Team:IIT Madras/Results

From 2009.igem.org

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(Fluorescent Imaging)
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===Fluorescent Imaging===
===Fluorescent Imaging===
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<p>The above panel of images show cells co-transformed with both constructs, namely expressing CFP with Ampicillin and RFP with Chloramphenicol.<br>
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</p><br></html>
[[Image:brightfield.jpg|center]]
[[Image:brightfield.jpg|center]]
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<html>(a) shows cells exposed to Bright Field.<br></html>
[[Image:RFP.jpg|center]]
[[Image:RFP.jpg|center]]
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<html>(b) shows cells exposed to Red filter.<br></html>
[[Image:CFP.jpg|center]]
[[Image:CFP.jpg|center]]
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<html>(c) shows cells exposed to Cyan filter.<br></html>
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<p>The above panel of images show cells co-transformed with both constructs, namely expressing CFP with Ampicillin and RFP with Chloramphenicol.<br>
<p>The above panel of images show cells co-transformed with both constructs, namely expressing CFP with Ampicillin and RFP with Chloramphenicol.<br>
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figure (a) shows cells exposed to Bright Field.<br>
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</p><br>
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figure (b) shows same cells exposed to Red filter.<br>
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figure (c) shows same cells exposed to Cyan filter. </p><br>
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For updated results, keep checking <a href="http://openwetware.org/wiki/IGEM:Indian_Institue_of_Technology_Madras/2009/Notebook/PLASMID_-_Plasmid_Locking_Assembly_for_Sustaining_Multiple_Insert_DNA/2009/10/31">here.</a>
For updated results, keep checking <a href="http://openwetware.org/wiki/IGEM:Indian_Institue_of_Technology_Madras/2009/Notebook/PLASMID_-_Plasmid_Locking_Assembly_for_Sustaining_Multiple_Insert_DNA/2009/10/31">here.</a>

Revision as of 18:16, 21 October 2009

Indian Institute of Technology,Madras

IIT Madras













Contents

Results

Comparing the differences in the growth rates of cells with and without plasmids in various media



Growth curves


DH5aall4cases.jpg
Fig 8.1: DH5a grown in LB containing no antibiotic, LB containing Ampicillin, LB containing Chloramphenicol, LB containing both antibiotics.


Rfpall4cases.jpg
Fig 8.2: RFP (pSB1C3) contanining cells grown in LB containing no antibiotic, LB containing Ampicillin, LB containing Chloramphenicol, LB containing both antibiotics.


Cfpall4cases.jpg
Fig 8.3: CFP (pSB1A2) contanining cells grown in LB containing no antibiotic, LB containing Ampicillin, LB containing Chloramphenicol, LB containing both antibiotics.



RC4cases.jpg
Fig 8.4: RFP (pSB1C3) - CFP (pSB1A2) contanining cells grown in LB containing no antibiotic, LB containing Ampicillin, LB containing Chloramphenicol, LB containing both antibiotics.



Noaball4.jpg
Fig 8.5: All 4 strains in media without antibiotics.



Corraball4.jpg
Fig 8.6: All 4 strains in their corresponding antibiotic media - DH5a in Lb without antibiotics, RFP (pSB1C3) in LB with Chloramphenicol, CFP (pSB1A2) in LB with Ampicillin, RFP (pSB1C3) - CFP (pSB1A2) cells in LB with Chloramphenicol and Ampicillin.



Logall4noab.jpg
Fig 8.7: log (OD600) vs Time plot for all 4 strains in media without antibiotics.



Logcorrab.jpg
Fig 8.8: log (OD600) vs Time plot for all 4 strains in their corresponding antibiotic media - DH5a in Lb without antibiotics, RFP (pSB1C3) in LB with Chloramphenicol, CFP (pSB1A2) in LB with Ampicillin, RFP (pSB1C3) - CFP (pSB1A2) cells in LB with Chloramphenicol and Ampicillin.

Modeling

For updated results, keep checking here.

Fluorescent Imaging

The above panel of images show cells co-transformed with both constructs, namely expressing CFP with Ampicillin and RFP with Chloramphenicol.


Brightfield.jpg

(a) shows cells exposed to Bright Field.

RFP.jpg

(b) shows cells exposed to Red filter.

CFP.jpg

(c) shows cells exposed to Cyan filter.

The above panel of images show cells co-transformed with both constructs, namely expressing CFP with Ampicillin and RFP with Chloramphenicol.


For updated results, keep checking here.