Difference between revisions of "Part:BBa K733003:Design"
(→Design Notes) |
(→Source) |
||
Line 10: | Line 10: | ||
===Source=== | ===Source=== | ||
− | + | We obtain this part from the genomic DNA of Bacillus subtilis 168 via PCR amplification. | |
+ | |||
+ | Forward primer: 5’-aaaggaggtgtatgttttttgtctg-3’ (Prefix not shown) | ||
+ | |||
+ | Reverse primer: 5’-TGATTATCCTCCGCTGACTA-3’ (Suffix not shown) | ||
===References=== | ===References=== |
Revision as of 17:04, 22 September 2012
RBS+ydcD: antitoxin gene
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
To easily building an antitoxin expression device, forward primer containing consensus RBS sequence in B. subtilis is designed, aiming at adding RBS directly to the upstream of ydcD gene through PCR.
Source
We obtain this part from the genomic DNA of Bacillus subtilis 168 via PCR amplification.
Forward primer: 5’-aaaggaggtgtatgttttttgtctg-3’ (Prefix not shown)
Reverse primer: 5’-TGATTATCCTCCGCTGACTA-3’ (Suffix not shown)