Team:Warsaw/Calendar-Main/13 August 2008

From 2008.igem.org

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<li>Washing.</li>
<li>Washing.</li>
<li>Anti-rabbit antibody binding.</li>
<li>Anti-rabbit antibody binding.</li>
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<li>Developing with BCIP and NBT.</li>
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<li>Developing with BCIP and NBT (see fig.1.).</li>
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</p>
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</p><img src="https://static.igem.org/mediawiki/2008/e/ec/Blot_OmpA_WAW.jpg" width=150/>
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<var><b>Fig. 1.</b>Protein A detection on the surface of bacteria.<br>
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1 - <i>E. coli</i> expressing <b>OmpA_Omega_A_Alpha</b>,<br>
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2 - <b>negative control</b> - <i>E. coli</i> expressing <b>OmpA_Z_Omega</b>,<br>
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3 - <i>E. coli</i> expressing <b>OmpA_A_Alpha</b>,<br>
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4 - <b>negative control</b> - <i>E. coli</i> carrying OmpA_Omega_A_Alpha without inducer,<br>
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5 - <i>E. coli</i> expressing <b>OmpA_A_Omega</b>,<br>
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6 - <b>negative control</b> - <i>E. coli</i> Top10 without plasmid.</var>
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[photo of the gel is to be placed here]
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<br><br>
<h3>Cloning of alpha to <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-A-omega>pACYC177+OmpA_A_omega</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a></h3><h4>Michał K.</h4>
<h3>Cloning of alpha to <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-A-omega>pACYC177+OmpA_A_omega</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a></h3><h4>Michał K.</h4>
<p> Inoculation of <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-A-omega>pACYC177+OmpA_A_omega</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a> plasmids to LB with kanamycin.</p>
<p> Inoculation of <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-A-omega>pACYC177+OmpA_A_omega</a> and <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a> plasmids to LB with kanamycin.</p>
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Revision as of 23:21, 25 October 2008

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Checking for presence of protein A on the cell membrane

Piotr

  1. Pouring bacteria by drops onto nitrocellulose.
  2. Drying.
  3. Blocking.
  4. Anti-A antibody binding.
  5. Washing.
  6. Anti-rabbit antibody binding.
  7. Developing with BCIP and NBT (see fig.1.).

Fig. 1.Protein A detection on the surface of bacteria.
1 - E. coli expressing OmpA_Omega_A_Alpha,
2 - negative control - E. coli expressing OmpA_Z_Omega,
3 - E. coli expressing OmpA_A_Alpha,
4 - negative control - E. coli carrying OmpA_Omega_A_Alpha without inducer,
5 - E. coli expressing OmpA_A_Omega,
6 - negative control - E. coli Top10 without plasmid.


Cloning of alpha to pACYC177+OmpA_A_omega and pACYC177+OmpA_Z_omega

Michał K.

Inoculation of pACYC177+OmpA_A_omega and pACYC177+OmpA_Z_omega plasmids to LB with kanamycin.