Team:Warsaw/Calendar-Main/22 May 2008
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<li> Gel electrophoresis (no proper colonies found). Fig. 1.</li> | <li> Gel electrophoresis (no proper colonies found). Fig. 1.</li> | ||
<img src="https://static.igem.org/mediawiki/2008/8/87/Aid_fusion_digests_WAW.jpg"width=300/> | <img src="https://static.igem.org/mediawiki/2008/8/87/Aid_fusion_digests_WAW.jpg"width=300/> | ||
- | <var>Fig. 1. 1-DNA ladder;<br> | + | <var><b>Fig. 1.</b> 1-DNA ladder;<br> |
2 and 3-hypothetical pMPM-T5 with transcription fusion digested with EcoRI (2 clones); <br> | 2 and 3-hypothetical pMPM-T5 with transcription fusion digested with EcoRI (2 clones); <br> | ||
4-pMPM-T5-AID digested with EcoRI; <br> | 4-pMPM-T5-AID digested with EcoRI; <br> |
Revision as of 15:28, 11 October 2008
Preparation of pMPMT5-AID+T7 and pMPMT5+AID-T7Piotr
Design of primers for sequencing something we want from pMPM-T5. Michał K.
2 and 3-hypothetical pMPM-T5 with transcription fusion digested with EcoRI (2 clones); 4-pMPM-T5-AID digested with EcoRI; 5-hypothetical pMPM with translation fusion digested with BamHI; 6-pMPM-T5-AID digested with BamHI. |