Team:Warsaw/Calendar-Main/2 September 2009
From 2009.igem.org
(Difference between revisions)
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<p>Task 2:</p> | <p>Task 2:</p> | ||
<ul><li>Prepare the bacterial cultures for isolation of on <a href="http://partsregistry.org/Part:pSB1A3"><span style="color: black">pSB1A3</a></span> plasmid containing <a href="http://partsregistry.org/Part:BBa_C0051"><span style="color: black">BBa_C0051</a></span> with <a href="http://partsregistry.org/Part:BBa_B0032"><span style="color: black">BBa_B0032</a></span></li> | <ul><li>Prepare the bacterial cultures for isolation of on <a href="http://partsregistry.org/Part:pSB1A3"><span style="color: black">pSB1A3</a></span> plasmid containing <a href="http://partsregistry.org/Part:BBa_C0051"><span style="color: black">BBa_C0051</a></span> with <a href="http://partsregistry.org/Part:BBa_B0032"><span style="color: black">BBa_B0032</a></span></li> | ||
- | <ul> | + | </ul> |
</html> | </html> | ||
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<br> | <br> | ||
+ | <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>Colonies transfer</li> | ||
+ | <li>Liquid cultures establishment</li> | ||
+ | </ul> | ||
+ | <br /> | ||
+ | <p>Methods:</p> | ||
+ | <ul> | ||
+ | <li>Appropriate colonies (both of them) were transferred to a new plate containing ampicilin</li> | ||
+ | <li>Liquid cultures were established in 5 ml LB medium supplemented with ampicilin and incubated overnight with areation</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>Colonies transfer</li> | ||
+ | <li>Liquid cultures establishment</li> | ||
+ | </ul> | ||
+ | <br /> | ||
+ | <p>Methods:</p> | ||
+ | <ul> | ||
+ | <li>Appropriate colonies (all 7 of them) were transferred to a new plate containing ampicilin</li> | ||
+ | <li>Liquid cultures were established in 5 ml LB medium supplemented with ampicilin and incubated overnight with areation</li> | ||
+ | </ul> | ||
+ | <br /> | ||
+ | </html> | ||
Revision as of 21:16, 8 September 2009
Assembly of endosomal detection operon
Marcin
Task 1:
- Restriction digest of followed costruct: BBa_C0051 with BBa_B0032 connected to BBa_E0022 with BBa_B0032 from the pSB1A3 plasmid
Methods:
- Reaction mixture composition:
1. μl purified plasmid DNA product 1 μl XbaI (Fermentas) 1 μl PstI (Fermentas) 2 μl Buffer Tango (Fermentas) 15 μl MQ water
Results
- All isolated plasmids have no insert
Task 2:
- Prepare the bacterial cultures for isolation of on pSB1A3 plasmid containing BBa_C0051 with BBa_B0032
Acquiring the internaline A gene from Listeria monocytogenes st. EDG-e genome
Jarek
Tasks:
- Preparation of PCR reaction with L.monocytogenes st. EGD-e genome DNA
- Separation of PCR products on the 0,8% agarose gel
- Acquiring the pure DNA sample from PCR reaction with Clean-Up kit
Cloning of the mgtc promoter into the pSB1A3 plasmid
Kamil
Tasks:
- Colonies transfer
- Liquid cultures establishment
Methods:
- Appropriate colonies (both of them) were transferred to a new plate containing ampicilin
- Liquid cultures were established in 5 ml LB medium supplemented with ampicilin and incubated overnight with areation
Cloning of the cro-box into the pSB1A3 plasmid
Kamil
Tasks:
- Colonies transfer
- Liquid cultures establishment
Methods:
- Appropriate colonies (all 7 of them) were transferred to a new plate containing ampicilin
- Liquid cultures were established in 5 ml LB medium supplemented with ampicilin and incubated overnight with areation
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