Types | DnaRegion
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Roles | Measurement
engineered_region
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Sequences | BBa_J119401_sequence (Version 1)
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Description
The BD2 C Dog RBS has a lower binding efficiency than BD18. PCR Amplification was used to amplify the J100255 plasmid, excluding BD18, and BD2 was inserted via Decoupled Golden Gate Assembly.
Notes
BD2 was inserted to the plasmid via Decoupled Golden Gate Assembly. Using iPCR, all of the J100255 plasmid was amplified, besides BD18.
Source
J100255, original tClone tet+PDB Riboswitch, is located in Campbell M Lab. BD2, located in Eckdahl Lab, is part number J119025.