Team:Copenhagen/Notebook
From 2012.igem.org
(Difference between revisions)
|
|
| Line 56: |
Line 56: |
| | <br> | | <br> |
| | <a name="Week 2b"></a><h2>Week 2: 9th-13th</h2> | | <a name="Week 2b"></a><h2>Week 2: 9th-13th</h2> |
| | + | <table id="graa" class=" " align="right"> |
| | + | <tr><td><img src=" " width="180px"><p>Info</p></td></tr> |
| | + | </table> |
| | | | |
| | We're still having trouble with both pSB1C3 and ProC. We're currently running a self-annealing programme for ProC because it is to small to do PCR. pSB1C3, on the other hand, seems too big so therefore we've lowered the annealing temperature and chosen a longer extension time. So far it has had no effect but we will keep optimizing. | | We're still having trouble with both pSB1C3 and ProC. We're currently running a self-annealing programme for ProC because it is to small to do PCR. pSB1C3, on the other hand, seems too big so therefore we've lowered the annealing temperature and chosen a longer extension time. So far it has had no effect but we will keep optimizing. |
Revision as of 14:05, 11 July 2012
Notebook
Follow our work here in the notebook.
We will post the most important of our findings from the lab-work. We will also post pictures from our great summer!!! The light at the department of Plant Biology will probably shine brighter than the Danish summer sun anyway ;)
June
Week 1: 4th-8th
Exam period starts :(
Week 2: 11th-15th
Exams for a lot of our team members but we start designing our primers.
Week 3: 18th-22nd
Primers are designed and ordered so we'll have them next week.
Week 4: 25th-29th
Exams are finally over and we can start some of the lab work! Yay!!! :D
We've divided our construct into two halfs and will in this week be doing PCR on the first half of our construct. We've designed primers for the second half of our construct and ordered them.
All our templates, kindly provided by Uppsala, are sent to sequencing in Holland.
July
Week 1: 2nd-6th
The sequencing results have come back, and everything was as we hoped.
It took more time than expected to get the new primers so the first days has been spend applying for sponsors, remaking our website, and deciding how to do the next experiments.
PCR on the backbone (pSB1C3), and our constitutive promoter has been unsuccessful while we have been able to amplify and cut out a fine band of YF1.
Week 2: 9th-13th
 Info |
We're still having trouble with both pSB1C3 and ProC. We're currently running a self-annealing programme for ProC because it is to small to do PCR. pSB1C3, on the other hand, seems too big so therefore we've lowered the annealing temperature and chosen a longer extension time. So far it has had no effect but we will keep optimizing.
Week 3: dato
JahDah JahDah ... Text ...
Week 4: dato
JahDah JahDah ... Text ...
August
Week 1: dato
JahDah JahDah ... Text ...
Week 2: dato
JahDah JahDah ... Text ...
Week 3: dato
JahDah JahDah ... Text ...
Week 4: dato
JahDah JahDah ... Text ...
September
Week 1: dato
JahDah JahDah ... Text ...
Week 2: dato
JahDah JahDah ... Text ...
Week 3: dato
JahDah JahDah ... Text ...
Week 4: dato
JahDah JahDah ... Text ...
October
Week 1: dato
JahDah JahDah ... Text ...
Week 2: dato
JahDah JahDah ... Text ...
Week 3: dato
JahDah JahDah ... Text ...
Week 4: dato
JahDah JahDah ... Text ...
This is our notebook, displaying how our work has progressed throughout the summer.
|
|
"
