Difference between revisions of "Part:BBa K176003:Design"
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===Source=== | ===Source=== | ||
| − | PCR from the plasmid pluxCcdB3(a gift from Prof. Lingchong You). | + | PCR from the plasmid pluxCcdB3<cite>You</cite (a gift from Prof. Lingchong You>). |
| + | |||
Forward Primer: GTTTCT TCTAG ATG accatgattacgg attcactggccgtcgttttac | Forward Primer: GTTTCT TCTAG ATG accatgattacgg attcactggccgtcgttttac | ||
| + | |||
Reverse Primer: GTTTCTTC CTGCAG CGGCCGC T ACTAGT A TTATTA tattccccagaacatcaggtta | Reverse Primer: GTTTCTTC CTGCAG CGGCCGC T ACTAGT A TTATTA tattccccagaacatcaggtta | ||
| + | |||
Digest with XbaI and SpeI, ligate into pSB1A3. | Digest with XbaI and SpeI, ligate into pSB1A3. | ||
===References=== | ===References=== | ||
<biblio> | <biblio> | ||
| − | # | + | #You pmid=15064770 |
</biblio> | </biblio> | ||
Revision as of 16:32, 3 July 2009
lacZalpha-ccdB coding sequence
Assembly Compatibility:
- 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 387
Design Notes
The part is similar to BBa_J32026 and the original coding sequence in pluxCcdB3, but the multiple cloning sites are eliminated in order to avoid site-specific mutagenesis. The multiple cloning sites are from lacZalpha in pZErO-2.
After eliminate the MCS, the lacZalpha part is identical to the N-terminal of the wild type gene(BBa_I732006 & BBa_I732005), and fused with the ccdB part (BBa_K145151) with a 3aa linker.
Source
PCR from the plasmid pluxCcdB3You).
Forward Primer: GTTTCT TCTAG ATG accatgattacgg attcactggccgtcgttttac
Reverse Primer: GTTTCTTC CTGCAG CGGCCGC T ACTAGT A TTATTA tattccccagaacatcaggtta
Digest with XbaI and SpeI, ligate into pSB1A3.
References
<biblio>
- You pmid=15064770
</biblio>