Part:BBa_K2943902:Experience
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UNIQ27d0db8a1ef1f2b6-partinfo-00000000-QINU UNIQ27d0db8a1ef1f2b6-partinfo-00000001-QINU
BBa_K2943902 TAU_Israel |
Part Characterization: Using PCR reaction, we amplified part of the plasmid, excluding part of the mRFP and RBS. This enabled us to insert the gblocks into the plasmid which included already the appropriate backbone and overlaps for the assembly. The gblock was inserted using Gibson Assembly. Before the assembly, we have done DPN1 to ensure no unwanted DNA template was present and used PCR clean kit to prepare the amplified backbone. Then we proceeded to the Gibson reaction and transformed the resulting plasmid into E. coli DH10beta. |