Difference between revisions of "Part:BBa K200009:Design"
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===Source=== | ===Source=== | ||
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+ | Streptococcus pneumoniae Hungary19A-6. | ||
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+ | The DNA sequence was then synthesised and includes a RBS preceding the coding region for DpnII. | ||
===References=== | ===References=== | ||
http://www.ncbi.nlm.nih.gov/nuccore/NC_010380.1?report=fasta&from=1825422&to=1826288 | http://www.ncbi.nlm.nih.gov/nuccore/NC_010380.1?report=fasta&from=1825422&to=1826288 |
Latest revision as of 08:12, 12 October 2009
DpnII Composite
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
NOTE: Unlike other restriction enzymes that show Star Activity at high pH 8.0, DpnII has Star Activity above approximately pH 6.5. The effect of pH on Star Activity of DpnII is very extreme, showing one-thousand-fold more Star Activity at pH 7.5 than at pH 6.0.
Source
Streptococcus pneumoniae Hungary19A-6.
The DNA sequence was then synthesised and includes a RBS preceding the coding region for DpnII.
References
http://www.ncbi.nlm.nih.gov/nuccore/NC_010380.1?report=fasta&from=1825422&to=1826288