Difference between revisions of "Team:Pittsburgh/Notebook"

m (table of contents styling)
Line 38: Line 38:
 
<ul>
 
<ul>
 
<li>Test efficiency of competent cells</li>
 
<li>Test efficiency of competent cells</li>
<li>Test cell free extract reaction with T7-GFP plasmid</li>
 
 
</ul>
 
</ul>
 +
<h3>Cell Free Extract</h3>
 +
    <ul><li>Test cell free extract reaction with T7-GFP plasmid</li></ul>
 
<h2>Dry Lab</h2>
 
<h2>Dry Lab</h2>
 
<ul>
 
<ul>
Line 50: Line 51:
 
<h1 class="nav"><a name="Week3" class="nav">Week 3: June 6 - June 12</a></h1>
 
<h1 class="nav"><a name="Week3" class="nav">Week 3: June 6 - June 12</a></h1>
 
<h2>Wet Lab</h2>
 
<h2>Wet Lab</h2>
 +
<h3>Reporter</h3>
 
<ul>
 
<ul>
 
<li>Transform T7 promoter, amilCP, and terminator</li>
 
<li>Transform T7 promoter, amilCP, and terminator</li>
Line 63: Line 65:
 
<h1 class="nav"><a name="Week4" class="nav">Week 4: June 13 - June 17</a></h1>
 
<h1 class="nav"><a name="Week4" class="nav">Week 4: June 13 - June 17</a></h1>
 
<h2>Wet Lab</h2>
 
<h2>Wet Lab</h2>
 +
<h3>Reporter</h3>
 
<ul>
 
<ul>
 
<li>Transform T7-GFP plasmid, lacZ alpha fragment, and eGFP</li>
 
<li>Transform T7-GFP plasmid, lacZ alpha fragment, and eGFP</li>

Revision as of 18:58, 26 June 2016

Our weekly progress

Week 1: May 23 - May 27

Wet Lab

  • Training begins
  • Grow Top 10 competent cells.

Dry Lab

  • Brainstorm genetic circuits for a thallium sensor
  • Lab safety training
Week 1 Notebook Back to Top

Week 2: May 31 - June 3

Wet Lab

  • Test efficiency of competent cells

Cell Free Extract

  • Test cell free extract reaction with T7-GFP plasmid

Dry Lab

  • Contact museums and summer programs for outreach opportunities
  • Lab safety training
Week 2 Notebook Back to Top

Week 3: June 6 - June 12

Wet Lab

Reporter

  • Transform T7 promoter, amilCP, and terminator
  • Begin assembly by ligating linearized T7 promoter and amilCP

Dry Lab

  • Contact museums and summer programs for outreach opportunities
Week 3 Notebook Back to Top

Week 4: June 13 - June 17

Wet Lab

Reporter

  • Transform T7-GFP plasmid, lacZ alpha fragment, and eGFP
  • Send promising T7 promoter -- amilCP ligations to be sequenced
  • Perform double digest of T7 promoter and terminator from last week
  • Ligate double-digested T7 promoter to new reporters (lacZ and eGFP)

Dry Lab

  • TECBio, DiSCoBio, and Tissue Engineering Camp outreach opportunities set
Week 4 Notebook Back to Top