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Uniform amplification of a mixture of deoxyribonucleic acids with varying GC content.
Author(s) -
Namadev Baskaran,
Rajendra P. Kandpal,
A.K. Bhargava,
Michael W. Glynn,
A. Bale,
S M Weissman
Publication year - 1996
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.6.7.633
Subject(s) - biology , gc content , multiple displacement amplification , dna , polymerase chain reaction , betaine , microbiology and biotechnology , polymerase , genetics , biochemistry , dna extraction , gene , genome
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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