Team:Warsaw/Calendar-Main/16 June 2008

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  primers (20 cycles, elongation duration 30 s, annealing temperature 58&deg;C).<br>
  primers (20 cycles, elongation duration 30 s, annealing temperature 58&deg;C).<br>
As a result we got three PCR products: OmpA_linker and two fragments of TEM1 beta-lactamese: linker_alpha and linker_omega. </li>
As a result we got three PCR products: OmpA_linker and two fragments of TEM1 beta-lactamese: linker_alpha and linker_omega. </li>
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<li> Gel electrophoresis of PCR products and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper bands (OmpA_linker - 500 bp, linker_alpha  - 600 bp and linker_omega - 350 bp).</li>
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<li> Gel electrophoresis of PCR products (<a href="https://2008.igem.org/wiki/index.php?title=Team:Warsaw/Calendar-Main/16_June_2008#fig1">Fig. 1</a>) and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper bands (OmpA_linker - 500 bp, linker_alpha  - 600 bp and linker_omega - 350 bp).</li>
<li>Electrophoresis to estimate the concentration of isolated DNA.</li>
<li>Electrophoresis to estimate the concentration of isolated DNA.</li>
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<li>Sequencing of proper fragments using primer <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a>.</li></ol>
<li>Sequencing of proper fragments using primer <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a>.</li></ol>
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<a name="fig1"><img src="https://static.igem.org/mediawiki/2008/a/a3/PCR_Ompa_Alpha_Omega_WAW.jpg" width=300/></a>
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<var>PCR products: linker_alpha (lane 2), linker_omega (lane 3), OmpA_linker (lane 4)</var>
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Revision as of 00:31, 12 October 2008

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Preparation of constructs with OmpA protein fusions

Michał K.

  1. PCR on pB30D plasmid with OmpaL_N and OmpaP_link primers (15 cycles, elongation duration 45 s, annealing temperature 63°C).
  2. PCR on pUC19 plasmid with AlphaL_link and AlphaP_XB primers (20 cycles, elongation duration 45 s, annealing temperature 63°C).
  3. PCR on pUC19 plasmid with OmegaL_link and OmegaP_EPB primers (20 cycles, elongation duration 30 s, annealing temperature 58°C).
    As a result we got three PCR products: OmpA_linker and two fragments of TEM1 beta-lactamese: linker_alpha and linker_omega.
  4. Gel electrophoresis of PCR products (Fig. 1) and gel-out of proper bands (OmpA_linker - 500 bp, linker_alpha - 600 bp and linker_omega - 350 bp).
  5. Electrophoresis to estimate the concentration of isolated DNA.

Blue/white and rifampicin test

Michał L., Ewa, Marcin

  1. Colony PCR.
    Template: DNA isolated from white colonies
    Primers: pZCseqL and pZCseqR

    Colony PCR program
    TemperatureTimeNo. of cycles
    94°C4:00
    94°C0:3028 cycles
    48°C0:45
    72°C1:30
    72°C10:00
    4°Cinfinite

  2. DNA gel electrophoresis of PCR products.
  3. Gel-out of proper products (~1200 bp).
  4. Sequencing of proper fragments using primer pZCseqL.
PCR products: linker_alpha (lane 2), linker_omega (lane 3), OmpA_linker (lane 4)