Team:Warsaw/Calendar-Main/29 August 2008
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<h4>Piotr</h4> | <h4>Piotr</h4> | ||
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- | + | Transformation of <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#rosetta">Rosetta</a> with <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BA-alpha>pET15b+A-alpha</a> plasmid. Plating on LB with chloramphenicol and ampicillin.</p> | |
<h3>Blue-white screening and rifampicin test in <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#gm">GM2163</a></h3> | <h3>Blue-white screening and rifampicin test in <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#gm">GM2163</a></h3> | ||
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<p>Transformants were selected on CTAXI plates (LB + Chloramphenicol + Tetracycline + IPTG + Ampicillin 30 μg/mL + X-Gal) because GM2163 are chloramphenicol resistant.</p> | <p>Transformants were selected on CTAXI plates (LB + Chloramphenicol + Tetracycline + IPTG + Ampicillin 30 μg/mL + X-Gal) because GM2163 are chloramphenicol resistant.</p> | ||
- | + | <h3>Cloning of protein A DNA to <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-alpha>pET15b+OmpA-alpha</a> plasmid</h3><h4>Michał K.</h4> | |
+ | <p><ol><li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation">Isolation</a> of <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BA-alpha>pET15b+A-alpha</a> plasmids.</li> | ||
+ | <li> Control <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">digest</a> of isolated plasmids with XbaI and BamHI (Tango buffer). </li> | ||
+ | <li>Gel electrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/29_August_2008#fig1">Fig. 1.</a>). Choice of proper clone. </li> | ||
+ | </ol></p> | ||
<a name="fig1"><img src=" | <a name="fig1"><img src=" | ||
- | https://static.igem.org/mediawiki/2008/a/a8/Kokodak.jpg" width=300/></a> <var><b>Fig. 1. Control XbaI/BamHI digests of plasmids isolated from transformants with colony PCR product. | + | https://static.igem.org/mediawiki/2008/a/a8/Kokodak.jpg" width=300/></a> <var><b>Fig. 1.</b> Control XbaI/BamHI digests of plasmids isolated from transformants with colony PCR product.<br> |
1. Marker<br> | 1. Marker<br> | ||
- | 2-4. | + | 2-4. Digested plasmids pET15b+A-alpha <br></var> |
Latest revision as of 20:58, 26 October 2008
Purification of proteins: A-alphaPiotrTransformation of Rosetta with pET15b+A-alpha plasmid. Plating on LB with chloramphenicol and ampicillin. Blue-white screening and rifampicin test in GM2163Michał L.GM2163 competent cells carrying pZC320 were transformed with following plasmids: Transformants were selected on CTAXI plates (LB + Chloramphenicol + Tetracycline + IPTG + Ampicillin 30 μg/mL + X-Gal) because GM2163 are chloramphenicol resistant. Cloning of protein A DNA to pET15b+OmpA-alpha plasmidMichał K.
1. Marker 2-4. Digested plasmids pET15b+A-alpha
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