In situ hybridization (ISH) for the detection of single- or low-copy s
equences, particularly large DNA fragments cloned into YAC or BAC vect
ors, generally requires the suppression or ''blocking'' of highly-repe
titive DNAs. C(0)t-1 DNA is enriched for repetitive DNA elements, high
or moderate in copy number, and can therefore be used more effectivel
y than total genomic DNA to prehybridize and competitively hybridize r
epetitive elements that would otherwise cause nonspecific hybridizatio
n. C(0)t-1 DNAs from several mammalian species are commercially availa
ble, however, none is currently available for plants to the best of ou
r knowledge. We have developed a simple 1-day procedure to generate C(
0)t-1 DNA without the use of specialized equipment.