Team:EPF-Lausanne/Notebook/June2011

From 2011.igem.org

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(Friday, 1st of July 2011)
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== Friday, 1st of July 2011==
 
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Alina and Lilia did MITOMI on His-tetR expressed from linear template, it was loaded on chip in ITT expression mix. DNA was spotted on June 29 in different concentrations for both: consensus (tetO1) sequence and a random sequence ((-)control).
 
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[[File:EPFL_1jully_MITOMI_His-TetR_concensus_vs_negctrl.png|600px|GFP-tetR and cy5 fluorescence‎]]
 
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Images: Green fluorescence comes from green-lysine and red fluorescence comes from DNA (cy-5 labeled).
 
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Although we don't observe much protein bound to the anti His-tag antibody, we can still see that it does bound TetO1 sequence and did not bind any (-)control sequence. 
 
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Some possible reasons for low protein fluorescence under the buttons: the expression yield from the linear template with T7 promoter might be too low, the His-tag to antibody binding is not strong enough or the concentration of antibody is too low.
 
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== Friday, 1st of July 2011==
 
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Alina and Lilia amplified the His-tetR linear template. After PCR sample was loaded on 1% agarose gel with Rad Safe, “1Kb Plus DNA Ladder” was used. 
 
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[[File:EPFL_His-tetR_linear_template_amplification_results.png|200px|Gel after PCR amplification of linear template His-tetR‎]]
 
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We also prepared about thirty LB-agar plates with ampicilin, they are in the BM fridge.
 
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Revision as of 22:09, 2 July 2011