Re: [DIYbio] Re: cheaper/better transformation - using ultrasound (sonoporation)


What would be fun to try: 

pGlo is relatively small, I think. Ori, AmpR and GFP. 

Why not use pVIB? If one of the LuxC,D,A,B,E genes is disturbed / damaged, it likely won't work any more. Because I imagine that bigger plasmids will rather be damaged than smaller ones. But just an assumption... 

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