Team:EPF Lausanne/Calendar/13 September 2013

From 2013.igem.org

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{{Template:EPFL2013Header}}
{{Template:EPFL2013Header}}
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<font size = "4"> Cell Surface Display </font> <BR>
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''Inverted Microscopy'' <BR>
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- All our constructs (ISA,ISD,ISI and competent cells as negative control) were incubated 1hr with TexRed conjugate nanoparticles.
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<br>- Visualization under the microscope with a cy5 filter.
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<br><br>
<font size = "4"> Sensing-Effector </font> <BR>
<font size = "4"> Sensing-Effector </font> <BR>
''Innoculation of Bacteria with our constructs'' <BR>
''Innoculation of Bacteria with our constructs'' <BR>
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-In order to characterize both the sensing and the effector plasmid I innoculated Bacteria in liquid LB cultures over-night.
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-In order to characterize both the sensing and the effector plasmid I inoculated Bacteria in liquid LB cultures over-night.
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''Biotinylation''<BR>
''Biotinylation''<BR>
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-We Biotinylated the two new nanoparticles batches.
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-We biotinylated the two new nanoparticles batches.
<BR>
<BR>
-End of the anti-strepta resistance check (sample mix, use of strepatavidin beads and microscopy)
-End of the anti-strepta resistance check (sample mix, use of strepatavidin beads and microscopy)

Latest revision as of 22:22, 4 October 2013

Taxi.Coli: Smart Drug Delivery iGEM EPFL

Header

Cell Surface Display

Inverted Microscopy
- All our constructs (ISA,ISD,ISI and competent cells as negative control) were incubated 1hr with TexRed conjugate nanoparticles.
- Visualization under the microscope with a cy5 filter.

Sensing-Effector

Innoculation of Bacteria with our constructs
-In order to characterize both the sensing and the effector plasmid I inoculated Bacteria in liquid LB cultures over-night.

Nanoparticles

Biotinylation
-We biotinylated the two new nanoparticles batches.
-End of the anti-strepta resistance check (sample mix, use of strepatavidin beads and microscopy)

DSL Measurements
-We did DLS measurements of the new biotinylated nanoparticles (before dialysis).