Difference between revisions of "Team:Austin UTexas/Results/Electroporations"

Line 5: Line 5:
 
background-color:#808080;
 
background-color:#808080;
 
}
 
}
 +
 
div.naviSection {
 
div.naviSection {
 +
}
 +
img.resize {
 +
  max-width:50%;
 +
  max-height:50%;
 +
    display: block;
 +
    margin-left: auto;
 +
    margin-right: auto;
 
}
 
}
  
Line 16: Line 24:
 
.w3-button:hover{color:#ff0000!important;background-color:#fff!important}
 
.w3-button:hover{color:#ff0000!important;background-color:#fff!important}
  
yeet {
 
  color: transparent; 
 
  text-shadow: #ffffff;
 
}
 
  
 
.w3-sidebar{height:100%;width:200px;background-color:#808080;position:fixed!important;z-index:1;overflow:auto}
 
.w3-sidebar{height:100%;width:200px;background-color:#808080;position:fixed!important;z-index:1;overflow:auto}
Line 76: Line 80:
 
::-webkit-file-upload-button{-webkit-appearance:button;font:inherit}
 
::-webkit-file-upload-button{-webkit-appearance:button;font:inherit}
 
/* End extract */
 
/* End extract */
html,body{font-family:Verdana,sans-serif;font-size:15px;line-height:1.5}html{overflow-x:hidden}
+
 
h1{font-size:36px}h2{font-size:30px}h3{font-size:24px}h4{font-size:20px}h5{font-size:18px}h6{font-size:16px}.w3-serif{font-family:serif}
+
 
h1,h2,h3,h4,h5,h6{font-family:"Segoe UI",Arial,sans-serif;font-weight:400;margin:10px 0}.w3-wide{letter-spacing:4px}
+
hr{border:0;border-top:1px solid #eee;margin:20px 0}
+
.w3-image{max-width:100%;height:auto}img{vertical-align:middle}a{color:inherit}
+
 
.w3-table,.w3-table-all{border-collapse:collapse;border-spacing:0;width:100%;display:table}.w3-table-all{border:1px solid #ccc}
 
.w3-table,.w3-table-all{border-collapse:collapse;border-spacing:0;width:100%;display:table}.w3-table-all{border:1px solid #ccc}
 
.w3-bordered tr,.w3-table-all tr{border-bottom:1px solid #ddd}.w3-striped tbody tr:nth-child(even){background-color:#f1f1f1}
 
.w3-bordered tr,.w3-table-all tr{border-bottom:1px solid #ddd}.w3-striped tbody tr:nth-child(even){background-color:#f1f1f1}
Line 107: Line 108:
 
.w3-dropdown-hover.w3-mobile,.w3-dropdown-hover.w3-mobile .w3-btn,.w3-dropdown-hover.w3-mobile .w3-button,.w3-dropdown-click.w3-mobile,.w3-dropdown-click.w3-mobile .w3-btn,.w3-dropdown-click.w3-mobile .w3-button{width:100%}}
 
.w3-dropdown-hover.w3-mobile,.w3-dropdown-hover.w3-mobile .w3-btn,.w3-dropdown-hover.w3-mobile .w3-button,.w3-dropdown-click.w3-mobile,.w3-dropdown-click.w3-mobile .w3-btn,.w3-dropdown-click.w3-mobile .w3-button{width:100%}}
 
.w3-button:hover{color:#000!important;background-color:#ccc!important}
 
.w3-button:hover{color:#000!important;background-color:#ccc!important}
 
  
  
Line 139: Line 139:
 
<div class="w3-black">
 
<div class="w3-black">
 
   <button id="openNav" class="w3-button w3-black w3-xlarge" onclick="w3_open()">&#9776;</button>
 
   <button id="openNav" class="w3-button w3-black w3-xlarge" onclick="w3_open()">&#9776;</button>
 
+
</div>
  
  

Revision as of 02:52, 15 October 2018


Electroporations


Results from One Test Tube Electroporations

At the core of the Broad Host Range Kit is the One Test Tube Method of testing plasmids in a host bacteria. This is how the majority of people who get our kit for the first time will begin their experiments. The idea here is that a researcher will be able to transform multiple assembled plasmids at once ,and then through selective plating see which works in the non-model organisms. This will give the researcher insight for what origin of replication works, which is the first step in building a plasmid to genetically engineering an organism. Results will be confirmed by one of two ways: assessing the phenotype produced by the reporter gene or sequencing at the barcode region . The reporter is either a fluorescent protein or chromoprotein specific and each color designates an origin. At a genomic level, a unique, non-coding sequence of DNA does the same thing, specifying which origin it is paired with. We created our one tube mixture of the initial assemblies by calculating an equimolar concentration.

Pictures