Literature DB >> 8574188

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

Y Shibasaki1, J C Maule, R S Devon, E M Slorach, J R Gosden, D J Porteous, A J Brookes.   

Abstract

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.

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Year:  1995        PMID: 8574188     DOI: 10.1101/gr.4.4.209

Source DB:  PubMed          Journal:  PCR Methods Appl        ISSN: 1054-9803


  3 in total

Review 1.  Coincidence cloning. Taking the coincidences out of genome analysis.

Authors:  R S Devon; A J Brookes
Journal:  Mol Biotechnol       Date:  1996-06       Impact factor: 2.695

2.  Rapid detection of IgH/BCL2 rearrangement in follicular lymphoma by interphase fluorescence in situ hybridization with bacterial artificial chromosome probes.

Authors:  Feng Jiang; Fan Lin; Roger Price; Jun Gu; L Jeffrey Medeiros; Hua Z Zhang; Su-Su Xie; Nancy P Caraway; Ruth L Katz
Journal:  J Mol Diagn       Date:  2002-08       Impact factor: 5.568

Review 3.  Pulsed-field gel electrophoresis.

Authors:  J Maule
Journal:  Mol Biotechnol       Date:  1998-04       Impact factor: 2.860

  3 in total

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