Types | DnaRegion
|
Roles | Regulatory
promoter
|
Sequences | BBa_J119381_sequence (Version 1)
|
Description
This part was designed and clone by students in the Missouri Western State University Genetics class of Spring 2015. It was cloned into the pClone Red vector (BBa_J119137) using Golden Gate Assembly and synthetic oligonucleotides. The mutation deletes TATAAT at position -12 to -7. The mutation had a large effect on the function of the promoter (see Experience page).
Notes
None
Source
Synthetic oligonucleotides