Team:Freiburg/Notebook/11 July
From 2011.igem.org
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<span style="color:blue;">Comments: No bands for M30-M32 and M36-M38. It should be repeated with a fresh gel.</span> | <span style="color:blue;">Comments: No bands for M30-M32 and M36-M38. It should be repeated with a fresh gel.</span> | ||
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+ | ==<span style="color:grey;">Transformation</span>== | ||
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+ | '''Investigators: Rüdiger''' | ||
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+ | To see the expression of the plastic-binding domain (pbd), the GFP-pbd plasmid was transformed in cells. |
Revision as of 11:41, 14 July 2011
Miniprep of Promotor-Ribosome-binding-site-constructs
As our PR-DNA run out Sophie inoculated LB with bacteria from our Glycerol-stocks and made two minipreps (a and b) per PR-strain The DNA-concentrations measured were (in ng/µL):
PR1a: 89,7 PR1b: 98,6
PR2a: 78,2 PR2b: 52,4
PR3a: 25,7 PR3b: 37,8
PR4a: 45,7 PR4b: 15,7
PR5a: 35,1 PR5b: 55,9
PR6a: 45,7 PR6b: 38,9
Test-digest
Investigators: Julia
14 samples:
- M30-M32, M 36-M38?????????????????
- S24-S29
Enzymes used:
- Enzyme 1: EcoRI
- Enzyme 2: PstI
Comments: No bands for M30-M32 and M36-M38. It should be repeated with a fresh gel.
Transformation
Investigators: Rüdiger
To see the expression of the plastic-binding domain (pbd), the GFP-pbd plasmid was transformed in cells.