The technique, now a staple of every molecular biology lab, uses the thermostable Taq DNA polymerase to extend short single-stranded synthetic primers using the target DNA or cDNA as a template ...

engineered proofreading DNA polymerase, providing superior fidelity and specificity to your PCR. With >300x Taq fidelity and buffer specially formulated for primer annealing at 60°C, Platinum SuperFi ...

Alone, the above two procedures are clearly very powerful. But if the procedures were to be combined so that the Bst DNA polymerase procedure of LAMP replaced the PCR of the tadpole procedure ...