Difference between revisions of "Part:BBa K1041000"
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| − | [[Image:WP 000051.jpg|thumb|(Left) BBa_K1041000 and (right) BBa_J04450 visualized under non-UV lightbox]] | + | [[Image:WP 000051.jpg|thumb|Fig 1:(Left) BBa_K1041000 and (right) BBa_J04450 visualized under non-UV lightbox]] |
| − | Both parts BBa_K1041000 and BBa_J04450 have colonies that appear red under natural light. The addition of a NdeI site has not effected the ability for the RFP gene to be transcribed. | + | Both parts BBa_K1041000 and BBa_J04450 have colonies that appear red under natural light ''fig.1''. The addition of a NdeI site has not effected the ability for the RFP gene to be transcribed. |
Revision as of 11:15, 24 August 2013
RFP Coding Device
Mutagenesis was used to add a Nde1 site at the start of the RFP coding region of the biobrick BBa_J04450. This enables a restriction digest with Nde1 to be performed allowing the RFP coding region to be excised from the plasmid.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 781
Illegal AgeI site found at 893 - 1000COMPATIBLE WITH RFC[1000]
Pictures
Both parts BBa_K1041000 and BBa_J04450 have colonies that appear red under natural light fig.1. The addition of a NdeI site has not effected the ability for the RFP gene to be transcribed.