From 2008.igem.org
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- | <h3>Cloning of protein A DNA to OmpA constructs</h3>
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- | <p><ol>
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- | <li>Colony PCR on colonies from plates with transformations pACYC177+OmpA_A_omega and pACYC177+OmpA_A_alpha. Primers used:
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- | <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AL+SacI">AL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AP+NotI">AP+NotI</a>
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- | </li>
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- | <li> Confirmed transformant colonies (found only on pACYC177+OmpA_A_alpha plate) inoculated to liquid LB with kanamycin. </li></ol>
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- | </p>
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| + | <h3>Cloning of protein A DNA to OmpA constructs</h3><h4>Michał K.</h4> |
| + | <ol><li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation">Isolation of plasmids</a> from cultures inocluated on previous day (pACYC177+OmpA_A_omega).</li> |
| + | <li>Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">digest</a> of isolated plasmids with BamHI and SacI. </li></ol> |
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Revision as of 18:54, 11 October 2008
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Cloning of omega_A DNA fragment to pACYC177+OmpA_alpha
- DNA fragment of omega_A isolated from gel on 20 July digestion with SacI and NotI.
- clean-upClean-up of digested DNA fragment.
- Digestion (SacI and NotI) and dephosphorylation (CIAP) of pACYC177+OmpA_alpha.
- Gel electrophoresis and gel-out of 4300 bp band.
- Ligation of DNA fragments from 2. and 4. (1 hr)
- Transformation of E. coli TOP10 strain with ligation.
- Transformants plating on LB + kanamycin.
Cloning of protein Z DNA to pET15b-OmpA-omega in place of OmpA
Paweł
- Results of ligation: 6 colonies grown.
- Each colony cultured overnight in LB + ampicillin
Cloning of protein Z DNA to pET15b-OmpA-omega in place of OmpA
Paweł
- Isolation of plasmids from cultures inocluated on previous day
- Control digest of isolated plasmids with NdeI and NotI. Two positives obtained (proper band: ~150 bp visible)
- One of positive plasmids transformed into TOP10 and plated on LB+amp, overnight, for further isolation of pET15b+Z+omega vector
Antoni
- Setup of overnight culture E. coli TOP10 (LB broth) for preparation of chemocompetent bacteria.
Cloning of protein A DNA to OmpA constructsMichał K.
- Isolation of plasmids from cultures inocluated on previous day (pACYC177+OmpA_A_omega).
- Control digest of isolated plasmids with BamHI and SacI.
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