Team:Warsaw/Calendar-Main/21 September 2009
From 2009.igem.org
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* Detailed protocol of transformation is described [https://2009.igem.org/Team:Warsaw/protocols here] | * Detailed protocol of transformation is described [https://2009.igem.org/Team:Warsaw/protocols here] | ||
+ | <html> | ||
+ | <h3><div style="text-align: center;">Cloning of the mgtc promoter into the pSB1A3 plasmid</div></h3> | ||
+ | <h4>Kamil</h4> | ||
+ | <br /> | ||
+ | <p>Tasks:</p> | ||
+ | <ul> | ||
+ | <li>Selection of the colonies</li> | ||
+ | </ul> | ||
+ | <br /> | ||
+ | <p>Methods:</p> | ||
+ | <ul> | ||
+ | <li>The appropriate colonies were transferred to a fresh agarose plate and liquid cultures were established.</li> | ||
+ | <li>The plate and the liquid cultures were incubated overnight in 37°C</li> | ||
+ | </ul> | ||
+ | <br /> | ||
+ | |||
+ | <h3><div style="text-align: center;">Cloning of the cro-box into the pSB1A3 plasmid</div></h3> | ||
+ | <h4>Kamil</h4> | ||
+ | <br /> | ||
+ | <p>Tasks:</p> | ||
+ | <ul> | ||
+ | <li>Selection of the colonies</li> | ||
+ | </ul> | ||
+ | <br /> | ||
+ | <p>Methods:</p> | ||
+ | <ul> | ||
+ | <li>The appropriate colonies were transferred to a fresh agarose plate and liquid cultures were established.</li> | ||
+ | <li>The plate and the liquid cultures were incubated overnight in 37°C</li> | ||
+ | </ul> | ||
+ | <br /> | ||
+ | </html> | ||
Latest revision as of 21:57, 2 October 2009
Assembly of endosome detection operon
Marcin
Task 1: Isolation of [http://partsregistry.org/Part:pSB1A3pSB1A3] plasmid containing [http://partsregistry.org/Part:BBa_K177044BBa_K177044]
Methods:
- Plasmids were isolated using the A&A plasmid mini kit. Detailed procedure of the isolation is described [http://aabiot.com/products/dna_purification/plasmid_dna/plasmid_mini/protocol_plasmid_mini.pdf here]
Task 2: Restriction digest of previously isolated plasmids:
Methods:
- Reaction mixture composition:
3 μl purified plasmid DNA product 1 μl XbaI (Fermentas) 1 μl PstI (Fermentas) 2 μl Buffer Tango (Fermentas) 13 μl MQ water
- Reactions were carried out 2 hour
Results:
Some sequences 1500 bp length are visible on the gel but I need to determine whether it is expected product or contamination (bacteria containing plasmid with listeriolysin were also presented on the same plate)
Task 3: PCR reaction to determine the identity of isolated (Task 1) DNA
Commment:
I decided to perform PCR reaction using primers for listeriolysin. If the plasmids contain [http://partsregistry.org/Part:BBa_K177044BBa_K177044] there will be no PCR product.
Methods:
- Reaction mixture composition:
0.1 μl purified plasmid DNA product 1.4 μl Opti Taq Polymerase (EURx) 1 μl dNTPs (EURx) 2 μl Opti Taq Buffer (Fermentas) 15.5 μl MQ water
Results:
All isolated plasmid contain listeriolysin. It is necessary to carry out ligation one more time
Task 4:
- Transformation of chemocompetent E. coli TOP10 strain
Construct to transform:
- [http://partsregistry.org/Part:BBa_K177044BBa_K177044]
Methods:
- Ligation mixture was thermally inactivated in 80 °C for 20 minutes
- Detailed protocol of transformation is described here
Cloning of the mgtc promoter into the pSB1A3 plasmid
Kamil
Tasks:
- Selection of the colonies
Methods:
- The appropriate colonies were transferred to a fresh agarose plate and liquid cultures were established.
- The plate and the liquid cultures were incubated overnight in 37°C
Cloning of the cro-box into the pSB1A3 plasmid
Kamil
Tasks:
- Selection of the colonies
Methods:
- The appropriate colonies were transferred to a fresh agarose plate and liquid cultures were established.
- The plate and the liquid cultures were incubated overnight in 37°C
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