Team:Warsaw/Calendar-Main/1 October 2008

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<li>Gel elctrophoresis and <a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper band: ??????. </li>  
<li>Gel elctrophoresis and <a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper band: ??????. </li>  
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<li>Inoculation of some colonies from <a href=http://partsregistry.org/wiki/index.php?title=Part:pSB2K3>pSB2K3</a>+<a href=http://partsregistry.org/wiki/index.php?title=Part:BBa_K103004>Z(BBa_K103004)</a> plate to LB with ampicillin.</li></ol>
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<li>Inoculation of some colonies from <a href=http://partsregistry.org/wiki/index.php?title=Part:pSB1A3>pSB1A3</a>+<a href=http://partsregistry.org/wiki/index.php?title=Part:BBa_K103004>Z(BBa_K103004)</a> plate to LB with ampicillin.</li></ol>

Revision as of 00:15, 26 October 2008

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Preparation of BioBricks

Michał K.

  1. Addition of 5 μl T4 ligase buffer and 2 μl of T4 ligase to digest of pLac_OmpA_omega fragment. Ligation for 1 hr.
  2. PCR on pMPMT5+AID plasmid using AIDl and AIDP_HindSpeNotPst primers (annealing temperature 58 °C; elongation length 60s) to obtain AID fragment.
  3. PCR on ligation of pLac_OmpA_omega fragment using PlacL_XNE and LinP_BS primers (annealing temperature 58 °C; elongation length 90s) to obtain pLac_OmpA_omega fragment without EcoRI.
  4. Gel electrophoresis of PCR products and gel-out of proper bands (AID - 600 bp and pLac_Omp_omega_ - 1200 bp).
  5. Isolation of pSB2K3 and BBa_I739204 (pACYC177 converted into BioBrick vector) plasmids.
  6. Digest of isolated plasmids with EcoRI and BcuI (BamHI buffer). Dephosphorylation (CIAP) of plasmids.
  7. Gel elctrophoresis and gel-out of proper band: ??????.
  8. Inoculation of some colonies from pSB1A3+Z(BBa_K103004) plate to LB with ampicillin.