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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: | ||
− | <li>BBa_K2857110</li> | + | <li>P71S: BBa_K2857110</li> |
− | <li>BBa_K2857106</li> | + | <li>P6S: BBa_K2857106</li> |
− | <li>BBa_K2857115</li> | + | <li>P5R: BBa_K2857115</li> |
− | <li>BBa_K2857105</li> | + | <li>P5S: BBa_K2857105</li> |
− | <li>BBa_K2857102</li> | + | <li>P2S: BBa_K2857102</li> |
− | <li>BBa_K2857120</li> | + | <li>P71R: BBa_K2857120</li> |
− | <li>BBa_K2857114</li> | + | <li>P4R: BBa_K2857114</li> |
− | <li>BBa_K2857116</li> | + | <li>P6R: BBa_K2857116</li> |
− | <li>BBa_K2857117</li> | + | <li>P70R: BBa_K2857117</li> |
− | <li>BBa_K2857118</li> | + | <li>P8R: BBa_K2857118</li> |
− | <li>BBa_K2857119</li> | + | <li>P9R: BBa_K2857119</li> |
− | <li>BBa_K2857111</li> | + | <li>P1R: BBa_K2857111</li> |
− | <li>BBa_K2857101</li> | + | <li>P1S: BBa_K2857101</li> |
− | <li>BBa_K2857113</li> | + | <li>P3R: BBa_K2857113</li> |
The results are summarized in the bar graph below. | The results are summarized in the bar graph below. |
Revision as of 02:48, 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: