Team:Warsaw/Calendar-Main/26 August 2008
From 2008.igem.org
(Difference between revisions)
MKrzyszton (Talk | contribs) |
|||
(18 intermediate revisions not shown) | |||
Line 4: | Line 4: | ||
<html> | <html> | ||
- | |||
- | |||
- | |||
- | <a href= | + | <h3>Tests for ampicillin resistance given by protein added to medium</h3><h4>Piotr</h4> |
- | <li> | + | <ol><li> |
+ | <p>Purification <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-alpha>pACYC177+OmpA_alpha</a> from antibiotic resistance contamination:<br> | ||
+ | Inoculation of <i>E. coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> carrying <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-alpha>pACYC177+OmpA_alpha</a> to liquid LB with kanamycin and with kanamycin and ampicillin.</li> | ||
+ | <li>Inoculation of all pACYC177+OmpA variants of constructs to LB + 0.25 mM IPTG, kanamycin, ampicillin (50 μg/ml) and 50 μg/ml of protein (Z_alpha and Z_omega; negative control without protein).</li> | ||
+ | <li>Measurement of growth after 5 hours and on next day.</li></ol> | ||
- | <h3>Cloning of protein A DNA to pET15b+ | + | |
+ | </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>Antoni</h4> | ||
<p><ol> | <p><ol> | ||
- | <li> | + | <li> Colony <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on colonies from plates with transformations <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pGeneart-A>pGeneart+A</a> Primers used: |
- | + | ||
- | + | ||
- | + | ||
- | + | ||
+ | <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AP+NotI">AP+NotI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AL+SacI">AL+SacI.</a></li> | ||
+ | <li> Lack of confirmed transformant colonies. </li></ol></p> | ||
+ | |||
+ | <h3>Cloning of alpha to <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-A-omega>pACYC177+OmpA_A_omega</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a></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 of plasmids</a> from cultures inocluated on previous day (both potential constructs). </li> | ||
+ | <li> Control | ||
+ | <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">digest</a> of isolated plasmids with FastBamHI and FastAcc65I (Fast Digest buffer).</li> <li> Gel electrophoresis - still no proper clones found.</li> | ||
</ol></p> | </ol></p> | ||
+ | |||
+ | |||
</html> | </html> | ||
Latest revision as of 20:56, 26 October 2008
Tests for ampicillin resistance given by protein added to mediumPiotr
Cloning of protein A DNA to pET15b+OmpA-alpha plasmidAntoni
Cloning of alpha to pACYC177+OmpA_A_omega and pACYC177+OmpA_Z_omegaMichał K.
|