With the help of the miniPCR, the 2-in-1 blueGel electrophoresis and LED light transilluminator and my own Samsung Galaxy Note 4, I first helped a well known and established laboratore located at McGill Goodman Cancer Center in Montreal. The project consisted in helping them convert the Taq from NEB and Qiagen they routinely used for mouse genotyping by PCR. This project became our very first PCR Success Story and EasyTaq would become our best selling product! Their group routinely performed EGFP, flox/src, NeuN, Cre, and Confetti mice genotyping by PCR. Notably, their ”Confetti” PCR was the most challenging, often failing at amplifying the mutant allele, even with the very expensive Taq DNA polymerase from Qiagen. Back in my NEB-days, it had taken about 2 years to convert this lab to OneTaq from NEB. But still then, they sometimes had to use the Qiagen Taq for difficult DNA amplifications. This time, it only took me 2 weeks to fully convert the lab exclusively to EasyTaq. How I did it? The lab gave me a couple of mouse DNA extracts and DNA primers. Starting off with their lab protocols, I replicated every reaction using miniPCR and EasyTaq. It was so easy, even for the difficulf mutant Confetti allele that the lab subsequently ordered thousands of units of EasyTaq DNA Polymerase!