Team:Paris/August 29

From 2008.igem.org

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(→Ligation)
(→Transformation of E. coli DH5 alpha competent cells)
 
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==Transformation of E. coli DH5 alpha competent cells==
==Transformation of E. coli DH5 alpha competent cells==
-
*defrosing of the cells on ice
+
* Defroze of the cells on ice
-
*adding of 5 µL of ligation products in 100 µL of competent cells in 14 mL falcon polypropylene tubes
+
* Add 5 µL of DNA in 100 µL of competent cells (ligation products or pUC19 for positive control)
-
*30 min on ice
+
* 30 min on ice
-
*thermal schock of 45 s at 42°C
+
* Heat schock 45sec at 42°C
-
*2 min on ice
+
* 2 min on ice
-
*adding of 900 µL of SOC
+
* Add 900 µL of SOC
-
*1 hour at 37°C
+
* Incubate 1h at 37°C
-
*contrifugation 5 min 6000 rpm
+
* Centrifugate 5 min at 6000 rpm
-
*removal of 800 µL
+
* Remove 800 µL
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*plating the 200 µL left on LB + amplicilline
+
* Plate the 200 µL left on LB + amplicilline
-
*overnight incubation at 37°C
+
* 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
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