im working with the yeast strain BY4741, the double mutant (cta,ctt) that i have previously transformed with 4 diferent catalase T variants insterted in the plasmid pRS316, which confers the ability to grow in media without uracil, and I have transformant colonies of each variant but theres one that, despite the uracil selection, shows no apparent catalase activity 

My advisor told me i could use paraquat or H2O2 to "force" the catalase to express, Im looking for media recipes and for the safety measures needed when manipulating paraquat, hope theres any...

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