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 salicylate. We tested two kind of needles (more or less thin) and three different concentrations of salicylate: 1mM, 10mM and 100mM. In each chemotaxis cubicle there were two needles: one with salicylate (S) and another with buffer, the control (C). This is a representation of the assay:</p>
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     <div class="table">

Latest revision as of 21:08, 26 October 2010

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September, 20th

Assay Team

We designed and prepared material to performance an assay to show Pseudomonas sp. G7 was chemotactic to salicylate. We tested two kind of needles (more or less thin) and three different concentrations of salicylate: 1mM, 10mM and 100mM. In each chemotaxis cubicle there were two needles: one with salicylate (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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