Team:Warsaw/Calendar-Main/13 October 2008
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<a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL+SacI">AlphaL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#LinP_BS2">LinP_BS2</a> | <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL+SacI">AlphaL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#LinP_BS2">LinP_BS2</a> | ||
- | primers (annealing temperature 58 °C; elongation length 60s) to obtain | + | primers (annealing temperature 58 °C; elongation length 60s) to obtain alpha2 fragment with proper restriction sites. </li> |
+ | <li>Gel electrophoresis and <a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper band 600 bp for alpha PCR products and 3000 bp for 3kb(????)+pLac_OmpA_. </li> | ||
+ | <li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>Digest</a> of | ||
+ | isolated PCR products: alpha2 fragment with SacI and BcuI (SacI buffer) and link_alpha with EcoRI and BcuI (BamHI buffer). </li> | ||
+ | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_purification_after_enzymatic_reaction">Clean-up</a> of digested PCR products. </li> | ||
+ | <li> Inoculation of colonies from plate with ligation of 5kb (??????) + pT7_omega_link to liquid LB + kanamycin and RFP(?????) + pT7_alpha fragment to liquid LB + ampicillin.</li> | ||
+ | <li> Inoculation of few more colonies from old plate with ligation of 3kb (??????) + OmpA_omega_link to liquid LB + kanamycin.</li> | ||
+ | <li> Overnight <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">ligation</a> of DNA fragments: 3kb(?????)+ link_alpha; 3kb(????)_pLac_OmpA_ + alpha2; RFP(?????) (from 6 October) + AraC+pBAD+AID.</li> | ||
+ | </ol> | ||
</html> | </html> | ||
Revision as of 17:37, 25 October 2008
Preparation of BioBricksMichał K.
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