Catch-linker + PCR labeling: a simple method to generate fluorescence in situ hybridization probes from yeast artificial chromosomes

Y Shibasaki, J C Maule, R S Devon, E M Slorach, J R Gosden, D J Porteous, A J Brookes

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)209-11
Number of pages3
JournalPCR methods and applications
Volume4
Issue number4
Publication statusPublished - 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

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