Difference between revisions of "Part:BBa K108001:Design"
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===Design Notes=== | ===Design Notes=== | ||
| − | cloned into pSB1AC3 | + | |
| + | PCR using primers with biobrick prefix and surfix, and then cloned into pSB1AC3. | ||
===Source=== | ===Source=== | ||
| − | Enterobacteria phage lambda | + | S, R and Rz were cloned from Enterobacteria phage lambda genome (reference 1 and 2). |
===References=== | ===References=== | ||
| − | 1. NCBI | + | 1. Construction and Selection of the Novel Recombinant Escherichia coli Strain for Poly(beta-Hydroxybutyrate) Production. Journal of Bioscience and Bioengineering. 2000, 89(4):307-311. |
| + | |||
| + | 2. NCBI | ||
Latest revision as of 07:32, 25 October 2008
SRRz
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
PCR using primers with biobrick prefix and surfix, and then cloned into pSB1AC3.
Source
S, R and Rz were cloned from Enterobacteria phage lambda genome (reference 1 and 2).
References
1. Construction and Selection of the Novel Recombinant Escherichia coli Strain for Poly(beta-Hydroxybutyrate) Production. Journal of Bioscience and Bioengineering. 2000, 89(4):307-311.
2. NCBI