Team:Warsaw/Calendar-Main/17 September 2008
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<p><ol><li>Plasmid <a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation>isolation</a> from previous day's cultures.</li> | <p><ol><li>Plasmid <a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation>isolation</a> from previous day's cultures.</li> | ||
- | <li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>Digest</a> with SacI and BamHI.</li><li>Electrophoresis.</li></ol></p> | + | <li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>Digest</a> with SacI and BamHI.</li><li>Electrophoresis (<a href="https://2008.igem.org/wiki/index.php?title=Team:Warsaw/Calendar-Main/17_September_2008#fig1">Fig. 1</a>).</li></ol></p> |
- | + | <a name="fig1"><img src="https://static.igem.org/mediawiki/2008/9/98/Konkurencja1.jpg" width=180/></a> | |
+ | <var><b>Fig. 1.</b> Result of competition test:<br> | ||
+ | 1 and 5 - DNA ladder,<br> | ||
+ | 2 - Insert from isolated plasmid refers to OmpA_A_Alpha <br>(Z_Omega protein added to the medium),<br> | ||
+ | 3 - Insert from isolated plasmid refers to OmpA_A_Omega <br>(Z_Alpha protein added to the medium),<br> | ||
+ | 4 - Insert from isolated plasmid refers to OmpA_Z_Omega <br>(A_Alpha protein added to the medium).</var> | ||
- | <p>Conclusion: cells with | + | <p>Conclusion: cells with interacting protein survive competition!</p> |
<h3>MutD5 testing</h3> | <h3>MutD5 testing</h3> | ||
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primers (elongation length 90s) to obtain OmpA_omega fragment. </li> | primers (elongation length 90s) to obtain OmpA_omega fragment. </li> | ||
<p>Each reaction was carried out with 25 cycles and in temperature gradient from 55 to 75 °C (four reactions).</p> | <p>Each reaction was carried out with 25 cycles and in temperature gradient from 55 to 75 °C (four reactions).</p> | ||
- | <li> Gel electrophoresis of PCR products (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/17_September_2008# | + | <li> Gel electrophoresis of PCR products (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/17_September_2008#fig2">Fig. 2.</a>).</li> |
</ol> | </ol> | ||
- | <a name=" | + | <a name="fig2"><img src="https://static.igem.org/mediawiki/2008/9/9e/Grad_17_09.jpg" width=300/></a><var><b>Fig. 2.</b> Gradient PCR (temperatures:55-75 °C)<br> |
1. Marker<br> | 1. Marker<br> | ||
2. 55 °C deltaA<br> | 2. 55 °C deltaA<br> |
Latest revision as of 15:15, 29 October 2008
'Hunter and prey' system tests: Competition testsPiotr
1 and 5 - DNA ladder, 2 - Insert from isolated plasmid refers to OmpA_A_Alpha (Z_Omega protein added to the medium), 3 - Insert from isolated plasmid refers to OmpA_A_Omega (Z_Alpha protein added to the medium), 4 - Insert from isolated plasmid refers to OmpA_Z_Omega (A_Alpha protein added to the medium). Conclusion: cells with interacting protein survive competition! MutD5 testingEmiliaInoculation of MutD5 into medium with tetracycline. Optimisation of primers for preparation of partsMichał K.
Each reaction was carried out with 25 cycles and in temperature gradient from 55 to 75 °C (four reactions). 1. Marker 2. 55 °C deltaA 3. 60 °C deltaA 4. 65 °C deltaA 5. 70 °C deltaA 6. 55 °C link_omega 7. 60 °C link_omega 8. 65 °C link_omega 9. 70 °C link_omega 10. 55 °C link_alpha 11. 60 °C link_alpha 12. 65 °C link_alpha 13. 70 °C link_alpha 14. 55 °C OmpA_omega 15. 60 °C OmpA_omega 16. 65 °C OmpA_omega 17. 70 °C OmpA_omega
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