Difference between revisions of "Team:Baltimore Bio-Crew/Team"

Line 2: Line 2:
 
{{Team:Baltimore Bio-Crew/JS}}
 
{{Team:Baltimore Bio-Crew/JS}}
 
{{Team:Baltimore Bio-Crew/templateReset}}
 
{{Team:Baltimore Bio-Crew/templateReset}}
−
 
−
 
 
<html>
 
<html>
 
<head>
 
<head>
 
<meta charset="utf8" />
 
<meta charset="utf8" />
 
<meta name="viewport" content="width=device-width, initial-scale=1">
 
<meta name="viewport" content="width=device-width, initial-scale=1">
−
<title>Team:Baltimore Bio-crew</title>
+
<title>Team Baltimore Bio-crew</title>
−
 
+
−
+
  
 +
<link rel="stylesheet" type="text/css" href="main.css" />
 
<style>
 
<style>
−
 
+
   
−
 
+
−
 
+
−
/*Slideshow*/
+
−
 
+
−
* {box-sizing:border-box}
+
−
 
+
−
/* Slideshow container */
+
 
.slideshow-container {
 
.slideshow-container {
 
   max-width: 100%;
 
   max-width: 100%;
Line 43: Line 33:
  
  
−
 
−
/*  text */
 
 
.text {
 
.text {
 
   color: #f2f2f2;
 
   color: #f2f2f2;
 +
  font-size: 15px;
 
   padding: 8px 12px;
 
   padding: 8px 12px;
 
   position: absolute;
 
   position: absolute;
−
   bottom: 80%;
+
   bottom: 50%;
 
   width: 100%;
 
   width: 100%;
 
   text-align: center;
 
   text-align: center;
Line 55: Line 44:
  
  
−
/* Fading animation */
+
 
 
.fade {
 
.fade {
 
   -webkit-animation-name: fade;
 
   -webkit-animation-name: fade;
Line 74: Line 63:
  
  
−
</style>
+
   
 +
   
 +
.profile {
 +
    box-shadow: 0 4px 8px 0 rgba(45, 132, 34, 1);
 +
    transition: 0.3s;
 +
    width: 40%;
 +
    border-radius: 5px;
 +
margin-top: 50px;
 +
    margin-bottom: 50px;
 +
    margin-right: 50%;
 +
    margin-left: 30%;
 +
}
 +
 
 +
.profile:hover {
 +
    box-shadow: 0 8px 16px 0 rgba(71, 232, 247, 1);
 +
}
 +
 
 +
.BioCrew img {
 +
    border-radius: 5px 5px 0 0;
 +
}
 +
 
 +
.profile-container {
 +
    padding: 2px 16px;
 +
 
 +
}
 +
   
 +
    .Ttopnav{
 +
background-color: #FF1493;
 +
 
 +
}
 +
.Ttopnav li {
 +
    display: inline;
 +
    float: right;
 +
    text-align: center;
 +
}
 +
.Ttopnav ul {
 +
    list-style-type: none;
 +
    margin: 0;
 +
    padding: 0;
 +
    overflow: hidden;
 +
height: 70px;
 +
}
 +
.Ttopnav li a {
 +
    display: block;
 +
    padding: 8px 20px;
 +
 
 +
    color: #000;
 +
    text-decoration: none;
 +
}
 +
 
 +
.Ttopnav li a:hover {
 +
    background-color: #54d3f9;
 +
}
 +
   
 +
</style>
 +
 
 
</head>
 
</head>
 
<body>
 
<body>
−
<section id="intro" class="pureGold">
 
  
  
 +
<section>
 +
    <header id="TeamHeader">
 +
 +
<div class="Ttopnav">
 +
<ul>
 +
 +
<li> <a href="#Advisors">Advisors</a></li>
 +
<li> <a href="#Students">Students</a></li>
 +
<li><a href="#Acknowledgement">Acknowledgement</a></li>
 +
</ul>
 +
</div>
 +
</header>
 
<div class="slideshow-container ">
 
<div class="slideshow-container ">
 
  <div class="mySlides fade">
 
  <div class="mySlides fade">
−
     <img src="https://static.igem.org/mediawiki/2017/8/83/Baltimore_biocrew1.jpeg">
+
     <img src="https://2017.igem.org/File:BioCrewTeam.jpeg">
−
     <div class="text"><h1 style="font-size: 100px; overflow: visible;"> Welcome </h1></div>
+
     <div class="text"><h1 style="font-size: 100px;"> Meet the Team</h1></div>
 
   </div>
 
   </div>
  
 
   <div class="mySlides fade">
 
   <div class="mySlides fade">
−
     <img src="https://static.igem.org/mediawiki/2017/archive/9/9c/20170930173029%21E2.jpeg" >
+
     <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" >
  
 
   </div>
 
   </div>
  
 
   <div class="mySlides fade">
 
   <div class="mySlides fade">
−
     <img src="https://static.igem.org/mediawiki/2017/0/01/E1.jpeg" >
+
     <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" >
  
 
   </div>
 
   </div>
  
−
 
+
 
 
</div>
 
</div>
 
</section>
 
</section>
  
 +
<section id="Advisors" class="BioCrew">
 +
    <h2 style= "font-size: 40px; text-align:center;">
 +
        Advisors
 +
    </h2>
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>hi</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
   
 +
          <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
   
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
   
 +
   
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
 +
    </section>
 +
       
 +
  <section id="Students" class="BioCrew">
 +
        <h2 style= "font-size: 40px; text-align:center;">
 +
        Students
 +
    </h2>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
        <div class="profile">
 +
  <img src="https://2017.igem.org/File:BioCrewTeam.jpeg" alt="picture" style="width:100%">
 +
  <div class="profile-container">
 +
    <h4  style="font-size: 30px; text-align:center;"><b>thou art nameless</b></h4>
 +
    <p> We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.</p>
 +
  </div>
 +
</div>
 +
     
 +
  </section>
 +
       
 +
        <section id="Acknowledgement" class="BioCrew">
 +
           
 +
          <h2 style= "font-size: 40px; text-align:center;">
 +
        Sponsers
 +
    </h2>
 +
           
 +
        </section>
 
</body>
 
</body>
 
<script>
 
<script>
Line 118: Line 306:
  
 
</script>
 
</script>
−
+
 
  
 
</html>
 
</html>

Revision as of 02:54, 18 October 2017


BUGSS Logo
Home Team Project Results Design Notebook Composite Part Safety HP Silver Experiment Attribution Collaborations Interlab Contributions
Team Baltimore Bio-crew

Meet the Team

Advisors

picture

hi

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

Students

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

picture

thou art nameless

We are evaluating our parts by verifying that they can be used to degrade PET plastic. We are setting up an experiment in which we will test for the the ability of E.coli bacteria engineered with each part to degrade PET plastic. Glass culture tubes were set up containing LB media and small squares of PET plastic that had been weighed beforehand. The approximate dimensions of the plastic squares were 20x15x0.5mm, and they weighed between 101 and 89 mg. After the bacteria with the gene have been added, the plastic will be weighed twice a week to check for lost material. Some tubes will be incubated at 30 degrees Celsius because that is the best growth temperature for the Ideonealla bacteria, and some will be incubated at 37 degrees Celsius because that is the best temperature for E. coli.

Sponsers