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Team:Valencia-CIPF/Introduction
From 2013.igem.org
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To try to develop our objective, we began with cDNA from Arabidopsis Thaliana and from <i>Clarkia Breweri</i> and with plasmids with cupper promoter and ADH promoter. (Raw material: ER85 (LIS), pBTM 116, pYEX-4T, restriction enzymes: BamHI, SalI, PstI, EcoRI). | To try to develop our objective, we began with cDNA from Arabidopsis Thaliana and from <i>Clarkia Breweri</i> and with plasmids with cupper promoter and ADH promoter. (Raw material: ER85 (LIS), pBTM 116, pYEX-4T, restriction enzymes: BamHI, SalI, PstI, EcoRI). | ||
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Revision as of 00:01, 5 October 2013
Introduction
The aim of our project was to create a biological platform within a model organism to develop an alternative method for the production of several aromatic monoterpenoids.
To try to develop our objective, we began with cDNA from Arabidopsis Thaliana and from Clarkia Breweri and with plasmids with cupper promoter and ADH promoter. (Raw material: ER85 (LIS), pBTM 116, pYEX-4T, restriction enzymes: BamHI, SalI, PstI, EcoRI).
To try to develop our objective, we began with cDNA from Arabidopsis Thaliana and from Clarkia Breweri and with plasmids with cupper promoter and ADH promoter. (Raw material: ER85 (LIS), pBTM 116, pYEX-4T, restriction enzymes: BamHI, SalI, PstI, EcoRI).
