Okay, so here I am waiting for my PCR product to be finished. The first one that Tim, the PhD student looking after my training on the job right now, and I did failed... we had no marks on the gel when exposed to UV light. So I asked him if I could do it with another sample, just to practice and to fill up some time... otherwise I'd be sitting around doing nothing again...
I know I've probably messed up the first 3 wells, which are ladder 1, sample 1 and sample 2. But hopefully I've gotten the other 8 wells done right.
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