Team:Warsaw/Calendar-Main/22 May 2008

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<a name="fig1"><img src="https://static.igem.org/mediawiki/2008/8/87/Aid_fusion_digests_WAW.jpg"width=300/></a>
<a name="fig1"><img src="https://static.igem.org/mediawiki/2008/8/87/Aid_fusion_digests_WAW.jpg"width=300/></a>
<var><b>Fig. 1.</b> 1-DNA ladder;<br>  
<var><b>Fig. 1.</b> 1-DNA ladder;<br>  
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2 and 3-hypothetical pMPM-T5 with transcription fusion digested with EcoRI (2 clones); <br>
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2 and 3-hypothetical pMPM-T5 with transcriptional fusion digested with EcoRI (2 clones); <br>
4-pMPM-T5-AID  digested with EcoRI; <br>
4-pMPM-T5-AID  digested with EcoRI; <br>
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5-hypothetical pMPM with translation fusion digested with BamHI; <br>
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5-hypothetical pMPM with translational fusion digested with BamHI; <br>
6-pMPM-T5-AID digested with BamHI.</var>
6-pMPM-T5-AID digested with BamHI.</var>
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Revision as of 16:30, 12 October 2008

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Preparation of pMPMT5-AID+T7 and pMPMT5+AID-T7

Piotr

Design of primers for sequencing something we want from pMPM-T5.
Primers:

Michał K.

  1. Isolation of hypothetical pMPM-T5 with transcriptional fusion.
  2. Isolation of hypothetical pMPM-T5 with translational fusion
  3. Control digest of pMPM-T5 with transcriptional fusion with EcoRI (EcoRI buffer).
  4. Control digest of pMPM-T5 with translational fusion with BamHI (BamHI buffer).
  5. Gel electrophoresis (no proper colonies found). Fig. 1.
  6. Fig. 1. 1-DNA ladder;
    2 and 3-hypothetical pMPM-T5 with transcriptional fusion digested with EcoRI (2 clones);
    4-pMPM-T5-AID digested with EcoRI;
    5-hypothetical pMPM with translational fusion digested with BamHI;
    6-pMPM-T5-AID digested with BamHI.