Imperial College/19 September 2008

From 2008.igem.org

(Difference between revisions)
m (Wet Lab)
 
Line 26: Line 26:
[[Image:Velocity_Distribution_90_Cells.jpg|thumb|center|300px|Run velocity distribution for 90 cells]]
[[Image:Velocity_Distribution_90_Cells.jpg|thumb|center|300px|Run velocity distribution for 90 cells]]
 +
<br>
 +
{{Imperial/EndPage|Notebook|Notebook}}

Latest revision as of 20:48, 28 October 2008

August
MTWTFSS
        1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30 31
September
MTWTFSS
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30
October
MTWTFSS
    1 2 3 4 5
6 7 8 9 10 11 12
13 14 15 16 17 18 19
20 21 22 23 24 25 26
27 28 29 30 31

19 September 2008

Wet Lab

  • A variety of ligations were carried out last week and to test there success we carried out single colony PCR using Psb primers to verify if an insert is present in the vector AK3. For each ligation thress seperate colonies were picked to carry out SCP and a negative colony where no DNA was present. The gel below shows the resuls of this experiment:
SCP-19.png
  • The conditions used were as follows:
    • 1 cycle - 95oC for 30 seconds
    • 30 cycles - 95oC for 30 seconds, 60oC for 30 seconds,72oC for 30 seconds
    • 1 cycle - 72oC for 2 minutes
  • The numbers of the ligations correspond to the following ligation reactions:
    • 5-Eps+AK3
    • 8-PgsiB-gsiB+AK3
    • 9-PgsiB-spoVG+AK3
    • 12-Pveg-spoVG

Dry Lab

  • Tracked a total ot 90 cells. Run velocity profile is shown below:
Run velocity distribution for 90 cells