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Nucleic Acids Symp Ser (Oxf) ; (52): 259-60, 2008.
Article in English | MEDLINE | ID: mdl-18776352

ABSTRACT

Several 3'-ether and 3'-ester derivatives of 2'-deoxyribonucleoside 5'-triphosphates (dNTPs) were prepared. These dNTP derivatives were not substrates for DNA polymerase and did not support primer extension at room temperature. However, by short pre-heating to 95 degrees C in PCR buffer, these 3'-modified dNTPs can be converted to corresponding unmodified natural dNTPs that efficiently support PCR amplification. The analysis of PCR products obtained with 3'-modified dNTPs revealed a significant improvement in PCR performance resulting in higher amplicon yield and reduced formation of off-target products (mis-priming and primer dimer). Among the studied 3'-modified dNTPs, the 3'-tetrahydrofuranyl derivatives showed the best results.


Subject(s)
Deoxyribonucleotides/chemistry , Hot Temperature , Polymerase Chain Reaction , Bacteriophage lambda/genetics , DNA, Viral/biosynthesis , DNA-Directed DNA Polymerase/metabolism , Deoxyribonucleotides/chemical synthesis , Deoxyribonucleotides/metabolism , HIV-1/genetics , Humans , Kinetics
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