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Team:Warsaw/Calendar-Main/18 August 2009
From 2009.igem.org
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<li>All samples were inactivated via heating in 80 °C for 20 minutes | <li>All samples were inactivated via heating in 80 °C for 20 minutes | ||
<li>All gel-outs were performed using the EurX gel-out kit according to the manual</a></li></ul> | <li>All gel-outs were performed using the EurX gel-out kit according to the manual</a></li></ul> | ||
| - | <p>Results</p> | + | <p>Results:</p> |
| + | <img src="https://static.igem.org/mediawiki/2009/7/7d/PSB_p53_R0080_C0040%2BRBS_gel_out_ocena_18_08_09.png"></br> | ||
<ul><li>All gel-outs (except C0040 with RBS) were successful. One isolation failed because of very low DNA concentration</ul></li></br> | <ul><li>All gel-outs (except C0040 with RBS) were successful. One isolation failed because of very low DNA concentration</ul></li></br> | ||
<p>Task 2:</p> | <p>Task 2:</p> | ||
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1 μl XbaI (Fermentas) | 1 μl XbaI (Fermentas) | ||
0.5 μl SpeI (Fermentas) | 0.5 μl SpeI (Fermentas) | ||
| - | 5 μl Buffer Tango (Fermentas)</pre> | + | 5 μl Buffer Tango (Fermentas)</pre></ul> |
<br/> | <br/> | ||
<p>Task 3:</p> | <p>Task 3:</p> | ||
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</ul> | </ul> | ||
<br /> | <br /> | ||
| - | + | <h3><div style="text-align: center;">Cloning switch 1 regulatory parts [ | |
| + | <a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K177012">K177012</a>-PcI.RBS.LacI, | ||
| + | <a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K177033">K177033</a>-PcI.RBS.LacI.PcI.RBS.RFP.terminator, | ||
| + | <a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K177011">K177011</a>-PLacI.RBS.cI.terminator, | ||
| + | <a href="http://partsregistry.org/Part:BBa_K177038">K177038</a>-PLacI.RBS.cI.terminator.PLacI.RBS.GFP.terminator | ||
| + | ] | ||
| + | into two compatible low copy number plasmids of different antibiotic resistance</div></h3> | ||
| + | <h4>Ania</h4> | ||
| + | <br/> | ||
| + | <p>Tasks:</p> | ||
| + | <ul> | ||
| + | <li> | ||
| + | </li> | ||
| + | </ul> | ||
| + | <br/> | ||
</html> | </html> | ||
Latest revision as of 21:29, 13 September 2009
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Assembly of endosomal detection operon
Marcin
Task 1:
- Gel-outs of following constructs digested on 17.08.09:
Methods:
- All samples were inactivated via heating in 80 °C for 20 minutes
- All gel-outs were performed using the EurX gel-out kit according to the manual
Results:
- All gel-outs (except C0040 with RBS) were successful. One isolation failed because of very low DNA concentration
Task 2:
- Digest pKSII plasmid with cro CDS
Methods:
- Reaction mixture composition:
45 μl purified plasmid DNA product 1 μl XbaI (Fermentas) 0.5 μl SpeI (Fermentas) 5 μl Buffer Tango (Fermentas)
Task 3:
Methods:
- Reaction mixture composition:
10 μl p53 CDS 7 μl vector 2.3 μl Buffer Tango (Fermentas) 3 μl dNTPs mixture (EurX) 1 μl T4 ligase (Fermentas)
Making of plac-RBS-llo part
Jarek
Tasks:
- Preparation of 20 liquid cultures, from colonies that grew from ligation, in 3 ml of LB+Amp nad incubating them in 37C degree
Ania
Tasks:
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