Abstract
A multiplex PCR assay consisting of 13 Rapidly Mutating Y STR loci called RM-Yplex was previously developed. Platinum® Taq DNA polymerase was used to amplify the 13 Y STR loci in a single reaction at an amplification time of approximately 2.5 h. In order to shorten the process with reliable results, two DNA polymerases were tested with the multiplex. Phusion® Flash High Fidelity, TAKARA Z-taqTM, and Platinum® Taq DNA polymerases were investigated for conducting RM-Yplex assay at various PCR cycling conditions. Rapid, robust, and efficient amplification of all the markers within the multiplex were achieved. The amplification time was reduced from 2.5 h to less than 28 min with Phusion® Flash High Fidelity DNA polymerase using Veriti® PCR thermal cycler.
| Original language | English |
|---|---|
| Pages (from-to) | 2817-2821 |
| Number of pages | 5 |
| Journal | Electrophoresis |
| Volume | 37 |
| Issue number | 21 |
| DOIs | |
| Publication status | Published - Oct 1 2016 |
| Externally published | Yes |
Keywords
- DNA typing
- Fast DNA polymerases
- Forensic science
- Rapid PCR
- Rapidly mutating Y-short tandem repeats
ASJC Scopus subject areas
- Biochemistry
- Clinical Biochemistry
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