IGEM:IMPERIAL/2007/Notebook/2007-8-30: Difference between revisions

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[[Image:ICGEMS_T7GEL2.bmp|250px]]
[[Image:ICGEMS_T7GEL2.bmp|250px]]


Protocols can be found at Protocols can be found at [[IGEM:IMPERIAL/2007/Notebook/General_Protocols#Electrophoresis|Electrophoresis]] in the general protocols page
Protocols can be found at [[IGEM:IMPERIAL/2007/Notebook/General_Protocols#Electrophoresis|Electrophoresis]] in the general protocols page




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#Gel extract purified insert re-digest
#Gel extract purified insert re-digest


Protocols can be found at Protocols can be found at [[IGEM:IMPERIAL/2007/Notebook/General_Protocols#DNA Extraction/Purification|DNA Extaction/Purification]] in the general protocols page
Protocols can be found at [[IGEM:IMPERIAL/2007/Notebook/General_Protocols#DNA Extraction/Purification|DNA Extaction/Purification]] in the general protocols page




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[[Image:ICGEMS_T7GEL3.bmp|250px]]
[[Image:ICGEMS_T7GEL3.bmp|250px]]


Protocols can be found at Protocols can be found at [[IGEM:IMPERIAL/2007/Notebook/General_Protocols#Electrophoresis|Electrophoresis]] in the general protocols page
Protocols can be found at [[IGEM:IMPERIAL/2007/Notebook/General_Protocols#Electrophoresis|Electrophoresis]] in the general protocols page





Revision as of 16:00, 30 August 2007

<calendar> name=iGEM:IMPERIAL/2007/Notebook date=2007/09/24 view=threemonths format=%name/%year-%month-%day weekstart=7 </calendar>

Construction of pT7-GFP

  1. Insert re-digest was run on 1% agarose gel
    • 1. 30 μl insert re-digest
    • 2. 5 μl uncut insert
    • 3. 2 μl 1 kb DNA ladder

Protocols can be found at Electrophoresis in the general protocols page


  1. PCR purified vector digest
  2. Gel extract purified insert re-digest

Protocols can be found at DNA Extaction/Purification in the general protocols page


  1. Purified vector and insert were run on 1% agarose gel
    • 1. 6 μl purified insert
    • 2. 3 μl purified vector
    • 3. 2 μl 1 kb DNA ladder

Protocols can be found at Electrophoresis in the general protocols page


  1. Ligated vector and insert at 14°C overnight
    • 7 μl purified insert
    • 1 μl purified vector
    • 1 μl T4 ligase
    • 1 μl T4 ligation buffer
  2. A negative control with ddH20 instead of insert was also set up

Cell by date - Operating Temperature Range

Construct - pTet-GFP BBa_I13522
Temperatures - 37 °C and 20°C Aims: To test for the behaviour of the DNA construct (pTet) at temperatures 20oC and 37oC by observing the amount of fluorescence produced over a period of 24 hours.

  • For each temperature two experiments carried out at staggered time points to minimize the time points not measured over night.
  • Sampling was initially every 10 minutes however, this was reaccessed and changed to 20 and 30 minute time intervals.
  • Measurements will carry on over tomorrow day to give ~30hours of measurements.

Protocol can be found here under Phase 2-Operating Temperature Range on the experimental design page.

Results can here under Results on the experimental design page.

Degradation of GFP

  • Tested GFP degradation at 37 °C and 20°C
  • The tests were carried out on the same plate as the Operating Temperature Ranges and so the sampling was the same as that for the individual temperatures
  • Measurements will carry on over tomorrow day to give ~30hours of measurements