Things That we Have Done

From 2006.igem.org

(Difference between revisions)
Jump to: navigation, search
(Cloning)
(Cloning)
Line 16: Line 16:
-
<font color="red">'''KanB'''
+
<font color="red">'''KanB'''</font color>
*Kan backwards is the only gene that we are completely positive has not been cloned into a plasmid. Further testing is needed to see if it has indeed been cloned.
*Kan backwards is the only gene that we are completely positive has not been cloned into a plasmid. Further testing is needed to see if it has indeed been cloned.

Revision as of 18:50, 12 July 2006

Cloning

We have been able to successfully clone the following antibiotic pancakes

  • Hin
  • Hin with LVA degredation tag
  • Cmr- forward
  • Kan-forward
  • Tet-forward
  • Tet-backwards
  • Cmr-backwards
    • The sample contains the insert but it is very faint as can be seen hereSNR CB8 and Kan.jpg


  • The lane farthest from the ladder contains the Cmr Backwards.
  • Cmr is 659 bp long
  • The Cmr was cut with EcoRI and PstI to ensure that it had full BioBrick ends.


KanB

  • Kan backwards is the only gene that we are completely positive has not been cloned into a plasmid. Further testing is needed to see if it has indeed been cloned.

RE and Hix

We have been able to clone RE into cells. The RE that we are using has two point mutations but they should not compromise the activity of the Fis-binding sites please see the page for part Part BBa_J3101 [http://partsregistry.org/Part:BBa_J3101] for further details.

  • As per the [http://2006.igem.org/Davidson_Assembly_Plan| assembly plan] we will be attaching the RE downstream of the double terminator BBa_B0015 [http://partsregistry.org/Part:BBa_B0015]
  • We also have two cultures with the correct sequences for Hix C.
  • We have sent a "Master Plate" with cultures of all of the things that we have cloned to the Mammoths.
Personal tools
Past/present/future years