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Team:Tsinghua/Result1
From 2009.igem.org
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We have successfully cloned the Nu1-A, W-B, C and D-E-FI-FII gene segments from the bacteriophage lambda genome. | We have successfully cloned the Nu1-A, W-B, C and D-E-FI-FII gene segments from the bacteriophage lambda genome. | ||
| - | [[Image:j22.png| | + | [[Image:j22.png|400px|center|j22]] |
| - | [[Image:j23.png| | + | [[Image:j23.png|400px|center|j23]] |
| + | Positive clones of the two linkage groups of the GenSniper genome have been achieved. After PCR of the purified recombinant plasmids, we can get the desired bands on the gels. Nonspecific bands are due to the low annealing temperature. | ||
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[[Image:j24.png|300px|center|j24]] | [[Image:j24.png|300px|center|j24]] | ||
[[Image:j26.png|600px|center|j26]] | [[Image:j26.png|600px|center|j26]] | ||
Revision as of 04:53, 12 October 2009
Contents |
Synthesis of the Genome of GenSniper
Bottom-Up Approach
Showed above are the maps of the GenSniper using bottom-up approach. The genes of Nu1, A, W, B and lysis genes (S, R, Rz) are incorporated into pET-28a, while C, D, E, FI and FII are synthesized into pACYCDuet-1. In other word, the GenSniper will have two linkage groups.
We have successfully cloned the Nu1-A, W-B, C and D-E-FI-FII gene segments from the bacteriophage lambda genome.
Positive clones of the two linkage groups of the GenSniper genome have been achieved. After PCR of the purified recombinant plasmids, we can get the desired bands on the gels. Nonspecific bands are due to the low annealing temperature.
Top-Down Approach
GenSniper Production Evaluation
