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09:55, 3 September 2013 (diff | hist) N 3 September 2013 ‎ (Created page with "The optical density of yesterday culture was measured, however it was not sufficient enough to put it into sporulation media. so the cultures we left for further incubation for 3...") (top)
09:50, 3 September 2013 (diff | hist) N 2 September 2013 ‎ (Created page with "all cultures of yeast left for prorulation 5 days ago were not appropriate for further manipulations. After observing each sample microscopically, we could see either non-meiotic...")
11:39, 15 July 2013 (diff | hist) N 15 July 2013 ‎ (Created page with "<html>TOPO TA cloning of our PCR products of DNA aptamers from SELEX cycle 8 was done. For this procedure we used pGEMTII Vector. The following steps were done: <div>Ligation re...") (top)
11:34, 15 July 2013 (diff | hist) N 15 March 2013 ‎ (Created page with "<html> <ol> Today we performed TOPO TA cloning of our PCR products of DNA aptamers from SELEX cycle 8. For this procedure we used pGEMTII Vector. The following steps were done: <...") (top)
20:27, 14 July 2013 (diff | hist) N 13 July 2013 ‎ (Created page with "<html> Every sample has grown in LB broth without antibiotic. Therefore the problem is not in the cells themselves but in transformation. Another transformation should be done. ...") (top)
11:34, 12 July 2013 (diff | hist) N 12 July 2013 ‎ (Created page with "<html> No growth was observed on the plates made yesterday. Possible reasons: <div>- transformation did not occur</div> <div>- cells used were not competent</div> <div>To test t...") (top)