Team:Warsaw/Calendar-Main/3 September 2008
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<p><ol><li>Samples were resuspended in PBS, sonicated and centrifuged.</li> | <p><ol><li>Samples were resuspended in PBS, sonicated and centrifuged.</li> | ||
<li>Lysis buffer was added separately to pellet and supernatant, then samples were boiled for 10 min. </li> | <li>Lysis buffer was added separately to pellet and supernatant, then samples were boiled for 10 min. </li> | ||
- | <li>Lysates loaded on 12% polyacrylamide gel (Fig. 1.) (amount relating to 100 μl of OD=1.0 culture).</li> | + | <li>Lysates were loaded on 12% polyacrylamide gel (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/3_September_2008#fig1">Fig. 1.</a>) (amount relating to 100 μl of OD=1.0 culture).</li> |
- | <li>Gel stained with Coomassie Blue. Optimal induction conditions chosen.</li> | + | <li>Gel was stained with Coomassie Blue. Optimal induction conditions chosen.</li> |
- | <li>A-alpha | + | <li>A-alpha in Rosetta strain was cultured overnight.</li></ol></p> |
- | <img src="https://static.igem.org/mediawiki/2008/b/bd/September_3_rd.jpg" width=300 /><var>Fig. 1. <b>Supernatants from A-alpha induction with various IPTG concentrations<br> | + | <a name="fig1"><img src="https://static.igem.org/mediawiki/2008/b/bd/September_3_rd.jpg" width=300 /></a><var><b>Fig. 1.</b> Supernatants from A-alpha induction with various IPTG concentrations<br> |
- | The arrow shows place of our overexpressed protein: | + | The arrow shows place of our overexpressed protein:<br> |
1. 22°C 0.5 mM IPTG 5 h<br> | 1. 22°C 0.5 mM IPTG 5 h<br> | ||
2. Marker<br> | 2. Marker<br> |
Latest revision as of 21:04, 26 October 2008
Purification of proteins: A-alphaPiotr, Emilia
The arrow shows place of our overexpressed protein: 1. 22°C 0.5 mM IPTG 5 h 2. Marker 3. 22°C 0.5 mM IPTG overnight 4. 22°C 1 mM IPTG 5 h 5. 22°C 1 mM IPTG overnight 6. 37°C 0.5 mM IPTG 5 h 7. 37°C 0.5 mM IPTG overnight 8. 37°C 1 mM IPTG 5 h 9. 37°C 1 mM IPTG overnight 10. Marker
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