Team:UPO-Sevilla/Notebook/09 20

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       <h2>Assay Team</h2>
       <h2>Assay Team</h2>
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       <p>We designed and prepared material to performance an assay to show Pseudomonas sp. G7 was chemotactic to salicilate. We tested two kind of needles (more or less thin) and three different concentrations of salicilate: 1mM, 10mM and 100mM. In each chemotaxis cubicle there were two needles: one with salicilate and another with buffer, the control. This is a representation of the assay:</p>
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       <p>We designed and prepared material to performance an assay to show <i>Pseudomonas sp</i>. G7 was chemotactic to salicilate. We tested two kind of needles (more or less thin) and three different concentrations of salicilate: 1mM, 10mM and 100mM. In each chemotaxis cubicle there were two needles: one with salicilate (S) and another with buffer, the control (C). This is a representation of the assay:</p>
     <div class="table">
     <div class="table">

Revision as of 12:18, 26 October 2010

September, 20th

Assay Team

We designed and prepared material to performance an assay to show Pseudomonas sp. G7 was chemotactic to salicilate. We tested two kind of needles (more or less thin) and three different concentrations of salicilate: 1mM, 10mM and 100mM. In each chemotaxis cubicle there were two needles: one with salicilate (S) and another with buffer, the control (C). This is a representation of the assay:

  1mM 10mM 100mM
thin needle
S        C
S        C
S        C
thick needle
S        C
S        C
S        C
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