Difference between revisions of "Part:BBa K3788013:Experience"

 
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This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
 
This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
 
how you used this part and how it worked out.
 
how you used this part and how it worked out.
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===Applications of BBa_K3788025===
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===Cell visualization with confocal microscope===
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<p>We wanted to determine whether the fluorescence is located in the periplasm or in the cytoplasm, so we used a confocal microscope to visualize our cells.</p>
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<p>We transformed E.Coli MG1655 strains with an empty J04500 vector or with the BBa_K3788013 plasmid. We then prepared 3mL 2YT growing medium with chloramphenicol and then put MG1655 containing either J04500 or BBa_K3788025 plasmids.</p>
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<p>After 3 hours of incubation at 37°C, we prepared the plates and visualized our cells </p>
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https://2021.igem.org/wiki/images/d/d6/T--Aix-Marseille--Microscopie_J04500.jpeg
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<i><b>Figure :</b> Visualisation of MG1655 E.coli strains containing J04500</i>
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https://2021.igem.org/wiki/images/3/31/T--Aix-Marseille--Microscopie_J04500%2BPelBsfGFP.jpeg
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<i><b>Figure :</b> Visualisation of MG1655 E.coli strains containing BBa_K3788013</i>
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<p>We can see that bacteria containing J04500 do not emit light, contrary to the ones containing J04500_PelBsfGFP, which are green under a confocal microscope.</p>
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<p>However, we are not able to determine whether the light is located at the surface of the bacteria or if it is located in all the cells.</p>
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===Applications of BBa_K3788013===
 
===Applications of BBa_K3788013===

Revision as of 15:37, 21 October 2021


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K3788025

Cell visualization with confocal microscope

We wanted to determine whether the fluorescence is located in the periplasm or in the cytoplasm, so we used a confocal microscope to visualize our cells.

We transformed E.Coli MG1655 strains with an empty J04500 vector or with the BBa_K3788013 plasmid. We then prepared 3mL 2YT growing medium with chloramphenicol and then put MG1655 containing either J04500 or BBa_K3788025 plasmids.

After 3 hours of incubation at 37°C, we prepared the plates and visualized our cells


T--Aix-Marseille--Microscopie_J04500.jpeg Figure : Visualisation of MG1655 E.coli strains containing J04500


T--Aix-Marseille--Microscopie_J04500%2BPelBsfGFP.jpeg Figure : Visualisation of MG1655 E.coli strains containing BBa_K3788013


We can see that bacteria containing J04500 do not emit light, contrary to the ones containing J04500_PelBsfGFP, which are green under a confocal microscope.

However, we are not able to determine whether the light is located at the surface of the bacteria or if it is located in all the cells.


Applications of BBa_K3788013

User Reviews

UNIQ932b1b568f875685-partinfo-00000000-QINU UNIQ932b1b568f875685-partinfo-00000001-QINU