Team:Warsaw/Calendar-Main/15 July 2008
From 2008.igem.org
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- | <h3><a href= | + | <h3>Cloning omega-A fusion on <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pKSII%2B>pKS</a> (second attempt)</h3> |
<h4>Michał L., Ewa, Marcin</h4> | <h4>Michał L., Ewa, Marcin</h4> | ||
- | <p> | + | <p><b><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcl">Polymerase Chain Ligation</a> on linker-A and omega-linker</b> |
<ul> | <ul> | ||
<li>reisolated PCR product omega-linker - 4 µl<br> | <li>reisolated PCR product omega-linker - 4 µl<br> |
Revision as of 12:21, 26 October 2008
Cloning of protein Z DNA to OmpA constructsMichał K.Two colonies (pACYC177+OmpA_Z_omega) was inoculated to liquid LB with kanamycin. Preparation of alpha+A conctructAntoni
Cloning omega-A fusion on pKS (second attempt)Michał L., Ewa, MarcinPolymerase Chain Ligation on linker-A and omega-linker
Fig. 1.Gradient PCR on alpha+A products. Lanes 1-3, 5, 6 - annealing temperature 68°C and DMSO concentration of 2%, 4%, 6%, 8% and 10% respectively. Lanes 7-11 - 72°C and DMSO concentration increasing in the same maner. Lane 4 and 12 GeneRuler DNA Ladder Mix 1 μg and 0.5 μg respectively. |