Team:Colombia/Interlab

From 2014.igem.org

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<h2><center> Interlab Study </center></h2>
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This year Colombia Team-iGEM is participating in Interlab Study! We are glad of share our results and measurements. You can find them in the tabs below, you can find the specifications of our equipments and the methodology we used as well.
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<center><b><h1  class="curs1">Interlab Study</h1></b></center>
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Methods And Validation
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<h3>Methods</h3>
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<p>
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This year Colombia Team-iGEM is participating in Interlab Study! We are glad of share our results and measurements. You can find them in the tabs below, you can find the specifications of our equipments and the methodology we used as well.
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</p>
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<b> <font size="10"> Methods </font> </b>
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<br><br><br>
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<b><font color="#8A0808" size="5" >Strains and culture</font></b>
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<h4>Strains and culture</h4>
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<p>
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All transformations were carried out in ''E. coli'' TOP10. This bacterium was cultured in LB (suplemented with the appropiate antibiotic for each case) at 37 °C.  
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All transformations were carried out in ''E. coli'' TOP10. This bacterium was cultured in LB (supplemented with the appropriate antibiotic for each case) at 37 °C.  
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</p>
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<h4>Transformations and plasmidic DNA extration</h4>
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<b><font color="#8A0808" size="5" >Transformations and plasmid DNA extraction</font></b>
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This process was carried out as it is indicated in our <html><a href="https://2014.igem.org/Team:Colombia/Protocols" target="_blank">protocols page</a>.</html>
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<p>
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This process was carried out as indicated in our <html><a href="https://2014.igem.org/Team:Colombia/Protocols" target="_blank">protocols page</a>.</html>
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</p>
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<h4>Fluorescence Microscopy</h4>
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<b><font color="#8A0808" size="5" >Fluorescence Microscopy</font></b>
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<p>
All the pictures shown here were taken using a <html><a href="http://www.nikoninstruments.com/Products/Microscope-Systems/Inverted-Microscopes/Eclipse-Ti" target="_blank">Eclipse-Ti Nikon® ECLIPSE Ti inverted microscope</a></html> equiped with an <html><a href="http://www.andor.com/scientific-cameras/ixon-emccd-camera-series/ixon-ultra-897" target="_blank">ANDOR iXon Ultra 897</a></html> camera. The filter used was FITC.
All the pictures shown here were taken using a <html><a href="http://www.nikoninstruments.com/Products/Microscope-Systems/Inverted-Microscopes/Eclipse-Ti" target="_blank">Eclipse-Ti Nikon® ECLIPSE Ti inverted microscope</a></html> equiped with an <html><a href="http://www.andor.com/scientific-cameras/ixon-emccd-camera-series/ixon-ultra-897" target="_blank">ANDOR iXon Ultra 897</a></html> camera. The filter used was FITC.
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</p>
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<h4>Fluorometry</h4>
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<b><font color="#8A0808" size="5" >Fluorometry</font></b>
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The fluorometric measures were taken using a DGEASGAES. The measures  were carried out three times while 10 min with an ON culture diluted in a 1:10 proportion in 2mL of fresh LB, with a previous measuring of OD.
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<p>
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The fluorometric measurements were taken using a DGEASGAES. The measurements were carried out three times while 10 min with an ON culture diluted in a 1:10 proportion in 2mL of fresh LB, with a previous measuring of OD.
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</p>
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<h4>Image Analysis</h4>
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<b><font color="#8A0808" size="5" >Image Analysis</font></b>
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The image analysis were performed with ImageJ 1.46r using Nikon ND Reader and interactive 3D Surface Plot pluggins. We used ''Analyzing fluorescence microscopy images with ImageJ'' (Queen's University Belfast 2014) as guide. You can download this useful material <html><a href="https://static.igem.org/mediawiki/2014/9/94/Guide_Fluoresence_ImageJ.pdf" target="_blank">here</a>.</html>
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<p>
 +
Image analyses were performed with ImageJ 1.46r using Nikon ND Reader and interactive 3D Surface Plot pluggins. We used ''Analyzing fluorescence microscopy images with ImageJ'' (Queen's University Belfast 2014) as guide. You can download this useful material <a href="https://static.igem.org/mediawiki/2014/9/94/Guide_Fluoresence_ImageJ.pdf" target="_blank">here</a>.
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<br><br><br>
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<b> <font size="10"> Validation </font> </b>
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<br><br>
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<h3>Validation</h3>
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<p>
The following gel shows respectively the plasmids with the devices and the restriction profiles for each of the tree devices digested with EcoRI and PstI. For restrictions we obtained two bands (the plasmid and the device) with the expected sizes in all cases.
The following gel shows respectively the plasmids with the devices and the restriction profiles for each of the tree devices digested with EcoRI and PstI. For restrictions we obtained two bands (the plasmid and the device) with the expected sizes in all cases.
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</p>
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<p>
GELES :)
GELES :)
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</p>
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<p>
You can check the size of each device with the next table:
You can check the size of each device with the next table:
