BIOTEC Dresden/Notepad/19 October 2010

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(New page: {{Biotec_Dresden/Header}} <html> <head> <style type="text/css"> #bodyContent p, #bodyContent pre, #bodyContent table { margin:10px 30px; } </style> </head> </html> '''Parts Assembly''' ...)
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The digested parts were purified by gel purification and nanodropped.
The digested parts were purified by gel purification and nanodropped.
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'''Fusion Protein'''
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50 colonies were picked from the ligation plates of the fusion protein for colony PCR. Colonies were picked for the overnight cultures.

Revision as of 12:21, 23 October 2010

Parts Assembly

All the parts need to be ligated into the plasmid backbone containing chloramphenicol as per iGeM requirement. The following parts were restriction digested with EcoRI and PstI for 1 hour 15 min at 37 degrees.

52b, 52c, 53a, 53b, 53c, 54a, 54b, 54c, 55a, 55b, 55c, backbone, 6e-4a

The digested parts were purified by gel purification and nanodropped.

Fusion Protein

50 colonies were picked from the ligation plates of the fusion protein for colony PCR. Colonies were picked for the overnight cultures.




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