Boston University/Plasmid Customization
From 2007.igem.org
(Difference between revisions)
(→Overview) |
(→Overview) |
||
| Line 18: | Line 18: | ||
The native sacB gene was excised from the plasmid pJQ200 with the restriction enzymes EcoRI and HindIII. In the presence of 10% sucrose, the sacB gene acts as a suicide gene. After ligating a gene into this multiple cloning site, the plasmid pJQ200 should no longer be sucrose sensitive and should retain the gentamicin antibiotic resistance gene. Positive transformants will survive in the presence of gentamicin and sucrose. | The native sacB gene was excised from the plasmid pJQ200 with the restriction enzymes EcoRI and HindIII. In the presence of 10% sucrose, the sacB gene acts as a suicide gene. After ligating a gene into this multiple cloning site, the plasmid pJQ200 should no longer be sucrose sensitive and should retain the gentamicin antibiotic resistance gene. Positive transformants will survive in the presence of gentamicin and sucrose. | ||
| + | |||
| + | |||
Revision as of 15:02, 30 July 2007
Contents |
Overview
Excising the sacB gene from plasmid pJQ200
|
|
|
The native sacB gene was excised from the plasmid pJQ200 with the restriction enzymes EcoRI and HindIII. In the presence of 10% sucrose, the sacB gene acts as a suicide gene. After ligating a gene into this multiple cloning site, the plasmid pJQ200 should no longer be sucrose sensitive and should retain the gentamicin antibiotic resistance gene. Positive transformants will survive in the presence of gentamicin and sucrose.
Verifying the presence of the lacZ promoter in the plasmid pJQ200
|
|
|
|
|
PCR amplification of the global transcription factors SO1415, SO4157, hlyU
|
|
