Team:Caltech/week6

From 2014.igem.org

(Difference between revisions)
m
Line 109: Line 109:
</td>
</td>
<td valign="top">
<td valign="top">
-
<ul>
+
<b>Export Systems</b>
 +
3 of our 5 constructs were not properly cloned, so we are going to redo them:
 +
<ul><li>PCRed out backbones for pTG002, pTG003, and pTG006 with overhangs</li>
 +
    <li>PCR product was then DpnI digested and PCR-purified. A gel was run with processed and unprocessed product to verify backbone creation</li>
 +
    <li>Gibson assembly of pTG002, pTG003, and pTG006 (pTG006 had 2 reactions: 1 with the backbone created last week, since it had been verified to work for cloning pTG005, and another with backbone created today)</li>
 +
    <li>Assemblies were transformed into JM109, plated on carbenicillin plates, and incubated overnight</li>
</ul>
</ul>
</td>
</td>

Revision as of 06:10, 22 July 2014


Home Team Official Team Profile Project Parts Modeling Notebook Safety Attributions
Notebook
Overview

Week 1

Week 2

Week 3

Week 4

Week 5

Week 6

Week 7

Week 8

Week 9

Week 10

Week 11

Week 12

Week Six

Monday, 7/21/14

Export Systems 3 of our 5 constructs were not properly cloned, so we are going to redo them:
  • PCRed out backbones for pTG002, pTG003, and pTG006 with overhangs
  • PCR product was then DpnI digested and PCR-purified. A gel was run with processed and unprocessed product to verify backbone creation
  • Gibson assembly of pTG002, pTG003, and pTG006 (pTG006 had 2 reactions: 1 with the backbone created last week, since it had been verified to work for cloning pTG005, and another with backbone created today)
  • Assemblies were transformed into JM109, plated on carbenicillin plates, and incubated overnight

Tuesday, 7/22/14

Wednesday, 7/23/14


Thursday, 7/24/14

Friday, 7/25/14