Team:Warsaw/Calendar-Main/31 July 2008
From 2008.igem.org
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9. supernatant 37°C 0.5 mM IPTG<br></var> | 9. supernatant 37°C 0.5 mM IPTG<br></var> | ||
- | <img src="https://static.igem.org/mediawiki/2008/2/2e/31_july.jpg" width= | + | <img src="https://static.igem.org/mediawiki/2008/2/2e/31_july.jpg" width=250/> <var><b>Fig. 3. Control SacI/BamHI digests of isolated plasmids</b><br> |
1-4. digested plasmids pACYC177 + OmpA-omega-deltaA-alpha<br> | 1-4. digested plasmids pACYC177 + OmpA-omega-deltaA-alpha<br> | ||
5. Marker<br></var> | 5. Marker<br></var> |
Revision as of 17:25, 25 October 2008
Purification of proteins: Z-alpha and Z-omegaPiotr, Emilia
Cloning of omega_ΔA DNA fragment to pACYC177+OmpA_alphaMichał K.
Cloning of truncated fragment of protein AMichał K.
The arrow shows place of our overexpressed protein: 1. 22°C 0.5 mM IPTG 2. 22°C 0.1 mM IPTG 3. 22°C 1 mM IPTG 4. Marker 5. negative control 6. 37°C 0.1 mM IPTG 7. 37°C 0.5 mM IPTG 8. 37°C 1 mM IPTG Fig. 2. Pellets and supernatants from Z-alpha induction with various IPTG concentrations The arrow shows place of our overexpressed protein: 1. Marker 2. pellet negative control 3. supernatant negative control 4. pellet 37°C 0.1 mM IPTG 5. supernatant 37°C 0.1 mM IPTG 6. sonicate 22°C 0.1 mM IPTG 7. sonicate 22°C 0.5 mM IPTG 8. pellet 37°C 0.5 mM IPTG 9. supernatant 37°C 0.5 mM IPTG Fig. 3. Control SacI/BamHI digests of isolated plasmids 1-4. digested plasmids pACYC177 + OmpA-omega-deltaA-alpha 5. Marker
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