Types | DnaRegion
|
Roles | Reporter
engineered_region
|
Sequences | BBa_J31011_sequence (Version 1)
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Description
BBa_J31010 was created by PCR amplification of the RBS-RFP portion of BBa_I13507.
Notes
The primers were designed to add PstI-NotI-SpeI to the left and XbaI-NotI-EcoRI to the right (reversal of standard BioBrick cloning sites) so that this part could be cloned in the reverse orientation. Placement of a promoter (reverse) to the right of this part should convey RFP expression.
Source
BBa_I13507