Difference between revisions of "Part:BBa K215002"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K215002 short</partinfo> | <partinfo>BBa_K215002 short</partinfo> | ||
− | + | For example, assume our gene (E0040) starts with: | |
+ | 5'-atgcgtaaaggagaagaacttt...-3' | ||
+ | |||
+ | The design process would be: | ||
+ | # Start with the XbaI site: 5'-TCTAGA-3' | ||
+ | # Add ~20bp of the gene immediately after the XbaI site, starting _after_ the start codon (atg), and try to end on a G or C: 5'-TCTAGAcgtaaaggagaagaacttt-3' for E0040 from above. These ~20bp will determine the melting temperature for the primer. | ||
+ | # Add 6-8 random nucleotides at the start. Try to balance out the primer to ~%50 g&c to a&t: 5'-cgggcTCTAGAcgtaaaggagaagaacttt-3' | ||
+ | # Tweak the number of nucleotides until the melting point roughly matches that of Vr. | ||
+ | |||
+ | Then to add the gene to the construct, again assuming the gene is a biobrick with standard suffix: | ||
+ | # PCR with the designed forward primer and Vr | ||
+ | # Then run the PCR product in a digest with XbaI and PstI, and digest this part (the display construct) with NheI and PstI. The XbaI site has a sticky end that binds with NheI. | ||
+ | # Standard ligation and transformation. | ||
+ | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 05:17, 1 October 2009
pLac+RBS+Secretion Signal and Streptavidin Binding Tags
For example, assume our gene (E0040) starts with: 5'-atgcgtaaaggagaagaacttt...-3'
The design process would be:
- Start with the XbaI site: 5'-TCTAGA-3'
- Add ~20bp of the gene immediately after the XbaI site, starting _after_ the start codon (atg), and try to end on a G or C: 5'-TCTAGAcgtaaaggagaagaacttt-3' for E0040 from above. These ~20bp will determine the melting temperature for the primer.
- Add 6-8 random nucleotides at the start. Try to balance out the primer to ~%50 g&c to a&t: 5'-cgggcTCTAGAcgtaaaggagaagaacttt-3'
- Tweak the number of nucleotides until the melting point roughly matches that of Vr.
Then to add the gene to the construct, again assuming the gene is a biobrick with standard suffix:
- PCR with the designed forward primer and Vr
- Then run the PCR product in a digest with XbaI and PstI, and digest this part (the display construct) with NheI and PstI. The XbaI site has a sticky end that binds with NheI.
- Standard ligation and transformation.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 196
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]