Abstract / Description of output
A simple and efficient method to generate hapten-labeled DNA fragments from a trace amount of YAC DNA isolated by PFGE is described. After agarase digestion of the gel slice containing the resolved YAC recombinant, the purified DNA is digested with Sau3Al and a compatible CL oligonucleotide duplex ligated on. A probe is generated by PCR amplification using a primer complementary to the CL with a single biotin moiety incorporated at the 5' end. When used as a FISH probe, this material yields mapping results superior to Alu-PCR or whole YAC labeling methods and allows sensitive detection of chimerism.
Original language | English |
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Pages (from-to) | 209-11 |
Number of pages | 3 |
Journal | PCR methods and applications |
Volume | 4 |
Issue number | 4 |
Publication status | Published - 1995 |
Keywords / Materials (for Non-textual outputs)
- Base Sequence
- Chimera
- Chromosomes, Artificial, Yeast
- DNA Ligases
- DNA, Fungal
- Humans
- In Situ Hybridization, Fluorescence
- Molecular Sequence Data
- Mutagenesis, Insertional
- Oligodeoxyribonucleotides
- Polymerase Chain Reaction
- Sensitivity and Specificity