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</p>
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<p>
{| border="2" align="center"
{| border="2" align="center"
|+'''Devices and their size'''
|+'''Devices and their size'''
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| style="text-align: left;" |2070
| style="text-align: left;" |2070
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<b> <font size="10"> Parts tested </font> </b>
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<b><font color="#8A0808" size="5" >BBa_I20260 (J23101-B0032-E0040-B0015)</font></b>
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This part corresponds to GFP under the constitutive promoter J23101, with B0032 as RBS and two stops (B001 and B0010). The backbone of this already constructed device is pSB3K3 with kandamycin resistance.
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</p>
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<div class="accordion" id="accordion2">
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<b>Fluorescence microscopy</b>
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<p>
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BBa_I20260 (J23101-B0032-E0040-B0015)
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<h3>Measures</h3>
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This part corresponds to GFP under the constitutive promoter J23101, with B0032 as RBS and two stops (B001 and B0010). The backbone of this already constructed device is pSB3K3 with kanamycin resistance.
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<h4>Fluorescence microscopy</h4>
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Here are the images of the transformed cells with this device:
Here are the images of the transformed cells with this device:
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</p>
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<center>
[[File:IL1comp.jpg|700px|thumb|center|Light (left) and FITC (right)]]
[[File:IL1comp.jpg|700px|thumb|center|Light (left) and FITC (right)]]
[[File:IL1acomp.jpg|700px|thumb|center|Light (left) and FITC (right)]]
[[File:IL1acomp.jpg|700px|thumb|center|Light (left) and FITC (right)]]
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</center>
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<p>
And the analysis for relative fluorescence among them performed from the last image above:
And the analysis for relative fluorescence among them performed from the last image above:
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</p>
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<center>
[[File:IL1c3d.jpg|700px|thumb|center|Relative fluorescence among cells]]
[[File:IL1c3d.jpg|700px|thumb|center|Relative fluorescence among cells]]
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</center>
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<b>Fluorometry</b>
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<h4>Fluorometry</h4>
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dtgdxhedh
dtgdxhedh
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<b><font color="#8A0808" size="5" >BBa_J23115 + BBa_E0240 (B0032-E0040-B0015)</font></b>
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This part is identical to the last one, but built by us on a pSB1C3 backbone.
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BBa_J23115 + BBa_E0240 (B0032-E0040-B0015)
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<b>Fluorescence microscopy</b>
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<h3>Measures</h3>
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This part is identical to the last one, but built by us in pSB1C3.
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<h4>Fluorescence microscopy</h4>
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Here are the images of the transformed cells with this device:
Here are the images of the transformed cells with this device:
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+
</p>
 +
<center>
[[File:IL2comp.jpg|700px|thumb|center|Light (left) and FITC (right)]]
[[File:IL2comp.jpg|700px|thumb|center|Light (left) and FITC (right)]]
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</center>
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<p>
And the analysis for relative fluorescence among them performed from the last image above:
And the analysis for relative fluorescence among them performed from the last image above:
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</p>
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<center
[[File:IL23d.jpg|700px|thumb|center|Relative fluorescence among cells]]
[[File:IL23d.jpg|700px|thumb|center|Relative fluorescence among cells]]
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</center>
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<b>Fluorometry</b>
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<h4>Fluorometry</h4>
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<p>
Ejemplillo
Ejemplillo
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BBa_J23101 + BBa_E0240 (B0032-E0040-B0015)
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<h3>Measures</h3>
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<br><br><br>
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The only difference between this part and the last one is the consitutive promoter, that in this case is J23115. The plasmid, RBS and stops are all the same.
+
<b><font color="#8A0808" size="5" >BBa_J23101 + BBa_E0240 (B0032-E0040-B0015)</font></b>
 +
<p>
 +
The only difference between this part and the last one is the constitutive promoter, which in this case is J23115. The plasmid, RBS and stops are all the same.
 +
</p>
-
<h4>Fluorescence microscopy</h4>
+
<b>Fluorescence microscopy</b>
 +
<p>
Here are the images of the transformed cells with this device:
Here are the images of the transformed cells with this device:
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+
</p>
 +
<center>
[[File:IL4comp.jpg|700px|thumb|center|Light (left) and FITC (right)]]
[[File:IL4comp.jpg|700px|thumb|center|Light (left) and FITC (right)]]
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</center>
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<p>
And the analysis for relative fluorescence among them performed from the last image above:
And the analysis for relative fluorescence among them performed from the last image above:
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</p>
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<center>
[[File:IL43d.jpg|700px|thumb|center|Relative fluorescence among cells]]
[[File:IL43d.jpg|700px|thumb|center|Relative fluorescence among cells]]
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</center>
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<b>Fluorometry</b>
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<h4>Fluorometry</h4>
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<p>
dtgdxhedh
dtgdxhedh
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Revision as of 22:24, 28 September 2014

