Hello everyone!
I'm starting a project involving phage display and the protocols largely sound like I can do my panning on the bench top, instead of in a biosafety cabinet. Do I need to pan aseptically? Or how do I prevent contamination downstream when I infect my E. coli cultures with the selected phages if the solution the phages are in is not sterile? Do you filter the recovered phages before infecting? Any suggestions? General knowledge?
- Badges
- Science topic
- Similar topics
- Biological Science
- Molecular Biology
- Molecular Biological Techniques
More Stephanie Morphet's questions See All
Similar questions and discussions