clin. Chem. 55 (2009) 670.

Google Scholar

[2] Information on http: /www. invitrogen. com/site/us/en/home/References/Molecular-Probes- The-Handbook. html.

Google Scholar

[3] H.A. Crissman and G. T. Hirons, Methods Cell Biol. 41 (1994) 195.

Google Scholar

[4] T. Deligeorgiev, N. Gadjev, A. Vasilev, K. -H. Drexhage and S.M. Yarmoluk, Dyes Pigments. 70 (2006) 185.

DOI: 10.1016/j.dyepig.2005.05.010

Google Scholar

[5] G.R. Rosania, J.W. Lee, L. Ding, H. -S. Yoon and Y. -T. Chang, J. Am. Chem. Soc. 125 (2003) 1130.

Google Scholar

[6] J.W. Lee, M. Jung, G.R. Rosania and Y. -T. Chang, Chem. Commun. (2003) 1852.

Google Scholar

[7] S. Feng, Y.K. Kim, Q. Yang, Y. -T. Chang, Chem. Commun. 6 (2010) 436.

Google Scholar

[8] R.A. Velapoldi and H.H. Tønnesen, J. Fluoresc. 14 (2004) 465.

Google Scholar

[9] M.J. Frisch: Gaussian 09, Revision A. 02, Gaussian, Inc., Wallingford CT (2009).

Google Scholar

[10] L.C. Zhou, G.J. Zhao, J.F. Liu, K.L. Han, Y.K. Wu, X.J. Peng, M.T. Sun, J. Photochem. Photobiol. A: Chemistry. 187 (2007) 305.

Google Scholar

[11] M.R. Dreizler, E.K.U. Gross: Density Functional Theory, Springer Verlag, Heidelberg (1990).

Google Scholar

[12] E.K.U. Gross, W. Kohn, Phys. Rev. Lett. 55 (1985) 2850.

Google Scholar

[13] R.E. Stratmann, G.E. Scuseria, M.J. Frisch, J. Chem. Phys. 109 (1998) 8218.

Google Scholar

[14] G.L. Silva, V. Ediz, D. Yaron, B.A. Armitage, J. Am. Chem. Soc. 129 (2007) 5710.

Google Scholar

[15] J.T. Petty, J.A. Bordelon, M.E. Robertson, J. Phys. Chem. B. 104 (2000) 7221.

Google Scholar