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Interlab Study





This year Colombia Team-iGEM is participating in Interlab Study! We are glad of share our results and measurements. You can find them in the tabs below, you can find the specifications of our equipments and the methodology we used as well.

Methods


Strains and culture

All transformations were carried out in ''E. coli'' TOP10. This bacterium was cultured in LB (supplemented with the appropriate antibiotic for each case) at 37 °C.

Transformations and plasmid DNA extraction

This process was carried out as indicated in our protocols page. </p>

Fluorescence Microscopy

All the pictures shown here were taken using a Eclipse-Ti Nikon® ECLIPSE Ti inverted microscope equiped with an ANDOR iXon Ultra 897 camera. The filter used was FITC.

Fluorometry

The fluorometric measurements were taken using a DGEASGAES. The measurements were carried out three times while 10 min with an ON culture diluted in a 1:10 proportion in 2mL of fresh LB, with a previous measuring of OD.

Image Analysis

Image analyses were performed with ImageJ 1.46r using Nikon ND Reader and interactive 3D Surface Plot pluggins. We used Analyzing fluorescence microscopy images with ImageJ (Queen's University Belfast 2014) as guide. You can download this useful material <a href="https://static.igem.org/mediawiki/2014/9/94/Guide_Fluoresence_ImageJ.pdf" target="_blank">here</a>.


Validation

<p> The following gel shows respectively the plasmids with the devices and the restriction profiles for each of the tree devices digested with EcoRI and PstI. For restrictions we obtained two bands (the plasmid and the device) with the expected sizes in all cases.

GELES :)

You can check the size of each device with the next table:

Devices and their size
Name Backbone + device / bp Device / bp Linearized backbone / bp
BBa_I20260 3669 919 2750
BBa_J23101 + BBa_E0240(B0032-E0040-B0015) 2981 911 2070
BBa_J23115 + BBa_E0240 (B0032-E0040-B0015) 2981 911 2070

Parts tested


BBa_I20260 (J23101-B0032-E0040-B0015)

This part corresponds to GFP under the constitutive promoter J23101, with B0032 as RBS and two stops (B001 and B0010). The backbone of this already constructed device is pSB3K3 with kandamycin resistance.

Fluorescence microscopy

Here are the images of the transformed cells with this device:

Light (left) and FITC (right)
Light (left) and FITC (right)

And the analysis for relative fluorescence among them performed from the last image above:

Relative fluorescence among cells

Fluorometry dtgdxhedh





BBa_J23115 + BBa_E0240 (B0032-E0040-B0015)

This part is identical to the last one, but built by us on a pSB1C3 backbone.

Fluorescence microscopy

Here are the images of the transformed cells with this device:

Light (left) and FITC (right)

And the analysis for relative fluorescence among them performed from the last image above:

<center

Relative fluorescence among cells

</center>

Fluorometry

Ejemplillo




BBa_J23101 + BBa_E0240 (B0032-E0040-B0015)

The only difference between this part and the last one is the constitutive promoter, which in this case is J23115. The plasmid, RBS and stops are all the same.

Fluorescence microscopy

Here are the images of the transformed cells with this device:

Light (left) and FITC (right)

And the analysis for relative fluorescence among them performed from the last image above:

Relative fluorescence among cells

Fluorometry

dtgdxhedh





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