Team:Valencia/Parts

From 2009.igem.org

(Difference between revisions)
(Preparing inserts)
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PCR was conducted as follows:<br>
PCR was conducted as follows:<br>
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<ol>A first denaturation cycle
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<ol>A first denaturation cycle
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<ol>94º 3'</ol>
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<ol>94º 3min</ol>
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Followed by 30 amplification cycles:
Followed by 30 amplification cycles:
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<ol>94º 30''
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55º 1'
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<ol>94º 30s<br>
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72º 1'</ol>
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55º 1min<br>
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72º 1min<br></ol>
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And a final extension step:
And a final extension step:
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<ol>72º 7'</ol>
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<ol>72º 7min</ol>
</ol>
</ol>
'''Results:'''<br>
'''Results:'''<br>
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[[Image:.jpg]]<br>
 
1 = wt (1 microlitre)<br>
1 = wt (1 microlitre)<br>
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Competent cells were transformed and resulting colonies (Amp LB) screened with Fw and Rv primers to confirm the presence of inserts. <br>
Competent cells were transformed and resulting colonies (Amp LB) screened with Fw and Rv primers to confirm the presence of inserts. <br>
pSB1AK3 containing UCP-1, 175-deleted and 76-deleted were sent to the Registry <br>
pSB1AK3 containing UCP-1, 175-deleted and 76-deleted were sent to the Registry <br>
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</div>
 
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</div>
 

Revision as of 18:10, 7 October 2009















Preparing inserts

Total DNA was extracted from our yeast strains.
AEQ was amplified by PCR using oligonucleotides matching the sequence and bearing the appropriate Biobrick prefix and suffix.



And our oligos (EcoRI and XbaI sites in bold) were:
Forward: 5'gaattcgcggccgcttctagatgaccagcg 3’
Reverse: 5’tactagtagcggccgctgcagttaggggac 3’



PCR was conducted as follows:

    A first denaturation cycle
      94º 3min

    Followed by 30 amplification cycles:

      94º 30s
      55º 1min
      72º 1min

    And a final extension step:

      72º 7min


Results:

1 = wt (1 microlitre)
2 = wt (2 microlitres)
3 = Cch1 (1 microlitre)
4 = Mid1 (1 microlitre)
5 = Negative Control
6 = Possitive Control
(We used the same MWM)

We used wt 1 microlitre of PCR amplification product (career 1) to build the AEQ BioBrick.

Amplicons were digested (H buffer) with EcoRI y XbaI.


Preparing vectors

Competent cells were transformed with:


Plasmids were extracted (High pure miniprep plasmid isolation kit ROCHE)
Plasmid were digested with EcoRI and XbaI


Ligating Biobricks into plasmids

Both plasmids and inserts were run into 0.8% 0.5X TBE agarose gels and DNA bands excised with a clean scalpel. DNA was extracted from agarose blocks (ultra clean gel spin, DNA purification Kit, MO BIO laboratories).
T4 Ligase was used to ligate inserts and vectors for 1 h at room temperature (2X quick buffer was used).
Competent cells were transformed and resulting colonies (Amp LB) screened with Fw and Rv primers to confirm the presence of inserts.
pSB1AK3 containing UCP-1, 175-deleted and 76-deleted were sent to the Registry