From 2014.igem.org
(Difference between revisions)
|
|
Line 113: |
Line 113: |
| </td> | | </td> |
| </tr> | | </tr> |
| + | |
| + | <tr><td bgColor="#777777" colspan="2" height="1px"></td></tr> |
| | | |
| <tr> | | <tr> |
Line 124: |
Line 126: |
| </td> | | </td> |
| </tr> | | </tr> |
| + | |
| + | <tr><td bgColor="#777777" colspan="2" height="1px"></td></tr> |
| | | |
| <tr> | | <tr> |
Line 138: |
Line 142: |
| </td> | | </td> |
| </tr> | | </tr> |
| + | |
| + | <tr><td bgColor="#777777" colspan="2" height="1px"></td></tr> |
| | | |
| <tr> | | <tr> |
Revision as of 19:06, 3 July 2014
|
|
|
|
|
|
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 One |
Tuesday, 6/17/14
|
- Get acquainted with summer logistics and lab basics
- Clean up lab space, stock lab supplies
|
|
Wednesday, 6/18/14
|
- Continue to discuss project and clean up lab space
- Designed PCR primers for combinatorial promoters subproject
|
|
Thursday, 6/19/14
|
- Formulated plasmid design (pAA001) for the response regulation subproject
- PCR run on plasmid backbone and sfGFP to create constructs with the proper overhangs for Gibson assembly
- Gel electrophoresis for confirmation of PCR products' length
- With the exception of the lacI gene, PCR products were confirmed via gel electrophoresis
|
|
Friday, 6/20/14
|
- Purification of PCR products created yesterday
- Gibson assembly of purified products
- Transformation of Gibson-assembled plasmids into JM109 E. coli
- Meeting with Prof. Murray to discuss give an update on the project
- Colonies were found and picked after transformation and incubation.
|
|
|