BIOTEC Dresden/Notepad/20 October 2010

From 2010.igem.org

(Difference between revisions)
Line 20: Line 20:
'''Fusion Protein'''
'''Fusion Protein'''
-
Miniprep of the overnight cultures was done for the colonies.
+
Miniprep of the overnight cultures was done for the colonies of the fusion protein.
Ligation of the MBP in the backbone followed by its transformation chemically
Ligation of the MBP in the backbone followed by its transformation chemically
Line 26: Line 26:
Restriction digest was done to the pETMM43 vector followed by its gel purification.
Restriction digest was done to the pETMM43 vector followed by its gel purification.
 +
'''AHL Sensor'''
 +
 +
Kinetics of part 17+51 was measured in both Ampicillin and Chloramphenicol.
{{Biotec_Dresden/month}}
{{Biotec_Dresden/month}}
{{Biotec_Dresden/Bottom}}
{{Biotec_Dresden/Bottom}}

Revision as of 16:49, 27 October 2010

Parts Assembly

The digested parts were ligated into the plasmid backbone containing chloramphenicol.

52b, 52c, 53a, 53c, 54a, 54b, 54c, 55a, 55b, 55c

The ligation mix was heat inactivated at 65 degrees for 15 min. The mix was then transformed by chemical transformation method and plated for overnight growth of colonies.

Fusion Protein

Miniprep of the overnight cultures was done for the colonies of the fusion protein.

Ligation of the MBP in the backbone followed by its transformation chemically

Restriction digest was done to the pETMM43 vector followed by its gel purification.

AHL Sensor

Kinetics of part 17+51 was measured in both Ampicillin and Chloramphenicol.


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