On 12-01-24 08:39 AM, Regina Kettering wrote:
At some point we aspirated an _expression_ plasmid, let it sit in the tip for a while and then went through different washing protocols, water, high-salt, 0.1M NaOH, and then dispense a small volume of water into a PCR reaction. We found just a water wash got rid of most of the DNA, as long as the outside of the tip was also washed. After the high salt we could no longer detect the DNA by PCR. Although protein is not the same as DNA I would have no concern about protease contamination if you implement a good wash/strip protocol for the protein dispense tip. Bart |
- [ccp4bb] Biology infrastructure at the XFEL Victor Lamzin
- [ccp4bb] Crystallization robot and trypsin Horacio Botti
- Re: [ccp4bb] Crystallization robot and tryp... Regina Kettering
- Re: [ccp4bb] Crystallization robot and ... Bart Hazes
- Re: [ccp4bb] Crystallization robot and tryp... Sebastiano Pasqualato
