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Team:UPO-Sevilla/Notebook/09 20
From 2010.igem.org
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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> | + | <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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