Difference between revisions of "Part:BBa K245046"
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+ | {{Curation/ccdb}} | ||
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+ | All of RFC 37 vectors (BB-NIC-II-HisN - BBa_K245005, BB-NIC-II-NC - BBa_K245006, BB-NIC-II-HisC - BBa_K245007 and BB-NIC-III-HisN - BBa_K245008) have a ccdB gene inserted in their multiple cloning site. CcdB serves as positive selection marker since it is lethal to almost all BioBrick cell strains (E.coli DB3.1 strain is an exeption). While inserting BioBrick parts in plasmid, there exist a possibility of contamination of ligation mixture with uncut vector. If vector in which one plans to insert BioBrick part contains ccdB domain in multiple cloning site as the ones listed above, cells that were transformed with unmodified vector express ccdB protein which results in cell death. For this reason any vector containing ccdB could only be propagated in resistant cell strains like DB3.1. This part comprises only active ccdB part without inactive ccdA. | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 17:26, 9 July 2015
ccdB
All of RFC 37 vectors (BB-NIC-II-HisN - BBa_K245005, BB-NIC-II-NC - BBa_K245006, BB-NIC-II-HisC - BBa_K245007 and BB-NIC-III-HisN - BBa_K245008) have a ccdB gene inserted in their multiple cloning site. CcdB serves as positive selection marker since it is lethal to almost all BioBrick cell strains (E.coli DB3.1 strain is an exeption). While inserting BioBrick parts in plasmid, there exist a possibility of contamination of ligation mixture with uncut vector. If vector in which one plans to insert BioBrick part contains ccdB domain in multiple cloning site as the ones listed above, cells that were transformed with unmodified vector express ccdB protein which results in cell death. For this reason any vector containing ccdB could only be propagated in resistant cell strains like DB3.1. This part comprises only active ccdB part without inactive ccdA.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 216