Difference between revisions of "Part:BBa K525740:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | *This is the complete sequence of NAD<sup>+</sup> -dependent DNA ligase. | |
− | + | *It is designed in [https://parts.igem.org/Assembly_standard_25 RFC 25] -standard | |
− | + | **NgoMIV restriction site downstream the start codon to easily fuse an N-terminal domain to the coding sequence | |
===Source=== | ===Source=== | ||
− | Escherichia coli | + | *PCR on the '' Escherichia coli'' TOP 10 DNA cloned into BioBrick Vectors |
+ | *Primers with BioBrick Freiburg prefix in the fwd primer. Suffix and His-tag in the rev primer. | ||
+ | **fwd: 5'-acgtgaattcgcggccgcttctagatggccggcgaatcaatcgaacaacaactgac-3' | ||
+ | **rev: 5'-acgtctgcagcggccgctactagtaatgatgatgatgatgatggctacccagcaaacgc-3' | ||
===References=== | ===References=== |
Latest revision as of 21:59, 21 September 2011
DNA ligase from Escherichia coli (LigA) with His-tag
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1422
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 4
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 1636
Design Notes
- This is the complete sequence of NAD+ -dependent DNA ligase.
- It is designed in RFC 25 -standard
- NgoMIV restriction site downstream the start codon to easily fuse an N-terminal domain to the coding sequence
Source
- PCR on the Escherichia coli TOP 10 DNA cloned into BioBrick Vectors
- Primers with BioBrick Freiburg prefix in the fwd primer. Suffix and His-tag in the rev primer.
- fwd: 5'-acgtgaattcgcggccgcttctagatggccggcgaatcaatcgaacaacaactgac-3'
- rev: 5'-acgtctgcagcggccgctactagtaatgatgatgatgatgatggctacccagcaaacgc-3'