BIOTEC Dresden/Notepad/21 September 2010

From 2010.igem.org

Revision as of 14:10, 24 October 2010 by Lucas.schirmer (Talk | contribs)

Parts Assembly

PCR amplification of the following parts and the plasmid backbone containing chloramphenicol was done.

4a, 9b, 14f, 20f, 21f

The PCR products were run on an agarose gel. Due to difference in buffer usage, this step was once again repeated.

Fusion Protein

Ligation of the parts was carried out followed by their transformation. Gradient PCR for the fusion parts was done.


July
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
August
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
September
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
October
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
Share to Twitter Share to Facebook Share to Orkut Stumble It Email This More...