Source:
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: David Caballero, Fernando Govantes
Date created: 2011-10-18 11:00:00
Date modified: 2015-05-08 01:12:30
pUC18Sfi-miniTn7BB-Gm-pBad/araC
| Types | DnaRegion |
| Roles | engineered_region Composite |
| Sequences | BBa_K510038_sequence (Version 1) |
Description
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The BBa_I0500 BioBrick was inserted within the BCS of pUC18Sfi-miniTn7BB-Gm by EcoRI and PstI clonning.In order to construct the pUC18Sfi-miniTn7BB-Gm delivery plasmid, the miniTn7BB-Gm transposon was cleaved from the commercial plasmid pMA (Mr. Gene) with SfiI and ligated to SfiI-digested pUC18Sfi. This strategy removes all multi-cloning restriction sites from pUC18Sfi, except for the flanking SfiI, thus guaranteeing that the unique sites in the transposon are not duplicated. The remove of the multi-cloning restriction sites was verify by analytic digestions.
Source
The miniTn7BB-Gm minitransposon was synthesized commercially and pUC18SfiI is a commercial vector.| Access | Instance | Definition |
| public public | BBa_K510000 BBa_I0500 | BBa_K510000 pBad/araC |
| Sequence Annotation | Location | Component / Role(s) |
| BBa_K510000 BBa_I0500 | 1,4388 4397,5606 | BBa_K510000 pBad/araC |