Plasmid_Backbone

Part:BBa_K516999:Experience

Designed by: Nicolo' Politi, Susanna Zucca, Tommaso Goggia, Paolo Magni   Group: iGEM11_UNIPV-Pavia   (2011-09-15)

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Applications of BBa_K516999

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UNIPV-Pavia iGEM 2011

This vector was designed and realized in order to facilitate the cloning of coding sequences downstream of the strong promoter pTet. This vector was assembled by ligating S-P excided mRFP coding sequence from BBa_J61002 and ligating it in BBa_R0040 cut with S and P. Thus, the resulting vector contains mRFP between S and P. pTet can be easily excided (E-P) and moved in the desired vector (E-P) and then the desired coding sequence can be easily assembled by digesting S-P the vector and X-P the coding sequence, thus obtaining a final part that is standard10-compatible.

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