Team:Warsaw/Calendar-Main/17 July 2008
From 2008.igem.org
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- | < | + | <h3>Cloning of protein A DNA to OmpA constructs</h3> |
- | + | <p><ol> | |
- | + | <li> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">Digest</a> of pKS-A plasmid, pACYC177+OmpA_omega and pACYC177+OmpA_alpha with NotI and SacI (pACYC177 were also dephosporylated with CIAP)</li> | |
- | + | <li> Gel electrophoresis and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper bands (420 bp - pKS-A lane, 4050 bp - pACYC177+OmpA_omega lane and 4300 bp pACYC177+OmpA_alpha lane). </li> | |
- | + | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of A DNA fragment with both pACYC177 vectors.</li> | |
- | + | <li> Transformation of <i>E. coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top">TOP10</a> strain with ligations. </li> | |
+ | <li>Transformants plating on LB + kanamycin. </li></ol> | ||
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- | <p> | + | <p>Paweł: pET15b vector transformed into TOP10 strain for plasmid purification </p> |
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+ | </html> | ||
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Revision as of 18:17, 1 October 2008
Cloning of protein A DNA to OmpA constructs
Paweł: pET15b vector transformed into TOP10 strain for plasmid purification
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