Team:Paris/August 29

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(Difference between revisions)
(Cloning of EnvZ*)
(Transformation of E. coli DH5 alpha competent cells)
 
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{|border="1" style="text-align: center"
{|border="1" style="text-align: center"
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|DNA concentration
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|'''DNA concentration'''
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|A260 / A2801
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|'''A260 / A2801'''
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|D159 (EnvZ*)
|D159 (EnvZ*)
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|rowspan="2"|control
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|rowspan="2"|'''control'''
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|colspan="2"|insert / vector ratio
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|colspan="2"|'''insert / vector ratio'''
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|3 / 1
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|'''3 / 1'''
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|4 / 1
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|'''4 / 1'''
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|D159 (EnvZ*)
|D159 (EnvZ*)
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|3,4 µL
|3,4 µL
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 +
*10 min at room temperature
 +
*followed by 7 hours at about 16°C.
 +
 +
==Transformation of E. coli DH5 alpha competent cells==
 +
* Defroze of the cells on ice
 +
* Add 5 µL of DNA in 100 µL of competent cells (ligation products or pUC19 for positive control)
 +
* 30 min on ice
 +
* Heat schock 45sec at 42°C
 +
* 2 min on ice
 +
* Add 900 µL of SOC
 +
* Incubate 1h at 37°C
 +
* Centrifugate 5 min at 6000 rpm
 +
* Remove 800 µL
 +
* Plate the 200 µL left on LB + amplicilline
 +
* Incubate O/N at 37°C

Latest revision as of 18:55, 16 September 2008

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Contents

Cloning of EnvZ*

Concentration measurement

DNA concentration A260 / A2801
D159 (EnvZ*) 9 µg/mL 1,59
D116 (pSB1A2) 13 µg/mL 1,29

Ligation

control insert / vector ratio
3 / 1 4 / 1
D159 (EnvZ*) 0 8,7 µL 11,6 µL
D116 (pSB1A2) 2 µL 2 µL 2 µL
T4 DNA ligase 10X buffer 2 µL 2 µL 2 µL
T4 DNA ligase 1 µL 1 µL 1 µL
H2O (qsp 20 µL) 15 µL 6,3 µL 3,4 µL
  • 10 min at room temperature
  • followed by 7 hours at about 16°C.

Transformation of E. coli DH5 alpha competent cells

  • Defroze of the cells on ice
  • Add 5 µL of DNA in 100 µL of competent cells (ligation products or pUC19 for positive control)
  • 30 min on ice
  • Heat schock 45sec at 42°C
  • 2 min on ice
  • Add 900 µL of SOC
  • Incubate 1h at 37°C
  • Centrifugate 5 min at 6000 rpm
  • Remove 800 µL
  • Plate the 200 µL left on LB + amplicilline
  • Incubate O/N at 37°C