23 September 2015 1 3K Report

Hi,

when I try to SILAC lable a yeast strain which is not arginine auxotrophic with heavy arginine I generally gel low labelling efficiencies. In mammalian cell culture people often starve their cells in medium without the amino acid before labelling. Would anyone have a protocol to do sth similar in S. cerevisiae? Or do you have any other suggestions how to increase label incorporation?

Thanks!

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