BIOTEC Dresden/Notepad/20 October 2010

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Revision as of 12:20, 23 October 2010 by Sarah Mansour (Talk | contribs)

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.

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.




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