Team:Warsaw/Calendar-Main/13 October 2008

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(Difference between revisions)
(New page: {{WarNotebook}} <!-- do not edit above me! --> <html> <h3>Preparation of BioBricks</h3> <h4>Michał K.</h4> <ol> <li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/p...)
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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>
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primers (annealing temperature 58 &deg;C; elongation length 60s) to obtain alpha fragment with proper restriction sites. </li>
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primers (annealing temperature 58 &deg;C; elongation length 60s) to obtain alpha2 fragment with proper restriction sites. </li>
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<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>
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<li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>Digest</a> of
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isolated PCR products: alpha2 fragment with SacI and BcuI (SacI buffer) and link_alpha with EcoRI and BcuI (BamHI buffer). </li>
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<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>
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<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>
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<li> Inoculation of few more colonies from old plate with ligation of 3kb (??????) + OmpA_omega_link to liquid LB + kanamycin.</li>
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<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>
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</ol>
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Revision as of 17:37, 25 October 2008

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Preparation of BioBricks

Michał K.

  1. Digest of 3kb(????)+pLac_OmpA_omega with BcuI and SacI (SacI buffer), dephosphorylation with CIAP.
  2. PCR on pACYC177+OmpA_omega_deltaA_alpha plasmid using LinLSXNE and AlfaPSpe primers (annealing temperature 58 °C; elongation length 60s) to obtain link_alpha fragment.
  3. PCR on alpha PCR product from 10 September using AlphaL+SacI and LinP_BS2 primers (annealing temperature 58 °C; elongation length 60s) to obtain alpha2 fragment with proper restriction sites.
  4. Gel electrophoresis and gel-out of proper band 600 bp for alpha PCR products and 3000 bp for 3kb(????)+pLac_OmpA_.
  5. Digest of isolated PCR products: alpha2 fragment with SacI and BcuI (SacI buffer) and link_alpha with EcoRI and BcuI (BamHI buffer).
  6. Clean-up of digested PCR products.
  7. 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.
  8. Inoculation of few more colonies from old plate with ligation of 3kb (??????) + OmpA_omega_link to liquid LB + kanamycin.
  9. Overnight ligation of DNA fragments: 3kb(?????)+ link_alpha; 3kb(????)_pLac_OmpA_ + alpha2; RFP(?????) (from 6 October) + AraC+pBAD+AID.