Team:Newcastle/Labwork/31 July 2009
From 2009.igem.org
Lab Session 31/07/2009
Previously
cinR ([http://partsregistry.org/Part:BBa_C0077 BBa_C0077]) and cinI ([http://partsregistry.org/Part:BBa_C0076 BBa_C0076]) coding sequences did not grow in LB + Kan media but they grew in plain LB media. We had overnight cultures prepared for CinR sensitive promoter([http://partsregistry.org/Part:BBa_R0077 BBa_R0077]), cI coding sequence([http://partsregistry.org/Part:BBa_B1002 BBa_B1002]) and the double terminator([http://partsregistry.org/Part:BBa_B1002 BBa_B1002]).
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