Team:Paris-Saclay/Project/Notebook/Week 10
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*Liquid culture of B1 in order to prepare a glycerol stock | *Liquid culture of B1 in order to prepare a glycerol stock | ||
- | ** | + | **Reception of new primers |
**2 Forward | **2 Forward | ||
**3 Reverse | **3 Reverse | ||
**Plasmid Reverse | **Plasmid Reverse | ||
- | |||
====8th August==== | ====8th August==== |
Latest revision as of 00:32, 27 September 2012
Week 10
6th August
- Sending of the B1 sample to sequencing with two pairs of primers
- K-274100 Forward and Reverse
- Plasmid pSB1A2 Forward and Reverse
7th August
- Liquid culture of B1 in order to prepare a glycerol stock
- Reception of new primers
- 2 Forward
- 3 Reverse
- Plasmid Reverse
8th August
Amplification of the plasmid pSB1A2, BBa_K274100 and BBa_K115017 by PCR with the new primers. Visualization by electrophoresis on a 2% Agarose gel for BBa_K115017 and a 0.8% Agarose gel for BBa_K274100 and the plasmid pSB1A2. We are expecting a band at 147 bp for BBa_K115017, 3408 bp for BBa_K274100 and 2079 for the plasmid. |
9th August
New amplification by PCR of the plasmid pSB1A2, BBa_K274100 and BBa_K115017 as it has been done the day before. |
- Digestion by EcoRI of the plasmid that contains BBa_K274100.
10th August
Amplification by PCR of BBa_K274100 already digested by EcoRI. Visualization by electrophoresis on a 0.8% Agarose gel. |
Miniprep of BBa_K274100 followed by Nanovue to determine the concentration of the sample | |
Miniprep of the Plasmid pSB1A2 followed by Nanovue to determine the concentration of the sample |
- Digestion by HindIII of the plasmid pSB1A2 in order to linearize it.
Digestion of BBa_K115017 by DPNI to eliminate the plasmid matrix. Visualization by electrophoresis on a 2% Agarose gel. We are expecting a band at 123 bp. |
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