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#Allow the bacteria to be absorbed into the media before you move them. About 30-60 minutes.
#Obtain 2 '''control''' plates - these plates contain the same NGM lite medium described above and the bacterial strain on them are identical to your RNAi feeder strain, ''except'' that the pL4440 plasmid is only expressing RNA from the vector - it lacks DNA specific to any worm genes.
#Stack all 6 dry plates carefully (without tilting them) - and put them in your lab section box with a labeled piece of your team color tape on top.
#The plates will be stored at 4°C until you are ready to add worms.


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