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Team:Warsaw/Calendar-Stage1/6 July 2010
From 2010.igem.org
(Difference between revisions)
| Line 26: | Line 26: | ||
[community RBSes], | [community RBSes], | ||
<a href="http://partsregistry.org/Part:BBa_J23100">J23100</a> | <a href="http://partsregistry.org/Part:BBa_J23100">J23100</a> | ||
| - | + | [synthetic promoter]. | |
<br>2. Alkaline lysis of part of liquid culture used to prepare stocks. Undigested plasmids run on the gel. Results seem to be correct. | <br>2. Alkaline lysis of part of liquid culture used to prepare stocks. Undigested plasmids run on the gel. Results seem to be correct. | ||
<br> | <br> | ||
Revision as of 22:39, 9 July 2010
Preparation of glycerol stocks
1.Glycerol stocks of folloeing biobricks: J61100, J61101, J61107, J61117, J61127 [Anderson's RBSes], B0030, B0031, B0032, B0033, B0034 [community RBSes], J23100 [synthetic promoter].
2. Alkaline lysis of part of liquid culture used to prepare stocks. Undigested plasmids run on the gel. Results seem to be correct.
Cloning of GFP-terminator behind RBSes - approach 2
1. Digest GFP-terminator in psb1A2 plazmid. [16 μl DNA, 6 μl buforu, 16 μl H2O, 0,5 μl Xba/ Pst]
2. Gel extraction of Gel-out GFP-terminator.
3. Ligation of GFPterminator with B0030, B0031, B0032, B0033, B0034 [community RBSes] [1 μl vector-RBSes, 10 μl < insert-GFPterminator, 2 μl buffer, 7 μl water]
4. Transformation with 20 μl ligation mixture
Cloning of GFP-terminator behind RBSes - approach 1
7. 05.07.2010 transformation results: contamination with ampicillin susceptible bacteria.
8. Set up one liquiquid culture fro each plate. Cultures inocculated with mix of all clones obtained on the plate.
