Difference between revisions of "Team:Paris Bettencourt/Project/Phytase"
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− | <p>We used the yeast <i>Saccharomyces cerevisiae</i>, more precisly the strain SK1 coming from the INSERM unit U1001. We create two primers to replace the two repressors genes of the phytase synthesis called PHO80 and PHO85 on the chromosoms 15 and 16. The plasmid used here | + | <p>We used the yeast <i>Saccharomyces cerevisiae</i>, more precisly the strain SK1 coming from the INSERM unit U1001. We create two primers to replace the two repressors genes of the phytase synthesis called PHO80 and PHO85 on the chromosoms 15 and 16. The plasmid used here was pSB1C3 within the gene of geneticin resistance or the gene of RFP that we take and put between two CRE-lox to replace PHO80 and between two FRT or the other localisation. </p> |
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Revision as of 20:18, 28 October 2015