✦ LIBER ✦

32P-postlabeling analysis of DNA adducts formed by leukotriene A4 (LTA4)

✍ Scribed by Dorothee Funk; Bernd L. Sorg; Sabine C. Lindner; Heinz H. Schmeiser

Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 252 KB
Volume: 51
Category: Article
ISSN: 0893-6692
DOI: 10.1002/em.20547

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Influences of DNA isolation and RNA cont

Influences of DNA isolation and RNA contamination on carcinogen-DNA adduct analysis by 32P-postlabeling

✍ R.W.L. Godschalk; L.M. Maas; J.C.S. Kleinjans; F.J. Van Schooten 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 148 KB 👁 2 views

P-Postlabeling is a widely applied assay for the analysis of carcinogen-DNA adducts. Optimization of most steps in this assay has been given attention, but influences of DNA isolation and DNA purity on adduct quantitation have not been investigated systematically. In this study, DNA was isolated fro

Total nucleotide analysis of Hydra DNA a

Total nucleotide analysis of Hydra DNA and RNA by MEKC with LIF detection and 32P-postlabeling

✍ Monika Hassel; Michael G. Cornelius; Jochen vom Brocke; Heinz H. Schmeiser 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 151 KB 👁 2 views

Comparative 32P-postlabeling analysis of

Comparative 32P-postlabeling analysis of exogenous and endogenous DNA adducts in mouse skin exposed to a wood-preserving waste extract, a complex mixture of polycyclic and polychlorinated chemicals

✍ K. Randerath; G.-D. Zhou; E. Randerath; S.H. Safe; K.C. Donnelly 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 154 KB 👁 2 views

Wood preserving waste (WPW) sites contain nu-electrophilic quinoid compounds, which presummerous toxic compounds, including phenols, poly-ably were formed from phenols by chemical reaccyclic aromatic hydrocarbons (PAHs), polychlori-tions of waste material or biologically by oxidative nated dibenzodi

Identification of N-(deoxyguanosin-8-yl)

Identification of N-(deoxyguanosin-8-yl)-4-azobiphenyl by 32P-postlabeling analyses of DNA in human uroepithelial cells exposed to proximate metabolites of the environmental carcinogen 4-aminobiphenyl

✍ James F. Hatcher; Santhanam Swaminathan 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 172 KB 👁 1 views

Polycyclic aromatic hydrocarbon-inducibl

Polycyclic aromatic hydrocarbon-inducible DNA adducts: Evidence by 32P-postlabeling and use of knockout mice for Ah receptor-independent mechanisms of metabolic activation in vivo

✍ Sudha R. Kondraganti; Pedro Fernandez-Salguero; Frank J. Gonzalez; Kenneth S. Ra 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 264 KB 👁 2 views

## Abstract There is significant human exposure to polycyclic aromatic hydrocarbons (PAHs), many of which are potent carcinogens in laboratory animals and are suspected human carcinogens. The PAHs are bioactivated by cytochrome P450 (CYP)1A1/1B1 enzymes to reactive intermediates that bind to DNA, a