Team:Warsaw/Calendar-Main/25 June 2008

From 2008.igem.org

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<h3>Change of the reporter from pZC with B-galactosidase to GFP or RFP</h3>
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<h3>Change of the reporter from <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pZC320>pZC320</a> with B-galactosidase to GFP or RFP</h3>
<h4>Piotr, Weronika</h4>
<h4>Piotr, Weronika</h4>
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<li>Inoculation of 10ml LB with E.coli TOP10 carrying pZC</li>
<li>Inoculation of 10ml LB with E.coli TOP10 carrying pZC</li>
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<li>Isolation and chemotransformation with plasmids nazwa (Gfp genetrator), nazwa (RFP generator)</li>
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<li>Isolation and chemotransformation with <a href=http://partsregistry.org/wiki/index.php?title=Part:pSB1A2>pSB1A2</a> standard plasmids carrying parts: <A href=http://partsregistry.org/wiki/index.php?title=Part:BBa_E0840>BBa_E0840</a>(Gfp genetrator) and <a href=http://partsregistry.org/wiki/index.php?title=Part:BBa_J04450>BBa_J04450</a> (RFP generator)</li>
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<li>We've run gradient <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> to obtain Alpha-link and link-A.
<li>We've run gradient <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> to obtain Alpha-link and link-A.
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<ul><li>Taq polymerase</li><li>buffer suplemented with (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub></li><li>MgCl<sub>2</sub> concentration gradient (from 1 to 4 mM)</li><li>annealing temp 55&deg;C</li><li>elongation time 1 - 2 minutes</li></ul></li>
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<ul><li>DNA template: pDRIVE-TAPTAG</li>
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<li>Taq polymerase</li><li>buffer suplemented with (NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub></li><li>MgCl<sub>2</sub> concentration gradient (from 1 to 4 mM)</li><li>annealing temp 55&deg;C</li><li>elongation time 1 - 2 minutes</li></ul></li>
<li>We have successfully amplified Alpha-link and link-A (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/25_June_2008#fig1">Fig. 1</a>). Now it's time for PCL (Polymerase Chain Ligation) to create fusions  Alpha-A and Omega-A.</li></ol>
<li>We have successfully amplified Alpha-link and link-A (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/25_June_2008#fig1">Fig. 1</a>). Now it's time for PCL (Polymerase Chain Ligation) to create fusions  Alpha-A and Omega-A.</li></ol>

Revision as of 16:27, 24 October 2008

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Change of the reporter from pZC320 with B-galactosidase to GFP or RFP

Piotr, Weronika

  1. Inoculation of 10ml LB with E.coli TOP10 carrying pZC
  2. Isolation and chemotransformation with pSB1A2 standard plasmids carrying parts: BBa_E0840(Gfp genetrator) and BBa_J04450 (RFP generator)
  3. Plating of chemotransformants on LB+ampicillin

Preparation of constructs with OmpA protein fusions

Michał K.

Repetition of PCRs and gel-out purifications from 16 June.

PCR of Alpha-link and link-A

Michał L. Marcin and Ewa

  1. We've run gradient PCR to obtain Alpha-link and link-A.
    • DNA template: pDRIVE-TAPTAG
    • Taq polymerase
    • buffer suplemented with (NH4)2SO4
    • MgCl2 concentration gradient (from 1 to 4 mM)
    • annealing temp 55°C
    • elongation time 1 - 2 minutes
  2. We have successfully amplified Alpha-link and link-A (Fig. 1). Now it's time for PCL (Polymerase Chain Ligation) to create fusions Alpha-A and Omega-A.
Fig. 1. PCR product - link-A.

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