Difference between revisions of "Team:IIT-Madras/Part Collection"

(Undo revision 484108 by Sathvik A (talk))
 
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One of the major objectives of our project is to make a Synthetic promoter library for Acinetobacter baylyi ADP1. This can very helpful to scientists working on synthetic biology and metabolic engineering areas. Traditional approaches work on extremes of knocking out a gene or over expression. However, in Synthetic biology experiments, we require stringent promoters that have tight control over the gene expression rate.
 
One of the major objectives of our project is to make a Synthetic promoter library for Acinetobacter baylyi ADP1. This can very helpful to scientists working on synthetic biology and metabolic engineering areas. Traditional approaches work on extremes of knocking out a gene or over expression. However, in Synthetic biology experiments, we require stringent promoters that have tight control over the gene expression rate.
 
<p>
 
<p>
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We have taken T5-GFP-pBAV1k(BBa_K1321309) as control and normalized the fluorometry data with respect of it.
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We have taken T5-GFP-pBAV1k(BBa_K1321309) as control and normalized the fluorometry data with respect of it.<br><br>
  
  
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The parts belonging to this collection are:
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The parts belonging to this collection are:<br>
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<li>P71S: BBa_K2857110</li>
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P71S: BBa_K2857110<br>
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<li>P6S:  BBa_K2857106</li>
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P6S:  BBa_K2857106<br>
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<li>P5R:  BBa_K2857115</li>
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P5R:  BBa_K2857115<br>
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<li>P5S:  BBa_K2857105</li>
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P5S:  BBa_K2857105<br>
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<li>P2S:  BBa_K2857102</li>
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P2S:  BBa_K2857102<br>
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<li>P71R: BBa_K2857120</li>
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P71R: BBa_K2857120<br>
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<li>P4R:  BBa_K2857114</li>
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P4R:  BBa_K2857114<br>
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<li>P6R:  BBa_K2857116</li>
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P6R:  BBa_K2857116<br>
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<li>P70R: BBa_K2857117</li>
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P70R: BBa_K2857117<br>
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<li>P8R:  BBa_K2857118</li>
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P8R:  BBa_K2857118<br>
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<li>P9R:  BBa_K2857119</li>
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P9R:  BBa_K2857119<br>
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<li>P1R:  BBa_K2857111</li>
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P1R:  BBa_K2857111<br>
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<li>P1S:  BBa_K2857101</li>
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P1S:  BBa_K2857101<br>
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<li>P3R:  BBa_K2857113</li>
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P3R:  BBa_K2857113<br>
  
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The results are summarized in the bar graph below.
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The results are summarized in the bar graph below.<br>
 
<img src="https://static.igem.org/mediawiki/parts/9/96/T--IIT-Madras-Promoter-characterization.png" style="width:inherit;">
 
<img src="https://static.igem.org/mediawiki/parts/9/96/T--IIT-Madras-Promoter-characterization.png" style="width:inherit;">
  
 
</html>
 
</html>

Latest revision as of 02:57, 18 October 2018

iGEM Collaborations Page

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Part Collection

One of the major objectives of our project is to make a Synthetic promoter library for Acinetobacter baylyi ADP1. This can very helpful to scientists working on synthetic biology and metabolic engineering areas. Traditional approaches work on extremes of knocking out a gene or over expression. However, in Synthetic biology experiments, we require stringent promoters that have tight control over the gene expression rate.

We have taken T5-GFP-pBAV1k(BBa_K1321309) as control and normalized the fluorometry data with respect of it.

The parts belonging to this collection are:
P71S: BBa_K2857110
P6S: BBa_K2857106
P5R: BBa_K2857115
P5S: BBa_K2857105
P2S: BBa_K2857102
P71R: BBa_K2857120
P4R: BBa_K2857114
P6R: BBa_K2857116
P70R: BBa_K2857117
P8R: BBa_K2857118
P9R: BBa_K2857119
P1R: BBa_K2857111
P1S: BBa_K2857101
P3R: BBa_K2857113
The results are summarized in the bar graph below.