Array comparative genomic hybridization with cyanin cis-platinum-labeled DNAs
Author(s) -
Anton K. Raap,
Marja J.M. van der Burg,
Jeroen Knijnenburg,
Eric J. Meershoek,
Carla Rosenberg,
Joe W. Gray,
J. Wiegant,
John Hodgson,
Hans J. Tanke
Publication year - 2004
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/04371dd03
Subject(s) - platinum , nucleic acid , guanine , dna , microbiology and biotechnology , chemistry , fluorescence , enzyme , nucleotide , biology , genomic dna , hybridization probe , nucleic acid thermodynamics , biochemistry , gene , base sequence , physics , quantum mechanics , catalysis
Fluorescent cis-platinum compounds that react with the N7 atom of guanine are useful for labeling nucleic acids influorescence hybridization applications. Here we report that cyanin (CyN) cis-platinum labeling of DNA samples for array comparative genomic hybridizations (arrayCGH) can be achieved reproducibly and reliably. We demonstrate that degrees of labeling of approximately 1% of all nucleotides in test and reference DNA samples with CyN3- and CyN5-cis-platinum produces arrayCGH signal-to-background ratios ranging from 30 to 40. The arrayCGH results achieved during analyses of mouse and human tumor samples were comparable to those achieved using enzymatic labeling. Thus, we conclude that Cy-cis-platinum labeling is an alternative to enzymatic labeling for arrayCGH.
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