Team:Warsaw/Calendar-Main/22 August 2008

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<h3>Cloning of protein A DNA to GeneArt plasmid</h3><h4>Antoni</h4><ol>
<h3>Cloning of protein A DNA to GeneArt plasmid</h3><h4>Antoni</h4><ol>
<li> Control <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">digest</a> of <A href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pGeneart-A>pGeneart+A</a> plasmids with NdeI and NotI (Orange buffer). </li>
<li> Control <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">digest</a> of <A href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pGeneart-A>pGeneart+A</a> plasmids with NdeI and NotI (Orange buffer). </li>
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<li>Gel elctrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/22_August_2008#fig1">Fig. 1.</a>). Choice of proper clone. </li></ol>
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<li>Gel electrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/22_August_2008#fig1">Fig. 1.</a>). Choice of proper clone. </li></ol>
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<a name=fig1><img src="https://static.igem.org/mediawiki/2008/d/d0/PGA%2BAtraw.jpg"></a>
<a name=fig1><img src="https://static.igem.org/mediawiki/2008/d/d0/PGA%2BAtraw.jpg"></a>
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<var><b>Fig. 1.</b>Control digest of freshly ligated pKS+A (lines 1-3). Line 4 - 0.5&mu;g of DNA ladder mix.  </var>  
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<var><b>Fig. 1.</b>Control digest of freshly ligated pKS+A (lanes 1-3). Lane 4 - 0.5&mu;g of DNA ladder mix.  </var>  
<h3>Cloning of protein A DNA to <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-alpha>pET15b+OmpA-alpha</a> plasmid</h3><h4>Antoni</h4>
<h3>Cloning of protein A DNA to <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-alpha>pET15b+OmpA-alpha</a> plasmid</h3><h4>Antoni</h4>

Revision as of 20:49, 26 October 2008

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Tests for ampicillin resistance given by protein added to medium

Piotr

Purification of pACYC177+OmpA_alpha from antibiotic resistance contamination:
Transformation of E. coli TOP10 strain with pACYC177+OmpA_alpha.

Cloning of alpha to pACYC177+OmpA_A_omega and pACYC177+OmpA_Z_omega

Michał K.

  1. Ligation of digested vectors from 14 August and alpha DNA fragment from 19 August (more vectors added).
  2. Electroporation of E. coli TOP10 with ligations products.
  3. Transformants plating on LB + kanamycin.

Cloning of protein A DNA to GeneArt plasmid

Antoni

  1. Control digest of pGeneart+A plasmids with NdeI and NotI (Orange buffer).
  2. Gel electrophoresis (Fig. 1.). Choice of proper clone.

Fig. 1.Control digest of freshly ligated pKS+A (lanes 1-3). Lane 4 - 0.5μg of DNA ladder mix.

Cloning of protein A DNA to pET15b+OmpA-alpha plasmid

Antoni

  1. Digest of pGeneart+A with NdeI and NotI (Orange buffer).
  2. Gel electrophoresis of digested plasmid and gel-out of 470 bp band.
  3. Overnight ligation of pET15b+alpha and A (pET15b+alpha from 19 August).


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