Difference between revisions of "Part:BBa K2012009"
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− | <p>Figure 1.<i>E.coli</i> with BBa_K2012009 was observed under light field.Figure 2.<i>E.coli</i> with BBa_K2012009 was observed under | + | <p>Figure 1.<i>E.coli</i> with BBa_K2012009 was observed under light field.Figure 2.<i>E.coli</i> with BBa_K2012009 was observed under fluorescence field;</p> |
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 16:01, 15 October 2016
RBS(J61100) and CheZ with fused with a GS linker and GFP in C teminal
Biobrick 5' XbaI J23100 XbaI K2012009 Biobrick 3'
gaattcgcggccgcttctagaGTTGACGGCTAGCTCAGTCCTAGGTACAGTGCTAGCTtctaga...................................actagtagcggccgctgcag
This feature in no way prevents the use of these parts in standard Biobrick assembly. Normal prefix insertion into EcoRI/XbaI will delete this promoter element. Suffix insertion into SpeI/PstI will retain this promoter, but it can of course be removed later by a prefix insertion.
Note also that the base 5' to the SpeI site is allowed to float in these parts and is therefore rarely "T". The "G" downstream of the XbaI site obeys the standard. Because the database does not permit variation at this position, the predicted sequences of composite parts derived from these parts will be incorrect at this position.(some content are cited from J61100 part(BBa_J61100))
Figure 1.E.coli with BBa_K2012009 was observed under light field.Figure 2.E.coli with BBa_K2012009 was observed under fluorescence field;
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.rc site found at 1321