Abstract
An efficient, PCR based method for the selective amplification of DNA target sequences that differs by a single base pair is described. The method utilises the high affinity and specificity of PNA for their complementary nucleic acids and that PNA cannot function as primers for DNA polymerases.
Cite
CITATION STYLE
APA
Orum, H. (2000). PCR clamping. Current Issues in Molecular Biology. https://doi.org/10.1002/9783527678679.dg09253
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