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Team:UC Chile/Cyano/Labook/week5
From 2012.igem.org
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<p><font face="Calibri"><font size="4">Tuesday</font></font></p> | <p><font face="Calibri"><font size="4">Tuesday</font></font></p> | ||
| + | <br> | ||
| + | <p><font face="Calibri"> | ||
| + | *Electrophoresis gel was done with water instead of TAE. | ||
| + | *PCR for parts to build C2. | ||
| + | </font></p> | ||
| + | <br> | ||
| + | <p><font face="Calibri"><font size="4">Wednesday</font></font></p> | ||
| + | <br> | ||
| + | <p><font face="Calibri"> | ||
| + | *Transformation of part K325005 (Lux operon). | ||
| + | *Gibson assembly of C2. | ||
| + | </font></p> | ||
| + | <br> | ||
| + | <p><font face="Calibri"><font size="4">Thursday</font></font></p> | ||
| + | *Synechocystis PCC6803 culture was examined with acridine orange dye. It was axenic. Synechocystis was reinoculated in BG11 medium: 10 mL bacteria + 90 mL BG medium. | ||
| + | *E. coli was transformed with Gibson products. | ||
| + | </font> | ||
| + | <br> | ||
Revision as of 20:03, 13 August 2012
April 2 - April 8
Tuesday
Wednesday
Thursday
- Synechocystis PCC6803 culture was examined with acridine orange dye. It was axenic. Synechocystis was reinoculated in BG11 medium: 10 mL bacteria + 90 mL BG medium.
- E. coli was transformed with Gibson products.
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