Chemically Modified Primers for Improved Multiplexed PCR
Poster Jan 08, 2010
Elena Hidalgo Ashrafi, Tony Le, Alexandre Lebedev, Richard Hogrefe, Victor Timoshchuk, Sabrina Shore, Inna Koukhareva and Natasha Paul
Multiplex PCR is an advantageous technique used in PCR applications to amplify multiple targets in a single reaction. As useful as it is, this technique presents a new set of challenges that further complicates PCR setup. For example, reactions are more prone to off-target amplifications such as mis-priming and primer dimer due to the increased number of primer pairs. Furthermore, preferential amplification of certain targets leads to an unequal distribution of amplicon products, making quantification and detection of problematic targets extremely difficult. To improve upon the problems specific to multiplex PCR, we evaluated Hot Start modified primers which contain either one or two thermolabile 4-oxo-tetradecyl (OXT) modifications to prevent DNA polymerase extension at low-stringent temperatures, and that are released after a Hot Start activation step. Herein, we find that the singly-modified primers provide greater amplification efficiency, specificity, and yield in the multiplex amplification of DNA targets. In reverse transcriptase PCR (RT-PCR), the doubly-modified primers have been proven to be the optimal choice. The presence of two thermolabile protecting groups allows for an efficient one-step RT-PCR reaction that provides high specificity for multiple targets. TriLink’s innovative technology represents a convenient tool for multiplex PCR amplification of DNA and RNA samples.
When there is a need to quickly analyze samples using a number of different PCR assays, it is likely that optimal conditions for each assay will not be the same. First, different assays often will require different annealing temperatures for their primers. In addition, amplicons may be designed to be of different lengths and therefore require varying durations of the extension step.READ MORE