Team:BAU-Indonesia/Modeling

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<h2>Abstract Project</h2>
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<h2><b>Modeling</b></h2>
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                                        Biobrick parts that we have been using  is <b> Coming Soon </b> (in progress) because the Protein Coding Site (Cutinase gene) is in sequencing process. so we're not be able to post our parts.<br>
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We use cutinase gene (LC cutinase) which is homolog with Thermobifidafuscacutinase. We align some cutinase gene that we got from the gene bank, and create the DNA primer from it. Our forward primer is
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5' AACCCCTACGAGCGCGGCCCC 3' and our reverse primer is5' AGAACGGGCAGGTGGAGCGGT 3'.<br>
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<div class="read"><a href="#">read more &raquo;</a></div>
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We use strong constitutive promoter, and we cut it from PET 14 plasmids then we'll connect it to the plasmid vector pSB1C3. We use the strong constitutive promoter because we want the enzyme secreted continuously.<br>
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We just use one modul, <b>The Degradation Modul </b><br><br><br>
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<h2>Introduction</h2>
 
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Latest revision as of 22:37, 26 September 2012


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Modeling


Biobrick parts that we have been using is Coming Soon (in progress) because the Protein Coding Site (Cutinase gene) is in sequencing process. so we're not be able to post our parts.
We use cutinase gene (LC cutinase) which is homolog with Thermobifidafuscacutinase. We align some cutinase gene that we got from the gene bank, and create the DNA primer from it. Our forward primer is 5' AACCCCTACGAGCGCGGCCCC 3' and our reverse primer is5' AGAACGGGCAGGTGGAGCGGT 3'.
We use strong constitutive promoter, and we cut it from PET 14 plasmids then we'll connect it to the plasmid vector pSB1C3. We use the strong constitutive promoter because we want the enzyme secreted continuously.
We just use one modul, The Degradation Modul



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