Template:Team:KULeuven/18 August 2009/VanillinProduction

From 2009.igem.org

(Difference between revisions)
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* Re-plated the ligation products (SAMS and EF)
* Re-plated the ligation products (SAMS and EF)
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* We propose 3 tests to check if the restriction digest (esp. between EcoRI and XbaI, because they lie very close to each other) works properly:
+
* We propose 3 tests to check if the restriction digest (esp. between EcoRI and XbaI, because they lie very close together) works properly:
** Cut every plasmid (Sam8, Sam5, Ech, Fcs) separately with EcoRI, XbaI and -only Sam8 and Fcs- with SpeI.
** Cut every plasmid (Sam8, Sam5, Ech, Fcs) separately with EcoRI, XbaI and -only Sam8 and Fcs- with SpeI.
** Cut subsequently with EcoRI and XbaI, leaving an incubation period of 1h between two digests. Total: 30µl
** Cut subsequently with EcoRI and XbaI, leaving an incubation period of 1h between two digests. Total: 30µl
** Use pUC18 vector
** Use pUC18 vector
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* Made fluid cultures of Sam8, Sam5, Ech, Fcs
* Made fluid cultures of Sam8, Sam5, Ech, Fcs

Revision as of 13:14, 19 August 2009

  • Cells didn't grow. Yet again...
  • Re-plated the ligation products (SAMS and EF)
  • We propose 3 tests to check if the restriction digest (esp. between EcoRI and XbaI, because they lie very close together) works properly:
    • Cut every plasmid (Sam8, Sam5, Ech, Fcs) separately with EcoRI, XbaI and -only Sam8 and Fcs- with SpeI.
    • Cut subsequently with EcoRI and XbaI, leaving an incubation period of 1h between two digests. Total: 30µl
    • Use pUC18 vector
  • Made fluid cultures of Sam8, Sam5, Ech, Fcs