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<h1> Part Collection </h1> | <h1> Part Collection </h1> | ||
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We have taken T5-GFP-pBAV1k(BBa_K1321309) as control and normalized the fluorometry data with respect of it. | We have taken T5-GFP-pBAV1k(BBa_K1321309) as control and normalized the fluorometry data with respect of it. | ||
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The parts belonging to this collection are: | The parts belonging to this collection are: | ||
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<li>BBa_K2857101</li> | <li>BBa_K2857101</li> | ||
<li>BBa_K2857113</li> | <li>BBa_K2857113</li> | ||
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+ | The results are summarized in the bar graph below. | ||
+ | <img src="https://static.igem.org/mediawiki/parts/9/96/T--IIT-Madras-Promoter-characterization.png" style="width:inherit;"> | ||
</html> | </html> |
Revision as of 02:41, 18 October 2018
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: