Uniform amplification of a mixture of deoxyribonucleic acids with varying GC content.

  1. N Baskaran,
  2. R P Kandpal,
  3. A K Bhargava,
  4. M W Glynn,
  5. A Bale, and
  6. S M Weissman
  1. Boyer Center for Molecular Medicine, Yale University School of Medicine, New Haven, Connecticut 06536, USA.

Abstract

A PCR method for uniform amplification of a mixture of DNA templates differing in GC content is described using the two enzyme approach (Klentaq1 and Pfu DNA polymerase) and a combination of DMSO and betaine. This method was applied to amplify the CGG repeat region from the fragile X region.

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