I have tried multiple protocols with varying ratios of DCM and SDS but was not successful in preparing PLA emulsified Agar media.

Problems faced ,

1. Plates are too transparent to see any clearance produced by bacteria

2. Adding more PLA to make the plates turbid doesn't work because upon autoclaving the PLA clumps together and deposits at the bottom.

It would be really helpful if anyone has some good working protocol for the same.

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