From 2007.igem.org

07/30/07

• We control bacterial grew (link).
• Transformation for C0012 and J52034 and B0015.
• We get along with the ligation R0051+I13507 (I763007) (vector 2 ul, insert 6 ul) and the ligation J04500+ C0051 (I763005) (vector 2 ul, insert 10 ul).

07/31/07

• There isn’t any colony for C0012, so we inoculate I52034 and B0015 colony in 5 ml.
• We plate 30/07 ligations.
• We get along with the J04431 fluorescence test:

-From the glycerol stock we sprout 1 ml at 37°C for 1 hour in agitation.

-We verify the OD and the fluorescence every 15 minutes. The fluorescence compare at the istance t=210min and at the OD=0.5.

• At the end of this test we decide to repeat it to see if we can switch off the fluorescent cells with a major quantity of glucose to confirm our assumptions.

We will attend this test on 07/08.

08/01/07

• We get along with:

-Miniprep of I52034 and B0015;

-Digestion of B0015 with Xba/Pst1

                     I52034 with Spe/Pst1;

-extraction from gel (we can’t see B0015);

-R0015+I13507 (I763007) ligation which doesn’t give colonies so we transform with the other 10 ul of ligation;

-J04500+C0051 (I763005) ligation which gives colonies so we inoculate in 5ml;

-transformation for C0012 (4ul) and for J22101 (2ul);

-a new R0051+ I13507 (I763007) (vector 4ul, insert 8ul) ligation.

08/02/07

08/03/07

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