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Identification and extraction of parts

We have already successfully extracted and cultured 4 parts (All from Plate 1)

A further 16 parts were identified as being necessary for use in our project. (From Plate 1 unless stated)


Preformed electroporation on competent cells with the following plasmids and set in 37C incubator overnight to grow. All except 17K were incubated on ampicillin plates since they all had ampicillin resistance gene.