| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5517111 | Biomolecular Detection and Quantification | 2017 | 5 Pages |
Abstract
Reducing the time taken to run qPCR assays on today's qPCR cyclers is rather straightforward and requires no specialised reagents or instruments. As the first article in a new series of short technical reports, I demonstrate that it is possible to reduce significantly both denaturation temperatures and cycling times, whilst retaining sensitivity and specificity of the original qPCR conditions.
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Agricultural and Biological Sciences (General)
Authors
Stephen A. Bustin,