Difference between revisions of "Team:Lethbridge/Improve"

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{{Team:Lethbridge/assets/reset.css}}
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{{Team:Lethbridge/navbar}}
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<html>
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<head>
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<style>
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/*SIDE MENU FOR IGEM STUFF*/
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#sideMenu{width: 200px;position: absolute;top: 20px;left: 1020px;z-index: 10;padding-top: 0px;padding-bottom: 15px;padding-left: 15px;padding-right: 15px;background-color: white;text-align: left;display: none;z-index: 9996;}
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#content{width: 100%;padding: 0px;margin-left: 0px;}
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#top_title{overflow: hidden;display: none;}
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#top_menu_14{height: 20px;}
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#top_menu_under{height: 0px;}
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/*#globalWrapper{padding-bottom: 200px;}*/
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/*VISIBLE CONTENT STYLING BEGINS HERE*/
 
/*VISIBLE CONTENT STYLING BEGINS HERE*/
 
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  <body>

Revision as of 05:35, 19 October 2017

/*VISIBLE CONTENT STYLING BEGINS HERE*/

<body>

Composite Parts

Part BBa_K1791001

Part BBa_K1791001 contains two modules, a standard ribosome binding site (RBS) expressing MS2 coat protein and a theophylline ribozyme with a MS2 aptamer at the 3’ end. To express MS2 coat protein the part utilizes expression of c-terminal 6x His tagged MS2 coat protein under the regulation of a T7 promoter and a standard Shine Dalgarno sequence followed by a double terminator (BBa_0015). Downstream of the RBS is a T7 promoter followed by a theophylline ribozyme and a MS2 aptamer at the 3’ end. Coexpression of the two modules results in MS2 binding to the 3’ end of the theophylline ribozyme module which allows for MS2-RNA purification by nickel affinity chromatography, RNA can then be eluted from the MS2-RNA complex by addition of theophylline.

Check it out on the Registry

Part BBa_K1791002

Part BBa_K17910012 contains two modules, a low efficiency ribosome binding site (RBS) expressing MS2 coat protein and a theophylline ribozyme with a MS2 aptamer at the 3’ end. To express MS2 coat protein the part utilizes expression of c-terminal 6x His tagged MS2 coat protein under a T7 promoter and a standard Shine Dalgarno sequence followed by a double terminator (BBa_0015). Downstream of the RBS is a T7 promoter followed by a theophylline ribozyme and a MS2 aptamer at the 3’ end. Coexpression of the two modules results in MS2 binding to the 3’ end of the theophylline ribozyme construct which allows for MS2-RNA purification by nickel affinity chromatography, RNA can then be eluted from the MS2-RNA complex by addition of theophylline.

Check it out on the Registry